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3-AMINO-3,4-DIHYDRO-1,5-NAPHTHYRIDIN-2(1H)-ONE is a heterocyclic chemical compound belonging to the naphthyridinone class. It features a distinctive naphthyridine ring system with an incorporated amino group and a dihydro-1,5-naphthyridin-2-one moiety. 3-AMINO-3,4-DIHYDRO-1,5-NAPHTHYRIDIN-2(1H)-ONE has garnered interest due to its potential pharmaceutical properties, such as being a prospective anti-inflammatory and anti-tumor agent. Its unique chemical structure and properties render it a promising candidate for further research and possible drug development.

600157-67-3

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600157-67-3 Usage

Uses

Used in Pharmaceutical Industry:
3-AMINO-3,4-DIHYDRO-1,5-NAPHTHYRIDIN-2(1H)-ONE is used as a potential anti-inflammatory agent for its capacity to modulate inflammatory responses, which could be beneficial in treating various inflammatory conditions.
3-AMINO-3,4-DIHYDRO-1,5-NAPHTHYRIDIN-2(1H)-ONE is also used as a potential anti-tumor agent due to its ability to target and inhibit the growth of tumor cells, making it a candidate for cancer therapy and potentially leading to the development of new anticancer drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 600157-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,0,1,5 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 600157-67:
(8*6)+(7*0)+(6*0)+(5*1)+(4*5)+(3*7)+(2*6)+(1*7)=113
113 % 10 = 3
So 600157-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O/c9-5-4-7-6(11-8(5)12)2-1-3-10-7/h1-3,5H,4,9H2,(H,11,12)

600157-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-3,4-dihydro-1H-1,5-naphthyridin-2-one

1.2 Other means of identification

Product number -
Other names -

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:600157-67-3 SDS

600157-67-3Relevant academic research and scientific papers

HETEROCYCLIC AMIDE DERIVATIVES WHICH POSSES GLYCOGEN PHOSPHORYLASE INHIBITORY ACTIVITY

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Page/Page column 71, (2010/02/11)

Heterocyclic amides of formula (1) wherein: B is selected from R4 and R 5 together are either -S-C(R 6)=C(R 7)_ or _C(R7)=C(R6)_SA is a pyridylene ring; m is 0, 1 or 2; n is 0 or 1; R 2 is for example selected from (I -4C)alkyl, hydroxy(l -4C)alkyl, dihydroxy(2-4C)alkyl and (1 -4C)aIkoxy(1 -4C)alkyl. or a pharmaceutically acceptable salt possess glycogen phosphorylase inhibitory activity and accordingly have value in the treatment of disease states associated with increased glycogen phosphorylase activity. Processes for the manufacture of said heterocyclic amide derivatives, intermediates in said processes and pharmaceutical compositions containing the heterocyclic amide derivatives are described.

HETEROCYCLIC AMIDE DERIVATIVES AS INHIBITORS OF GLYCOGEN PHOSPHORYLASE

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Page/Page column 108, (2010/02/07)

Heterocyclic amides of formula (1) wherein: X is N or CH; R4 and R5together are either -S-C(R6)=C(R7)- or -C(R7)=C(R6)-S-; R6 and R7 are independently selected from, f

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