Identification |
Name: | 6H-Oxireno[e][2]benzoxacyclotetradecin-6,12(7H)-dione,8-chloro-1a,14,15,15a-tetrahydro-9,11-dihydroxy-14-methyl-,(1aR,2Z,4E,14R,15aR)- |
Synonyms: | Monorderne; |
CAS: | 12772-57-5 |
Molecular Formula: | C18H17ClO6 |
Molecular Weight: | 364.77698 |
InChI: | InChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2+,5-3+ |
Molecular Structure: |
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Properties |
Transport: | UN 2811 6.1/PG 3 |
Density: | 1.364 g/cm3 |
Refractive index: | 1.583 |
Water Solubility: | ethanol: 10 mg/mL ,Soluble in DMSO (20 mg/ml-clear colorless solution) |
Solubility: | ethanol: 10 mg/mL ,Soluble in DMSO (20 mg/ml-clear colorless solution) |
Appearance: | White/yellow powder |
Biological Activity: | Antifungal antibiotic. Inhibits heat shock protein 90 (Hsp90) activity by binding to the ATP-binding pocket, subsequently suppressing cell transformation induced by src, ras and mos. Represses estrogen receptor transcriptional activity and inhibits angiogenesis. |
Storage Temperature: | −20°C |
Color: | yellow |
Safety Data |
Hazard Symbols |
Xn: Harmful
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