Reaction Details |
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Target | Thermolysin |
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Ligand | BDBM50035235 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_210393 (CHEMBL814123) |
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IC50 | 175±n/a nM |
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Citation | Bihovsky, R; Levinson, BL; Loewi, RC; Erhardt, PW; Polokoff, MA Hydroxamic acids as potent inhibitors of endothelin-converting enzyme from human bronchiolar smooth muscle. J Med Chem38:2119-29 (1995) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Thermolysin |
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Name: | Thermolysin |
Synonyms: | THER_BACTH | npr |
Type: | PROTEIN |
Mol. Mass.: | 60097.54 |
Organism: | Bacillus thermoproteolyticus |
Description: | ChEMBL_1468794 |
Residue: | 548 |
Sequence: | MKMKMKLASFGLAAGLAAQVFLPYNALASTEHVTWNQQFQTPQFISGDLLKVNGTSPEEL
VYQYVEKNENKFKFHENAKDTLQLKEKKNDNLGFTFMRFQQTYKGIPVFGAVVTSHVKDG
TLTALSGTLIPNLDTKGSLKSGKKLSEKQARDIAEKDLVANVTKEVPEYEQGKDTEFVVY
VNGDEASLAYVVNLNFLTPEPGNWLYIIDAVDGKILNKFNQLDAAKPGDVKSITGTSTVG
VGRGVLGDQKNINTTYSTYYYLQDNTRGNGIFTYDAKYRTTLPGSLWADADNQFFASYDA
PAVDAHYYAGVTYDYYKNVHNRLSYDGNNAAIRSSVHYSQGYNNAFWNGSQMVYGDGDGQ
TFIPLSGGIDVVAHELTHAVTDYTAGLIYQNESGAINEAISDIFGTLVEFYANKNPDWEI
GEDVYTPGISGDSLRSMSDPAKYGDPDHYSKRYTGTQDNGGVHINSGIINKAAYLISQGG
THYGVSVVGIGRDKLGKIFYRALTQYLTPTSNFSQLRAAAVQSATDLYGSTSQEVASVKQ
AFDAVGVK
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BDBM50035235 |
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n/a |
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Name | BDBM50035235 |
Synonyms: | CHEMBL2372437 | N-[1-(Carbamoylmethyl-carbamoyl)-ethyl]-N''-hydroxy-2-isobutyl-malonamide |
Type | Small organic molecule |
Emp. Form. | C12H22N4O5 |
Mol. Mass. | 302.3269 |
SMILES | CC(C)C[C@H](C(=O)NO)C(=O)N[C@@H](C)C(=O)NCC(N)=O |r| |
Structure |
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