6-Mercaptopurine
Based on 18 publication(s) in Google Scholar
6-Mercaptopurine is a purine analogue which acts as an antagonist of the endogenous purines and has been widely used as antileukemic agent and immunosuppressive drug.
Para uso exclusivo en investigación. No vendemos a pacientes.
- Pureza: 99.93%
- No. CAS: 50-44-2
- Fòrmula: C5H4N4S
- Peso molecular:152.18
-
Almacenamiento:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Publications Citing Use of MedChemExpress (MCE) 6-Mercaptopurine
More- Nat Commun. 2022 Nov 17;13(1):7031. [Abstract]
- Adv Sci (Weinh). 2025 Dec 5:e20444. [Abstract]
- Adv Sci (Weinh). 2024 Dec 4:e2408373. [Abstract]
- Cell Rep Med. 2025 Apr 2:102053. [Abstract]
- Cell Death Dis. 2024 Mar 14;15(3):216. [Abstract]
- Pharmacol Res. 2024 Feb:200:107082. [Abstract]
- ACS Environ Au. 2025 Aug 5;5(6):573-582. [Abstract]
- Int J Biol Macromol. 2024 Sep 15:135698. [Abstract]
- Cell Rep. 2025 Mar 25;44(4):115466. [Abstract]
- Anal Chem. 2025 Jun 3;97(21):11099-11109. [Abstract]
- Life Sci. 2026 Mar 15:389:124236. [Abstract]
- Int J Pharm. 2026 Mar 10:692:126648. [Abstract]
- Commun Biol. 2024 Oct 30;7(1):1416. [Abstract]
- J Mol Med (Berl). 2019 Aug;97(8):1183-1193. [Abstract]
- Cancers (Basel). 2022 Oct 19;14(20):5127. [Abstract]
- PLoS Negl Trop Dis. 2019 Aug 20;13(8):e0007681. [Abstract]
- Front Oncol. 2024 Jul 19:14:1440650. [Abstract]
- Res Sq. 2026 Jun 15.
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WB
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In Vivo Efficacy Study
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In Vivo Efficacy Study
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Cell Proliferation/Viability Assay
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WB
Ver todos los productos específicos de isoformas Endogenous Metabolite
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Actividad biológica
endogenous purines[1]
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
47 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human A549 cells at lag phase of growth after 48 hrs by MTT assay
Cytotoxicity against human A549 cells at lag phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| A549 | IC50 |
49.3 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human A549 cells at exponential phase of growth after 48 hrs by MTT assay
Cytotoxicity against human A549 cells at exponential phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| A549 | IC50 |
47 μM
Compound: C2
|
Cytotoxicity against human A549 cells assessed as cell viability after 48 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as cell viability after 48 hrs by MTT assay
|
[PMID: 22705001] |
| A549 | IC50 |
47 μM
Compound: C2
|
Cytotoxicity against human A549 cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| A549 | IC50 |
49.4 μM
Compound: C2
|
Cytotoxicity against human A549 cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| ASPC1 | IC50 |
2.45 μM
Compound: 6-MP
|
Cytotoxicity against human Aspc-1 cells by crystal violet staining
Cytotoxicity against human Aspc-1 cells by crystal violet staining
|
[PMID: 20930123] |
| B16 | IC50 |
0.8 μg/mL
Compound: 6-MP
|
Cytotoxicity against mouse B16 cells after 72 hrs by MTT assay
Cytotoxicity against mouse B16 cells after 72 hrs by MTT assay
|
[PMID: 7807120] |
| C6 | IC50 |
30.2 μg/mL
Compound: 6-MP
|
Cytotoxicity against rat C6 cells assessed as cell viability after 96 hrs by MTT assay
Cytotoxicity against rat C6 cells assessed as cell viability after 96 hrs by MTT assay
|
[PMID: 11087619] |
| CCRF-CEM | IC50 |
1 μM
Compound: 6MP
|
Antiproliferative activity against human CCRF-CEM cells by MTT assay
Antiproliferative activity against human CCRF-CEM cells by MTT assay
|
[PMID: 17254669] |
| CCRF-CEM | CC50 |
1 μM
Compound: 6MP
|
Antiproliferative activity against human CCRF-CEM cells after 96 hrs by MTT assay
Antiproliferative activity against human CCRF-CEM cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
| CCRF-SB | IC50 |
1 μM
Compound: 6MP
|
Antiproliferative activity against human CCRF-SB cells by MTT assay
Antiproliferative activity against human CCRF-SB cells by MTT assay
|
[PMID: 17254669] |
| CCRF-SB | CC50 |
1.1 μM
Compound: 6MP
|
Antiproliferative activity against human CCRF-SB cells after 96 hrs by MTT assay
Antiproliferative activity against human CCRF-SB cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
| CHO | ED50 |
50 μM
Compound: 6MP
|
Cytotoxicity against CHO cells
Cytotoxicity against CHO cells
|
[PMID: 23411915] |
| COLO357 | IC50 |
6.12 μM
Compound: 6-MP
|
Cytotoxicity against human Colo-357 cells by crystal violet staining
Cytotoxicity against human Colo-357 cells by crystal violet staining
