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70465-86-0

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70465-86-0 Usage

Medication Purpose

Treats HIV infection

Drug Class

Non-nucleoside reverse transcriptase inhibitors (NNRTIs)

Mechanism of Action

Interferes with the enzyme reverse transcriptase, which is used by the HIV virus to replicate its genetic material

Effect on HIV

Reduces the amount of virus in the body and helps to improve the immune system

Usage

Often used in combination with other HIV medications for effective management of the infection

Available Forms

Tablets and capsules

Dosage

Usually taken once daily

Potential Side Effects

Dizziness, drowsiness, vivid dreams

Drug Interactions

May interact with other medications

Professional Guidance

Should be used under the guidance of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 70465-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,6 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70465-86:
(7*7)+(6*0)+(5*4)+(4*6)+(3*5)+(2*8)+(1*6)=130
130 % 10 = 0
So 70465-86-0 is a valid CAS Registry Number.

70465-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2R,4S,5R)-4-ethylsulfanyl-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names Thymidine,3'-S-ethyl-3'-thio

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:70465-86-0 SDS

70465-86-0Downstream Products

70465-86-0Relevant articles and documents

Artificial nucleosides possessing metal binding sites at the 3′- and 5′-positions of the deoxyribose moieties

Chiba, Jun-ya,Tanaka, Kentaro,Ohshiro, Yukinori,Miyake, Ryosuke,Hiraoka, Shuichi,Shiro, Motoo,Shionoya, Mitsuhiko

, p. 331 - 338 (2007/10/03)

This paper describes a convenient synthetic procedure for nucleoside mimics, 1-6, in which the 3′,5′-hydroxy groups of natural 2′-deoxythymidine or 2′-deoxyadenosine are replaced by thiol, amine, or alkylthiol groups. Such nucleosides would be built up into a single DNA strand with cooperative participation of metal coordination, where internucleoside linkages are replaced by metal complexation motifs. The X-ray crystal structure and complexation behaviors of 3′,5′-dithiothymidine, 1, with AuI are also reported.

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