Reaction Details |
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Target | Urease subunit alpha |
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Ligand | BDBM50229993 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Urease Inhibition Assay |
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Temperature | 303.15±n/a K |
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IC50 | 2.1e+4± 1.1e+2 nM |
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Comments | extracted |
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Citation | Rashid, U; Rahim, F; Taha, M; Arshad, M; Ullah, H; Mahmood, T; Ali, M Synthesis of 2-acylated and sulfonated 4-hydroxycoumarins: In vitro urease inhibition and molecular docking studies. Bioorg Chem66:111-6 (2016) [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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BDBM50229993 |
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n/a |
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Name | BDBM50229993 |
Synonyms: | 2-thiourea | CHEMBL260876 | Thiocarbamid | Thioharnstoff | Thiokarbamid | carbonothioic diamide | thiocarbamide | thiocarbonic acid diamide | thiourea |
Type | Small organic molecule |
Emp. Form. | CH4N2S |
Mol. Mass. | 76.121 |
SMILES | NC(N)=S |
Structure |
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