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Details

Stereochemistry ACHIRAL
Molecular Formula 2C6H5O7.Bi.3K
Molecular Weight 704.4747
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BISMUTH SUBCITRATE

SMILES

[K+].[K+].[K+].[Bi+3].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O.OC(CC([O-])=O)(CC([O-])=O)C([O-])=O

InChI

InChIKey=ZQUAVILLCXTKTF-UHFFFAOYSA-H
InChI=1S/2C6H8O7.Bi.3K/c2*7-3(8)1-6(13,5(11)12)2-4(9)10;;;;/h2*13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);;;;/q;;+3;3*+1/p-6

HIDE SMILES / InChI

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 K
Molecular Weight 39.0983
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C6H5O7
Molecular Weight 189.0997
Charge -3
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.drugs.com/international/bibrocathol.html | https://clinicaltrials.gov/ct2/show/NCT01357538 | https://www.drugs.com/international/noviform.html | https://www.ncbi.nlm.nih.gov/pubmed/17003947

Bibrocathol (trade names Noviform and Posiformin) is a well-established topical antiseptic for the treatment of acute eyelid diseases like blepharitis. Eye ointments containing 2 or 5 % bibrocathol and the excipients liquid paraffin, white soft paraffin, and lanolin have been marketed since 1967 for the treatment of eye irritation, chronic blepharitis, and uninfected corneal injuries. Reports of clinical experience with bibrocathol for inflammation of the edge of the palpebra exist since the beginning of the 20th century. Until recently, no controlled, randomized clinical studies according to the guidelines for Good Clinical Practice for Trials on Medical Products for Human Use (GCP) as defined by the International Conference on Harmonisation (ICH) have been performed with bibrocathol 2 % ointment, as these were not required for marketing authorization in the 1960s. A first double-blind, prospective, controlled, GCP-compliant clinical study was recently performed to assess the efficacy of bibrocathol 5 % (Noviform®) in acute blepharitis. It demonstrated superior efficacy of bibrocathol 5 % ointment as compared to an ointment vehicle (placebo) after 2 weeks of treatment as assessed by a combined measure of slit-lamp examination results and patients’ subjective complaints.

Originator

Sources: Medizinische Klinik (Muenchen, Germany) (1913), 8, 992.

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Noviform

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Successful treatment of blepharitis with bibrocathol (Posiformin® 2 %).
2012 Dec
Patents

Sample Use Guides

A strip of 5 mm eye ointment applied 3 times per day to the eye lid
Route of Administration: Topical
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:04:58 GMT 2023
Edited
by admin
on Fri Dec 15 18:04:58 GMT 2023
Record UNII
HS813P8QPX
Record Status Validated (UNII)
Record Version
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Name Type Language
BISMUTH SUBCITRATE
VANDF   WHO-DD  
Common Name English
COLLOIDAL BISMUTH SUBCITRATE
MI  
Common Name English
BISMUTH POTASSIUM CITRATE
Systematic Name English
COLLOIDAL BISMUTH SUBCITRATE [MI]
Common Name English
BISMUTH SUBCITRATE [VANDF]
Common Name English
1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-, BISMUTH(3+) POTASSIUM SALT (2:1:3)
Common Name English
BISMUTH TRIPOTASSIUM DICITRATE
Systematic Name English
Tripotassium dicitratobismuthate [WHO-DD]
Common Name English
BISMUTH SUBCITRATE, COLLOIDAL
Common Name English
TRIPOTASSIUM DICITRATOBISMUTHATE
WHO-DD  
Common Name English
Bismuth subcitrate [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QA02BD08
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
NCI_THESAURUS C29701
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
WHO-VATC QA02BX05
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
NCI_THESAURUS C2080
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
WHO-ATC A02BX05
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
WHO-ATC A02BD08
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
Code System Code Type Description
RXCUI
47181
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
260-872-5
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
NCI_THESAURUS
C1351
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY NCIT
DRUG CENTRAL
4355
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
FDA UNII
HS813P8QPX
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
CAS
57644-54-9
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
PUBCHEM
10101269
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
MESH
C002791
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
EVMPD
SUB22602
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
EVMPD
SUB13089MIG
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY
MERCK INDEX
m3739
Created by admin on Fri Dec 15 18:04:58 GMT 2023 , Edited by admin on Fri Dec 15 18:04:58 GMT 2023
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY