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Reaction Details
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TargetMevalonate kinase
LigandBDBM38527
Substrate/Competitorn/a
Meas. Tech.Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - MK Dose Response
IC50>9999000±n/a nM
Citation PubChem, PC Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - MK Dose Response PubChem Bioassay(2007)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Mevalonate kinase
Name:Mevalonate kinase
Synonyms:n/a
Type:Enzyme Catalytic Domain
Mol. Mass.:31420.64
Organism:Streptococcus pneumoniae D39
Description:A0A0H2ZQX9
Residue:292
Sequence:
MTKKVGVGQAHSKIILIGEHAVVYGYPAISLPLLEVEVTCKVVPAESPWRLYEEDTLSMA
VYASLEYLNITEACIRCEIDSAIPEKRGMGSSAAISIAAIRAVFDYYQADLPHDVLEILV
NRAEMIAHMNPSGLDAKTCLSDQPIRFIKNVGFTELEMDLSAYLVIADTGVYGHTREAIQ
VVQNKGKDALPFLHALGELTQQAEIAISQKDAEGLGQILSQAHLHLKEIGVSSLEADSLV
ETALSHGALGAKMSGGGLGGCIIALVTNLTHAQELAERLEEKGAVQTWIESL
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  Blast E-value cutoff:
BDBM38527
n/a
NameBDBM38527
Synonyms:4-[3-(3-Chloro-benzyl)-7-hydroxy-3H-[1,2,3]triazolo[4,5-d]pyrimidin-5-yl]-piperidine-1-carboxylic acid (4-fluoro-phenyl)-amide | 4-[3-(3-chlorobenzyl)-7-keto-2H-triazolo[4,5-d]pyrimidin-5-yl]-N-(4-fluorophenyl)piperidine-1-carboxamide | 4-[3-[(3-chlorophenyl)methyl]-7-oxidanylidene-2H-[1,2,3]triazolo[4,5-d]pyrimidin-5-yl]-N-(4-fluorophenyl)piperidine-1-carboxamide | 4-[3-[(3-chlorophenyl)methyl]-7-oxo-2H-triazolo[4,5-d]pyrimidin-5-yl]-N-(4-fluorophenyl)-1-piperidinecarboxamide | 4-[3-[(3-chlorophenyl)methyl]-7-oxo-2H-triazolo[4,5-d]pyrimidin-5-yl]-N-(4-fluorophenyl)piperidine-1-carboxamide | MLS000035382 | SMR000007388 | cid_649776
TypeSmall organic molecule
Emp. Form.C23H21ClFN7O2
Mol. Mass.481.91
SMILESFc1ccc(NC(=O)N2CCC(CC2)c2nc3n(Cc4cccc(Cl)c4)nnc3c(=O)[nH]2)cc1
Structure
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