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AEG 3482 is an antiapoptotic compound that inhibits Jun Kinase Activity (JNK) and cell death through induced expression of heat shock protein 70.

63735-71-7

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63735-71-7 Usage

Uses

Used in Pharmaceutical Industry:
AEG 3482 is used as a therapeutic agent for the treatment of neurological disorders due to its ability to inhibit JNK and promote cell survival through the expression of heat shock protein 70.

Biological Activity

Inhibitor of c-jun N-terminal kinase (JNK) signaling. Binds Hsp90 and facilitates HSF1 release, induces expression of Hsp70, which in turn blocks JNK activation and JNK-dependent apoptosis. Antiapoptotic; inhibits NGF withdrawal-induced death in SCG neurons (EC 50 = 20 μ M).

references

[1]salehi ah, morris sj, ho wc, etal. , aeg3482 is an antiapoptotic compound that inhibits jun kinase activity and cell death through induced expression of heat shock protein 70. chem biol. 2006 feb;13(2):213-23.[2] gallo ka. targeting hsp90 to halt neurodegeneration. chem biol. 2006 feb;13(2):115-6.

Check Digit Verification of cas no

The CAS Registry Mumber 63735-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63735-71:
(7*6)+(6*3)+(5*7)+(4*3)+(3*5)+(2*7)+(1*1)=137
137 % 10 = 7
So 63735-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N4O2S2/c11-18(15,16)10-13-14-6-8(12-9(14)17-10)7-4-2-1-3-5-7/h1-6H,(H2,11,15,16)

63735-71-7 Well-known Company Product Price

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  • Sigma

  • (SML0264)  AEG 3482  ≥98% (HPLC)

  • 63735-71-7

  • SML0264-5MG

  • 1,077.57CNY

  • Detail
  • Sigma

  • (SML0264)  AEG 3482  ≥98% (HPLC)

  • 63735-71-7

  • SML0264-25MG

  • 4,351.23CNY

  • Detail

63735-71-7SDS

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 6-phenylimidazo[2,1-b][1,3,4]thiadiazole-2-sulfonamide

1.2 Other means of identification

Product number -
Other names HMS1538B12

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 -
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More Details:63735-71-7 SDS

63735-71-7Downstream Products

63735-71-7Relevant academic research and scientific papers

USE OF IMIDAZO[2,1-b)]-1,3,4-THIADIAZOLE-2-SULFONAMIDE COMPOUNDS TO TREAT NEUROPATHIC PAIN

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Page/Page column 52, (2008/06/13)

Disclosed herein are methods and compositions for treating and/or prophylaxis of neuropathic pain in a subject. The methods comprise administering to the subject suffering from neuropathic pain, a therapeutically effective amount of a compound, according

ACYLATED AND NON-ACYLATED IMIDAZO[2,1-b]-1,3,4,-THIADIAZOLE-2-SULFONAMIDES, AND USES THEREOF

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Page 44, (2008/06/13)

This invention relates to novel compounds of Formula (I): and the use of compounds of Formula (I) in the treatment of neuronal disorders of the central and peripheral nervous systems and for the treatment of proliferative diseases, such as cancer.

Cerebrovasodilatation through selective inhibition of the enzyme carbonic anhydrase. 2. Imidazo[2,1-b]thiadiazole and imidazo[2,1-b]thiazolesulfonamides.

Barnish,Cross,Dickinson,Gadsby,Parry,Randall,Sinclair

, p. 117 - 121 (2007/10/02)

A series of imidazo[2,1-b]thiadiazole and imidazo[2,1-b]thiazolesulfonamide carbonic anhydrase inhibitors is described and their anticonvulsant activities are listed. Many of the compounds have the same degree of ionization as acetazolamide and methazolam

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