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Cardiovascular Disease

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  • YN250042 BRD-6929 849234-64-6

    BRD-6929 (Cpd-60) is a brain-penetrant, selective inhibitor of HDAC1 and HDAC2(IC50= 1 and 8nM), extracted from patent US2018360927. BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 with Kiof 0.2 ...

  • YN372705 Alogliptin Benzoate 850649-62-6

    Alogliptin is a potent, selective inhibitor of DPP-4 with IC50 of <10 nM, exhibits greater than 10,000-fold selectivity over DPP-8 and DPP-9.

  • YN450103 GSK269962A 850664-21-0

    GSK269962A (GSK 269962) is a potentROCKinhibitor with IC50s of 1.6 and 4nM for recombinant humanROCK1 and ROCK2respectively. GSK269962A has anti-inflammatory and vasodilatory activities.

  • YN320680 MK-0354 851776-28-8

    MK-0354 is a partial agonist of GPR109a receptor, for hGPR109a/ mGPR109a with EC50 of 1.65/1.08μM, showed no activation of GPR109b.

  • YN360805 Ropivacaine mesylate 854056-07-8

    Ropivacaine Mesilate is the mesylate form of ropivacaine, which is a member of the amino amide class of local anesthetics.

  • YN370962 Kurarinol 855746-98-4

    Kurarinol is a flavanone found in the root ofSophora flavescens. Kurarinol is a competitivetyrosinaseinhibitor, with IC50 of 0.1μM for mushroom tyrosinase.

  • YN330291 Choline Fenofibrate 856676-23-8

    Choline fenofibrate is a newly developed choline salt of fenofibric acid, a synthetic phenoxy-isobutyric acid derivate with antihyperlipidemic activity that acts as an PPARα agonist.

  • YN300029 (-)-Blebbistatin 856925-71-8

    (-)-Blebbistatin is a cell-permeable inhibitor for non muscle myosin II ATPase with IC50 of ~2 μM in cell-free assays, does not inhibit myosin light chain kinase, inhibits contraction of the cleavage furrow without disrupting mito...

  • YN340042 BMS-690514 859853-30-8

    BMS-690514 is a potent and orally active inhibitor ofEGFR and VEGFR; hasIC50s of 5, 20 and 60nM for EGFR, HER 2 and HER 4, respectively.

  • YN483839 M617 860790-38-1

    M617 is a selective galanin receptor 1(GAL1)agonist, with Kis of 0.23 and 5.71nM for GAL1 and GAL2, respectively. M617, acting through its central GAL1, can promote GLUT4 expression and enhance GLUT4 content in...

  • YN320903 Azilsartan medoxomil 863031-21-4

    Azilsartan Medoxomil is a potent angiotensin II type 1 (AT1) receptor antagonist, inhibits the RAAS, with an IC50 of 2.6 nM, exhibits >10,000-fold selectivity over AT2.

  • YN360151 Zoniporide hydrochloride hydr... 863406-85-3

    Zoniporide (CP-597396) hydrochloride hydrate is a potent and selective inhibitor ofsodium-hydrogen exchanger type 1 (NHE-1). Zoniporide hydrochloride hydrate inhibits human NHE-1 (IC50=14nM), and has >150-fold selectivity v...

  • YN321038 Revefenacin 864750-70-9

    Revefenacin (TD-4208) is a potent, lung-selective, long-acting muscarinic antagonist that may be for the treatment of respiratory disease.

  • YN480717 Aladorian 865433-00-7

    Aladorian (ARM036) is a benzothiazepine derivative, with anti-arrhythmia effect. Aladorian is used for the research of heart failure and catecholaminergic polymorphic ventricular tachycardia.

  • YN372684 5-R-Rivaroxaban 865479-71-6

    5-R-Rivaroxaban is (R)-enantiomer of Rivaroxaban. Rivaroxaban (BAY 59-7939) is a highly potent and selective, directFactor Xa(FXa) inhibitor, achieving a strong gain in anti-FXa potency (IC500.7nM;Ki0.4nM).

  • YN310059 CMPD101 865608-11-3

    CMPD101 is a potent, highly selective and membrane-permeable small-molecule inhibitor ofGRK2/3with IC50 of 18nM and 5.4nM, respectively. CMPD101 exhibits less selectively against GRK1, GRK5, ROCK-2 and PKC...

  • YN320994 PRX-08066 866206-54-4

    PRX-08066 is a selective 5-hydroxytryptamine receptor 2B (5-HT2BR, IC50= 3.4nM) antagonist that causes selective vasodilation of pulmonary arteries.

  • YN450021 ROCK-IN-2 867017-68-3

    Azaindole 1 (TC-S 7001) is a selective Rho-associated protein kinase (ROCK) inhibitor with IC50 of 0.6 and 1.1 nM for human ROCK-1 and ROCK-2 in an ATP-competitive manner.

  • YN481405 Tecarfarin 867257-26-9

    Tecarfarin (ATI-5923) is an orally active and non-competitive vitamin K epoxide reductase (VKOR) antagonist, and impairs the activation of the vitamin K-dependent clotting factors II, VII, IX and X. Tecarfarin has t...

  • YN321901 Obestatin(rat) 869705-22-6

    Obestatin(rat), encoded by the Ghrelin gene, is a cpeptide, comprised of 23 amino acids. Obestatin(rat) suppresses food intake, inhibits jejunal contraction, and decreases body-weight gain. Obestatin is an endogenous lig and of G-pr...

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