Details of the Drug-Related molecule(s) Interaction Atlas

General Information of Drug (ID: DMZI7O1)

Drug Name

2-phenyl-1H-imidazole-4-carboxylic acid Drug Info

Synonyms

2-Phenyl-1H-imidazole-4-carboxylic acid; 77498-98-7; 2-phenyl-1H-imidazole-5-carboxylic acid; 1H-Imidazole-5-carboxylic acid, 2-phenyl-; CHEMBL1232889; 1H-Imidazole-4-carboxylic acid, 2-phenyl-; UNII-HGH57KDY8T; HGH57KDY8T; 2-phenylimidazole-4-carboxylic acid; G14; 2-phenyl-3H-imidazole-4-carboxylic Acid; AC1MC8EL; SCHEMBL1080850; CTK4I4538; CTK2I0991; XCAXKZJNJCKTQH-UHFFFAOYSA-N; MolPort-000-146-264; HMS3604D08; ZINC164985; CS-D0591; ALBB-012261; CP-011; BDBM50329857; STK897779; ANW-57703; AKOS007930827; AKOS005173647; NE61009

Indication

Disease Entry	ICD 11	Status	REF
Discovery agent	N.A.	Investigative	[1]

Cross-matching ID

PubChem CID: 2738139
CAS Number: CAS 77498-98-7
TTD Drug ID: DMZI7O1

Molecule-Related Drug Atlas

Molecule Type:

DTT

Drug Status:

Approved Drug(s)

Clinical Trial Drug(s)

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Drug(s) Targeting Staphylococcus Beta-lactamase (Stap-coc blaZ)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
Tazobactam	DM3XNUI	Appendicitis	DB10	Approved	[2]
Clavulanate	DM2FGRT	Bacteremia	1A73	Approved	[3]
CAZ AVI	DMPG4OM	Serious infection	1H0Z	Phase 3	[4]
Enmetazobactam	DMZKTYJ	Urinary tract infection	GC08	Phase 3	[5]
Vaborbactam	DMDCFXJ	Urinary tract infection	GC08	Phase 3	[6]
MK-7655	DMLMV0O	Bacterial infection	1A00-1C4Z	Phase 2	[7]
CXL	DM3JFZ2	Methicillin-resistant staphylococci infection	1A00-1A09	Phase 2	[8]
RASV-Sp	DM4VTX6	Streptococcus infection	1B53	Phase 1	[9]
ME-1071	DMEMQ5J	Bacterial infection	1A00-1C4Z	Phase 1	[10]
OP-0595	DMECVP9	Bacterial infection	1A00-1C4Z	Phase 1	[11]
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Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

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Drug Therapeutic Target (DTT)

DTT Name	DTT ID	UniProt ID	MOA	REF
Staphylococcus Beta-lactamase (Stap-coc blaZ)	TTHI19T	BLAC_STAAU	Inhibitor	[1]

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References

1	The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42.
2	Selection of TNF-alpha binding affibody molecules using a beta-lactamase protein fragment complementation assay. N Biotechnol. 2009 Nov 30;26(5):251-9.
3	A sensitive coupled HPLC/electrospray mass spectrometry assay for SPM-1 metallo-beta-lactamase inhibitors. Assay Drug Dev Technol. 2009 Apr;7(2):170-9.
4	NXL104 irreversibly inhibits the -lactamase from Mycobacterium tuberculosis. Biochemistry. 2012 Jun 5;51(22):4551-7.
5	Pharmacodynamics of Cefepime Combined with the Novel Extended-Spectrum--Lactamase (ESBL) Inhibitor Enmetazobactam for Murine Pneumonia Caused by ESBL-Producing Klebsiella pneumoniae. Antimicrob Agents Chemother. 2020 May 21;64(6):e00180-20.
6	Vaborbactam: Spectrum of Beta-Lactamase Inhibition and Impact of Resistance Mechanisms on Activity in Enterobacteriaceae. Antimicrob Agents Chemother. 2017 Oct 24;61(11):e01443-17.
7	Discovery of MK-7655, a beta-lactamase inhibitor for combination with Primaxin . Bioorg Med Chem Lett. 2014 Feb 1;24(3):780-5.
8	Beta-Lactam Antibiotics Renaissance. Antibiotics. 2014, 3(2), 193-215.
9	WO patent application no. 2010,0456,20, Recombinant bacterium capable of eliciting an immune response against streptococcus pneumoniae.
10	Multidrug-resistant Gram-negative bacterial infections: are you ready for the challenge. Curr Clin Pharmacol. 2014 Feb;9(1):27-38.
11	OP0595, a new diazabicyclooctane: mode of action as a serine -lactamase inhibitor, antibiotic and -lactam 'enhancer'. J Antimicrob Chemother. 2015 Oct;70(10):2779-86.