|
[PMID: 20930123] |
| CRL-7065 cell line | IC50 |
>100 μM
Compound: 6MP
|
Antiproliferative activity against human CRL7065 cells by MTT assay
Antiproliferative activity against human CRL7065 cells by MTT assay
|
[PMID: 17254669] |
| DAN-G | IC50 |
4.06 μM
Compound: 6-MP
|
Cytotoxicity against human DAN-G cells by crystal violet staining
Cytotoxicity against human DAN-G cells by crystal violet staining
|
[PMID: 20930123] |
| Daudi | IC50 |
>200 μM
Compound: 6-MP
|
Antiproliferative activity against human Daudi cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
Antiproliferative activity against human Daudi cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
|
[PMID: 18467007] |
| DU-145 | IC50 |
2 μM
Compound: 6MP
|
Antiproliferative activity against human DU145 cells by MTT assay
Antiproliferative activity against human DU145 cells by MTT assay
|
[PMID: 17254669] |
| DU-145 | CC50 |
2 μM
Compound: 6MP
|
Antiproliferative activity against human DU145 cells after 96 hrs by MTT assay
Antiproliferative activity against human DU145 cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
| HEK293 | IC50 |
0.007 μM
Compound: 6-MP
|
Antiproliferative activity against HEK293 cells assessed as reduction of cell growth after 72 hrs by MTT method
Antiproliferative activity against HEK293 cells assessed as reduction of cell growth after 72 hrs by MTT method
|
[PMID: 10757708] |
| HEK293 | IC50 |
0.007 μM
Compound: 6-MP
|
Antiproliferative activity against HEK293 cells after 3 days by MTT conversion assay
Antiproliferative activity against HEK293 cells after 3 days by MTT conversion assay
|
[PMID: 16643040] |
| HEK293 | IC50 |
0.007 μM
Compound: 6-MP
|
Antiproliferative activity against HEK293 cells after 72 hrs by MTT conversion assay
Antiproliferative activity against HEK293 cells after 72 hrs by MTT conversion assay
|
[PMID: 16989528] |
| HEK293 | IC50 |
0.007 μM
Compound: 6-MP
|
Antiproliferative activity against human HEK293 cells after 72 hrs by MTT conversion assay
Antiproliferative activity against human HEK293 cells after 72 hrs by MTT conversion assay
|
[PMID: 18442289] |
| HEK293 | IC50 |
7.1 x 10-7 mg/mL
Compound: 6-mercaptopurine
|
Cytotoxicity against HEK293 cells by rapid colorimetric assay
Cytotoxicity against HEK293 cells by rapid colorimetric assay
|
[PMID: 19133758] |
| HeLa | IC50 |
>200 μM
Compound: 6-MP
|
Antiproliferative activity against human HeLa cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
Antiproliferative activity against human HeLa cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
|
[PMID: 18467007] |
| HeLa | IC50 |
2.9 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human HeLa cells at lag phase of growth after 48 hrs by MTT assay
Cytotoxicity against human HeLa cells at lag phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| HeLa | IC50 |
4.1 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human HeLa cells at exponential phase of growth after 48 hrs by MTT assay
Cytotoxicity against human HeLa cells at exponential phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| HeLa | IC50 |
2.9 μM
Compound: C2
|
Cytotoxicity against human HeLa cells assessed as cell viability after 48 hrs by MTT assay
Cytotoxicity against human HeLa cells assessed as cell viability after 48 hrs by MTT assay
|
[PMID: 22705001] |
| HeLa | IC50 |
2.9 μM
Compound: C2
|
Cytotoxicity against human HeLa cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against human HeLa cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| HeLa | IC50 |
4.1 μM
Compound: C2
|
Cytotoxicity against human HeLa cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against human HeLa cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| HeLa | ED50 |
0.1 μg/mL
Compound: 6-mercaptopurine
|
Cytostatic activity against human HeLa cells after 72 hrs by FCR-based colorimetric method
Cytostatic activity against human HeLa cells after 72 hrs by FCR-based colorimetric method
|
[PMID: 448680] |
| HeLa | ED50 |
0.1 μg/mL
Compound: 6-mercaptopurine
|
In vitro cytostatic activity against human HeLa cells assessed as cell growth after 72 hrs by colorimetric method
In vitro cytostatic activity against human HeLa cells assessed as cell growth after 72 hrs by colorimetric method
|
[PMID: 458800] |
| HeLa | ED50 |
0.1 μg/mL
Compound: 6-Mercaptopurine
|
Cytostatic activity against human HeLa cells assessed as growth inhibition after 72 hrs by colorimetric method
Cytostatic activity against human HeLa cells assessed as growth inhibition after 72 hrs by colorimetric method
|
[PMID: 671455] |
| HEp-2 | IC50 |
317.8 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human Hep2 cells at exponential phase of growth after 48 hrs by MTT assay
