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240122-30-9

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240122-30-9 Usage

General Description

Griffithazanone A is a natural product extracted from the marine-derived fungus Aspergillus Griffithii. It is a complex molecule with a unique chemical structure, and it has been found to exhibit various biological activities. Griffithazanone A shows potent cytotoxicity against cancer cells, making it a promising candidate for the development of anti-cancer drugs. Additionally, it has also demonstrated inhibitory effects on certain enzymes, suggesting potential applications in enzyme-targeted therapy. Overall, Griffithazanone A is a significant chemical compound with diverse pharmacological properties, and it has attracted attention from researchers in the fields of drug discovery and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 240122-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,1,2 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 240122-30:
(8*2)+(7*4)+(6*0)+(5*1)+(4*2)+(3*2)+(2*3)+(1*0)=69
69 % 10 = 9
So 240122-30-9 is a valid CAS Registry Number.

240122-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Griffithazanone A

1.2 Other means of identification

Product number -
Other names -

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:240122-30-9 SDS

240122-30-9Upstream product

240122-30-9Downstream Products

240122-30-9Relevant articles and documents

Photoelectrocyclization Reactions of Amidonaphthoquinones

Landward, Michael B.,Rainier, Jon D.,Yin, Jinya

, p. 4298 - 4311 (2020)

Readily available acrylamide naphthoquinones can be converted into the corresponding aza-anthraquinones using 6?-photoelectrocyclization reactions. Not only do these reactions not proceed thermally but, as demonstrated here, they can also be used to generate a range of aza-anthraquinone and aza-tetracycline derivatives including the natural products griffithazanone A and marcanine A. Several of the aza-anthraquinones generated in this work showed antibacterial activity.

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