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162648-46-6

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162648-46-6 Usage

General Description

1-Methyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid is a chemical compound with potential pharmaceutical applications. It is a carboxylic acid derivative of tetrahydroquinoline, which is a heterocyclic compound containing a quinolone ring. 1-METHYL-1,2,3,4-TETRAHYDRO-QUINOLINE-6-CARBOXYLIC ACID has been studied for its potential medicinal properties, including as an anti-inflammatory agent and a potential treatment for neurodegenerative diseases. Its structure and functional groups make it a promising candidate for further pharmaceutical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 162648-46-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,6,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162648-46:
(8*1)+(7*6)+(6*2)+(5*6)+(4*4)+(3*8)+(2*4)+(1*6)=146
146 % 10 = 6
So 162648-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO2/c1-12-6-2-3-8-7-9(11(13)14)4-5-10(8)12/h4-5,7H,2-3,6H2,1H3,(H,13,14)

162648-46-6Relevant articles and documents

INHIBITORS OF ENL/AF9 YEATS

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Paragraph 00137; 00139, (2021/06/26)

Methods and compositions for treating leukemia are disclosed. Acylated 6-aminoindoles, acylated 6-aminopyrrolopyridines and acylated 3-aminopyrrolo[3,2-c]pyridazines of the following formula inhibit ENL/AF9 YEATS and are therefore useful for treating leukemia.

FUSED 1,4-DIHYDRODIOXIN DERIVATIVES AS INHIBITORS OF HEAT SHOCK TRANSCRIPTION FACTOR 1

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, (2015/04/22)

The present invention relates to compounds of formula I wherein A1, A2 R4 and Q are as defined herein. The compounds of the present invention are inhibitors of heat shock factor 1 (HSF1). In particular, the present invention relates to the use of these compounds as therapeutic agents for the treatment and/or prevention of proliferative diseases, such as cancer. The present invention also relates to processes for the preparation of these compounds, and to pharmaceutical compositions comprising them.

Heterocyclic esters of rapamycin

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, (2008/06/13)

A compound of the structure STR1 wherein R and R1 are each, independently, STR2 or hydrogen, R2 is a heterocyclic radical which may be optionally substituted; n=0-6; with the proviso that R and R1 are both not hydrogen, or a pharmaceutically acceptable salt thereof which is useful as an immunosuppressive, antiinflammatory, antifungal, antiproliferative, and antitumor agent.

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