Cytotoxicity against human Hep2 cells at exponential phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| HEp-2 | IC50 |
431 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human Hep2 cells at lag phase of growth after 48 hrs by MTT assay
Cytotoxicity against human Hep2 cells at lag phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| HepG2 | IC50 |
8 μM
Compound: 6MP
|
Antiproliferative activity against human HepG2 cells by MTT assay
Antiproliferative activity against human HepG2 cells by MTT assay
|
[PMID: 17254669] |
| HepG2 | CC50 |
8 μM
Compound: 6MP
|
Antiproliferative activity against human HepG2 cells after 96 hrs by MTT assay
Antiproliferative activity against human HepG2 cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
| HT-29 | IC50 |
>200 μM
Compound: 6-MP
|
Antiproliferative activity against multidrug-resistant human HT-29 cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
Antiproliferative activity against multidrug-resistant human HT-29 cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
|
[PMID: 18467007] |
| HT-29 | IC50 |
0.87 μg/mL
Compound: 6-MP
|
Cytotoxicity against human HT-29 cells after 72 hrs by MTT assay
Cytotoxicity against human HT-29 cells after 72 hrs by MTT assay
|
[PMID: 7807120] |
| IGR-1 | IC50 |
1.1 μg/mL
Compound: 6-MP
|
Antiproliferative activity against human IGR-1 cells after 72 hrs by MTT assay
Antiproliferative activity against human IGR-1 cells after 72 hrs by MTT assay
|
[PMID: 9358643] |
| IGR-1 | IC50 |
12.3 μg/mL
Compound: 6-MP
|
Antiproliferative activity against human IGR-1 cells after 48 hrs by MTT assay
Antiproliferative activity against human IGR-1 cells after 48 hrs by MTT assay
|
[PMID: 9358643] |
| IGR-1 | IC50 |
51.7 μg/mL
Compound: 6-MP
|
Cytotoxicity against human IGR-1 cells after 24 hrs by MTT assay
Cytotoxicity against human IGR-1 cells after 24 hrs by MTT assay
|
[PMID: 9358643] |
| J774 | IC50 |
0.003 μM
Compound: 6-MP
|
Antiproliferative activity against mouse J774 cells assessed as reduction of cell growth after 72 hrs by MTT method
Antiproliferative activity against mouse J774 cells assessed as reduction of cell growth after 72 hrs by MTT method
|
[PMID: 10757708] |
| J774 | IC50 |
0.5 μg/mL
Compound: 6-MP
|
Antiproliferative activity against mouse J774 cells after 72 hrs by MTT assay
Antiproliferative activity against mouse J774 cells after 72 hrs by MTT assay
|
[PMID: 9358643] |
| J774 | IC50 |
3.6 μg/mL
Compound: 6-MP
|
Antiproliferative activity against mouse J774 cells after 48 hrs by MTT assay
Antiproliferative activity against mouse J774 cells after 48 hrs by MTT assay
|
[PMID: 9358643] |
| J774 | IC50 |
61 μg/mL
Compound: 6-MP
|
Cytotoxicity against mouse J774 cells after 24 hrs by MTT assay
Cytotoxicity against mouse J774 cells after 24 hrs by MTT assay
|
[PMID: 9358643] |
| J774.A1 | IC50 |
0.003 μM
Compound: 6-MP
|
Antiproliferative activity against mouse J774.A1 cells after 3 days by MTT conversion assay
Antiproliferative activity against mouse J774.A1 cells after 3 days by MTT conversion assay
|
[PMID: 16643040] |
| J774.A1 | IC50 |
0.003 μM
Compound: 6-MP
|
Antiproliferative activity against mouse J774A1 cells after 72 hrs by MTT conversion assay
Antiproliferative activity against mouse J774A1 cells after 72 hrs by MTT conversion assay
|
[PMID: 16989528] |
| J774.A1 | IC50 |
0.003 μM
Compound: 6-MP
|
Antiproliferative activity against mouse J774.A1 cells after 72 hrs by MTT conversion assay
Antiproliferative activity against mouse J774.A1 cells after 72 hrs by MTT conversion assay
|
[PMID: 18442289] |
| J774.A1 | IC50 |
5.1 ng/mL
Compound: 6-mercaptopurine
|
Cytotoxicity against mouse J774A1 cells by rapid colorimetric assay
Cytotoxicity against mouse J774A1 cells by rapid colorimetric assay
|
[PMID: 19133758] |
| J774.A1 | IC50 |
5.1 x 10-6 mg/mL
Compound: 6-mercaptopurine
|
Cytotoxicity against mouse J774A1 cells by rapid colorimetric assay
Cytotoxicity against mouse J774A1 cells by rapid colorimetric assay
|
[PMID: 19133758] |
| Jurkat | IC50 |
>200 μM
Compound: 6-MP
|
Antiproliferative activity against human Jurkat cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
Antiproliferative activity against human Jurkat cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
|
[PMID: 18467007] |
| K562 | IC50 |
0.4 μg/mL
Compound: 6-mercaptopurine
|
Cytotoxicity against chronic myelogenous leukemia cell line K-562 was determined by measuring [3H]thymidine incorporation after 48 h
Cytotoxicity against chronic myelogenous leukemia cell line K-562 was determined by measuring [3H]thymidine incorporation after 48 h
|
[PMID: 11844673] |
| K562 | IC50 |
8.5 μg/mL
Compound: 6-mercaptopurine
|
