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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T5458 | Darusentan | Lu-135252 | Endothelin Receptor |
Darusentan (Lu-135252) is a potent inhibitor of endothelin signaling and function in both large and small arteries | |||
TN1969 | N-(p-Coumaroyl) serotonin | PDGFR | |
N-(p-Coumaroyl) Serotonin is a polyphenol isolated from the seeds of safflower. N-(p-Coumaroyl) serotonin has antioxidant, cardioprotective effects after ischemia and antitumor activity, it may be beneficial in improving... | |||
TQ0003 | 740 Y-P | 740YPDGFR,PDGFR 740Y-P | PI3K , Autophagy |
740 Y-P (740YPDGFR) is a potent and cell-permeable activator of PI3K. | |||
T3965 | Fevipiprant | QAW039,NVP-QAW039 | GPR , Prostaglandin Receptor |
Fevipiprant (NVP-QAW039) is a selective, potent, reversible competitive CRTh2 antagonist. | |||
T13475 | β-Aminopropionitrile | 3-Aminopropionitrile,BAPN | Others , Endogenous Metabolite |
β-Aminopropionitrile (3-Aminopropionitrile) is a selective inhibitor of lysyl oxidase. | |||
T7437 | 3-(3-Hydroxyphenyl)propionic Acid | m-Hydroxyphenylpropionic acid,3-Hydroxyhydrocinnamic acid | Others , Endogenous Metabolite |
3-(3-Hydroxyphenyl)propionic Acid (m-Hydroxyphenylpropionic acid) is one of the major metabolites of ingested caffeic acid.it inhibited osteoclastogenesis and bone osteoclastic resorptive activity. | |||
T6991 | Nitroprusside disodium dihydrate | Sodium Nitroferricyanide(III) Dihydrate,Sodium Nitroprusside Dihydrate | Guanylate cyclase , Autophagy |
Nitroprusside disodium dihydrate (Sodium Nitroprusside Dihydrate) is a potent vasodilator working through releasing NO spontaneously in blood. | |||
T10101 | Calcium channel-modulator-1 | Others , Calcium Channel | |
Calcium channel-modulator-1 is a calcium channel-modulator (IC50:0.8 μM) with specialisation to block aortic constriction. | |||
T33868 | Palmitoyl glutamic acid | N-Palmitoyl-L-glutamic acid,Palmitoylglutaminic acid | |
Palmitoyl glutamic acid (N-Palmitoyl-L-glutamic acid) is an acyl amino acid that blocks aortic constriction and antagonizes haloperidol-induced oral motility disorders. | |||
T62893 | SM-2470 | Adrenergic Receptor | |
SM-2470 is an α1-adrenoceptor antagonist with antihypertensive activity that decreases anterior ganglionic adrenal nerve activity and aortic descending nerve activity.SM-2470 has hypocholesterolemic activity and inhibits... | |||
TQ0057 | AVE 0991 | Others | |
AVE 0991, a nonpeptide analog of angiotensin-(1-7) [Ang-(1-7)], is an orally active Mas agonist with inhibitory effects on [125I]-Ang-(1-7) binding to bovine aortic endothelial cell membranes, and inhibits astrocyte-medi... | |||
T6102 | 2'-acetylacteoside | Antioxidant , Reductase | |
2'-Acetylacteoside has antioxidative activity. It can significantly attenuate glutamate-induced neurotoxicity at concentrations ranging from 0.1 to 10 μM. 2'-Acetylacteoside shows antiproliferative effects on aortic smoo... | |||
T11598 | IAXO-102 | TLR | |
IAXO-102 is a TLR4 antagonist that negatively regulates TLR4 signaling. It inhibits MAPK and p65 NF-κB phosphorylation and expression of TLR4 dependent proinflammatory protein. IAXO-102 also prevents experimental abdomin... | |||
T7284 | Argipressin acetate (113-79-1(free base)) | Others | |
Vasopressin acetate is a peptide hormone with vasoconstrictive and antidiuretic activities that binds to the vascular arginine vasopressin receptor, V1, with Kd values of 1.31 and 1.44 nM in A7r5 rat aortic smooth muscle... | |||
T11076 | Dooku1 | Others | |
Dooku1 is an analog of Yoda1 and a selective antagonist of endogenous Piezo1 channels. Dooku1 inhibits Ca2+ entry induced by 2μMYoda1 with IC50 values of 1.3μM (in HEK 293 cells) and 1.5μM (in HUVEC). Dooku1 inhibits Yod... | |||
T30140 | Arotinolol hydrochloride | Arotinolol HCl | 5-HT Receptor , Adrenergic Receptor |
Arotinolol hydrochloride(Arotinolol HCl) is a non-selective α/β-adrenergic receptor blocker.Arotinolol hydrochloride inhibits the binding of the radioligand 125I-ICYP to the 5HT1B-hydroxytryptamine receptor. Arotinolol h... | |||
TN1724 | Harmalol hydrochloride | Harmidol hydrochloride | P450 , Antioxidant |
Harmalol hydrochloride (Harmidol hydrochloride) is a β-carboline alkaloid that can be extracted from the seeds of Peganum harmala L. Harmalol hydrochloride is the major metabolite of Harmaline and significantly inhibits ... | |||
T68123 | Oxodipine | Calcium Channel | |
Oxodipine, a dihydropyridine-type calcium antagonist , inhibited KCl-induced aortic contraction in rabbits and reduced cardiac force in less potent rat ventricular test-paper contractions. In rat cultured neonatal ventri... | |||
T33440 | MK785 | MK-785,MK 785 | |
MK785 is part of the association between inhibition of aortic histamine formation, aortic albumin permeability, and atherosclerosis. Aortic histamine synthesis was inhibited by partial inhibition of aortic histidine deca... | |||
T32406 | KMUP-4 | KMUP 4 | |
Kmup-4 is an enhancer of cGMP activity and an aortic smooth muscle relaxant. |