STF-118804
Based on 3 publication(s) in Google Scholar
STF-118804 is a highly specific NAMPT inhibitor. STF-118804 activates AMPK and inhibits mTOR pathways. STF-118804 has antitumor activity against pancreatic cancer.
For research use only. We do not sell to patients.
- Purity: 99.72%
- CAS No.: 894187-61-2
- Formula: C25H23N3O4S
- Molecular Weight:461.54
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) STF-118804
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Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| B-ALL | EC50 |
0.061 μM
Compound: 1
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Antiproliferative activity against mouse B-ALL BCR-ABL double knockout cells assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against mouse B-ALL BCR-ABL double knockout cells assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| B-ALL | EC50 |
0.072 μM
Compound: 1
|
Antiproliferative activity against mouse B-ALL cells expressing wild type BCR-ABL assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against mouse B-ALL cells expressing wild type BCR-ABL assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| BJ | EC50 |
2.4938 μM
Compound: 1
|
Antiproliferative activity against human BJ assessed as cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against human BJ assessed as cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| K562 | EC50 |
4.6 μM
Compound: 1
|
Antiproliferative activity against human K562 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against human K562 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| KOPN-8 | EC50 |
1.23 μM
Compound: 1
|
Antiproliferative activity against human KOPN8 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against human KOPN8 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| MV4-11 | EC50 |
3.8 μM
Compound: 1
|
Antiproliferative activity against human MV411 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against human MV411 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| NALM-6 | EC50 |
0.026 μM
Compound: 1
|
Antiproliferative activity against human NALM6 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against human NALM6 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| SUP-B15 | EC50 |
1.1 μM
Compound: 1
|
Antiproliferative activity against human SUP-B15 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against human SUP-B15 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
| UoC-B1 | EC50 |
>54.98 μM
Compound: 1
|
Antiproliferative activity against human UOCB1 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
Antiproliferative activity against human UOCB1 assessed as reduction in cell viability after 72 hrs by CellTiter-Glo assay
|
[PMID: 30611980] |
STF-118804 (6.25-25 nM, 72 h) reduces viability and growth of different pancreatic ductal adenocarcinoma cells (PaTu8988t, Panc-1, Su86.86, Panc04.03)[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:PaTu8988t, Panc-1, Su86.86, Panc04.03
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Concentration:6.25, 12.5, 25 nM
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Incubation Time:72 h
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Result:Showed more sensitivity to Panc-1 and PaTu8988t cells.
STF-118804 (50 mg/kg, s.c., 20 days) improves survival in an orthotopic xenotransplant mouse model of high-risk acute lymphoblastic leukemia[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Nude mice (gender not specified, age 4 - 6 weeks) inoculated with Panc-1 cells expressing GFP-luciferase to establish an orthotopic pancreatic cancer model[1]
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Dosage:25 mg/kg
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Administration:Intraperitoneal injection (i.p.), 3 weeks
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Result:Reduced tumor growth as demonstrated by decreased luminescence, tumor weight and size.
Had no significant toxicity.
Chemical Information
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CAS No. 894187-61-2
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Appearance Solid
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Molecular Weight 461.54
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Formula C25H23N3O4S
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Color White to light yellow
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SMILES
O=C(NCC1=CC=CN=C1)C2=CC=C(C3=NC(CS(=O)(C4=CC=C(C)C=C4)=O)=C(C)O3)C=C2
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (3)
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Journal Impact Factor
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Most Recent
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PLoS Pathog
Nicotinamide metabolism is essential for Hepatitis C Virus replication and the production of infectious Lipo-Viro-Particles. [Abstract]2026 Apr 22;22(4):e1014165. PMID: 42018568 -
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Solvent & Solubility
DMSO : 25 mg/mL (54.17 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Purity & Documentation
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Data Sheet (274 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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Handling Instructions (2659 KB)
References
[1]. Espindola-Netto JM, et al. Preclinical efficacy of the novel competitive NAMPT inhibitor STF-118804 in pancreatic cancer. Oncotarget. 2017 Jun 29;8(49):85054-85067. [Content Brief]
[2]. Matheny CJ, et al. Next-generation NAMPT inhibitors identified by sequential high-throughput phenotypic chemical and functional genomic screens. Chem Biol. 2013 Nov 21;20(11):1352-63. [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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 2.1667 mL | 10.8333 mL | 21.6666 mL | 54.1665 mL |
| 5 mM | 0.4333 mL | 2.1667 mL | 4.3333 mL | 10.8333 mL | |
| 10 mM | 0.2167 mL | 1.0833 mL | 2.1667 mL | 5.4166 mL | |
| 15 mM | 0.1444 mL | 0.7222 mL | 1.4444 mL | 3.6111 mL | |
| 20 mM | 0.1083 mL | 0.5417 mL | 1.0833 mL | 2.7083 mL | |
| 25 mM | 0.0867 mL | 0.4333 mL | 0.8667 mL | 2.1667 mL | |
| 30 mM | 0.0722 mL | 0.3611 mL | 0.7222 mL | 1.8055 mL | |
| 40 mM | 0.0542 mL | 0.2708 mL | 0.5417 mL | 1.3542 mL | |
| 50 mM | 0.0433 mL | 0.2167 mL | 0.4333 mL | 1.0833 mL |