Cytotoxicity against chronic myelogenous leukemia cell line K-562 was determined by measuring [3H]thymidine incorporation after 5 h
Cytotoxicity against chronic myelogenous leukemia cell line K-562 was determined by measuring [3H]thymidine incorporation after 5 h
|
[PMID: 11844673] |
| K562 | IC50 |
>10 μg/mL
Compound: 6-MP
|
Inhibitory concentration required against human chronic myelogenous leukemic K-562 cell line after 5h, using [3H]thymidine incorporation assay
Inhibitory concentration required against human chronic myelogenous leukemic K-562 cell line after 5h, using [3H]thymidine incorporation assay
|
[PMID: 12617912] |
| K562 | IC50 |
0.6 μg/mL
Compound: 6-MP
|
Inhibitory concentration required against human chronic myelogenous leukemic K-562 cell line after 48h, using [3H]thymidine incorporation assay
Inhibitory concentration required against human chronic myelogenous leukemic K-562 cell line after 48h, using [3H]thymidine incorporation assay
|
[PMID: 12617912] |
| KB | ED50 |
0.1 μg/mL
Compound: 6-Mercaptopurine
|
Cytostatic activity against human KB cells assessed as growth inhibition after 72 hrs by colorimetric method
Cytostatic activity against human KB cells assessed as growth inhibition after 72 hrs by colorimetric method
|
[PMID: 671455] |
| KB | IC50 |
0.55 μg/mL
Compound: 6-MP
|
Cytotoxicity against human KB cells after 72 hrs by MTT assay
Cytotoxicity against human KB cells after 72 hrs by MTT assay
|
[PMID: 7807120] |
| KB | ED50 |
0.54 μg/mL
Compound: mercaptopurine
|
Cytotoxicity against human KB cells
Cytotoxicity against human KB cells
|
[PMID: 8277314] |
| L1210 | IC50 |
0.02 μM
Compound: 6-MP
|
Inhibitory concentration on parentral (sensitive) L1210 leukemia cells.
Inhibitory concentration on parentral (sensitive) L1210 leukemia cells.
|
[PMID: 1906107] |
| L1210 | IC50 |
0.024 μM
Compound: 6-MP
|
Inhibitory concentration on multidrug-resistant L1210 leukemia cells.
Inhibitory concentration on multidrug-resistant L1210 leukemia cells.
|
[PMID: 1906107] |
| MCF7 | IC50 |
3 μM
Compound: 6MP
|
Antiproliferative activity against human MCF7 cells by MTT assay
Antiproliferative activity against human MCF7 cells by MTT assay
|
[PMID: 17254669] |
| MCF7 | IC50 |
1.4 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human MCF7 cells at lag phase of growth after 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells at lag phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| MCF7 | IC50 |
5.8 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against human sMCF7 cells at exponential phase of growth after 48 hrs by MTT assay
Cytotoxicity against human sMCF7 cells at exponential phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| MCF7 | CC50 |
3.2 μM
Compound: 6MP
|
Antiproliferative activity against human MCF7 cells after 96 hrs by MTT assay
Antiproliferative activity against human MCF7 cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
| MCF7 | IC50 |
1.4 μM
Compound: C2
|
Cytotoxicity against human MCF7 cells assessed as cell viability after 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as cell viability after 48 hrs by MTT assay
|
[PMID: 22705001] |
| MCF7 | IC50 |
2.79 μM
Compound: 6MP
|
Cytotoxicity against human MCF7 cells
Cytotoxicity against human MCF7 cells
|
[PMID: 23411915] |
| MCF7 | IC50 |
1.4 μM
Compound: C2
|
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| MCF7 | IC50 |
5.8 μM
Compound: C2
|
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| MOLT-4 | IC50 |
50.5 μM
Compound: 6-MP
|
Antiproliferative activity against human MOLT4 cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
Antiproliferative activity against human MOLT4 cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
|
[PMID: 18467007] |
| MT4 | IC50 |
0.1 μM
Compound: 6MP
|
Antiproliferative activity against human MT4 cells by MTT assay
Antiproliferative activity against human MT4 cells by MTT assay
|
[PMID: 17254669] |
| MT4 | CC50 |
0.1 μM
Compound: 6MP
|
Cytotoxicity against human MT4 cells infected with HTLV-1 after 96 hrs by MTT assay
Cytotoxicity against human MT4 cells infected with HTLV-1 after 96 hrs by MTT assay
|
[PMID: 21741130] |
| P388 | IC50 |
0.26 μg/mL
Compound: 6-MP
|
Cytotoxicity against mouse doxorubicin resistant P388 cells after 72 hrs by MTT assay
Cytotoxicity against mouse doxorubicin resistant P388 cells after 72 hrs by MTT assay
|
[PMID: 7807120] |
| P388 | IC50 |
0.7 μg/mL
Compound: 6-MP
|
Cytotoxicity against mouse P388 cells after 72 hrs by MTT assay
Cytotoxicity against mouse P388 cells after 72 hrs by MTT assay
|
[PMID: 7807120] |
| P388 | ED50 |
0.25 μg/mL
Compound: mercaptopurine
|
Cytotoxicity against mouse doxorubicin-resistant P388 cells
Cytotoxicity against mouse doxorubicin-resistant P388 cells
|
[PMID: 8277314] |
| P388 | ED50 |
0.7 μg/mL
Compound: mercaptopurine
|
Cytotoxicity against mouse P388 cells
Cytotoxicity against mouse P388 cells
|
[PMID: 8277314] |
| P388 | IC50 |
0.3 μg/mL
Compound: 6-MP
|
Antiproliferative activity against mouse P388 cells after 72 hrs by MTT assay
Antiproliferative activity against mouse P388 cells after 72 hrs by MTT assay
|
[PMID: 9358643] |
| P388 | IC50 |
2.1 μg/mL
Compound: 6-MP
|
Antiproliferative activity against mouse P388 cells after 48 hrs by MTT assay
Antiproliferative activity against mouse P388 cells after 48 hrs by MTT assay
|
[PMID: 9358643] |
| P388 | IC50 |
37 μg/mL
Compound: 6-MP
|
Cytotoxicity against mouse P388 cells after 24 hrs by MTT assay
Cytotoxicity against mouse P388 cells after 24 hrs by MTT assay
|
[PMID: 9358643] |
| PANC-1 | IC50 |
6.39 μM
Compound: 6-MP
|
Cytotoxicity against human PANC1 cells by crystal violet staining
Cytotoxicity against human PANC1 cells by crystal violet staining
|
[PMID: 20930123] |
| PaTu 8988t | IC50 |
4.09 μM
Compound: 6-MP
|
Cytotoxicity against human Patu-T cells by crystal violet staining
Cytotoxicity against human Patu-T cells by crystal violet staining
|
[PMID: 20930123] |
| PBMC | IC50 |
149.5 nM
Compound: 6-MP
|
Inhibition of T cell mitogen-induced blastogenesis in human PBMC after 4 days
Inhibition of T cell mitogen-induced blastogenesis in human PBMC after 4 days
|
[PMID: 18467007] |
| REH | IC50 |
2.94 μM
Compound: 6TP
|
Cytotoxicity against human REH cells assessed as reduction in cell viability after 48 hrs by Alamar Blue assay
Cytotoxicity against human REH cells assessed as reduction in cell viability after 48 hrs by Alamar Blue assay
|
[PMID: 30774864] |
| S49 | EC50 |
8 μM
Compound: 6-MP
|
Cytotoxicity against wild type mouse S49 cells assessed as growth inhibition after 72 hrs by trypan blue exclusion assay
Cytotoxicity against wild type mouse S49 cells assessed as growth inhibition after 72 hrs by trypan blue exclusion assay
|
[PMID: 221658] |
| S49 | EC50 |
>1000 μM
Compound: 6-MP
|
Cytotoxicity against HGPRTase-deficient mouse S49 cells assessed as growth inhibition after 72 hrs by trypan blue exclusion assay
Cytotoxicity against HGPRTase-deficient mouse S49 cells assessed as growth inhibition after 72 hrs by trypan blue exclusion assay
|
[PMID: 221658] |
| SK-MEL-28 | IC50 |
15 μM
Compound: 6MP
|
Antiproliferative activity against human SK-MEL-28 cells by MTT assay
Antiproliferative activity against human SK-MEL-28 cells by MTT assay
|
[PMID: 17254669] |
| SK-MEL-28 | CC50 |
15 μM
Compound: 6MP
|
Antiproliferative activity against human SK-MEL-28 cells after 96 hrs by MTT assay
Antiproliferative activity against human SK-MEL-28 cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
| SK-MES-1 | IC50 |
58 μM
Compound: 6MP
|
Antiproliferative activity against human SKMES1 cells by MTT assay
Antiproliferative activity against human SKMES1 cells by MTT assay
|
[PMID: 17254669] |
| SK-MES-1 | CC50 |
58 μM
Compound: 6MP
|
Antiproliferative activity against human SKMES1 cells after 96 hrs by MTT assay
Antiproliferative activity against human SKMES1 cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
| U-937 | IC50 |
>200 μM
Compound: 6-MP
|
Antiproliferative activity against human U937 cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
Antiproliferative activity against human U937 cells assessed as [methyl-3H]thymidine incorporation after 16 hrs by XTT assay
|
[PMID: 18467007] |
| Vero | IC50 |
118.6 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against african green monkey Vero cells at exponential phase of growth after 48 hrs by MTT assay
Cytotoxicity against african green monkey Vero cells at exponential phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| Vero | IC50 |
67.5 μM
Compound: 6-mercaptopurine
|
Cytotoxicity against african green monkey Vero cells at lag phase of growth after 48 hrs by MTT assay
Cytotoxicity against african green monkey Vero cells at lag phase of growth after 48 hrs by MTT assay
|
[PMID: 19711987] |
| Vero | IC50 |
67.6 μM
Compound: C2
|
Cytotoxicity against african green monkey Vero cells assessed as cell viability after 48 hrs by MTT assay
Cytotoxicity against african green monkey Vero cells assessed as cell viability after 48 hrs by MTT assay
|
[PMID: 22705001] |
| Vero | IC50 |
>117 μM
Compound: C2
|
Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability using compound addition to cell culture cells in log phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| Vero | IC50 |
67.6 μM
Compound: C2
|
Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability using compound addition to cell culture cells in lag phase of growth and incubated for 48 hrs by MTT assay
