Reaction Details |
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Target | Urease subunit alpha |
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Ligand | BDBM173602 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Urease Inhibition Assay |
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pH | 7±n/a |
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IC50 | 2.31e+3± 2 nM |
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Comments | extracted |
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Citation | Rahim, F; Zaman, K; Ullah, H; Taha, M; Wadood, A; Javed, MT; Rehman, W; Ashraf, M; Uddin, R; Uddin, I; Asghar, H; Khan, AA; Khan, KM Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents. Bioorg Chem63:123-31 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Urease subunit alpha |
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Name: | Urease subunit alpha |
Synonyms: | URE1_SPOPA | Urea Amidohydrolase Subunit alpha | Urease | ureC |
Type: | Enzyme Subunit |
Mol. Mass.: | 61384.55 |
Organism: | Bacillus pasteurii |
Description: | n/a |
Residue: | 569 |
Sequence: | MKINRQQYAESYGPTVGDRVRLADTDLGEVEKDYYYLGDEVNFGGGKVLREGMGENGTYT
RTENVLDLLLTNALILDYTGIYKADIGVKDGYIVGIGKGGNPDIMDGVTPNMIVGTATEV
IAAEGKIVTAGGIDTHVHFINPDQVDVALANGITTLFGGGTGPAEGSKATTVTPGPWNIE
KMLKSTEGLPINVGILGKGHGSSIAPIMEQIDAGAAGLKIHEDWGATPASIDRSLTVADE
ADVQVAIHSDTLNEAGFLEDTVRAINGRVIHSFHVEGAGGGHAPDIMAMAGHPNVLPSST
NPTRPFTVNTIDEHLDMLMVCHHLKQNIPEDVAFADSRIRPETIAAEDILHDLGIISMMS
TDALAMGRAGEMVLRTWQTADKMKKQRGPLAEEKNGSDNFRLKRYVSKYTINPAIAQGMA
HEVGSIEEGKFADLVLWEPKFFGVKADRVIKGGIIAYAQIGDPSASIPTPQPVMGRRMYG
TVGDLIHDTNITFMSKSSIQQGVPAKLGLKRRIGTVKNCRNIGKKDMKWNDVTTDIDINP
ETYEVKVDGEVLTCEPVKELPMAQRYFLF
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BDBM173602 |
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n/a |
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Name | BDBM173602 |
Synonyms: | (Z)-2-((Z)-(1-(2-Bromo-4-nitrophenyl)ethylidene)hydrazono)thiazolidine-4-one (15) |
Type | Small organic molecule |
Emp. Form. | C11H9BrN4O3S |
Mol. Mass. | 357.183 |
SMILES | C\C(=N\N=C1/NC(=O)CS1)c1ccc(cc1Br)[N+]([O-])=O |
Structure |
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