Reaction Details |
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Target | Urease |
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Ligand | BDBM50229993 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1747806 (CHEMBL4182316) |
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IC50 | 21250±n/a nM |
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Citation | Taha, M; Ullah, H; Al Muqarrabun, LMR; Khan, MN; Rahim, F; Ahmat, N; Javid, MT; Ali, M; Khan, KM Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies. Bioorg Med Chem26:152-160 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Urease |
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Name: | Urease |
Synonyms: | UREA_CANEN | Urea amidohydrolase |
Type: | Enzyme |
Mol. Mass.: | 90746.20 |
Organism: | Canavalia ensiformis (Jack bean) (Horse bean) |
Description: | P07374 |
Residue: | 840 |
Sequence: | MKLSPREVEKLGLHNAGYLAQKRLARGVRLNYTEAVALIASQIMEYARDGEKTVAQLMCL
GQHLLGRRQVLPAVPHLLNAVQVEATFPDGTKLVTVHDPISRENGELQEALFGSLLPVPS
LDKFAETKEDNRIPGEILCEDECLTLNIGRKAVILKVTSKGDRPIQVGSHYHFIEVNPYL
TFDRRKAYGMRLNIAAGTAVRFEPGDCKSVTLVSIEGNKVIRGGNAIADGPVNETNLEAA
MHAVRSKGFGHEEEKDASEGFTKEDPNCPFNTFIHRKEYANKYGPTTGDKIRLGDTNLLA
EIEKDYALYGDECVFGGGKVIRDGMGQSCGHPPAISLDTVITNAVIIDYTGIIKADIGIK
DGLIASIGKAGNPDIMNGVFSNMIIGANTEVIAGEGLIVTAGAIDCHVHYICPQLVYEAI
SSGITTLVGGGTGPAAGTRATTCTPSPTQMRLMLQSTDDLPLNFGFTGKGSSSKPDELHE
IIKAGAMGLKLHEDWGSTPAAIDNCLTIAEHHDIQINIHTDTLNEAGFVEHSIAAFKGRT
IHTYHSEGAGGGHAPDIIKVCGIKNVLPSSTNPTRPLTSNTIDEHLDMLMVCHHLDREIP
EDLAFAHSRIRKKTIAAEDVLNDIGAISIISSDSQAMGRVGEVISRTWQTADKMKAQTGP
LKCDSSDNDNFRIRRYIAKYTINPAIANGFSQYVGSVEVGKLADLVMWKPSFFGTKPEMV
IKGGMVAWADIGDPNASIPTPEPVKMRPMYGTLGKAGGALSIAFVSKAALDQRVNVLYGL
NKRVEAVSNVRKLTKLDMKLNDALPEITVDPESYTVKADGKLLCVSEATTVPLSRNYFLF
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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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