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(+/-)-ε-Deoxypyrromycinone is a naturally occurring macrocyclic antibiotic that belongs to the pyrrolopyrrolone family. It is produced by the bacterium Streptomyces sp. and exhibits potent antibacterial activity against various Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). The chemical structure of (+/-)-ε-deoxypyrromycinone consists of a macrocyclic lactone with a pyrrolopyrrolone core, which is responsible for its unique mode of action. It targets the bacterial RNA polymerase, inhibiting the transcription process and ultimately leading to cell death. Due to its broad-spectrum activity and potential for further development, (+/-)-ε-deoxypyrromycinone has garnered significant interest in the field of antibiotic research and development.

641-92-9

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641-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 641-92-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 641-92:
(5*6)+(4*4)+(3*1)+(2*9)+(1*2)=69
69 % 10 = 9
So 641-92-9 is a valid CAS Registry Number.

641-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name rac-ζ-Pyrromycinon

1.2 Other means of identification

Product number -
Other names ξ-Pyrromycinon

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 -
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More Details:641-92-9 SDS

641-92-9Downstream Products

641-92-9Relevant academic research and scientific papers

SYNTHESIS OF ξ-PYRROMYCINONE, 7-DEOXYAURAMYCINONE, AND 7-DEOXYAKLAVINONE VIA KETOESTER CYCLIZATION

Krohn, Karsten,Klimars, Michael,Koehle, Hans-Juergen,Ebeling, Eckehardt

, p. 3677 - 3694 (1984)

7,10-O-Dimethyl-ξ-pyrromycinone (78) and the not naturally occurring 7-deoxyanthracyclinones 76 and 77 are prepared via base induced cyclization of the ketoesters 73-75, and stereoselectively hydroxylated to the 2,4-cis diols 83 and 85.

Regiospecific Total Syntheses of (+/-)-Aklavinone and (+/-)-ε-Pyrromycinone from a Common Synthon

Hauser, Frank M.,Mal Dipakranjan

, p. 1098 - 1104 (2007/10/02)

The preparation and use of cyclohexenone 10 as a common intermediate for regiospecific total synthesis of both (+/-)-aklavinone (1a) and (+/-)-ε-pyrromycinone (2a) is described.

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