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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H9AsNO5.Bi.O
Molecular Weight 499.0622
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCOBIARSOL

SMILES

[O--].[Bi+3].OCC(=O)NC1=CC=C(C=C1)[As](O)([O-])=O

InChI

InChIKey=UPCVPFKBUJAADX-UHFFFAOYSA-M
InChI=1S/C8H10AsNO5.Bi.O/c11-5-8(12)10-7-3-1-6(2-4-7)9(13,14)15;;/h1-4,11H,5H2,(H,10,12)(H2,13,14,15);;/q;+3;-2/p-1

HIDE SMILES / InChI
Glycobiarsol was known under the brand name Milibis. Glycobiarsol is found to be very effective in intestinal infections. Milibis is an antiprotozoal agent that has been used in humans as well as in dogs.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Milibis

Approved Use

Antiprotozoal agent, amebicide
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

220 mg of the drug per kilogram body weight
Route of Administration: Oral
GLYCOBIARSOL was reported to be effective in vitro at about 30 ug/ml in egg-infusion medium
Name Type Language
GLYCOBIARSOL
GREEN BOOK   INN   MART.   MI   WHO-DD  
INN  
Official Name English
MILIBIS
Brand Name English
GLYCOBIARSOL [MI]
Common Name English
glycobiarsol [INN]
Common Name English
GLYCOBIARSOL [MART.]
Common Name English
(Hydrogen N-glycoloylarsanilato)oxobismuth
Common Name English
BISMUTH, ((4-((HYDROXYACETYL)AMINO)PHENYL)ARSONATO(1-))OXO-
Common Name English
BISMUTH GLYCOLLYLARSANILATE
Common Name English
GLYCOBIARSOL [GREEN BOOK]
Common Name English
Glycobiarsol [WHO-DD]
Common Name English
NSC-221709
Code English
Classification Tree Code System Code
WHO-ATC P01AR03
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
WHO-VATC QP51AD53
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
WHO-ATC P01AR53
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
WHO-VATC QP51AD03
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
Code System Code Type Description
CAS
116-49-4
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
PUBCHEM
76957520
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
SMS_ID
100000084212
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
NSC
221709
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
DRUG CENTRAL
4849
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
NCI_THESAURUS
C76421
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
EVMPD
SUB07950MIG
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
WIKIPEDIA
GLYCOBIARSOL
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-143-1
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
INN
16
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
MERCK INDEX
M204
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID1048754
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY
FDA UNII
E3U8347QWJ
Created by admin on Wed Jul 05 22:46:11 UTC 2023 , Edited by admin on Wed Jul 05 22:46:11 UTC 2023
PRIMARY