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1-pentofuranosyl-1H-imidazo[4,5-d]pyridazin-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75909-15-8

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75909-15-8 Usage

Chemical class

Imidazo[4,5-d]pyridazine derivatives

Type of compound

Purine analog

Pharmacological activities

Potential anti-cancer properties

Mechanism of action

Inhibits DNA synthesis and cancer cell proliferation

Structure

Contains a pentofuranosyl group

Potential applications

Nucleoside analog for antiviral and antiparasitic drugs

Significance

Important target for research and development in medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 75909-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,0 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75909-15:
(7*7)+(6*5)+(5*9)+(4*0)+(3*9)+(2*1)+(1*5)=158
158 % 10 = 8
So 75909-15-8 is a valid CAS Registry Number.

75909-15-8SDS

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 2-(4-aminoimidazo[4,5-d]pyridazin-1-yl)-5-(hydroxymethyl)oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names 2-(5-amino-3,4,7,9-tetrazabicyclo[4.3.0]nona-1,3,5,7-tetraen-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

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:75909-15-8 SDS

75909-15-8Downstream Products

75909-15-8Relevant academic research and scientific papers

Synthesis and Biological Evaluation of N4-Substituted Imidazo- and v-Triazolopyridazine Nucleosides

Bussolari, Jacqueline C.,Ramesh, Kakarla,Stoeckler, Johanna D.,Chen, Shih-Fong,Panzica, Raymond P.

, p. 4113 - 4120 (1993)

The chemical synthesis of certain N4-substituted imidazopyridazine and v-triazolopyridazine nucleosides is described.In both series, the 4-chloro analogues, i.e., 4-chloro-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)imidazopyri

Purine nucleoside analogues for treating flaviviridae including hepatitis C

-

Page/Page column 67; 68, (2016/02/05)

This invention is directed to a method for treating a host, especially a human, infected with hepatitis C, flavivirus and/or pestivirus, comprising administering to that host an effective amount of an anti-HCV biologically active pentofuranonucleoside whe

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