AMPYRIMINE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C12H11N7
Molecular Weight	253.2626
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of AMPYRIMINE

Structure Search

SMILES

NC1=NC2=NC(N)=NC(C3=CC=CC=C3)=C2C(N)=N1

InChI

InChIKey=KTPVSQNBBGUGAJ-UHFFFAOYSA-N

InChI=1S/C12H11N7/c13-9-7-8(6-4-2-1-3-5-6)16-11(14)18-10(7)19-12(15)17-9/h1-5H,(H6,13,14,15,16,17,18,19)

HIDE SMILES / InChI

Molecular Formula	C12H11N7
Molecular Weight	253.2626
Charge	0
Count

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

Description
Sources: https://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&ns=NCI_Thesaurus&code=C81072 | https://books.google.ru/books?id=0vXTBwAAQBAJ&pg=PA1229&lpg=PA1229&dq=AMPYRIMINE retrieved from The Dictionary of Drugs: Chemical Data. Chemical Data, Structures and Bibliographies. Editors: Elks, J., p.1229

Ampyrimine is a diuretic agent.

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:20:04 GMT 2025` Edited by `admin` on `Mon Mar 31 18:20:04 GMT 2025`
Record UNII	X26VF7L4AL
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

SKF 13338

Preferred Name

English

AMPYRIMINE

Official Name

English

2,4,7-TRIAMINO-5-PHENYLPYRIMIDO(4,5-D)PYRIMIDINE

Systematic Name

English

SKF-13338

Code

English

5-Phenylpyrimido[4,5-d]pyrimidine-2,4,7-triamine

Systematic Name

English

ampyrimine [INN]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C448

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

Code System Code Type Description

NCI_THESAURUS

C81072

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

INN

1516

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

ChEMBL

CHEMBL2107705

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

FDA UNII

X26VF7L4AL

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

PUBCHEM

21779

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

CAS

5587-93-9

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

EVMPD

SUB05490MIG

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

SMS_ID

100000086935

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

EPA CompTox

DTXSID00204465

Created by admin on Mon Mar 31 18:20:04 GMT 2025 , Edited by admin on Mon Mar 31 18:20:04 GMT 2025

PRIMARY

Related Record Type Details


					X26VF7L4AL

ACTIVE MOIETY