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2-(1H-INDAZOL-3-YL)-ACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103755-46-0

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103755-46-0 Usage

Chemical Class

Acetamides

Contains an indazole ring

Provides potential for diverse interactions with biological targets

Used in research and pharmaceutical applications

Due to potential pharmacological properties

Biological activities

Antiviral, anticancer, and antibacterial properties

Interaction with biological systems

Potential to act as a pharmaceutical agent

Promising candidate for further study and drug development

Due to its diverse range of interactions and potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 103755-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,5 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103755-46:
(8*1)+(7*0)+(6*3)+(5*7)+(4*5)+(3*5)+(2*4)+(1*6)=110
110 % 10 = 0
So 103755-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O/c10-9(13)5-8-6-3-1-2-4-7(6)11-12-8/h1-4H,5H2,(H2,10,13)(H,11,12)

103755-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2H-indazol-3-yl)acetamide

1.2 Other means of identification

Product number -
Other names indazole-3-acetamide

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:103755-46-0 SDS

103755-46-0Relevant academic research and scientific papers

Novel indolylindazolylmaleimides as inhibitors of protein kinase C-β: Synthesis, biological activity, and cardiovascular safety

Zhang, Han-Cheng,Derian, Claudia K.,McComsey, David F.,White, Kimberly B.,Ye, Hong,Hecker, Leonard R.,Li, Jian,Addo, Michael F.,Croll, Diane,Eckardt, Annette J.,Smith, Charles E.,Li, Quan,Cheung, Wai-Man,Conway, Bruce R.,Emanuel, Stuart,Demarest, Keith T.,Andrade-Gordon, Patricia,Damiano, Bruce P.,Maryanoff, Bruce E.

, p. 1725 - 1728 (2005)

Novel indolylindazolylmaleimides were synthesized and examined for kinase inhibition. We identified low-nanomolar inhibitors of PKC-β with good to excellent selectivity vs other PKC isozymes and GSK-3β. In a cell-based functional assay, 8f and 8i effectiv

SUBSTITUTED PYRROLINES AS KINASE INHIBITORS

-

Page 70, (2008/06/13)

The present invention is directed to novel substituted pyrroline compounds useful as kinase or dual-kinase inhibitors, methods for producing such compounds and methods for treating or ameliorating a kinase or dual-kinase mediated disorder.

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