CAMYLOFIN HYDROCHLORIDE

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 Search

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	C19H32N2O2
Molecular Weight	320.4696
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

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

Description
Sources: http://www.drugsupdate.com/generic/view/753/Camylofin
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

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Muscarinic acetylcholine receptor 162 Target ID: CHEMBL2094109 Sources: http://www.genome.jp/dbget-bin/www_bget?dr:D07076	Antagonist 2849

Conditions

Condition	Modality	Targets	Highest Phase	Product
Labor complications 8 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22895986 https://www.ncbi.nlm.nih.gov/pubmed/23737030 https://www.ncbi.nlm.nih.gov/pubmed/24179892 http://www.ijrcog.org/index.php/ijrcog/article/view/1419	Primary		Approved 8583	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.
Spasm 18 Sources: http://www.druginfosys.com/drug.aspx?drugcode=833&type=1 http://www.medclik.com/General/pages/Drugmanual/BrandSearch/ANAFORTAN.asp	Primary		Approved 8583	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.

Doses

Dose	Population	Adverse events
120 mg single, intramuscular Higher than recommended Dose: 120 mg Route: intramuscular Route: single Dose: 120 mg Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M Food Status: UNKNOWN Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/	Other AEs: Skin rash, Tachycardia... Other AEs: Skin rash (18.8%) Tachycardia (12.5%) Drowsiness (6.25%) Facial flushing (6.25%) Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/

AEs

AE	Significance	Dose	Population
Tachycardia	12.5%	120 mg single, intramuscular Higher than recommended Dose: 120 mg Route: intramuscular Route: single Dose: 120 mg Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M Food Status: UNKNOWN Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/
Skin rash	18.8%	120 mg single, intramuscular Higher than recommended Dose: 120 mg Route: intramuscular Route: single Dose: 120 mg Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M Food Status: UNKNOWN Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/
Drowsiness	6.25%	120 mg single, intramuscular Higher than recommended Dose: 120 mg Route: intramuscular Route: single Dose: 120 mg Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M Food Status: UNKNOWN Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/
Facial flushing	6.25%	120 mg single, intramuscular Higher than recommended Dose: 120 mg Route: intramuscular Route: single Dose: 120 mg Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/	unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M Food Status: UNKNOWN Sources: https://pubmed.ncbi.nlm.nih.gov/1729516/

PubMed

Title	Date	PubMed
Antispasmodics for labour.	2012-08-15	22895986
Development and characterization of colon specific drug delivery system bearing 5-ASA and Camylofine dihydrochloride for the treatment of ulcerative colitis.	2010-09	20088681
Determination of the analgesic components of Spasmomigraine tablet by liquid chromatography with ultraviolet detection.	2007-03-22	17373440
A study of metabolism of isoamyl alpha-[N-(beta-diethylamino-ethyl)]-aminophenylacetate (avacan).	1956-03	13331655
[Pharmacology of Avacan].	1951-04-06	14831430

Patents

Sample Use Guides

In Vivo Use Guide

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 `Mon Mar 31 17:59:47 GMT 2025` Edited by `admin` on `Mon Mar 31 17:59:47 GMT 2025`
Record UNII	MO02H82C7M
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

CAMYLOFIN HYDROCHLORIDE

Common Name

English

ACAMYLOPHENINE HYDROCHLORIDE

Preferred 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

NSC-759249

Code

English

CAMYLOPHENINE DIHYDROCHLORIDE

Common Name

English

CAMYLOFINE HYDROCHLORIDE

Common Name

English

Code System Code Type Description

MESH

C004644