Reaction Details |
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Target | Urease [D459Y,K653P] |
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Ligand | BDBM123720 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Urease Inhibition Assay |
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Temperature | 303.15±0 K |
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IC50 | 4.10e+4± 1.3e+3 nM |
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Citation | Akhtar, T; Khan, MA; Iqbal, J; Jones, PG; Hameed, S A facile one-pot synthesis of 2-arylamino-5-aryloxylalkyl-1,3,4-oxadiazoles and their urease inhibition studies. Chem Biol Drug Des84:92-8 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Urease [D459Y,K653P] |
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Name: | Urease [D459Y,K653P] |
Synonyms: | UREA_CANEN | Urea amidohydrolase | Urease |
Type: | Protein |
Mol. Mass.: | 90763.23 |
Organism: | Canavalia ensiformis (Jack bean) |
Description: | P07374[D459Y,K653P] |
Residue: | 840 |
Sequence: | MKLSPREVEKLGLHNAGYLAQKRLARGVRLNYTEAVALIASQIMEYARDGEKTVAQLMCL
GQHLLGRRQVLPAVPHLLNAVQVEATFPDGTKLVTVHDPISRENGELQEALFGSLLPVPS
LDKFAETKEDNRIPGEILCEDECLTLNIGRKAVILKVTSKGDRPIQVGSHYHFIEVNPYL
TFDRRKAYGMRLNIAAGTAVRFEPGDCKSVTLVSIEGNKVIRGGNAIADGPVNETNLEAA
MHAVRSKGFGHEEEKDASEGFTKEDPNCPFNTFIHRKEYANKYGPTTGDKIRLGDTNLLA
EIEKDYALYGDECVFGGGKVIRDGMGQSCGHPPAISLDTVITNAVIIDYTGIIKADIGIK
DGLIASIGKAGNPDIMNGVFSNMIIGANTEVIAGEGLIVTAGAIDCHVHYICPQLVYEAI
SSGITTLVGGGTGPAAGTRATTCTPSPTQMRLMLQSTDYLPLNFGFTGKGSSSKPDELHE
IIKAGAMGLKLHEDWGSTPAAIDNCLTIAEHHDIQINIHTDTLNEAGFVEHSIAAFKGRT
IHTYHSEGAGGGHAPDIIKVCGIKNVLPSSTNPTRPLTSNTIDEHLDMLMVCHHLDREIP
EDLAFAHSRIRKKTIAAEDVLNDIGAISIISSDSQAMGRVGEVISRTWQTADPMKAQTGP
LKCDSSDNDNFRIRRYIAKYTINPAIANGFSQYVGSVEVGKLADLVMWKPSFFGTKPEMV
IKGGMVAWADIGDPNASIPTPEPVKMRPMYGTLGKAGGALSIAFVSKAALDQRVNVLYGL
NKRVEAVSNVRKLTKLDMKLNDALPEITVDPESYTVKADGKLLCVSEATTVPLSRNYFLF
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BDBM123720 |
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n/a |
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Name | BDBM123720 |
Synonyms: | 2-(4-Methylphenyl)amino-5-(1-(3,4-dichlorophenoxy)ethyl)-1,3,4-oxadiazole (3d) |
Type | Small organic molecule |
Emp. Form. | C17H15Cl2N3O2 |
Mol. Mass. | 364.226 |
SMILES | CC(Oc1ccc(Cl)c(Cl)c1)c1nnc(Nc2ccc(C)cc2)o1 |
Structure |
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