2'-O-METHYLADENOSINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C11H15N5O4
Molecular Weight	281.2679
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of 2'-O-METHYLADENOSINE

Structure Search

SMILES

CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N2C=NC3=C2N=CN=C3N

InChI

InChIKey=FPUGCISOLXNPPC-IOSLPCCCSA-N

InChI=1S/C11H15N5O4/c1-19-8-7(18)5(2-17)20-11(8)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17-18H,2H2,1H3,(H2,12,13,14)/t5-,7-,8-,11-/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary Target	Pharmacology	Condition	Potency
RNA 19 Target ID: RNA Sources: https://www.ncbi.nlm.nih.gov/pubmed/9383369 \| https://www.ncbi.nlm.nih.gov/pubmed/22496660	Modulator 828

PubMed

PubMed

Title	Date	PubMed
The role of magnesium ions and 2'-hydroxyl groups in the VS ribozyme-substrate interaction.	2002 Nov 22	12441101
Use of nucleotide analogs by class I and class II CCA-adding enzymes (tRNA nucleotidyltransferase): deciphering the basis for nucleotide selection.	2003 Aug	12869708

Name

Type

Language

2'-O-METHYLADENOSINE

Systematic Name

English

ADENOSINE, 2'-O-METHYL-

Systematic Name

English

Code System Code Type Description

MESH

C024341

Created by admin on Fri Dec 15 18:41:54 GMT 2023 , Edited by admin on Fri Dec 15 18:41:54 GMT 2023

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FDA UNII

02YX82IHZ5

Created by admin on Fri Dec 15 18:41:54 GMT 2023 , Edited by admin on Fri Dec 15 18:41:54 GMT 2023

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PUBCHEM

102213

Created by admin on Fri Dec 15 18:41:54 GMT 2023 , Edited by admin on Fri Dec 15 18:41:54 GMT 2023

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CAS

2140-79-6

Created by admin on Fri Dec 15 18:41:54 GMT 2023 , Edited by admin on Fri Dec 15 18:41:54 GMT 2023

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CHEBI

69426

Created by admin on Fri Dec 15 18:41:54 GMT 2023 , Edited by admin on Fri Dec 15 18:41:54 GMT 2023

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EPA CompTox

DTXSID50175671

Created by admin on Fri Dec 15 18:41:54 GMT 2023 , Edited by admin on Fri Dec 15 18:41:54 GMT 2023

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SUBSTANCE RECORD


					02YX82IHZ5

2'-O-METHYLADENOSINE