U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C15H16N6O.2C2H6O4S
Molecular Weight 548.59
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMICARBALIDE DIISETHIONATE

SMILES

OCCS(O)(=O)=O.OCCS(O)(=O)=O.NC(=N)C1=CC=CC(NC(=O)NC2=CC=CC(=C2)C(N)=N)=C1

InChI

InChIKey=PWUMRNFCZFZXAE-UHFFFAOYSA-N
InChI=1S/C15H16N6O.2C2H6O4S/c16-13(17)9-3-1-5-11(7-9)20-15(22)21-12-6-2-4-10(8-12)14(18)19;2*3-1-2-7(4,5)6/h1-8H,(H3,16,17)(H3,18,19)(H2,20,21,22);2*3H,1-2H2,(H,4,5,6)

HIDE SMILES / InChI

Molecular Formula C15H16N6O
Molecular Weight 296.3271
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C2H6O4S
Molecular Weight 126.132
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Amicarbalide (Diampron) is an aromatic diamidine exerting piroplasmocidal properties. It is effective against bovine and equine babesiosis and anaplasmosis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Cationic antitrypanosomal and other antimicrobial agents in the therapy of experimental Pneumocystis carinii pneumonia.
1988 Jun
Treatment of experimental pneumocystosis: review of 7 years of experience and development of a new system for classifying antimicrobial drugs.
1992 Sep
New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii.
1995 Nov 24
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:07:47 GMT 2023
Edited
by admin
on Sat Dec 16 08:07:47 GMT 2023
Record UNII
FCC0RF48XI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMICARBALIDE DIISETHIONATE
MI  
Common Name English
ETHANESULFONIC ACID, 2-HYDROXY-, COMPD. WITH 3,3'-(CARBONYLDIIMINO)BIS(BENZENECARBOXIMIDAMIDE) (2:1)
Systematic Name English
AMICARBALIDE DIISETHIONATE [MI]
Common Name English
M&B-5062A
Code English
DIAMPRON
Brand Name English
DIAMPRONE
Brand Name English
NSC-528032
Code English
Code System Code Type Description
FDA UNII
FCC0RF48XI
Created by admin on Sat Dec 16 08:07:48 GMT 2023 , Edited by admin on Sat Dec 16 08:07:48 GMT 2023
PRIMARY
NSC
528032
Created by admin on Sat Dec 16 08:07:48 GMT 2023 , Edited by admin on Sat Dec 16 08:07:48 GMT 2023
PRIMARY
CAS
3671-72-5
Created by admin on Sat Dec 16 08:07:48 GMT 2023 , Edited by admin on Sat Dec 16 08:07:48 GMT 2023
PRIMARY
EPA CompTox
DTXSID80190175
Created by admin on Sat Dec 16 08:07:48 GMT 2023 , Edited by admin on Sat Dec 16 08:07:48 GMT 2023
PRIMARY
ECHA (EC/EINECS)
222-937-6
Created by admin on Sat Dec 16 08:07:48 GMT 2023 , Edited by admin on Sat Dec 16 08:07:48 GMT 2023
PRIMARY
PUBCHEM
12883609
Created by admin on Sat Dec 16 08:07:48 GMT 2023 , Edited by admin on Sat Dec 16 08:07:48 GMT 2023
PRIMARY
MERCK INDEX
m556
Created by admin on Sat Dec 16 08:07:48 GMT 2023 , Edited by admin on Sat Dec 16 08:07:48 GMT 2023
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY