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Cardiovascular Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN372754 Nafamostat 81525-10-2

    Nafamostat, a synthetic serine protease inhibitor, is an anticoagulant. Nafamostat supresses T cell auto-reactivity by decreasing granzyme activity and CTL cytolysis. Nafamostat blocks activation of SARS-CoV-2.

  • YN360069 Sodium ionophore III 81686-22-8

    Sodium ionophore III (ETH2120) is aNa+ionophore suitable for the assay of sodium activity in blood, plasma, serum. etc.

  • YN330452 Zofenopril calcium 81938-43-4

    Zofenopril calcium is an angiotensin-converting enzyme (ACE) inhibitor that protects the heart and helps reduce high blood pressure.

  • YN321493 Ozagrel 82571-53-7

    Ozagrel is a selective thromboxane A(2) (TXA(2)) synthetase inhibitor with IC50 of 11 nM for rabbit platelet, used for the improvement of postoperative cerebrovascular contraction and accompanying cerebral ischaemia.

  • YN372788 Moexipril hydrochloride 82586-52-5

    Moexipril HCl is a potent orally active nonsulfhydryl angiotensin converting enzyme (ACE) inhibitor, used for the treatment of hypertension and congestive heart failure.

  • YN372809 Quinapril hydrochloride 82586-55-8

    Quinapril HCl is the hydrochloride salt of quinapril that is an angiotensin-converting enzyme inhibitor with a Ki of 20 μM.

  • YN484381 Vanillyl butyl ether 82654-98-6

    Vanillyl butyl ether, an ether of monohydroxybenzoic acid, is added to food products as a flavoring agent. It is also present in cosmetics and personal care products as a fragrance ingredient, oral care agent, hair conditioning agent, and...

  • YN372735 Perindopril 82834-16-0

    Perindopril (S-9490) is a long-acting ACE inhibitor of which is used to treat high blood pressure, heart failure or stable coronary artery disease. Perindopril is a long-acting ACE inhibitor. It is used to treat high blood pressur...

  • YN372755 Nafamostat mesylate 82956-11-4

    Nafamostat mesilate is a synthetic serine protease inhibitor, used as an anticoagulant during hemodialysis.

  • YN483968 Platelet Factor 4 (58-70), h... 82989-21-7

    Platelet Factor 4 (58-70), human, a peptide based on the amino acid sequence corresponding to residues 58-70 of platelet factor-4 (PF-4), contains the major heparin-binding domain, which is not sufficient for full antiangiogenic activit...

  • YN321783 Octreotide 83150-76-9

    Octreotide is a somatostatin analog that binds to thesomatostatin receptor, mainly subtypes 2, 3, and 5, increases Gi activity, and reduces intracellular cAMP production.

  • YN361059 Anipamil 83200-10-6

    Anipamil is a long-actingcalcium channelblocker, used for the treatment of cardiovascular disease.

  • YN370351 Delapril hydrochloride 83435-67-0

    an agonist of the RXR signaling pathway

  • YN482939 Ginsenoside Ra1 83459-41-0

    Ginsenoside Ra1 is a component from ginseng, inhibits protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation.

  • YN483765 α-CGRP, rat 83651-90-5

    α-CGRP, rat, a neuropeptide (calcitonin gene-related peptide (CGRP)), is a potent vasodilator, with the potential in cardiovascular, pro-inflammatory and metabolic studies.

  • YN484225 Ipramidil 83656-38-6

    Ipramidil (C80-1324) is a furoxan compound. Ipramidil (C80-1324) reveals marked dilator activity in the coronary circulation of isolated working hearts.

  • YN322069 Tertatolol 83688-84-0

    Tertatolol is a potent antagonist ofbeta-adrenoceptor and 5-HT receptor, with unique renal vasodilatatory effects.

  • YN372473 Lisinopril dihydrate 83915-83-7

    Lisinopril is an angiotensin-converting enzyme (ACE) inhibitor, used in treatment of hypertension, congestive heart failure, and heart attacks, and also in preventing renal and retinal complications of diabetes.

  • YN321960 Urotensin I 83930-33-0

    Urotensin I is, 41-aa neuropeptide, acts as an agonist ofCRF receptor withpEC50s of 11.46, 9.36 and 9.85 for human CRF1, human CRF2 and rat CRF2αreceptors in CHO cells, and Kis of 0.4, 1.8, and 5.7nM for hCRF1...

  • YN360802 Ropivacaine 84057-95-4

    Ropivacaine hydrochloride is an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM.

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