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(E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfamoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylamide is a complex organic compound characterized by its yellow solid appearance. It is a derivative of acrylamide with a unique structure that includes a sulfamoyl group attached to a phenyl ring, a methoxypyrazinyl moiety, and a nitrothiophene group. (E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfaMoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylaMide is of interest due to its potential applications in various fields, particularly in the pharmaceutical and chemical industries.

432531-71-0

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  • (E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfaMoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylaMide

    Cas No: 432531-71-0

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432531-71-0 Usage

Uses

Used in Pharmaceutical Industry:
(E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfamoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylamide is used as a potential therapeutic agent for targeting programmed necrosis (necroptosis). (E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfaMoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylaMide specifically blocks necrosis downstream of receptor-interacting serine-threonine kinase 3 (RIP3) activation, which is a key signaling molecule in the necroptosis pathway. By inhibiting this pathway, the compound may offer a novel approach to treating conditions associated with uncontrolled cell death and inflammation.
Used in Chemical Research:
In the field of chemical research, (E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfamoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylamide can be utilized as a starting material or intermediate for the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable building block for the development of new compounds with diverse applications, such as in materials science, pharmaceuticals, and agrochemicals.
Used in Drug Design and Development:
(E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfaMoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylaMide's ability to modulate the RIP3 signaling pathway makes it a promising candidate for drug design and development. Researchers can use (E)-N-[4-[N-(3-Methoxypyrazin-2-yl)sulfaMoyl]phenyl]-3-(5-nitrothiophene-2-yl)acrylaMide as a template to design new molecules with improved potency, selectivity, and pharmacokinetic properties. This could lead to the development of more effective therapies for a range of diseases, including those involving dysregulated cell death and inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 432531-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,5,3 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 432531-71:
(8*4)+(7*3)+(6*2)+(5*5)+(4*3)+(3*1)+(2*7)+(1*1)=120
120 % 10 = 0
So 432531-71-0 is a valid CAS Registry Number.

432531-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Necrosulfonamide

1.2 Other means of identification

Product number -
Other names (E)-N-[4-[(3-methoxypyrazin-2-yl)sulfamoyl]phenyl]-3-(5-nitrothiophen-2-yl)prop-2-enamide

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:432531-71-0 SDS

432531-71-0Downstream Products

432531-71-0Relevant articles and documents

Necrosulfonamide inhibits necroptosis by selectively targeting the mixed lineage kinase domain-like protein

Liao, Daohong,Sun, Liming,Liu, Weilong,He, Sudan,Wang, Xiaodong,Lei, Xiaoguang

, p. 333 - 337 (2014/03/21)

Through high-throughput screening of 200000 compounds and subsequent structure-activity relationship (SAR) studies we identified necrosulfonamide (NSA) as a potent small molecule inhibitor for necroptosis, induced by a combination of TNF-a, Smac mimetic, and z-VAD-fmk (T/S/Z). Applying a forward chemical genetic approach, we utilized an NSA based chemical probe to further reveal that NSA selectively targeted the Mixed Lineage Kinase Domain-like Protein (MLKL) to block the necrosome formation.

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