Reaction Details |
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Target | Thromboxane-A synthase |
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Ligand | BDBM50110456 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_210290 |
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IC50 | 41±n/a nM |
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Citation | Fujita, M; Seki, T; Inada, H; Shimizu, K; Takahama, A; Sano, T Novel agents combining platelet activating factor (PAF) receptor antagonist with thromboxane synthase inhibitor (TxSI). Bioorg Med Chem Lett12:771-4 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Thromboxane-A synthase |
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Name: | Thromboxane-A synthase |
Synonyms: | CYP5 | CYP5A1 | Cytochrome P450 5A1 | P450 TxA2 | TBXAS1 | THAS_HUMAN | TXA synthase | TXAS | TXS | Thromboxane A2 Synthase | Thromboxane A2 Synthase (P450 TxA2) | Thromboxane Alpha | Thromboxane prostanoid | Thromboxane synthase | Thromboxane-A synthase |
Type: | Enzyme |
Mol. Mass.: | 60524.67 |
Organism: | Homo sapiens (Human) |
Description: | P24557 |
Residue: | 533 |
Sequence: | MEALGFLKLEVNGPMVTVALSVALLALLKWYSTSAFSRLEKLGLRHPKPSPFIGNLTFFR
QGFWESQMELRKLYGPLCGYYLGRRMFIVISEPDMIKQVLVENFSNFTNRMASGLEFKSV
ADSVLFLRDKRWEEVRGALMSAFSPEKLNEMVPLISQACDLLLAHLKRYAESGDAFDIQR
CYCNYTTDVVASVAFGTPVDSWQAPEDPFVKHCKRFFEFCIPRPILVLLLSFPSIMVPLA
RILPNKNRDELNGFFNKLIRNVIALRDQQAAEERRRDFLQMVLDARHSASPMGVQDFDIV
RDVFSSTGCKPNPSRQHQPSPMARPLTVDEIVGQAFIFLIAGYEIITNTLSFATYLLATN
PDCQEKLLREVDVFKEKHMAPEFCSLEEGLPYLDMVIAETLRMYPPAFRFTREAAQDCEV
LGQRIPAGAVLEMAVGALHHDPEHWPSPETFNPERFTAEARQQHRPFTYLPFGAGPRSCL
GVRLGLLEVKLTLLHVLHKFRFQACPETQVPLQLESKSALGPKNGVYIKIVSR
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BDBM50110456 |
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n/a |
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Name | BDBM50110456 |
Synonyms: | 5-([3-{1-[6-(2-chlorophenyl)-1,4-dimethyl-7,8,9,10-tetrahydro-4H-pyrido[4',3':4,5]thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-9-yl]-1-butanone-4-yl}-phenyl]-pyridin-3-yl-methyleneaminooxy)-pentanoic acid ethyl ester | CHEMBL165359 |
Type | Small organic molecule |
Emp. Form. | C42H44ClN7O4S |
Mol. Mass. | 778.361 |
SMILES | CCOC(=O)CCCCO\N=C(\c1cccnc1)c1cccc(CCCC(=O)N2CCc3c(C2)sc-2c3C(=NC(C)c3nnc(C)n-23)c2ccccc2Cl)c1 |c:40| |
Structure |
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