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5-Hydroxypyridine-2-carbaldehyde pyrrolizino(thiocarbonyl)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53222-90-5

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53222-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53222-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53222-90:
(7*5)+(6*3)+(5*2)+(4*2)+(3*2)+(2*9)+(1*0)=95
95 % 10 = 5
So 53222-90-5 is a valid CAS Registry Number.

53222-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-((5-hydroxypyridin-2-yl)methylene)pyrrolidine-1-carbothiohydrazide

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:53222-90-5 SDS

53222-90-5Upstream product

53222-90-5Downstream Products

53222-90-5Relevant academic research and scientific papers

Potential antitumor agents. 11. Inhibitors of alkaline phosphatase, an enzyme involved in the resistance of neoplastic cells to 6 thiopurines

Agrawal,Lee,Booth,Moore,Sartorelli

, p. 934 - 938 (2007/10/09)

A series of 4' substituted derivatives of 5 hydroxy 2 formylpyridine thiosemicarbazone (5 HP) has been synthesized and evaluated as inhibitors of alkaline phosphatase partially purified from a murine ascitic cell line of Sarcoma 180 resistant to the antileukemic agents 6 mercaptopurine and 6 thioguanine. These agents were also tested as inhibitors of ribonucleoside diphosphate reductase from rat Novikoff hepatoma and for antineoplastic activity in mice bearing either 6 thiopurine sensitive or resistant cells of Sarcoma 180. Structure activity relationship studies have delineated the bulk requirement for a 5 membered ring at the 4' position for optimum phosphatase inhibitor interaction. Similar bulk produced loss of activity by α (N) heterocyclic carboxaldehyde thiosemicarbazones as inhibitors of ribonucleoside diphosphate reductase. Some of these agents were found to possess potent tumor inhibitory potential.

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