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604-25-1

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604-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 604-25-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 604-25:
(5*6)+(4*0)+(3*4)+(2*2)+(1*5)=51
51 % 10 = 1
So 604-25-1 is a valid CAS Registry Number.

604-25-1SDS

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 androst-4-ene-3,6-dione

1.2 Other means of identification

Product number -
Other names Androst-4-en-3,6-dion

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:604-25-1 SDS

604-25-1Upstream product

604-25-1Downstream Products

604-25-1Relevant articles and documents

Synthesis and biological evaluation of steroidal derivatives as selective inhibitors of AKR1B10

Zhang, Wei,Wang, Ling,Zhang, Liping,Chen, Wenli,Chen, Xinying,Xie, Minyu,Yan, Guangmei,Hu, Xiaopeng,Xu, Jun,Zhang, Jingxia

, p. 39 - 44 (2014/06/09)

AKR1B10 is a member of human aldo-keto reductase superfamily, and a promising anti-cancer therapeutic target. In this paper, androst-5-ene-3β- ol, dehydroepiandrosterone, pregnenolone and cholesterol were used as reactants, sixteen products were obtained through Jones reaction and reduction reaction using NaBH4. Their inhibitory activities against AKR1B10 and AKR1B1 were measured. The most active compound (3a) has the IC50 of 0.50 μM for AKR1B10, and the most AKR1B10 selective compound (2a) has the IC 50 of 0.81 μM with AKR1B1/AKR1B10 selectivity of 195. In addition, the binding modes of 2a and 3a in the active site of human AKR1B10 were identified by docking.

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