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Kazusamycin A_Molecular_structure_CAS_92090-94-3)
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Kazusamycin A

Catalog No. K1764 Name Sigma Aldrich
CAS Number 92090-94-3 Website http://www.sigmaaldrich.com
M. F. C33H48O7 Telephone 1-800-521-8956
M. W. 556.73002 Fax
Purity ≥95% (HPLC) Email
Storage Chembase ID: 131740

SYNONYMS

IUPAC name
(2E,10E,12E,16E,18E)-17-ethyl-6-hydroxy-9-(hydroxymethyl)-3,5,7,11,15-pentamethyl-19-(3-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-8-oxononadeca-2,10,12,16,18-pentaenoic acid
IUPAC Traditional name
(2E,10E,12E,16E,18E)-17-ethyl-6-hydroxy-9-(hydroxymethyl)-3,5,7,11,15-pentamethyl-19-(3-methyl-6-oxo-2,3-dihydropyran-2-yl)-8-oxononadeca-2,10,12,16,18-pentaenoic acid

DATABASE IDS

MDL Number MFCD03265635
CAS Number 92090-94-3

PROPERTIES

Biological Source from Streptomyces sp.
Purity ≥95% (HPLC)
Shipped in dry ice
Apperance aqueous methanol solution
Flash Point 15 °C
Flash Point 59 °F
Solubility methanol: water: soluble7:3
Solubility DMSO: soluble
Solubility H2O: insoluble
Solubility chloroform: soluble
Solubility ethanol: soluble
Solubility hexane: insoluble
Solubility methanol: soluble
GHS Pictograms GHS02
GHS Pictograms GHS06
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H225-H301-H311-H331-H370
European Hazard Symbols Flammable Flammable (F)
European Hazard Symbols Toxic Toxic (T)
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P210-P260-P280-P301 + P310-P311
RID/ADR UN 1230 3/PG 2
Risk Statements 11-23/24/25-39/23/24/25
Safety Statements 16-36/37-45
Storage Temperature -20°C
Hazard Class 3
UN Number 1230
Packing Group 2
German water hazard class 1

DETAILS

Description (English)
Biochem/physiol Actions
Kazusamycin A, an unsaturated branched chain fatty acid with a terminal lactone ring, is a hydroxy analog of Leptomycin B. It has significant in vitro cytotoxic activity against various human and mouse tumor lines encompassing a wide range of tissue types. Kazusamycin A exhibits in vivo antitumor activity against experimental murine tumors. It inhibits nuclear export and Rev translocation, a regulatory gene product in the HIV genome, at nanomolar concentrations.
Physical form
70% methanol solution.

REFERENCES