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Details

Stereochemistry ACHIRAL
Molecular Formula C20H15NO3
Molecular Weight 317.338
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXYPHENISATIN

SMILES

OC1=CC=C(C=C1)C2(C(=O)NC3=CC=CC=C23)C4=CC=C(O)C=C4

InChI

InChIKey=SJDACOMXKWHBOW-UHFFFAOYSA-N
InChI=1S/C20H15NO3/c22-15-9-5-13(6-10-15)20(14-7-11-16(23)12-8-14)17-3-1-2-4-18(17)21-19(20)24/h1-12,22-23H,(H,21,24)

HIDE SMILES / InChI

Molecular Formula C20H15NO3
Molecular Weight 317.338
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Oxyphenisatin is a stimulant laxative that has been used by mouth and as an enema. Oxyphenisatin was introduced as Lavema by Winthrop in US in 1959. Oxyphenisatin was used as a cleansing enema apart from x-ray studies and prior to urinary, gastro-intestinal and cholecystography x-ray examination. Oxyphenisatin was also used for preoperative preparation of the large intestine and colon. May be mixed with barium for x-ray examination of the large intestine. Oxyphenisatin may cause jaundice. Oxyphenisatin-induced liver damage usually occurs when the drug has been taken for at least six months and usually two years. Oxyphenisatin was withdrawn in most countries in the early 1970s.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
LAVEMA

Approved Use

Indications.-May be used as a cleansing enema apart from x-ray studies and prior to urinary, gastro-intestinal and cholecystography x-ray examination. Also preoperative preparation of the large intestine and colon. May be mixed with barium for x-ray examination of the large intestine.
Diagnostic
LAVEMA

Approved Use

Indications.-May be used as a cleansing enema apart from x-ray studies and prior to urinary, gastro-intestinal and cholecystography x-ray examination. Also preoperative preparation of the large intestine and colon. May be mixed with barium for x-ray examination of the large intestine.
Doses

Doses

DosePopulationAdverse events​
5 mg 2 times / day multiple, oral
Dose: 5 mg, 2 times / day
Route: oral
Route: multiple
Dose: 5 mg, 2 times / day
Sources:
unhealthy, 19-84 years
n = 32
Health Status: unhealthy
Condition: chronic non-alcoholic liver disease
Age Group: 19-84 years
Sex: M+F
Population Size: 32
Sources:
Other AEs: Liver damage...
Other AEs:
Liver damage
Sources:
7.5 mg 1 times / day multiple, oral
Dose: 7.5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 7.5 mg, 1 times / day
Sources:
unhealthy, 65 years
n = 1
Health Status: unhealthy
Age Group: 65 years
Sex: F
Population Size: 1
Sources:
Disc. AE: Hepatitis...
AEs leading to
discontinuation/dose reduction:
Hepatitis
Sources:
AEs

AEs

AESignificanceDosePopulation
Liver damage
5 mg 2 times / day multiple, oral
Dose: 5 mg, 2 times / day
Route: oral
Route: multiple
Dose: 5 mg, 2 times / day
Sources:
unhealthy, 19-84 years
n = 32
Health Status: unhealthy
Condition: chronic non-alcoholic liver disease
Age Group: 19-84 years
Sex: M+F
Population Size: 32
Sources:
Hepatitis Disc. AE
7.5 mg 1 times / day multiple, oral
Dose: 7.5 mg, 1 times / day
Route: oral
Route: multiple
Dose: 7.5 mg, 1 times / day
Sources:
unhealthy, 65 years
n = 1
Health Status: unhealthy
Age Group: 65 years
Sex: F
Population Size: 1
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: https://www.ncbi.nlm.nih.gov/pubmed/5024726
Cleansing enema: Lavema (Oxyphenisatin) in a dosage of from 1.5 to 3 g. should be thoroughly mixed in 1 to 2 quarts of water. Radiopaque (barium) enema adjuvant: Lavema in a dosage of from 1.5 to 3 g. should be added to the usu-al 1 to 2 quarts of barium enema suspension and well mixed, preferably in an electric mixer, to obtain uniform dispersion (1/2 packet for elderly and debilitated patients).
Route of Administration: Other
In Vitro Use Guide
Oxyphenisatin (10(-5) M, mucosal side) and deoxycholate (3 X 10(-4) M, mucosal side) completely blocked net water and sodium absorption in an everted sac preparation of stripped rat colon.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:04:37 GMT 2023
Edited
by admin
on Fri Dec 15 15:04:37 GMT 2023
Record UNII
3BT0VQG2GQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OXYPHENISATIN
Common Name English
NSC-59814
Code English
OXYPHENISATINE [MART.]
Common Name English
3,3-BIS(P-HYDROXYPHENYL)-2-INDOLINONE
Common Name English
Oxyphenisatine [WHO-DD]
Common Name English
oxyphenisatine [INN]
Common Name English
OXYPHENISATINE
INN   MART.   WHO-DD  
INN  
Official Name English
ISAPHEN
Brand Name English
Classification Tree Code System Code
WHO-ATC A06AB01
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
WHO-VATC QA06AB01
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
NCI_THESAURUS C29697
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
WHO-ATC A06AB20
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID5044528
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
FDA UNII
3BT0VQG2GQ
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-728-1
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
NCI_THESAURUS
C80953
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
PUBCHEM
31315
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
RXCUI
8136
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY RxNorm
DRUG CENTRAL
2038
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
NSC
59814
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
SMS_ID
100000082755
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
WIKIPEDIA
OXYPHENISATINE
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
ChEMBL
CHEMBL1402684
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
EVMPD
SUB09574MIG
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
INN
774
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
CAS
125-13-3
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
DRUG BANK
DB04823
Created by admin on Fri Dec 15 15:04:37 GMT 2023 , Edited by admin on Fri Dec 15 15:04:37 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY