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Details

Stereochemistry RACEMIC
Molecular Formula C19H32N2O2.2ClH
Molecular Weight 393.391
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAMYLOFIN HYDROCHLORIDE

SMILES

Cl.Cl.CCN(CC)CCNC(C(=O)OCCC(C)C)C1=CC=CC=C1

InChI

InChIKey=ZHRVNCCPAKIGRH-UHFFFAOYSA-N
InChI=1S/C19H32N2O2.2ClH/c1-5-21(6-2)14-13-20-18(17-10-8-7-9-11-17)19(22)23-15-12-16(3)4;;/h7-11,16,18,20H,5-6,12-15H2,1-4H3;2*1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C19H32N2O2
Molecular Weight 320.4696
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: Description was created based on several sources, including http://www.ijrcog.org/index.php/ijrcog/article/view/1419

Camylofin is an antimuscarinic. This medication is used as antispasmodic in biliary colic, renal and ureteric colic, dysmenorrhoea, peptic ulcer and chronic enterocolitis. It is used to treat stomach ache in infants and children. Camylofin should be the first choice and may be preferred over other drugs for cervical dilatation and acceleration of active phase of labor.

Originator

Curator's Comment: refernce retrieved from https://www.ncbi.nlm.nih.gov/pubmed/13331655

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ANAFORTAN

Approved Use

Camylofin is used as an anti-spasmodic. Camylofin is primarily indicated in conditions like Angina, Biliary colic, Dysmenorrhoea, Migraine, Myocardial infarction, Pancreatitis, Renal colic, Spasticity.
Primary
ANAFORTAN

Approved Use

Camylofin is used as an anti-spasmodic. Camylofin is primarily indicated in conditions like Angina, Biliary colic, Dysmenorrhoea, Migraine, Myocardial infarction, Pancreatitis, Renal colic, Spasticity.
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

0.285 to 0.857 mg/kg to be taken every 8 hrs.
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:31:08 GMT 2023
Edited
by admin
on Fri Dec 15 15:31:08 GMT 2023
Record UNII
MO02H82C7M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAMYLOFIN HYDROCHLORIDE
MART.   WHO-DD  
Common Name English
CAMYLOFINE DIHYDROCHLORIDE [MI]
Common Name English
ISOPENTYL 2-(2-DIETHYLAMINOETHYLAMINO)-2-PHENYLACETATE DIHYDROCHLORIDE
Systematic Name English
CAMYLOFIN HCL
Common Name English
ACAMYLOPHENINE HYDROCHLORIDE [JAN]
Common Name English
Camylofin hydrochloride [WHO-DD]
Common Name English
CAMYLOFIN HYDROCHLORIDE [MART.]
Common Name English
ACAMYLOPHENINE HYDROCHLORIDE
JAN  
Common Name English
NSC-759249
Code English
CAMYLOPHENINE DIHYDROCHLORIDE
Common Name English
CAMYLOFINE HYDROCHLORIDE
Common Name English
Code System Code Type Description
MESH
C004644
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-571-0
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
RXCUI
236175
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY RxNorm
NSC
759249
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
PUBCHEM
22182
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
CAS
5892-41-1
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
ChEMBL
CHEMBL253592
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
MERCK INDEX
m99
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID70974421
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
SMS_ID
100000084848
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
EVMPD
SUB01018MIG
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
FDA UNII
MO02H82C7M
Created by admin on Fri Dec 15 15:31:08 GMT 2023 , Edited by admin on Fri Dec 15 15:31:08 GMT 2023
PRIMARY
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