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6-Carbamimidoyl-1H-indazole-3-carboxylic acid is a chemical compound with the molecular formula C9H7N5O2, belonging to the class of indazole derivatives. It features a carbamimidoyl group and a carboxylic acid group, which contribute to its potential pharmaceutical applications. 6-Carbamimidoyl-1H-indazole-3-carboxylic acid is known for its reported biological activities, such as antiviral and antitumor properties, making it a promising candidate for drug development and medicinal chemistry research. Its unique structure and properties render it an interesting target for further study and potential therapeutic applications.

199609-47-7

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199609-47-7 Usage

Uses

Used in Pharmaceutical Industry:
6-Carbamimidoyl-1H-indazole-3-carboxylic acid is used as a pharmaceutical candidate for its antiviral and antitumor properties. 6-Carbamimidoyl-1H-indazole-3-carboxylic acid's functional groups and unique structure allow it to target specific biological pathways, making it a valuable asset in the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 6-Carbamimidoyl-1H-indazole-3-carboxylic acid serves as a key compound for studying its potential interactions with biological targets. Its unique structure and functional groups provide insights into the design and synthesis of novel drugs with improved efficacy and selectivity.
Used in Drug Development:
6-Carbamimidoyl-1H-indazole-3-carboxylic acid is utilized in drug development as a lead compound for the creation of new therapeutic agents. Its antiviral and antitumor properties, along with its unique chemical structure, make it a promising starting point for the design of innovative medications to treat various diseases.
Used in Antiviral Applications:
6-Carbamimidoyl-1H-indazole-3-carboxylic acid is employed as an antiviral agent, targeting specific viral mechanisms to inhibit viral replication and reduce the severity of viral infections. Its unique structure and functional groups enable it to interact with viral proteins, making it a valuable tool in the development of antiviral therapies.
Used in Antitumor Applications:
In the context of antitumor applications, 6-Carbamimidoyl-1H-indazole-3-carboxylic acid is used to target and inhibit the growth of cancer cells. Its biological activities and unique structure allow it to interfere with tumor progression and potentially lead to the development of novel anticancer drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 199609-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,6,0 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199609-47:
(8*1)+(7*9)+(6*9)+(5*6)+(4*0)+(3*9)+(2*4)+(1*7)=197
197 % 10 = 7
So 199609-47-7 is a valid CAS Registry Number.

199609-47-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CARBAMIMIDOYL-1H-INDAZOLE-3-CARBOXYLIC ACID

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:199609-47-7 SDS

199609-47-7Downstream Products

199609-47-7Relevant academic research and scientific papers

Fibrinogen receptor (GPIIb-IIIa) antagonists derived from 5,6-bicyclic templates. Amidinoindoles, amidinoindazoles, and amidinobenzofurans containing the N-α-sulfonamide carboxylic acid function as potent platelet aggregation inhibitors

Su, Ting,Naughton, Mary Ann H.,Smyth, Mark S.,Rose, Jack W.,Arfsten, Ann E.,McCowan, Jefferson R.,Jakubowski, Joseph A.,Wyss, Virginia L.,Ruterbories, Kenneth J.,Sall, Daniel J.,Scarborough, Robert M.

, p. 4308 - 4318 (1997)

A series of highly potent and specific fibrinogen receptor antagonists have been discovered and optimized through structural modification of the novel amidinoindole and benzofuran compounds, I and II. Systematic linker optimization afforded the amidinoben

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