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TargetThromboxane-A synthase
LigandBDBM50280073
Substrate/Competitorn/a
Meas. Tech.ChEBML_209929
IC50 50±n/a nM
Citation Faull, AWGaskin, HHadfield, PSJessup, RRussell, KWatkins, WJWayne, M Dual-acting thromboxane receptor antagonist/synthase inhibitors: heterocyclic variations Bioorg Med Chem Lett2:1181-1186 (1992)    Article
More Info.:Get all data from this article,  Assay Method
 
Thromboxane-A synthase
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50280073
n/a
NameBDBM50280073
Synonyms:(Z)-6-{(2S,4S,5R)-4-(3-Methyl-3H-imidazol-4-yl)-2-[1-methyl-1-(4-methyl-2-nitro-phenoxy)-ethyl]-[1,3]dioxan-5-yl}-hex-4-enoic acid | CHEMBL278714
TypeSmall organic molecule
Emp. Form.C24H31N3O7
Mol. Mass.473.5188
SMILESCc1ccc(OC(C)(C)[C@H]2OC[C@@H](C\C=C/CCC(O)=O)[C@H](O2)c2cncn2C)c(c1)[N+]([O-])=O
Structure
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