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568570-13-8

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568570-13-8 Usage

Also known as

Lamivudine

Type

Synthetic nucleoside analogue
Antiviral properties

Uses

Treatment of HIV and hepatitis B infections

Mechanism of action

Inhibits the reverse transcriptase enzyme
Reduces viral load in the body
Slows down disease progression

Administration

Oral

Tolerance

Generally well-tolerated

Common side effects

Nausea, headache, fatigue
Component of combination antiretroviral therapy for HIV management
First-line treatment for chronic hepatitis B

Check Digit Verification of cas no

The CAS Registry Mumber 568570-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,8,5,7 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 568570-13:
(8*5)+(7*6)+(6*8)+(5*5)+(4*7)+(3*0)+(2*1)+(1*3)=188
188 % 10 = 8
So 568570-13-8 is a valid CAS Registry Number.

568570-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(Chloromethyl)-N-(2-methylphenyl)-1,3,5-triazine-2,4-diamine

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:568570-13-8 SDS

568570-13-8Relevant articles and documents

Synthesis and antiviral activity of benzimidazolyl-and triazolyl-1,3,5- triazines

Maarouf, Azza R.,Farahat, Abdelbasset A.,Selim, Khalid B.,Eisa, Hassan M.

, p. 703 - 710 (2012/09/22)

A novel series of 1,3,5-triazine analogs was successfully synthesized through conjugation with benzimidazole or 1,2,4-triazole derivatives via a methylenethio linker. The new analogs were in vitro evaluated against HSV-1 in Vero cells; among these analogs, two compounds exhibited good effect in inhibiting HSV-1 replication (for compound 5p: EC50 = 3.5 μg/ml, SI = 358; for compound 5r: EC50 = 5.0 μg/ml, SI = 300) in comparison to acyclovir. Springer Science+Business Media, LLC 2011.

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