|
[PMID: 28923386] |
| WEHI-164 | IC50 |
0.017 μM
Compound: 6-MP
|
Antiproliferative activity against mouse WEHI164 cells assessed as reduction of cell growth after 72 hrs by MTT method
Antiproliferative activity against mouse WEHI164 cells assessed as reduction of cell growth after 72 hrs by MTT method
|
[PMID: 10757708] |
| WEHI-164 | IC50 |
1.3 μg/mL
Compound: 6-MP
|
Cytotoxicity against mouse WEHI164 cells assessed as cell viability after 96 hrs by MTT assay
Cytotoxicity against mouse WEHI164 cells assessed as cell viability after 96 hrs by MTT assay
|
[PMID: 11087619] |
| WEHI-164 | IC50 |
1.3 μg/mL
Compound: 6-MP
|
Antiproliferative activity against mouse WEHI164 cells assessed as cell viability after 96 hrs by MTT assay
Antiproliferative activity against mouse WEHI164 cells assessed as cell viability after 96 hrs by MTT assay
|
[PMID: 11430005] |
| WEHI-164 | IC50 |
0.015 μM
Compound: 6-MP
|
Antiproliferative activity against mouse WEHI164 cells after 3 days by MTT conversion assay
Antiproliferative activity against mouse WEHI164 cells after 3 days by MTT conversion assay
|
[PMID: 16643040] |
| WEHI-164 | IC50 |
0.015 μM
Compound: 6-MP
|
Antiproliferative activity against mouse WEHI164 cells after 72 hrs by MTT conversion assay
Antiproliferative activity against mouse WEHI164 cells after 72 hrs by MTT conversion assay
|
[PMID: 16989528] |
| WEHI-164 | IC50 |
0.015 μM
Compound: 6-MP
|
Antiproliferative activity against mouse WEHI164 cells after 72 hrs by MTT conversion assay
Antiproliferative activity against mouse WEHI164 cells after 72 hrs by MTT conversion assay
|
[PMID: 18442289] |
| WEHI-164 | IC50 |
2.5 ng/mL
Compound: 6-mercaptopurine
|
Cytotoxicity against mouse WEHI164 cells by rapid colorimetric assay
Cytotoxicity against mouse WEHI164 cells by rapid colorimetric assay
|
[PMID: 19133758] |
| WEHI-164 | IC50 |
2.5 x 10-6 mg/mL
Compound: 6-mercaptopurine
|
Cytotoxicity against mouse WEHI164 cells by rapid colorimetric assay
Cytotoxicity against mouse WEHI164 cells by rapid colorimetric assay
|
[PMID: 19133758] |
| WEHI-164 | IC50 |
2.7 μg/mL
Compound: 6-MP
|
Antiproliferative activity against mouse WEHI164 cells after 72 hrs by MTT assay
Antiproliferative activity against mouse WEHI164 cells after 72 hrs by MTT assay
|
[PMID: 9358643] |
| WEHI-164 | IC50 |
42 μg/mL
Compound: 6-MP
|
Antiproliferative activity against mouse WEHI164 cells after 48 hrs by MTT assay
Antiproliferative activity against mouse WEHI164 cells after 48 hrs by MTT assay
|
[PMID: 9358643] |
| WEHI-164 | IC50 |
83 μg/mL
Compound: 6-MP
|
Cytotoxicity against mouse WEHI164 cells after 24 hrs by MTT assay
Cytotoxicity against mouse WEHI164 cells after 24 hrs by MTT assay
|
[PMID: 9358643] |
| WIL2-NS | IC50 |
3 μM
Compound: 6MP
|
Antiproliferative activity against human WIL-2NS cells by MTT assay
Antiproliferative activity against human WIL-2NS cells by MTT assay
|
[PMID: 17254669] |
| WIL2-NS | CC50 |
3 μM
Compound: 6MP
|
Antiproliferative activity against human WIL2-NS cells after 96 hrs by MTT assay
Antiproliferative activity against human WIL2-NS cells after 96 hrs by MTT assay
|
[PMID: 21741130] |
6-Mercaptopurine hydrate (6-MP) induces NR4A3 transcriptional activity 1.6- to 11-fold (P<0.01) in a dose-responsive manner. It is found that 6-Mercaptopurine hydrate leads to a dose-dependent increase in NR4A3 protein levels. 6-MP treatment increases cell surface GLUT4 in both basal cells 1.8- to 3.6-fold (P<0.01) and insulin-stimulated cells 2.9- to 4.4-fold (P<0.01) over that in controls. It is also found that 6-Mercaptopurine hydrate increases phospho-AS160 significantly in a dose-responsive manner under both basal and insulin-stimulated conditions[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
-
No. CAS 50-44-2
-
Appearance Solid
-
Peso molecular 152.18
-
Fòrmula C5H4N4S
-
Color Light yellow to yellow
-
SMILES
S=C1NC=NC2=C1NC=N2
-
Synonyms
Mercaptopurine; 6-MP
-
Structure Classification
-
Initial Source
-
Envío
Room temperature in continental US; may vary elsewhere.
-
Almacenamiento
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Publications (18)
-
Journal Impact Factor
-
Most Recent
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Nat Commun
Identification of purine biosynthesis as an NADH-sensing pathway to mediate energy stress. [Abstract]2022 Nov 17;13(1):7031. PMID: 36396642
6-Mercaptopurine purchased from MedChemExpress. Usage Cited in: Nat Commun. 2022 Nov 17;13(1):7031. [Abstract]
6-Mercaptopurine (6-MP; 300 µM; pretreatment for 2 h) significantly inhibits EcSTH-induced phosphorylation of AMPK and ACC1 in HeLaTet-on EcSTH and MDA-MB-231Tet-on EcSTH cells.
