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Kazusamycin A, a hydroxylated analogue of leptomycin B, is a minor member of the leptomycin complex isolated from Streptomyces species. It is known for its potent antitumor activity, as well as strong antibacterial and antifungal properties.
Used in Pharmaceutical Industry:
Kazusamycin A is used as an anticancer agent for its potent antitumor activity both in vitro and in vivo against P388 and L1210 cell lines. It is effective in inducing G2 cell cycle arrest and delaying the M phase, which contributes to its ability to combat cancer cells.
Used in Antibacterial Applications:
Kazusamycin A is used as a potent antibiotic due to its strong antibacterial activity, making it a valuable tool in treating bacterial infections.
Used in Antifungal Applications:
Kazusamycin A is used as an antifungal agent for its strong antifungal properties, helping to combat fungal infections.

92090-94-3

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92090-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92090-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,9 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92090-94:
(7*9)+(6*2)+(5*0)+(4*9)+(3*0)+(2*9)+(1*4)=133
133 % 10 = 3
So 92090-94-3 is a valid CAS Registry Number.
InChI:InChI=1/C33H48O7/c1-8-27(13-14-29-24(5)12-15-31(37)40-29)17-21(2)10-9-11-22(3)18-28(20-34)33(39)26(7)32(38)25(6)16-23(4)19-30(35)36/h9,11-15,17-19,21,24-26,28-29,32,34,38H,8,10,16,20H2,1-7H3,(H,35,36)/b11-9+,14-13+,22-18+,23-19+,27-17-

92090-94-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,10,12,16,18-Nonadecapentaenoic acid, 19-[(2S,3S)-3,6-dihydro-3-methyl-6-oxo-2H-pyran-2-yl]-17-ethyl-6-hydroxy-9-(hydroxymethyl)-3,5,7,11,15-pentamethyl-8-oxo-, (2E,5S,6R,7S,9S,10E,12E,15R,16Z,18E)-

1.2 Other means of identification

Product number -
Other names Antibiotic CL 1957B

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92090-94-3 SDS

92090-94-3Upstream product

92090-94-3Downstream Products

92090-94-3Relevant academic research and scientific papers

First total synthesis of the antitumor compound (-)-kazusamycin A and absolute structure determination

Arai, Noriyoshi,Chikaraishi, Noriko,Omura, Satoshi,Kuwajima, Isao

, p. 2845 - 2848 (2007/10/03)

(Equation Presented) The first total synthesis of kazusamycin A, a potent antitumor compound from an actinomycete, has been achieved, and its absolute structure was determined. Paterson's stereoselective aldol reaction was successfully applied to construct the contiguous chiral centers by using an originally designed optically active 2-acyl-1,3-propanediol derivative.

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