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4,7-diphenyl[1,2,5]oxadiazolo[3,4-d]pyridazine 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140410-59-9

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140410-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140410-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,4,1 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140410-59:
(8*1)+(7*4)+(6*0)+(5*4)+(4*1)+(3*0)+(2*5)+(1*9)=79
79 % 10 = 9
So 140410-59-9 is a valid CAS Registry Number.

140410-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxido-4,7-diphenyl-[1,2,5]oxadiazolo[3,4-d]pyridazin-3-ium

1.2 Other means of identification

Product number -
Other names [1,2,5]Oxadiazolo[3,4-d]pyridazine,diphenyl-,1-oxide

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:140410-59-9 SDS

140410-59-9Relevant academic research and scientific papers

Diacylfuroxans Are Masked Nitrile Oxides That Inhibit GPX4 Covalently

Eaton, John K.,Kramm, Anneke,Ruberto, Richard A.,Schreiber, Stuart L.,Viswanathan, Vasanthi S.

, (2020/01/02)

GPX4 represents a promising yet difficult-to-drug therapeutic target for the treatment of, among others, drug-resistant cancers. Although most GPX4 inhibitors rely on a chloroacetamide moiety to modify covalently the protein's catalytic selenocysteine residue, the discovery and mechanistic elucidation of structurally diverse GPX4-inhibiting molecules have uncovered novel electrophilic warheads that bind and inhibit GPX4. Here, we report our discovery that diacylfuroxans can act as masked nitrile oxide prodrugs that inhibit GPX4 covalently with unique cellular and biochemical reactivity compared to existing classes of GPX4 inhibitors. These observations illuminate a novel molecular mechanism of action for biologically active furoxans and also expand the collection of reactive groups capable of targeting GPX4.

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