-
Adv Sci (Weinh)
NADH-Reductive Stress Induced by Dihydrolipoamide Dehydrogenase Activation Contributes to Cuproptosis. [Abstract]2025 Dec 5:e20444. PMID: 41346305
6-Mercaptopurine purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2025 Dec 5:e20444. [Abstract]
Viability of SH‐SY5Y cells treated with 500 µM CuSO4 and 100 µM 6-Mercaptopurine (6-MP) , 400 µM AICAR for 24 h (n = 3, unpaired t‐test).
-
Adv Sci (Weinh)
Targeting Caveolin-1 in Multiple Myeloma Cells Enhances Chemotherapy and Natural Killer Cell-Mediated Immunotherapy. [Abstract]2024 Dec 4:e2408373. PMID: 39630017
6-Mercaptopurine purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2024 Dec 4:e2408373. [Abstract]
MM1S cells were treated with 6-Mercaptopurine (6-MP, 1.25-10 µM) or daidzin at the indicated concentrations for 48 h and the expression of CAV1 was detected using western blot. The results showed that 6-MP significantly inhibited the expression of CAV1 protein.
6-Mercaptopurine purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2024 Dec 4:e2408373. [Abstract]
B‐NDG mice were inoculated with MM1S‐Luc cells and randomly divided into six groups (n = 5–7). After 11 days of inoculation, these mice were intraperitoneally injected with 6-Mercaptopurine (6-MP) (10-20 mg/kg), daidzin (30 mg/kg), or vehicle daily until day 67. After 15 days of inoculation, mice were intraperitoneally injected with bortezomib (0.5 mg/kg) three times a week until day 67. The distribution of MM1S‐Luc cells in these mice was measured at the indicated days after inoculation using a living imaging system.
6-Mercaptopurine purchased from MedChemExpress. Usage Cited in: Adv Sci (Weinh). 2024 Dec 4:e2408373. [Abstract]
B‐NDG mice were inoculated with MM1S‐Luc cells and randomly divided into six groups (n = 5–7). After 11 days of inoculation, these mice were intraperitoneally injected with 6‐MP (10-20 mg/kg), daidzin (30 mg/kg), or vehicle daily until day 67. After 15 days of inoculation, mice were intraperitoneally injected with bortezomib (0.5 mg/kg) three times a week until day 67. Kaplan–Meier curve showing mice survival. The results showed that 6-MP further promoted the bortezomib‐mediated survival of MM‐bearing mice.
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Cell Rep Med
CAN-Scan: A multi-omic phenotype-driven precision oncology platform identifies prognostic biomarkers of therapy response for colorectal cancer. [Abstract]2025 Apr 2:102053. PMID: 40187357 -
Cell Death Dis
Histidine re-sensitizes pediatric acute lymphoblastic leukemia to 6-mercaptopurine through tetrahydrofolate consumption and SIRT5-mediated desuccinylation. [Abstract]2024 Mar 14;15(3):216. PMID: 38485947 -
Pharmacol Res
Identification of Fasudil as a collaborator to promote the anti-tumor effect of lenvatinib in hepatocellular carcinoma by inhibiting GLI2-mediated hedgehog signaling pathway. [Abstract]2024 Feb:200:107082. PMID: 38280440 -
ACS Environ Au
Machine Learning-Assisted Recognition of Environmental Sulfur-Containing Chemicals in Nontargeted Mass Spectrometry Analysis of Inadequate Mass Resolution. [Abstract]2025 Aug 5;5(6):573-582. PMID: 41277996 -
Int J Biol Macromol
circE2F1-encoded peptide inhibits circadian machinery essential for nucleotide biosynthesis and tumor progression via repressing SPIB/E2F1 axis. [Abstract]2024 Sep 15:135698. PMID: 39288851 -
Cell Rep
Structural basis for the reversal of human MRP4-mediated multidrug resistance by lapatinib. [Abstract]2025 Mar 25;44(4):115466. PMID: 40138312 -
Anal Chem
Exposome-Scale Investigation of Cl-/Br-Containing Chemicals Using High-Resolution Mass Spectrometry, Multistage Machine Learning, and Cloud Computing. [Abstract]2025 Jun 3;97(21):11099-11109. PMID: 40401576 -
Life Sci
A protective role of ECSIT in chemotherapy-induced intestinal mucositis by maintaining Lgr5+ intestinal stem cells and gut homeostasis. [Abstract]2026 Mar 15:389:124236. PMID: 41611204 -
Int J Pharm
Physicochemical characterization and clinical evaluation of 3D-printed subdivided tablets of 6-Mercaptopurine with broad dosage variations. [Abstract]2026 Mar 10:692:126648. PMID: 41644072 -
Commun Biol
Ferroptosis-related gene signature for predicting prognosis and identifying potential therapeutic drug in EGFR wild-type lung adenocarcinoma. [Abstract]2024 Oct 30;7(1):1416. PMID: 39478024 -
J Mol Med (Berl)
2019 Aug;97(8):1183-1193. PMID: 31201471 -
Cancers (Basel)
Association between Dysfunction of the Nucleolar Stress Response and Multidrug Resistance in Pediatric Acute Lymphoblastic Leukemia. [Abstract]2022 Oct 19;14(20):5127. PMID: 36291909 -
PLoS Negl Trop Dis
Identification of anti-flaviviral drugs with mosquitocidal and anti-Zika virus activity in Aedes aegypti. [Abstract]2019 Aug 20;13(8):e0007681. PMID: 31430351 -
