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

Details

Stereochemistry ACHIRAL
Molecular Formula C25H38N2O
Molecular Weight 382.582
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUNAMIDINE

SMILES

CCCCCCOC1=C2C=CC=CC2=C(C=C1)C(=N)N(CCCC)CCCC

InChI

InChIKey=FGGFIMIICGZCCJ-UHFFFAOYSA-N
InChI=1S/C25H38N2O/c1-4-7-10-13-20-28-24-17-16-23(21-14-11-12-15-22(21)24)25(26)27(18-8-5-2)19-9-6-3/h11-12,14-17,26H,4-10,13,18-20H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C25H38N2O
Molecular Weight 382.582
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Bunamidine is a anti-parasitic drug, which was approved by FDA for the treatment of tapeworms in cats and dogs (Scolaban 400 tablets).

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
SCOLABAN 400

Approved Use

The drug is intended for oral administration to dogs for the treatment of the tapeworms Dipylidium caninum, Taenia pisiformis and Echinococcus granulosus and cats for the treatment of the tapeworms Dipylidium caninum and Taenia taeniaeformis.
PubMed

PubMed

TitleDatePubMed
The Hymenolepis diminuta-golden hamster (Mesocricetus auratus) model for the evaluation of gastrointestinal anticestode activity.
2004-08
The Styx Field Trial: effect of treatment of the definitive host for tapeworms on larval forms in the intermediate host.
1978
Evaluation of selected drugs for the treatment of canine echinococcosis.
1968
A NEW TAENIACIDE, BUNAMIDINE HYDROCHLORIDE: ITS EFFICIENCY AGAINST TAENIA PISIFORMIS AND DIPYLIDIUM CANINUM IN THE DOG AND HYDATIGERA TAENIAEFORMIS IN THE CAT.
1965-04-10

Sample Use Guides

It is administered to dogs at the rate of 25 to 50 milligrams per kilogram of body weight. The drug should be given on an empty stomach and food should not be given for 3 hours following treatment.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:49:36 GMT 2025
Edited
by admin
on Mon Mar 31 18:49:36 GMT 2025
Record UNII
A9IW1G3P6C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUNAMIDINE [MI]
Preferred Name English
BUNAMIDINE
INN   MI  
INN  
Official Name English
1-NAPHTHALENECARBOXIMIDAMIDE, N,N-DIBUTYL-4-(HEXYLOXY)-
Systematic Name English
N,N-DIBUTYL-4-(HEXYLOXY)-1-NAPHTHAMIDINE
Systematic Name English
bunamidine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C250
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
Code System Code Type Description
INN
2043
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
ChEMBL
CHEMBL1355596
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
CAS
3748-77-4
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
DRUG BANK
DB11501
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
NCI_THESAURUS
C81513
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
MESH
C100222
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
SMS_ID
100000088462
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
EVMPD
SUB05974MIG
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
PUBCHEM
13986
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
MERCK INDEX
m597
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY Merck Index
FDA UNII
A9IW1G3P6C
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
EPA CompTox
DTXSID4048272
Created by admin on Mon Mar 31 18:49:36 GMT 2025 , Edited by admin on Mon Mar 31 18:49:36 GMT 2025
PRIMARY
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY