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Digitonin is a natural product of the glycoside family and is a detergent. Digitonin has antitumor activity, binds to cholesterol molecules to increase the permeability of cell membranes, and is active in the cleavage of cell membranes in a wide range of cells.

L-701324 is an NMDA receptor with high affinity and selectivity for the glycine site, used as an orally active and long-acting anticonvulsant.

Mildronate (Meldonium) is an inhibitor of biosynthesis of L-carnitine by gamma-butyrobetaine (GBB) hydroxylase and as a competitive inhibitor of renal carnitine reabsorption.

Mildronate dihydrate is an inhibitor of biosynthesis of L-carnitine by gamma-butyrobetaine (GBB) hydroxylase and as a competitive inhibitor of renal carnitine reabsorption.

Lemildipine is a new blocker of dihydropyridine calcium entry.

Mildiomycin, an antibiotic produced by Streptoverticillium rimofaciens, effectively targets powdery mildew in barley. It also suppresses the growth of certain Mycobacterium and Rhodotorula species, though it is ineffective against most fungi and bacteria [1].

Mildronate-D3 hydrochloride is a deuterated compound of Mildronate hydrochloride.

Lecanemab (BAN-2401) is an IgG1 monoclonal antibody targeting soluble aggregated β-amyloid (Abeta) with activity against oligomers, protofibrils, and insoluble protofibrils, and may be useful in the study of Alzheimer's disease (AD)-induced mild cognitive impairment and mild AD dementia.

Norverapamil-D7 is a deuterium labeled Norverapamil (T12244) . Norverapamil (T12244) is a blocker of L-type calcium channel and an inhibitor of P-glycoprotein (P-gp) function .

Nedocromil sodium is a pharmacologic stabilizer of mast cells, has been shown to normalize cytokine levels and attenuate cardiac remodeling.

Verapamil-D7 is the deuterated form of Verapamil. Verapamil (T20656) ( (±)-Verapamil) acts as a calcium channel blocker and serves as an effective oral first-generation P-glycoprotein (P-gp) inhibitor. It also inhibits CYP3A4 and is utilized in research related to hypertension, arrhythmias, and angina.

Verapamil D3 is a deuterated compound of verapamil. Verapamil (CP-16533-1) is a non-dihydropyridine calcium channel blocker, a P-gp inhibitor, and a CYP3A4 inhibitor with oral activity. Verapamil can be used for the treatment of hypertension, angina pectoris, and myocardial infarction.

Norverapamil-D7 hydrochloride is a 2H-labeled Norverapamil hydrochloride (TMSM-3613), a calcium channel blocker and P-glycoprotein (P-gp) inhibitor, used in cardiovascular and neurodegenerative disease research.

R-Verapamil-D7 hydrochloride is a deuterated compound of R-Verapamil hydrochloride (TMSM-6393). R-Verapamil hydrochloride has a CAS number of 1188265-55-5.

S-Verapamil-D7 hydrochloride is a deuterated compound of S-Verapamil hydrochloride (TMSM-6393). S-Verapamil hydrochloride has a CAS number of 1188265-55-5.

Verapamil-D7 hydrochloride is a deuterated compound of Verapamil Hydrochloride. Verapamil Hydrochloride (T1010) has a CAS number of 152-11-4. Verapamil hydrochloride is a calcium channel blocker that is a class IV anti-arrhythmia agent.

Verapamil-D7 Hydrochloride (Standard) is a reference standard of Verapamil-D7 Hydrochloride intended for quantitative analysis, quality control, and related biochemical research applications. Verapamil-d7 Hydrochloride is a deuterated compound of Verapamil Hydrochloride. Verapamil Hydrochloride has a CAS number of 152-11-4. Verapamil hydrochloride is a calcium channel blocker that is a class IV anti-arrhythmia agent.

Norverapamil-D7 Hcl (Standard) is a reference standard of Norverapamil-D7 Hcl intended for quantitative analysis, quality control, and related biochemical research applications. Norverapamil-d7 HCl (D591-d7 HCl) is a 2H-labeled Norverapamil HCl, a calcium channel blocker and P-glycoprotein (P-gp) inhibitor, used in cardiovascular and neurodegenerative disease research.

Semaglutide TFA is a glucagon-like peptide-1 congener that induces weight loss, lowers blood glucose levels, and reduces cardiovascular risk in diabetic patients.Semaglutide TFA induces mild-to-moderate and transient gastrointestinal disturbances, and may be used in the study of type 2 diabetes and obesity.

ABT-288 is a selective and potent H3 antagonist for the treatment of mild to moderate Alzheimer's dementia.

Nanterinone (UK 61260), an orally available partial phosphodiesterase inhibitor, is a novel positive inotropic and balanced vasodilator compound.Nanterinone, when administered orally, results in significant improvements in acute haemodynamics, which may depend on pre-existing left ventricular filling pressures.Nanterinone is a novel positive inotropic and balanced vasodilator that has demonstrated acute hemodynamic effects in patients with mild to moderate heart failure.

Nolomirole HCl (CHF 1035) is a novel selective dopamine agonist with oral activity and inhibitory effects on norepinephrine release, which can be used to study mild chronic heart failure.

F13714 fumarate is a selective 5-HT1A receptor-biased agonist with antidepressant-like properties after a single dose in a mouse model of chronic mild stress.

Carprazidil is a potent vasodilator used to treat severe hypertension and mild heart failure.