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

Details

Stereochemistry ACHIRAL
Molecular Formula C18H18ClNO4
Molecular Weight 347.793
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLANOBUTIN

SMILES

COC1=CC=C(C=C1)N(CCCC(O)=O)C(=O)C2=CC=C(Cl)C=C2

InChI

InChIKey=VUPBWNXFSDRWJE-UHFFFAOYSA-N
InChI=1S/C18H18ClNO4/c1-24-16-10-8-15(9-11-16)20(12-2-3-17(21)22)18(23)13-4-6-14(19)7-5-13/h4-11H,2-3,12H2,1H3,(H,21,22)

HIDE SMILES / InChI

Molecular Formula C18H18ClNO4
Molecular Weight 347.793
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Clanobutin is a choleretic drug. It increases the secretion of bile by hepatocytes. Clanobutin sodium has been introduced as a choleretic and digestant agent for animals. It has been used in all domestic animals in which enhancement of digestion and all associated secretory processes are indicated. Clanobutin was reported to induce a demonstrable increase in the secretory activity of the exocrine digestive glands and in the excretion of the bile.

Approval Year

PubMed

PubMed

TitleDatePubMed
Nonfatal splenic haematoma and pancytopenia in an ass.
2004 Aug
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:02:10 GMT 2023
Edited
by admin
on Fri Dec 15 16:02:10 GMT 2023
Record UNII
W6Y945055S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLANOBUTIN
INN   MI  
INN  
Official Name English
CLANOBUTIN [MI]
Common Name English
4-(P-CHLORO-N-(P-METHOXYPHENYL)BENZAMIDO)BUTYRIC ACID
Common Name English
clanobutin [INN]
Common Name English
BYKAHEPAR
Brand Name English
Classification Tree Code System Code
WHO-VATC QA16QA05
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
NCI_THESAURUS C66913
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
Code System Code Type Description
EVMPD
SUB06639MIG
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
DRUG CENTRAL
3104
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
FDA UNII
W6Y945055S
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
SMS_ID
100000080169
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID10184628
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
MERCK INDEX
m3607
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
250-232-3
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
NCI_THESAURUS
C77837
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
INN
2907
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
PUBCHEM
35378
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107589
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
CAS
30544-61-7
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
MESH
C019159
Created by admin on Fri Dec 15 16:02:10 GMT 2023 , Edited by admin on Fri Dec 15 16:02:10 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY