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TargetThromboxane-A synthase
LigandBDBM50033293
Substrate/Competitorn/a
Meas. Tech.ChEMBL_209931 (CHEMBL813722)
IC50 2500±n/a nM
Citation Lee, SJKonishi, YYu, DTMiskowski, TARiviello, CMMacina, OTFrierson, MRKondo, KSugitani, MSircar, JC Discovery of potent cyclic GMP phosphodiesterase inhibitors. 2-Pyridyl- and 2-imidazolylquinazolines possessing cyclic GMP phosphodiesterase and thromboxane synthesis inhibitory activities. J Med Chem38:3547-57 (1995) [PubMed]
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:
BDBM50033293
n/a
NameBDBM50033293
Synonyms:Benzyl-(2-imidazol-1-yl-6-methoxy-quinazolin-4-yl)-amine; dihydrochloride | CHEMBL555463
TypeSmall organic molecule
Emp. Form.C19H17N5O
Mol. Mass.331.3712
SMILESCOc1ccc2nc(nc(NCc3ccccc3)c2c1)-n1ccnc1
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: