Chemical structure
Cat.No.
Product Name
CAS no.
Target
C16-PAF (PAF (C16)), a phospholipid mediator, is a platelet-activating factor and lig and for PAF G-protein-coupled receptor (PAFR). C16-PAF exhibits anti-apoptotic effect and inhibits caspase-dependent death by act...
Limaprost (OP1206) is aPGE1analogue and a potent and orally active vasodilator. Limaprost increases blood flow and inhibits platelet aggregation. Limaprost can be used for pain relief, has antianginal effects, and has potent...
Sauvagine, a 40-amino-acid neuropeptide from the skin of the frog, is amammalian CRFagonist. Sauvagine is effective at releasing ACTH from rat pituitary cells. Sauvagine possesses a number of pharmacological actions on diuresis, t...
Ro 363 is a potent and highly selectiveβ1-adrenoceptoragonist. RO 363 is an effective inotropic stimulant, and is a cardiovascular modulator that reduces diastolic blood pressure and pronounces increases in myocardial contractilit...
YN360598 Bepridil hydrochloride hydrat... 74764-40-2
Bepridil hydrochloride is an anti-anginal drug classified as a calcium channel blocker. It also blocks multiple other ion channels, including sodium and potassium channels.
YN372786 Argatroban 74863-84-6
Argatroban is a potent and selective synthetic thrombin inhibitor with Ki ranging from 5 nM to 39 nM, used as an anticoagulant.
YN251600 Kukoamine A 75288-96-9
Kukoamine A is a natural occurring spermine derivative, acts as a potent inhibitor oftrypanothione reductase(Ki, 1.8μM), with antihypertensive activity.
YN373122 Lovastatin 75330-75-5
Lovastatin is an inhibitor of HMG-CoA reductase with IC50 of 3.4 nM in a cell-free assay, used for lowering cholesterol (hypolipidemic agent).
YN320665 Cefminox sodium 75498-96-3
Cefminox Sodium is the sodium salt form of cefminox, a semi-synthetic, second-generation, beta-lactamase-stable cephalosporin with antibacterial activity.
YN360483 Nilvadipine 75530-68-6
Nilvadipine is a potent calcium channel blocker with an IC50 of 0.03 nM.
Imanixil (HOE-402 free base) is an inducer of the LDL receptor (LDLR). Imanixil (HOE-402 free base) is also a potent cholesterol-lowering compound, which inhibits very low density-lipoprotein (VLDL) production, and cons...
YN360751 Isradipine 75695-93-1
Isradipine is a potent and selective L-type voltage-gated calcium channel blocker, used to treat high blood pressure.
Ancarolol is abeta-adrenergicblocking agent.
Enalapril (MK-421) is an angiotensin converting enzyme (ACE) inhibitor.
YN370769 4-Hydroxynonenal 75899-68-2
4-Hydroxynonenal (4-HNE) is an α,β unsaturated hydroxyalkenal and an oxidative/nitrosative stress biomarker. 4-Hydroxynonenal is a substrate and an inhibitor ofacetaldehyde dehydrogenase 2 (ALDH2). 4-Hydroxynonenal can modu...
YN480823 (R)-Nicardipine 76093-35-1
(R)-Nicardipine ((R)-YC-93 free base) is the less active R enantiomer of Nicardipine. Nicardipine (YC-93) is acalcium channelblocker with an IC50 of 1μM for blocking cardiac calcium channels. Nicardipine acts as an agent for ...
YN480822 (S)-Nicardipine 76093-36-2
(S)-Nicardipine ((S)-YC-93 free base) is the less active S enantiomer of Nicardipine. Nicardipine is acalcium channelblocker with an IC50 of 1μM for blocking cardiac calcium channels. Nicardipine acts as an agent for chronic st...
YN372778 Enalapril maleate 76095-16-4
Enalapril Maleate is an angiotensin-converting enzyme (ACE) inhibitor, used in the treatment of hypertension, diabetic nephropathy, and chronic heart failure.
YN482073 Mildronate 76144-81-5
Mildronate (Meldonium) functions as a cardioprotective drug by cpmpetetively inhibitingBBOX1 and OCTN2. Mildronate (Meldonium) exhibitsIC50 values of 34-62μM for human recombinant BBOX and an EC50 of 21μM for human...
YN360037 Nicainoprol 76252-06-7
Nicainoprol is a fast-sodium-channelblocking drug, which is a potent antiarrhythmic agent.
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