| Weight | 507.693 g/mol |
|---|---|
| Formula | C27H41NO6S |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Epothilone B (152044-54-7)
Score:
#1125 in Biochemistry
,
#2870 in Biology
,
#3593 in Chemistry
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- Sigma-Aldrich - Epothilone B39.00 - 119.00 USD
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- Epothilone A and BNovel 16Membered Macrolides with Cytotoxic Activity: Isolation, Crystal Structure, and Conformation in Solution (Angewandte Chemie, 1996)
- Phase II Clinical Trial of Ixabepilone (BMS-247550), an Epothilone B Analog, in Patients With Taxane-Resistant Metastatic Breast Cancer (Journal of Clinical Oncology, 2007)
- Histone deacetylase inhibitor LAQ824 down-regulates Her-2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B (Molecular Cancer Therapeutics, 2003)
- Phase II Clinical Trial of Ixabepilone (BMS-247550), an Epothilone B Analog, in Metastatic and Locally Advanced Breast Cancer (Journal of Clinical Oncology, 2005)
- Phase II Clinical Trial of Ixabepilone (BMS-247550), an Epothilone B Analog, As First-Line Therapy in Patients With Metastatic Breast Cancer Previously Treated With Anthracycline Chemotherapy (Journal of Clinical Oncology, 2007)
- Multi-Institutional Randomized Phase II Trial of the Epothilone B Analog Ixabepilone (BMS-247550) With or Without Estramustine Phosphate in Patients With Progressive Castrate Metastatic Prostate Cancer (Journal of Clinical Oncology, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1CCCC2(C(O2)CC(OC(=O)CC(C(C(=O)C(C1O)C)(C)C)O)C(=CC3=CSC(=N3)C)C)C
-
InChIKeyQXRSDHAAWVKZLJ-UHFFFAOYSA-N
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