EMIMYCIN

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C4H4N2O2
Molecular Weight	112.0868
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of EMIMYCIN

Structure Search

SMILES

[O-][N+]1=CC(=O)NC=C1

InChI

InChIKey=PJILVKTWPIWODW-UHFFFAOYSA-N

InChI=1S/C4H4N2O2/c7-4-3-6(8)2-1-5-4/h1-3H,(H,5,7)

HIDE SMILES / InChI

Molecular Formula	C4H4N2O2
Molecular Weight	112.0868
Charge	0
Count

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

Approval Year

PubMed

PubMed

Title	Date	PubMed
Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.	1994-08-17	8080452
Toxoplasma gondii: the biochemical basis of resistance to emimycin.	1989-08	2526747

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:49:54 GMT 2025` Edited by `admin` on `Mon Mar 31 20:49:54 GMT 2025`
Record UNII	R14TE35LHD
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

NSC-119867

Preferred Name

English

EMIMYCIN

Common Name

English

4-OXIDO-1,3-DIHYDROPYRAZIN-2-ONE

Systematic Name

English

Code System Code Type Description

CAS

3735-46-4

Created by admin on Mon Mar 31 20:49:54 GMT 2025 , Edited by admin on Mon Mar 31 20:49:54 GMT 2025

PRIMARY

FDA UNII

R14TE35LHD

Created by admin on Mon Mar 31 20:49:54 GMT 2025 , Edited by admin on Mon Mar 31 20:49:54 GMT 2025

PRIMARY

NSC

119867

Created by admin on Mon Mar 31 20:49:54 GMT 2025 , Edited by admin on Mon Mar 31 20:49:54 GMT 2025

PRIMARY

PUBCHEM

274093

Created by admin on Mon Mar 31 20:49:54 GMT 2025 , Edited by admin on Mon Mar 31 20:49:54 GMT 2025

PRIMARY

EPA CompTox

DTXSID50958461

Created by admin on Mon Mar 31 20:49:54 GMT 2025 , Edited by admin on Mon Mar 31 20:49:54 GMT 2025

PRIMARY