Front Oncol
Hypoxanthine in the microenvironment can enable thiopurine resistance in acute lymphoblastic leukemia. [Abstract]2024 Jul 19:14:1440650. PMID: 39099696 -
Solvente y solubilidad
DMSO : 35.71 mg/mL (234.66 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (16.43 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (16.43 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
For the following dissolution methods, please prepare the working solution directly:
It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 50% PEG300 50% Saline
Solubility: 3.33 mg/mL (21.88 mM); Suspended solution; Need ultrasonic
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
-
+%Tween-80 + +
-
%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL. * In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Protocolo
L6 myotubes are treated with DMSO control or 6-Mercaptopurine hydrate (6-MP) for 24 h, with the final 3 h of incubation including treatments in serum-free DMEM, and further incubated in the absence or presence of 100 nM insulin for 60 min at 37°C. Then, protein lysates (50 μg) are collected and subjected to SDS-PAGE and immunoblotted with primary antibodies against overnight at 4°C. The proteins are finally quantified by densitometric analysis of scanned films using Image J software[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Cell viability is measured using Cell Viability Assay. L6 skeletal muscle cells are seeded in 96-well plates at a density of 10,000 cells/well and differentiated into myotubes within 7 days. Cells are treated with different doses of 6-Mercaptopurine hydrate (6-MP) for 24 h before the assay. For analysis of cell viability, plates are equilibrated at room temperature for 30 min; 50 μL of Cell Titer-Glo reagent is added to each well, and plates are mixed for 12 min on an orbital shaker. Luminescence is quantified using a luminometer[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Around thirteen-week-old pregnant rats are used in this study. The animals are housed individually in wire-mesh cages in an air-conditioned room (temperature, 23±3°C; humidity, 50±20%; ventilation, 10 times/hour; lighting, 12 h light to12 h dark cycle) and are given pelleted diet and water ad libitum. In the experiment, fifteen pregnant rats are injected i.p. with 50 mg/kg 6-Mercaptopurine hydrate (6-MP) on E13, and three dams each are sacrificed by exsanguination from the abdominal aorta under ether anesthesia at 12, 24, 36, 48, and 72 h. Fetuses are collected from each dam by Caesarean section. As controls, fifteen pregnant rats are injected i.p. with 2.0% methylcellulose solution in distilled water at E13, and three dams are sacrificed at each of the same time-points[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Pureza y Documentación
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Ficha de datos (282 KB)
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SDS (644 KB)
- English - EN (644 KB)
- Français - FR (644 KB)
- Deutsch - DE (644 KB)
- Norwegian - NO (644 KB)
- Español - ES (644 KB)
- Swedish - SV (644 KB)
- Italian - IT (644 KB)
- Korean - KR (644 KB)
- Portuguese - PT (644 KB)
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Instrucciones de manejo (2659 KB)
Referencias
[1]. Sahasranaman S, et al. Clinical pharmacology and pharmacogenetics of thiopurines. Eur J Clin Pharmacol. 2008 Aug;64(8):753-67. [Content Brief]
[2]. Liu Q, et al. 6-Mercaptopurine augments glucose transport activity in skeletal muscle cells in part via a mechanism dependent upon orphan nuclear receptor NR4A3. Am J Physiol Endocrinol Metab. 2013 Nov 1;305(9):E1081-92. [Content Brief]
[3]. Kanemitsu H, et al. 6-Mercaptopurine (6-MP) induces cell cycle arrest and apoptosis of neural progenitor cells in the developing fetal rat brain. Neurotoxicol Teratol. 2009 Mar-Apr;31(2):104-9. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 6.5712 mL | 32.8558 mL | 65.7117 mL | 164.2792 mL |
| 5 mM | 1.3142 mL | 6.5712 mL | 13.1423 mL | 32.8558 mL | |
| 10 mM | 0.6571 mL | 3.2856 mL | 6.5712 mL | 16.4279 mL | |
| 15 mM | 0.4381 mL | 2.1904 mL | 4.3808 mL | 10.9519 mL | |
| 20 mM | 0.3286 mL | 1.6428 mL | 3.2856 mL | 8.2140 mL | |
| 25 mM | 0.2628 mL | 1.3142 mL | 2.6285 mL | 6.5712 mL | |
| 30 mM | 0.2190 mL | 1.0952 mL | 2.1904 mL | 5.4760 mL | |
| 40 mM | 0.1643 mL | 0.8214 mL | 1.6428 mL | 4.1070 mL | |
| 50 mM | 0.1314 mL | 0.6571 mL | 1.3142 mL | 3.2856 mL | |
| 60 mM | 0.1095 mL | 0.5476 mL | 1.0952 mL | 2.7380 mL | |
| 80 mM | 0.0821 mL | 0.4107 mL | 0.8214 mL | 2.0535 mL | |
| 100 mM | 0.0657 mL | 0.3286 mL | 0.6571 mL | 1.6428 mL |