Reaction Details |
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Target | Thromboxane-A synthase |
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Ligand | BDBM50003776 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_209946 |
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IC50 | 2±n/a nM |
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Citation | Main, AJ; Bhagwat, SS; Boswell, C; Goldstein, R; Gude, C; Cohen, DS; Furness, P; Lee, W; Louzan, M Thromboxane receptor antagonism combined with thromboxane synthase inhibition. 3. Pyridinylalkyl-substituted 8-[(arylsulfonyl)amino]octanoic acids. J Med Chem35:4366-72 (1992) [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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BDBM50003776 |
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n/a |
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Name | BDBM50003776 |
Synonyms: | 8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-yl-propyl)-octanoic acid | CGS-22652 | CHEMBL65414 |
Type | Small organic molecule |
Emp. Form. | C22H29ClN2O4S |
Mol. Mass. | 452.995 |
SMILES | OC(=O)CCC(CCCCNS(=O)(=O)c1ccc(Cl)cc1)CCCc1cccnc1 |
Structure |
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