METHYLTHIOINOSINE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Investigational

Investigational

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C11H14N4O4S
Molecular Weight	298.318
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of METHYLTHIOINOSINE

Structure Search

SMILES

CSC1=NC=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O

InChI

InChIKey=ZDRFDHHANOYUTE-IOSLPCCCSA-N

InChI=1S/C11H14N4O4S/c1-20-10-6-9(12-3-13-10)15(4-14-6)11-8(18)7(17)5(2-16)19-11/h3-5,7-8,11,16-18H,2H2,1H3/t5-,7-,8-,11-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C11H14N4O4S
Molecular Weight	298.318
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	4 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

PubMed

Title	Date	PubMed
Molecular mechanisms underlying the enhanced sensitivity of thiopurine-resistant T-lymphoblastic cell lines to methyl mercaptopurineriboside.	2006-09-28	16859645
Synthesis and antiviral activity of certain carbamoylpyrrolopyrimidine and pyrazolopyrimidine nucleosides.	1982-11	7143371
Purine analogs as potential anticytomegalovirus agents.	1969-09	4309475

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 17:49:46 GMT 2025` Edited by `admin` on `Mon Mar 31 17:49:46 GMT 2025`
Record UNII	Y5G39SHR0V
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

METHYLTHIOINOSINE

Systematic Name

English

NCI-C04784

Preferred Name

English

INOSINE, 6-S-METHYL-6-THIO-

Systematic Name

English

NSC-49555

Code

English

NSC-40774

Code

English

SQ-21977

Code

English

6-METHYLMERCAPTOPURINE RIBOSIDE

Common Name

English

Code System Code Type Description

EVMPD

SUB179122

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

PRIMARY

CHEBI

44081

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

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FDA UNII

Y5G39SHR0V

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

PRIMARY

ECHA (EC/EINECS)

206-442-2

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

PRIMARY

PUBCHEM

9570

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

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EPA CompTox

DTXSID5030454

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

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NCI_THESAURUS

C2352

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

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CAS

342-69-8

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

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SMS_ID

100000164627

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

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DRUG BANK

DB02896

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

PRIMARY

NSC

49555

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

PRIMARY

NSC

40774

Created by admin on Mon Mar 31 17:49:46 GMT 2025 , Edited by admin on Mon Mar 31 17:49:46 GMT 2025

PRIMARY

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SOLVATE->ANHYDROUS