44 Results for "

Thromboxane receptor antagonists

" in MedChemExpress (MCE) Product Catalog:
Products (44)

44 Results for "Thromboxane receptor antagonists" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-B0774
CAS No.: 112665-43-7
Synonyms: AA 2414
Seratrodast (AA 2414), an orally active antiasthmatic agent, is a thromboxane A2 receptor (TP) antagonist and ferroptosis inhibitor. Seratrodast reduces lipid ROS production, modulates the systemic xc-/GSH/GPX4 axis, and inhibits JNK phosphorylation and p53 expression. Seratrodast exhibits anti-asthmatic and anti-epileptic activity .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-16991
CAS No.: 165538-40-9
Synonyms: S-18886
Terutroban (S-18886) is a selective and orally active thromboxane-prostaglandin (TP) receptor antagonist with an IC50 of 16.4 nM. Terutroban inhibits TXA2 and prostaglandin endoperoxide receptors. Terutroban is a potent antithrombotic agent and possesses anti-atherosclerotic and anti-vasoconstrictor properties .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-105218
CAS No.: 143443-90-7
Purity:  99.65%
Synonyms: BMS-180291
Ifetroban (BMS-180291) is an orally active antagonist of thromboxane A2 (TXA2) or prostaglandin H2 (PGH2) receptor. Ifetroban shows antiplatelet activity, and inhibits tumor cell migration without affecting cell proliferation. Ifetroban can be used for myocardial ischemia, hypertension, stroke, thrombosis, cardiomyopathy research .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-105218A
CAS No.: 156715-37-6
Purity:  99.83%
Synonyms: BMS-180291 sodium
Ifetroban (BMS-180291) sodium is an orally active antagonist of thromboxane A2 (TXA2) or prostaglandin H2 (PGH2) receptor. Ifetroban sodium shows antiplatelet activity, and inhibits tumor cell migration without affecting cell proliferation. Ifetroban sodium can be used for myocardial ischemia, hypertension, stroke, thrombosis, cardiomyopathy research .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-16991A
CAS No.: 609340-89-8
Synonyms: S-18886 sodium
Terutroban (S-18886) sodium is a selective and orally active thromboxane-prostaglandin (TP) receptor antagonist with an IC50 of 16.4 nM. Terutroban sodium inhibits TXA2 and prostaglandin endoperoxide receptors. Terutroban sodium is a potent antithrombotic agent and possesses anti-atherosclerotic and anti-vasoconstrictor properties .
loading...
    loading...
Cat. No.: HY-108972
CAS No.: 98672-91-4
Purity:  ≥99.0%
Research Areas:  

Metabolic Disease

SQ 29548 is a selective thromboxane-prostanoid (TP) receptor antagonist .
loading...
    loading...
Cat. No.: HY-129851
CAS No.: 2055599-51-2
Purity:  98.58%
Research Areas:  

Cardiovascular Disease

NTP42 is a thromboxane A2 (TXA2) receptor antagonist with an IC50 of 3.278 nM for antagonizing T prostanoid receptor (TP)- mediated [Ca 2+] mobilization following stimulation of cells with the alternative TP agonist U46619 . NTP42 can be used for the treatment of pulmonary arterial hypertension (PAH) .
loading...
    loading...
Cat. No.: HY-N2600
CAS No.: 76472-87-2
Kuwanon H is a selective non-peptide bombesin receptor antagonist and platelet activation inhibitor. Kuwanon H also acts as a specific antagonist of GRP-preferring receptors, with a Ki value of 290 nM for mouse GRP-R and 6500 nM for rat NMB-R. Kuwanon H inhibits the phosphorylation of AKT, mTOR, ERK, cPLA2 and p38, and upregulates TRIB3. It induces endoplasmic reticulum stress, apoptosis and autophagosome formation. Kuwanon H blocks calcium mobilization, mitogenic signaling, DNA synthesis, dense granule secretion, thromboxane A2 generation and integrin αIIb/β3 activity. It inhibits collagen-induced platelet aggregation and fibronectin adhesion, and delays clot retraction. Kuwanon H inhibits melanoma cell growth in vitro and in vivo, and enhances the sensitivity of melanoma cells to CDDP. It can be used in research related to melanoma, small cell lung cancer and thrombosis .
loading...
    loading...
Cat. No.: HY-121018
CAS No.: 79094-20-5
Synonyms: BM-13505; SKF 96148
Research Areas:  

Cardiovascular Disease

Daltroban (BM-13505) is a selective and specific thromboxane A2 (TXA2) receptor antagonist. Daltroban increase intracellular calcium in vascular smooth muscle cells. Daltroban shows protective effect in reperfusion injury .
loading...
    loading...
Cat. No.: HY-176990
CAS No.: 165537-72-4
TP receptor antagonist-3 (compound 51280) is a potent thromboxane A2 prostanoid (TP) receptor with an IC50 of 15.7 nM against Human TP. TP receptor antagonist-3 can be used for alzheimer's disease, cardiovascular and respiratory diseases, and cancer research .
loading...
    loading...
Cat. No.: HY-111271A
CAS No.: 1030017-51-6
Purity:  99.81%
L 888607 Racemate is a selective prostaglandin D2 receptor subtype 1 (DP1) antagonist, with Kis of 132 nM and 17 nM for DP1 and thromboxane A2 receptor (TP), respectively.
loading...
    loading...
Cat. No.: HY-B0774R
CAS No.: 112665-43-7
Synonyms: AA 2414 (Standard)
Seratrodast (Standard) is the analytical standard of Seratrodast. This product is intended for research and analytical applications. Seratrodast (AA 2414), an orally active antiasthmatic agent, is a thromboxane A2 receptor (TP) antagonist and ferroptosis inhibitor. Seratrodast reduces lipid ROS production, modulates the systemic xc-/GSH/GPX4 axis, and inhibits JNK phosphorylation and p53 expression. Seratrodast exhibits anti-asthmatic and anti-epileptic activity .
loading...
    loading...
Cat. No.: HY-13706
CAS No.: 844639-57-2
Purity:  99.00%
Synonyms: TM30089 Racemate
Research Areas:  

Endocrinology Cancer

CAY10471 Racemate (TM30089 Racemate) is a potent and highly selective prostaglandin D2 receptor CRTH2 antagonist, with a Ki of 0.6 nM for hCRTH2, selective over human thromboxane A2 receptor TP (Ki, >10000 nM) or PGD2 receptor DP (Ki, 1200 nM). CAY10471 Racemate also has effect on mouse and rat orthologs of CRTH2 .
loading...
    loading...
Cat. No.: HY-165587
CAS No.: 284464-83-1
Research Areas:  

Cardiovascular Disease

BM-573 is an orally active dual thromboxane A₂ (TXA₂) modulator with an IC50 of 1.3 nM. BM-573 possesses both thromboxane synthase (TxAS) inhibition and thromboxane receptor (TP) antagonistic effects. BM-573 can completely inhibit platelet aggregation induced by Arachidonic acid (HY-109590) or U-46619 (TXA₂ analogues). BM-573 completely blocks the generation of TXB₂ (the stable metabolite of TXA₂) in human platelets and does not inhibit cyclooxygenase (COX-1/COX-2), thus avoiding interference with other prostaglandin synthesis. BM-573 has an inhibitory effect on U-46619-induced contractions in rat gastric fundus smooth muscle (ED₅₀ = 4.2 μM), but has no effect on contractions caused by PGE₂, PGF₂α, or PGI₂. BM-573 can be used in the study of atherosclerosis, myocardial infarction, pulmonary hypertension and shock .
loading...
    loading...
Cat. No.: HY-19189
CAS No.: 149979-74-8
Synonyms: BIBV 308SE
Terbogrel is an orally available thromboxane A2 receptor antagonist and a thromboxane A2 synthase inhibitor, with both IC50s of about 10 nM.
loading...
    loading...
Cat. No.: HY-U00253
CAS No.: 217799-03-6
KP496 is a selective, dual antagonist for Leukotriene D4 receptor and Thromboxane A2 receptor.
loading...
    loading...
Cat. No.: HY-U00072
CAS No.: 207987-59-5
RS-601 is a novel leukotriene D4 (LTD4)/thromboxane A2 (TxA2) dual receptor antagonist, with antiasthmatic activities.
loading...
    loading...
Cat. No.: HY-19132
CAS No.: 134235-78-2
Research Areas:  

Cardiovascular Disease

CGS 22652 is a potent thromboxane A2 receptor antagonist. CGS 22652 has selective thromboxane A2 synthase inhibitory properties. CGS 22652 can be used in the research of coronary artery thrombosis .
loading...
    loading...
Cat. No.: HY-111304
CAS No.: 848188-18-1
MF266-1 is a selective E prostanoid receptor 1 (EP1) antagonist with an Ki value of 3.8 nM. MF266-1 also has moderate selectivity for thromboxane A2 receptor (TP). MF266-1 is promising for research of arthritis .
loading...
    loading...
Cat. No.: HY-101235
CAS No.: 106393-80-0
ICI 185282 is a potent, selective, orally active thromboxane A2 (TXA₂) receptor antagonist. ICI 185282 causes dose-dependent inhibition of U-46619 (HY-108566)-induced platelet aggregation ex-vivo in guinea-pig. ICI 185,282 inhibits bronchospasm induced by U-46619, PGD2 (HY-101988), PGF (HY-12956), arachidonic acid (HY-109590), LTD4 and PAF (HY-108635) in vivo. ICI 185282 can be used for bronchial asthma research .
loading...
    loading...