T-0902611

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C13H16N6O3.C6H6O3S
Molecular Weight	462.48
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OS(=O)(=O)C1=CC=CC=C1.C[C@H]2COCCN2C3=NC(C)=C(C(=N3)N4C=CN=C4)[N+]([O-])=O

InChI

InChIKey=GPJYNQNPOAOBPJ-FVGYRXGTSA-N

InChI=1S/C13H16N6O3.C6H6O3S/c1-9-7-22-6-5-18(9)13-15-10(2)11(19(20)21)12(16-13)17-4-3-14-8-17;7-10(8,9)6-4-2-1-3-5-6/h3-4,8-9H,5-7H2,1-2H3;1-5H,(H,7,8,9)/t9-;/m0./s1

HIDE SMILES / InChI

Molecular Formula	C6H6O3S
Molecular Weight	158.175
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C13H16N6O3
Molecular Weight	304.3045
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Tue Apr 01 16:28:43 GMT 2025` Edited by `admin` on `Tue Apr 01 16:28:43 GMT 2025`
Record UNII	YJN0IQX3S4
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

T-0902611

Code

English

T-902611

Preferred Name

English

T-2611

Code

English

T 611

Code

English

T-611

Code

English

2-(3S-3-METHYLMORPHOLINO)-4-(IMIDAZOL-1-YL)-6-METHYL-5-NITROPYRIMIDINE BENZENESULFONATE

Systematic Name

English

MORPHOLINE, 4-(4-(1H-IMIDAZOL-1-YL)-6-METHYL-5-NITRO-2-PYRIMIDINYL)-3-METHYL-, (3S)-, BENZENESULFONATE (1:1)

Systematic Name

English

BENZENESULFONIC ACID; (3S)-4-(4-IMIDAZOL-1-YL-6-METHYL-5-NITRO-PYRIMIDIN-2-YL)-3-METHYL-MORPHOLINE

Systematic Name

English

AIDS-111759

Code

English

AIDS111759

Code

English

Code System Code Type Description

MANUFACTURER PRODUCT INFORMATION

T-902611

Created by admin on Tue Apr 01 16:28:43 GMT 2025 , Edited by admin on Tue Apr 01 16:28:43 GMT 2025

PRIMARY

CAS

350595-61-8

Created by admin on Tue Apr 01 16:28:43 GMT 2025 , Edited by admin on Tue Apr 01 16:28:43 GMT 2025

PRIMARY

FDA UNII

YJN0IQX3S4

Created by admin on Tue Apr 01 16:28:43 GMT 2025 , Edited by admin on Tue Apr 01 16:28:43 GMT 2025

PRIMARY

PUBCHEM

9890530

Created by admin on Tue Apr 01 16:28:43 GMT 2025 , Edited by admin on Tue Apr 01 16:28:43 GMT 2025

PRIMARY

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Related Record Type Details


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T-0902611

ACTIVE MOIETY

Comments:

Class Antivirals: Small molecules; Mechanism of Action: Cytomegalovirus replication inhibitor; Highest Development Phase: Discontinued for Cytomegalovirus infection; Most Recent Events: 17 Jun 2002 Discontinued for Phase-II for Cytomegalovirus infections (PO)


					YJN0IQX3S4

T-0902611

ACTIVE MOIETY

Comments:

Synthesis of T-902611.


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ACTIVE MOIETY

Comments:

the nitropyrimidines (for example, T-0902611) inhibit HCMV.