Seratrodast

Seratrodast Basic information
Product Name:Seratrodast
Synonyms:50MG/200MG/1G;benzeneheptanoic acid, -(2,4,5-trimethyl-3,6-dioxo-1,4-cyclohexadien-1-yl)-;(+-)-7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoicacid;aa-2414;beta-(2,4,5-trimethyl-3,6-dioxo-1,4-cyclohexadien-1-yl)-bezeneheptanoicaci;Seratrodast(AA-2414,ABT-001);AA-2414;SERETRA;AA2414;AA 2414;Seretra
CAS:112665-43-7
MF:C22H26O4
MW:354.44
EINECS:692-169-8
Product Categories:ZAGAM;API;Heterocyclic Compounds;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:112665-43-7.mol
Seratrodast Structure
Seratrodast Chemical Properties
Melting point 118-120°C
Boiling point 522.3±49.0 °C(Predicted)
density 1.140±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Yellow-orange solid.
pka4.76±0.10(Predicted)
color Pale Orange to Yellow
Merck 14,8459
CAS DataBase Reference112665-43-7(CAS DataBase Reference)
Safety Information
RTECS DA1600050
HS Code 2918.30.3000
MSDS Information
Seratrodast Usage And Synthesis
DescriptionSeratrodast, a novel benzoquinone derivative, is the first thromboxane A2 (TxA2) receptor antagonist to reach the market. It is orally active for the treatment of bronchospastic disorders such as asthma. TxA2, a metabolite of the arachidonate cascade, is involved in several cardiovascular and respiratory diseases through its potent biological effects on platelet aggregation and constriction of vascular and respiratory smooth muscles. Seratrodast potently inhibits platelet aggregation and bronchoconstriction induced by a TxA2 mimic and by a variety of spasmogenic prostanoids including PGF, PGD2 and 9α,11β-PGF2. Seratrodast shows excellent efficacy in asthma and has been reported to be potentially useful in hyper-responsive disorder. The R-(+)- seratrodast was reported to be the active isomer.
Chemical PropertiesPale Orange Solid
OriginatorTakeda (Japan)
UsesThromboxane A2-receptor antagonist. Antiasthmatic.
Usesantibacterial
DefinitionChEBI: Seratrodast is an organic molecular entity.
Brand nameBronica
Biological ActivityThromboxane A 2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA 2 mimetic in guinea pigs.
in vitroseratrodast was found to inhibit the aggregation of guinea pig platelets induced by a prostaglandin endoperoxide analogue, u-44069 and the specific binding of another analogue, [3h]u-46619 to washed guinea pig platelets. seratrodast could competitively inhibit the contraction of rabbit aorta and pig coronary arteries induced by u-44069. seratrodast also inhibited the contraction of rabbit aorta induced by pgf2 alpha and the contraction of pig coronary arteries. however, seratrodast had no effect on the antiaggregatory effect of guinea pig platelets [1].
in vivoin experiments with guinea pigs, oral seratrodast at 0.1-1 mg/kg could dose-dependently inhibit the platelet aggregation induced by u-44069; the inhibition at 1 mg/kg was 100% at 1 hr and was 89% even at 24 hr after seratrodast administration [1].
IC 507.4 nm for guinea pig platelets
references[1] imura, y. ,terashita, z.,shibouta, y., et al. antagonistic action of aa-2414 on thromboxane a2/prostaglandin endoperoxide receptor in platelets and blood vessels. japanese journal of pharmacology 52(1), 35-53 (1990).
Seratrodast Preparation Products And Raw materials
Raw materialsPhenol-->Ferric chloride-->Heptanoic acid-->Trimethylhydroquinone-->(1S)-(+)-Camphor-10-sulphonic acid
Fexofenadine hydrochloride Acetaminophen Ozagrel Testosterone undecanoate Salbutamol Pemirolast potassium Cetirizine LACOSAMIDE Cyclophosphamide monohydrate Ketotifen fumarate Cetirizine hydrochloride (R*,S*)-(-)-8-Hydroxy-5-(1-hydroxy-2-((1-methylethyl)amino)butyl)-2(1H)-quinolinone Mesna BECLOMETHASONE Thionyl chloride 1,4-HEXADIENE 7-PHENYLHEPTANOIC ACID Heptanoic acid

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