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114748-67-3

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114748-67-3 Usage

Description

7-Iodo-2',3'-Dideoxy-7-Deaza-Guanosine is a chemical compound with the molecular formula C10H12IN5O3. It is a modified nucleoside analog of guanosine, featuring a deaza or deoxyriboside sugar moiety and an iodo substituent at the 7 position. 7-Iodo-2',3'-Dideoxy-7-Deaza-Guanosine has been studied for its potential antiviral activity, particularly against herpes simplex virus and human immunodeficiency virus (HIV), and is believed to inhibit viral replication by interfering with the synthesis of viral DNA. Additionally, due to its unique structure, 7-Iodo-2',3'-Dideoxy-7-Deaza-Guanosine is also being investigated for its potential use in cancer therapy. Overall, this chemical compound shows promise for various therapeutic applications due to its distinct structure and potential antiviral and anticancer properties.

Uses

Used in Antiviral Applications:
7-Iodo-2',3'-Dideoxy-7-Deaza-Guanosine is used as an antiviral agent for its potential activity against herpes simplex virus and human immunodeficiency virus (HIV). It functions by inhibiting the synthesis of viral DNA, thereby preventing viral replication and reducing the spread of the virus in the body.
Used in Cancer Therapy:
7-Iodo-2',3'-Dideoxy-7-Deaza-Guanosine is used as a potential therapeutic agent in cancer treatment. Its unique structure and properties are being investigated for their potential to target and inhibit the growth of cancer cells, offering a new avenue for cancer therapy.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 7-Iodo-2',3'-Dideoxy-7-Deaza-Guanosine is used as a research compound for the development of new antiviral and anticancer drugs. Its distinct structure and potential therapeutic properties make it a valuable candidate for further investigation and potential incorporation into novel therapeutic agents.
Used in Biomedical Research:
7-Iodo-2',3'-Dideoxy-7-Deaza-Guanosine is used as a research tool in biomedical research to study the mechanisms of viral replication and cancer cell growth. Its unique properties allow researchers to gain insights into the molecular processes involved in these diseases, potentially leading to the discovery of new targets for treatment and the development of more effective therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 114748-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,4 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114748-67:
(8*1)+(7*1)+(6*4)+(5*7)+(4*4)+(3*8)+(2*6)+(1*7)=133
133 % 10 = 3
So 114748-67-3 is a valid CAS Registry Number.

114748-67-3SDS

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 2-Amino-7-((S)-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-iodo-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-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:114748-67-3 SDS

114748-67-3Relevant articles and documents

The Use of Heterocyclic Chemistry in the Synthesis of Natural and Unnatural Products

Confalone, Pat. N.

, p. 31 - 46 (2007/10/02)

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