Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H9NO2 |
Molecular Weight | 151.1626 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(=CC=C1)C(N)=O
InChI
InChIKey=VKPLPDIMEREJJF-UHFFFAOYSA-N
InChI=1S/C8H9NO2/c1-11-7-4-2-3-6(5-7)8(9)10/h2-5H,1H3,(H2,9,10)
Approval Year
PubMed
Title | Date | PubMed |
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1,5-isoquinolinediol increases the frequency of gene targeting by homologous recombination in mouse fibroblasts. | 2003 Feb |
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Recoupled long-range C-H dipolar dephasing in solid-state NMR, and its use for spectral selection of fused aromatic rings. | 2003 May |
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In silico characterization of the family of PARP-like poly(ADP-ribosyl)transferases (pARTs). | 2005 Oct 4 |
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Antibacterial alkoxybenzamide inhibitors of the essential bacterial cell division protein FtsZ. | 2009 Jan 15 |
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Deciphering the stem cell machinery as a basis for understanding the molecular mechanism underlying reprogramming. | 2009 Nov |
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Characterization of ftsZ mutations that render Bacillus subtilis resistant to MinC. | 2010 Aug 11 |
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Creating an antibacterial with in vivo efficacy: synthesis and characterization of potent inhibitors of the bacterial cell division protein FtsZ with improved pharmaceutical properties. | 2010 May 27 |
Patents
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209527
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DB03073
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227-379-7
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5813-86-5
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M8502TLK98
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DTXSID00206848
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28589
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98487
Created by
admin on Sat Dec 16 06:35:03 GMT 2023 , Edited by admin on Sat Dec 16 06:35:03 GMT 2023
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SUBSTANCE RECORD