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

Approval Year

PubMed

PubMed

TitleDatePubMed
New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii.
1995-11-24
Treatment of experimental pneumocystosis: review of 7 years of experience and development of a new system for classifying antimicrobial drugs.
1992-09
Cationic antitrypanosomal and other antimicrobial agents in the therapy of experimental Pneumocystis carinii pneumonia.
1988-06
Name Type Language
Amicarbalide diisethionate
MI  
Common Name English
DIAMPRON
Preferred 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
DIAMPRONE
Brand Name English
NSC-528032
Code English
Code System Code Type Description
FDA UNII
FCC0RF48XI
Created by admin on Mon Mar 31 21:54:02 GMT 2025 , Edited by admin on Mon Mar 31 21:54:02 GMT 2025
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NSC
528032
Created by admin on Mon Mar 31 21:54:02 GMT 2025 , Edited by admin on Mon Mar 31 21:54:02 GMT 2025
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CAS
3671-72-5
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EPA CompTox
DTXSID80190175
Created by admin on Mon Mar 31 21:54:02 GMT 2025 , Edited by admin on Mon Mar 31 21:54:02 GMT 2025
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ECHA (EC/EINECS)
222-937-6
Created by admin on Mon Mar 31 21:54:02 GMT 2025 , Edited by admin on Mon Mar 31 21:54:02 GMT 2025
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PUBCHEM
12883609
Created by admin on Mon Mar 31 21:54:02 GMT 2025 , Edited by admin on Mon Mar 31 21:54:02 GMT 2025
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MERCK INDEX
m556
Created by admin on Mon Mar 31 21:54:02 GMT 2025 , Edited by admin on Mon Mar 31 21:54:02 GMT 2025
PRIMARY Merck Index