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

Details

Stereochemistry RACEMIC
Molecular Formula C11H14AsNO3S2
Molecular Weight 347.285
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ARSTHINOL

SMILES

CC(=O)NC1=C(O)C=CC(=C1)[As]2SCC(CO)S2

InChI

InChIKey=MRUDSZSRLQAPOG-UHFFFAOYSA-N
InChI=1S/C11H14AsNO3S2/c1-7(15)13-10-4-8(2-3-11(10)16)12-17-6-9(5-14)18-12/h2-4,9,14,16H,5-6H2,1H3,(H,13,15)

HIDE SMILES / InChI

Molecular Formula C11H14AsNO3S2
Molecular Weight 347.285
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

ARSTHINOL, an organoarsenical compound, is an antiprotozoal agent used for the treatment of mild or asymptomatic intestinal amebiasis. ARSTHINOL in complex with cyclodextrin displays an anticancer activity.

Approval Year

PubMed

PubMed

TitleDatePubMed
The treatment of amebiasis with arsthinol (N.N.R) (balarsen).
1954 Jun
Arsthinol (balarsen), a new trivalent arsenical for the treatment of intestinal amebiasis and other intestinal protozoa.
1954 Mar
Intestinal amebiasis; incidence, symptoms, and treatment with arsthinol (balarsen).
1956 Feb 4
The antitumor effects of an arsthinol-cyclodextrin complex in a heterotopic mouse model of glioma.
2013 Nov
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:14:54 GMT 2023
Edited
by admin
on Fri Dec 15 15:14:54 GMT 2023
Record UNII
QNT09A162Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ARSTHINOL
INN   MI   WHO-DD  
INN  
Official Name English
3-HYDROXYPROPYLENE ESTER OF 3-ACETAMIDO-4-HYDROXYDITHIOBENZENEARSONOUS ACID
Common Name English
ARSTHINOL [MI]
Common Name English
Arsthinol [WHO-DD]
Common Name English
arsthinol [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC P01AR01
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
WHO-VATC QP51AD01
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
Code System Code Type Description
DRUG CENTRAL
3007
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
FDA UNII
QNT09A162Y
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
EPA CompTox
DTXSID40861753
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
DRUG BANK
DB08928
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
PUBCHEM
8414
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
WIKIPEDIA
ARSTHINOL
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
INN
240
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
EVMPD
SUB05572MIG
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
SMS_ID
100000086623
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
NCI_THESAURUS
C76411
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
MESH
C546471
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
CAS
119-96-0
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
MERCK INDEX
m2072
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
204-361-7
Created by admin on Fri Dec 15 15:14:54 GMT 2023 , Edited by admin on Fri Dec 15 15:14:54 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY