Betulinic acid methyl ester
Based on 1 Customer Validation
Betulinic acid methyl ester, a betulinic acid derivative, possesses antiprotozoal activity.
For research use only. We do not sell to patients.
- Purity: 99.76%
- CAS No.: 2259-06-5
- Formula: C31H50O3
- Molecular Weight:470.73
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Storage:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
All Parasite Isoforms
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Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| 518A2 | IC50 |
16.93 μM
Compound: 15
|
Cytotoxicity against human 518A2 cells assessed as cell viability after 96 hrs by SRB assay
Cytotoxicity against human 518A2 cells assessed as cell viability after 96 hrs by SRB assay
|
[PMID: 23973824] |
| 518A2 | IC50 |
28.75 μM
Compound: 3
|
Cytotoxicity against human 518A2 cells after 96 hrs by SRB assay
Cytotoxicity against human 518A2 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| 8505C | IC50 |
17.17 μM
Compound: 15
|
Cytotoxicity against human 8505C cells assessed as cell viability after 96 hrs by SRB assay
Cytotoxicity against human 8505C cells assessed as cell viability after 96 hrs by SRB assay
|
[PMID: 23973824] |
| 8505C | IC50 |
23.67 μM
Compound: 3
|
Cytotoxicity against human 8505C cells after 96 hrs by SRB assay
Cytotoxicity against human 8505C cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| A253 cell line | IC50 |
18.51 μM
Compound: 3
|
Cytotoxicity against human A253 cells after 96 hrs by SRB assay
Cytotoxicity against human A253 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| A2780 | IC50 |
16.27 μM
Compound: 15
|
Cytotoxicity against human A2780 cells assessed as cell viability after 96 hrs by SRB assay
Cytotoxicity against human A2780 cells assessed as cell viability after 96 hrs by SRB assay
|
[PMID: 23973824] |
| A2780 | IC50 |
29.31 μM
Compound: 3
|
Cytotoxicity against human A2780 cells after 96 hrs by SRB assay
Cytotoxicity against human A2780 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| A-431 | IC50 |
26.99 μM
Compound: 3
|
Cytotoxicity against human A431 cells after 96 hrs by SRB assay
Cytotoxicity against human A431 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| A549 | IC50 |
17.17 μM
Compound: 15
|
Cytotoxicity against human A549 cells assessed as cell viability after 96 hrs by SRB assay
Cytotoxicity against human A549 cells assessed as cell viability after 96 hrs by SRB assay
|
[PMID: 23973824] |
| A549 | IC50 |
20.63 μM
Compound: 3
|
Cytotoxicity against human A549 cells after 96 hrs by SRB assay
Cytotoxicity against human A549 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| B16 | ED50 |
2.5 μM
Compound: 12
|
Induction of melanogenesis in mouse B16 2F2 cells assessed as intracellular melanin content after 3 days
Induction of melanogenesis in mouse B16 2F2 cells assessed as intracellular melanin content after 3 days
|
[PMID: 12027734] |
| B16 | IC50 |
4.9 μM
Compound: 12
|
Growth inhibition of mouse B16 2F2 cells after 3 days
Growth inhibition of mouse B16 2F2 cells after 3 days
|
[PMID: 12027734] |
| CCRF-CEM | IC50 |
150 μM
Compound: 2
|
Cytotoxicity against human CEM cells after 72 hrs by MTT assay
Cytotoxicity against human CEM cells after 72 hrs by MTT assay
|
[PMID: 15270560] |
| CHO | EC50 |
>10 μM
Compound: 34
|
Agonist activity at TGR5 expressed in CHO cells by CRE-driven luciferase reporter gene assay
Agonist activity at TGR5 expressed in CHO cells by CRE-driven luciferase reporter gene assay
|
[PMID: 19911773] |
| COS-1 | EC50 |
0 μM
Compound: 34
|
Agonist activity at human FXR expressed in COS1 cells by luciferase reporter gene assay
Agonist activity at human FXR expressed in COS1 cells by luciferase reporter gene assay
|
[PMID: 19911773] |
| DLD-1 | IC50 |
45.86 μM
Compound: 3
|
Cytotoxicity against human DLD1 cells after 96 hrs by SRB assay
Cytotoxicity against human DLD1 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| FaDu | IC50 |
20.33 μM
Compound: 3
|
Cytotoxicity against human FADU cells after 96 hrs by SRB assay
Cytotoxicity against human FADU cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| HCT-116 | IC50 |
20.47 μM
Compound: 3
|
Cytotoxicity against human HCT116 cells after 96 hrs by SRB assay
Cytotoxicity against human HCT116 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| HCT-8 | IC50 |
17.25 μM
Compound: 3
|
Cytotoxicity against human HCT8 cells after 96 hrs by SRB assay
Cytotoxicity against human HCT8 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| HT-29 | IC50 |
30.72 μM
Compound: 3
|
Cytotoxicity against human HT-29 cells after 96 hrs by SRB assay
Cytotoxicity against human HT-29 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| HT-29 | IC50 |
61 μM
Compound: 2
|
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: 15270560] |
| K562 | IC50 |
65 μM
Compound: 2
|
Cytotoxicity against paclitaxel-resistant human K562 cells after 72 hrs by MTT assay
Cytotoxicity against paclitaxel-resistant human K562 cells after 72 hrs by MTT assay
|
[PMID: 15270560] |
| K562 | IC50 |
71 μM
Compound: 2
|
Cytotoxicity against human K562 cells after 72 hrs by MTT assay
Cytotoxicity against human K562 cells after 72 hrs by MTT assay
|
[PMID: 15270560] |
| KB | ED50 |
11.8 μg/mL
Compound: 16
|
Cytotoxicity against human epidermoid carcinoma of the mouth (KB) cell line.
Cytotoxicity against human epidermoid carcinoma of the mouth (KB) cell line.
|
[PMID: 9873420] |
| MCF7 | IC50 |
16.93 μM
Compound: 15
|
Cytotoxicity against human MCF7 cells assessed as cell viability after 96 hrs by SRB assay
Cytotoxicity against human MCF7 cells assessed as cell viability after 96 hrs by SRB assay
|
[PMID: 23973824] |
| MCF7 | IC50 |
24.39 μM
Compound: 3
|
Cytotoxicity against human MCF7 cells after 96 hrs by SRB assay
Cytotoxicity against human MCF7 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| PC-3 | IC50 |
109 μM
Compound: 2
|
Cytotoxicity against human PC3 cells after 72 hrs by MTT assay
Cytotoxicity against human PC3 cells after 72 hrs by MTT assay
|
[PMID: 15270560] |
| SK-MEL-2 | ED50 |
8.3 μg/mL
Compound: 16
|
Cytotoxicity against cultured human melanoma (MEL-2) cell line.
Cytotoxicity against cultured human melanoma (MEL-2) cell line.
|
[PMID: 9873420] |
| SW-1736 | IC50 |
32.1 μM
Compound: 3
|
Cytotoxicity against human SW1736 cells after 96 hrs by SRB assay
Cytotoxicity against human SW1736 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
| SW480 | IC50 |
17.92 μM
Compound: 3
|
Cytotoxicity against human SW480 cells after 96 hrs by SRB assay
Cytotoxicity against human SW480 cells after 96 hrs by SRB assay
|
[PMID: 20451375] |
Chemical Information
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CAS No. 2259-06-5
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Appearance Solid
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Molecular Weight 470.73
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Formula C31H50O3
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Color White to off-white
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SMILES
COC([C@]12[C@@]([C@@H](CC2)C(C)=C)([H])[C@]3([H])[C@@](CC1)([C@]4([C@]([C@@]5([C@@](C(C)([C@H](CC5)O)C)([H])CC4)C)([H])CC3)C)C)=O
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Synonyms
Methyl betulinate
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Solvent & Solubility
DMSO : 5 mg/mL (10.62 mM; ultrasonic and warming and heat to 60°C; 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)
Purity & Documentation
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Data Sheet (271 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
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 | 2.1244 mL | 10.6218 mL | 21.2436 mL | 53.1090 mL |
| 5 mM | 0.4249 mL | 2.1244 mL | 4.2487 mL | 10.6218 mL | |
| 10 mM | 0.2124 mL | 1.0622 mL | 2.1244 mL | 5.3109 mL |