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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/12/21 12:53:13」(JST)

English Journal

Corrigendum: Repurposing the Chemical Scaffold of the Anti-Arthritic Drug Lobenzarit to Target Tryptophan Biosynthesis in Mycobacterium tuberculosis.

Evans GL, Gamage SA, Bulloch EM, Baker EN, Denny WA, Lott JS.
Chembiochem : a European journal of chemical biology.Chembiochem.2015 Mar 23;16(5):706. doi: 10.1002/cbic.201500098. Epub 2015 Mar 11.
PMID 26177917

Repurposing the chemical scaffold of the anti-arthritic drug Lobenzarit to target tryptophan biosynthesis in Mycobacterium tuberculosis.

Evans GL1, Gamage SA, Bulloch EM, Baker EN, Denny WA, Lott JS.
Chembiochem : a European journal of chemical biology.Chembiochem.2014 Apr 14;15(6):852-64. doi: 10.1002/cbic.201300628. Epub 2014 Mar 12.
PMID 24623674

Gregori-Puigjané E1, Setola V, Hert J, Crews BA, Irwin JJ, Lounkine E, Marnett L, Roth BL, Shoichet BK.
Proceedings of the National Academy of Sciences of the United States of America.Proc Natl Acad Sci U S A.2012 Jul 10;109(28):11178-83. doi: 10.1073/pnas.1204524109. Epub 2012 Jun 18.
PMID 22711801

Study of the Critical Points in Lobenzarit Disodium Hydrophilic Matrices for Controlled Drug Delivery

Application of a New Mathematical Method for the Estimation of the Mean Surface Area to Calculate the Percolation Threshold of Lobenzarit Dissodium Salt in Controlled Release Matrices

リンク元	「ロベンザリット」
拡張検索	「lobenzarit disodium」

Lobenzarit
Systematic (IUPAC) name
	2-[(2-Carboxyphenyl)amino]-4-chlorobenzoic acid
Clinical data
AHFS/Drugs.com	International Drug Names
Legal status	℞ (Prescription only);
Routes of; administration	Oral
Identifiers
CAS Number	63329-53-3
ATC code	None
PubChem	CID: 3946
ChemSpider	3809
UNII	915EE91P39
Chemical data
Formula	C14H10ClNO4
Molecular mass	291.68 g/mol
	SMILES C1=CC=C(C(=C1)C(=O)O)NC2=C(C=CC(=C2)Cl)C(=O)O ;
	InChI InChI=1S/C14H10ClNO4/c15-8-5-6-10(14(19)20)12(7-8)16-11-4-2-1-3-9(11)13(17)18/h1-7,16H,(H,17,18)(H,19,20) ; Key:UGDPYGKWIHHBMB-UHFFFAOYSA-N ;
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