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Cardiovascular Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN480167 Isoxsuprine-monoester-1 67160-74-1

    Isoxsuprine-monoester-1, a monoester of isoxsuprine, is a long acting peripheral vasodilator.

  • YN1570011 Fenoldopam 67227-56-9

    Fenoldopam(SKF 82526) is a drug and synthetic benzazepine derivative which acts as a selective D1 receptor partial agonist.

  • YN1570012 Fenoldopam mesylate 67227-57-0

    Fenoldopam is a selective dopamine-1 receptor (DA1) agonist with natriuretic/diuretic properties. It lowers blood pressure through arteriolar vasodilation.

  • YN361089 (±)-Naringenin 67604-48-2

    (±)-Naringenin is a naturally-occurring flavonoid. (±)-Naringenin displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCachannels in myocytes.

  • YN330178 S-Nitroso-N-acetyl-DL-pen... 67776-06-1

    S-Nitroso-N-acetyl-DL-penicillamine (SNAP) is a nitric oxide donor and acts as a stable inhibitor of platelet aggregation.

  • YN360047 Norverapamil hydrochloride 67812-42-4

    Norverapamil hydrochloride ((±)-Norverapamil hydrochloride), an N-demethylated metabolite of Verapamil, is aL-type calcium channelblocker and aP-glycoprotein (P-gp)function inhibitor.

  • YN483744 GPRP 67869-62-9

    GPRP (Pefa 6003) is a fibrin polymerization inhibitor that inhibits the interaction of fibrinogen with the platelet membrane glycoprotein IIb/IIIa complex (GPIIb/IIIa).

  • YN482406 Aurantio-obtusin 67979-25-3

    Inhibition of sEH (unknown origin) assessed as 6-methoxy-2-naphthaldehyde formation at 50 uM by fluorometry assay using 40 uM cyano-(6-methoxy-naphthalen-2-yl)-methyl ester as substrate

  • YN360130 Bepridil hydrochloride 68099-86-5

    Bepridil hydrochloride (CERM 1978) is acalcium channelblocker, with antianginal activity.

  • YN484217 Drobuline hydrochloride 68162-52-7

    Drobuline hydrochloride is an anti-arrhythmic agent with cardiac depressant.

  • YN320566 Arotinolol 68377-92-4

    Arotinolol is a nonselectiveα/β-adrenergic receptorblocker and a vasodilating β-blocker. Arotinolol also shows potency for inhibiting the binding of the radiolig and 125I-ICYP to5HT1B-serotonergic receptor sites. Arotinolol...

  • YN320810 Angiotensin II human acetat... 68521-88-0

    Angiotensin II (angII) is an octapeptide hormone which affects the activities of heart, kidney, vasculature and brain. It works via binding to specific receptors present on cell membranes.

  • YN370144 Cilostamide 68550-75-4

    Cilostamide is an inhibitor of type III phosphodiesterases with IC50 values of 27 nM and 50 nM for PDE3A and PDE3B, respectively.

  • YN480694 N-Feruloylserotonin 68573-23-9

    N-Feruloylserotonin, an antioxidative component and bioactive serotonin derivative, from the Seed of Carthamus tinctorius L., ameliorates atherosclerosis and distensibility of the aortic wall in Kurosawa and Kusanagi-hyperchole...

  • YN320115 Tiotidine 69014-14-8

    Tiotidine (ICI 125211) is a potent and selective antagonist ofhistamine H2-receptor(pA2=7.3-7.8 for guinea-pig right atrium). Tiotidine has low affinity for both the H1 and the H3 receptors.

  • YN481756 Sapropterin dihydrochloride 69056-38-8

    Sapropterin Dihydrochloride, a synthetic preparation of the dihydrochloride salt of naturally occurring tetrahydrobiopterin (BH4), is a phenylalanine hydroxylase activator.

  • YN482811 Pinoresinol 4-O-β-D-glucop... 69251-96-3

    Pinoresinol 4-O-β-D-glucopyranoside ((+)-Pinoresinol 4-O-β-D-glucopyranoside) is the major active furofuran type lignans in Fructus Forsythiae. Pinoresinol 4-O-β-D-glucopyranoside shows antioxidant, blood pressure reducing, a...

  • YN320453 Carbacyclin 69552-46-1

    Carbacyclin is a PGI2 analogue, acts as aprostacyclin (PGI2) receptoragonist and vasodilator, and potently inhibits platelet aggregation.

  • YN480017 RGH-5526 69579-13-1

    RGH-5526 (GYKI-11679) is a new antihypertensive agent.

  • YN360949 Tanshinone IIA sulfonate s... 69659-80-9

    Sodium tanshinone IIA sulfonate (STS) is a water-soluble derivative of tanshinone IIA isolated as the main pharmacologically active natural compound from a traditional Chinese herbal medicine, the dried root of Salvia miltiorrhi...

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