Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetAlpha-carbonic anhydrase domain-containing protein
LigandBDBM25914
Substrate/CompetitorBDBM10856
Meas. Tech.CA Inhibition Assay
pH7.4±n/a
Temperature298.15±n/a K
Ki 260±n/a nM
Citation Güzel, OInnocenti, AHall, RAScozzafava, AMühlschlegel, FASupuran, CT Carbonic anhydrase inhibitors. The nematode alpha-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides. Bioorg Med Chem17:3212-5 (2009) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Alpha-carbonic anhydrase domain-containing protein
Name:Alpha-carbonic anhydrase domain-containing protein
Synonyms:CAH-4b | alpha-Carbonic Anhydrase | ceCA
Type:Enzyme
Mol. Mass.:26169.24
Organism:Caenorhabditis elegans
Description:Q8WQD8
Residue:235
Sequence:
MAAAQRQSPIDIVPQHVCCDTDVCKADALNIDYKSGDCCDVLVSEGGFLVNVKRNCGTFL
TANHLPSSKFALAQFHAHWGSNSKEGSEHFLDGKQLSGEVHFVFWNTSYESFNVALSKPD
GLAVVGVFLKEGKYNDNYHGLIDTVRKATGNATPIAMPKDFHIEHLLPSPDKREFVTYLG
SLTTPPYNECVIWTLFTEPVEVSFGQLNVLRNIIPANHRACQDRCDREIRSSFNF
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM25914
BDBM10856
NameBDBM25914
Synonyms:3-(2-bromophenyl)-2-(hydrazinecarbonyl)-1H-indole-5-sulfonamide | BMC173212 Compound 2j | indole sulfonamide, 8j
TypeSmall organic molecule
Emp. Form.C15H13BrN4O3S
Mol. Mass.409.258
SMILESNNC(=O)c1[nH]c2ccc(cc2c1-c1ccccc1Br)S(N)(=O)=O |(3.59,5.07,;2.05,5.07,;1.28,3.73,;2.05,2.4,;-.26,3.73,;-1.17,2.49,;-2.63,2.96,;-3.97,2.19,;-5.3,2.96,;-5.3,4.5,;-3.97,5.27,;-2.63,4.5,;-1.17,4.98,;-.69,6.44,;.79,6.86,;1.17,8.36,;.06,9.43,;-1.42,9.01,;-1.8,7.52,;-3.28,7.1,;-6.63,5.27,;-7.97,6.04,;-5.86,6.61,;-7.4,3.94,)|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: