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2,4-Thiazolidinedione, 3-[(3-bromophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

848606-46-2

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848606-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848606-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,6,0 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 848606-46:
(8*8)+(7*4)+(6*8)+(5*6)+(4*0)+(3*6)+(2*4)+(1*6)=202
202 % 10 = 2
So 848606-46-2 is a valid CAS Registry Number.

848606-46-2Relevant academic research and scientific papers

PLASMINOGEN ACTIVATOR-1 INHIBITORS AND METHODS OF USE THEREOF

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Paragraph 00209-00212, (2014/05/24)

The invention relates to plasminogen activator- 1 (PAI-1) inhibitor compounds and uses thereof in the treatment of any disease or disorder associated with elevated PAI-1. The invention includes, but is not limited to, the use of such compounds to prevent or reduce thrombosis and fibrosis, to promote thrombolysis, and to modulate lipid metabolism and treat diseases or disorders associated with elevated PAI-1, cholesterol, or lipid levels.

Synthesis and biological evaluation of novel pyrazolyl-2,4-thiazolidinediones as anti-inflammatory and neuroprotective agents

Youssef, Amal M.,Sydney White,Villanueva, Erika B.,El-Ashmawy, Ibrahim M.,Klegeris, Andis

experimental part, p. 2019 - 2028 (2010/05/18)

Novel pyrazolyl-2,4-thiazolidinediones were prepared via the reaction of appropriate pyrazolecarboxaldehydes with 2,4-thiazolidinediones and substituted benzyl-2,4-thiazolidinediones. The resultant compounds were first evaluated for their anti-inflammatory and neuroprotective properties in vitro. The active compounds were further studied in vivo by using the formalin-induced paw edema and the turpentine oil-induced granuloma pouch bioassays. We identified four novel compounds that showed protective effects in vitro at non-toxic concentrations, and were also effective in the animal models of acute and sub-acute inflammation.

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