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(1S,2R,5R)-5-(6-amino-9H-purin-9-yl)-3-[(1S)-1-hydroxyethyl]cyclopent-3-ene-1,2-diol is a nucleoside that features a cyclopentene ring, a purine base with an amino group at the 6-position, and a hydroxyethyl group. As a stereoisomer, it has a specific configuration at the 1S, 2R, and 5R positions. (1S,2R,5R)-5-(6-amino-9H-purin-9-yl)-3-[(1S)-1-hydroxyethyl]cyclopent-3-ene-1,2-diol is integral to nucleic acids, playing a vital role in the storage and transfer of genetic information.

138662-99-4

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138662-99-4 Usage

Uses

Used in Pharmaceutical Industry:
(1S,2R,5R)-5-(6-amino-9H-purin-9-yl)-3-[(1S)-1-hydroxyethyl]cyclopent-3-ene-1,2-diol serves as a key component in the development of pharmaceuticals targeting various diseases. Its presence in nucleic acids makes it a potential candidate for drugs that interfere with genetic processes, such as antiviral or anticancer medications.
Used in Biochemical Research:
In the field of biochemical research, (1S,2R,5R)-5-(6-amino-9H-purin-9-yl)-3-[(1S)-1-hydroxyethyl]cyclopent-3-ene-1,2-diol is utilized for studying the structure and function of nucleic acids, as well as understanding the mechanisms of genetic information storage and transfer. It can also be employed in the synthesis of nucleic acid analogs for research purposes.
Used in Diagnostic Applications:
(1S,2R,5R)-5-(6-amino-9H-purin-9-yl)-3-[(1S)-1-hydroxyethyl]cyclopent-3-ene-1,2-diol can be applied in diagnostic assays to detect and monitor diseases related to nucleic acid abnormalities. Its specific interaction with genetic material allows for the development of sensitive and accurate diagnostic tools.
Used in Genetic Engineering:
In genetic engineering, (1S,2R,5R)-5-(6-amino-9H-purin-9-yl)-3-[(1S)-1-hydroxyethyl]cyclopent-3-ene-1,2-diol may be used as a building block for the synthesis of custom-designed nucleic acid sequences. Its incorporation into engineered genetic constructs can enable the development of novel therapies and research tools.

Check Digit Verification of cas no

The CAS Registry Mumber 138662-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138662-99:
(8*1)+(7*3)+(6*8)+(5*6)+(4*6)+(3*2)+(2*9)+(1*9)=164
164 % 10 = 4
So 138662-99-4 is a valid CAS Registry Number.

138662-99-4SDS

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 (1S,2R,5R)-5-(6-aminopurin-9-yl)-3-[(1S)-1-hydroxyethyl]cyclopent-3-ene-1,2-diol

1.2 Other means of identification

Product number -
Other names 9[(1R,2S,3R)-2,3-dihydroxy-4-(1-hydroxyethyl)-4-cyclopenten-1-yl]adenine

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:138662-99-4 SDS

138662-99-4Downstream Products

138662-99-4Relevant academic research and scientific papers

New neplanocin analogues. IX. A practical preparation of (6'R)-6'-C- methylneplanocin A (RMNPA), a potent antiviral agent, and the determination of its 6'-configuration. Diastereoselective deamination by adenosine deaminase

Shuto, Satoshi,Obara, Takumi,Yaginuma, Satoshi,Matsuda, Akira

, p. 138 - 142 (1997)

We previously synthesized (6'R)- and (6'S)-6'-C-methylneplanocin A's (2a and 2b, respectively), and found that one of them has a potent antiviral activity, though its 6'-configuration has not been confirmed. This report describes the determination of the

New neplanocin analogues. 1. Synthesis of 6'-modified neplanocin A derivatives as broad-spectrum antiviral agents

Shuto,Obara,Toriya,Hosoya,Snoeck,Andrei,Balzarini,De Clercq

, p. 324 - 331 (2007/10/02)

Novel neplanocin A analogues modified at the 6'-position, i.e., 6'-deoxy analogues (2, 3, 6, 9, 20), 6'-O-methylneplanocin A (15), and 6'-C- methylneplanocin A's (22a and 22b) have been synthesized and evaluated for their antiviral activity in a wide vari

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