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Thieno[3,2-b]pyridine-5-carboxylic acid is a heterocyclic compound featuring a thieno[3,2-b]pyridine ring fused with a carboxylic acid group. It is known for its unique chemical properties and potential applications in various fields due to its structural characteristics.

56473-92-8

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56473-92-8 Usage

Uses

Used in Pharmaceutical Industry:
Thieno[3,2-b]pyridine-5-carboxylic acid is used as a key intermediate in the synthesis of novel derivatives of echinomycin, an antibiotic. It serves as a replacement chromophore in the study of the biosynthesis process by Streptomyces echinatus, contributing to the development of new and potentially more effective antibiotic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 56473-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,7 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56473-92:
(7*5)+(6*6)+(5*4)+(4*7)+(3*3)+(2*9)+(1*2)=148
148 % 10 = 8
So 56473-92-8 is a valid CAS Registry Number.

56473-92-8Downstream Products

56473-92-8Relevant academic research and scientific papers

BICYCLIC HETEROAROMATIC CARBOXAMIDE COMPOUNDS USEFUL AS PIM KINASE INHIBITORS

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Page/Page column 137-138, (2016/02/26)

The present disclosure describes bicyclic heteroaromatic carboxamide derivatives of formula (I), as well as their compositions and methods of use. The compounds inhibit the activity of the Pim kinases, and are useful in the treatment of diseases related to the activity of Pim kinases including, e.g., cancer and other diseases.

ARYL SUBSTITUTED OLEFINIC COMPOUNDS AS PDE10A INHIBITORS

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Page/Page column 51-52, (2011/11/30)

The present invention provides aryl substituted olefinic compounds as Phosphodiesterase 1 0A (PDE 1 0A) inhibitors. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders by inhibiting Phospho

DIARYL 5,6-FUSED HETEROCYCLIC ACIDS AS LEUKOTRIENE ANTAGONISTS

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, (2008/06/13)

Compounds having the formula I: STR1 are antagonists of the actions of leukotrienes. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating angina, cerebral spasm, glomerular nephritis, hepatitis, endotoxemia, uveitis, and allograft rejection.

Furo[3,2-b]pyridines and thieno[3,2-b]pyridines as inhibitors of leukotriene biosynthesis

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, (2008/06/13)

Compounds having the formula I: STR1 are inhibitors of leukotriene biosynthesis. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating angina, cerebral spasm, glomemlar

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