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

Molecular Formula C8H8AsNO5
Molecular Weight 273.0744
Charge -2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Bi
Molecular Weight 208.9804
Charge 3
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Glycobiarsol for the control of Trichuris vulpis infection in the dog.
1969-08
[Treatment of trichocephaliasis with glycobiarsol].
1962-01
The trichomonacidal activity of milibis (glycobiarsol).
1954-11
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
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:51:33 GMT 2025
Edited
by admin
on Mon Mar 31 17:51:33 GMT 2025
Record UNII
E3U8347QWJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MILIBIS
Preferred Name English
GLYCOBIARSOL
GREEN BOOK   INN   MART.   MI   WHO-DD  
INN  
Official 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 Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
WHO-VATC QP51AD53
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
WHO-ATC P01AR53
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
WHO-VATC QP51AD03
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
Code System Code Type Description
CAS
116-49-4
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
PUBCHEM
76957520
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
SMS_ID
100000084212
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
NSC
221709
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
DRUG CENTRAL
4849
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
NCI_THESAURUS
C76421
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
EVMPD
SUB07950MIG
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
WIKIPEDIA
GLYCOBIARSOL
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-143-1
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
INN
16
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
MERCK INDEX
m204
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID1048754
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
FDA UNII
E3U8347QWJ
Created by admin on Mon Mar 31 17:51:33 GMT 2025 , Edited by admin on Mon Mar 31 17:51:33 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE