Antihypertensive drugs

Synonyms: D-ß-Phe(3-Cl)-OH(R)-3-Chloro-ß-phenylalanine Purity Limit: &ge 98% (HPLC) CAS No.: 262429-49-2 Molecular Formula: C9H10ClNO2 Molecular Weight: 199.

Synonyms: D-ß-Phe(3-Cl)-OH(R)-3-Chloro-ß-phenylalanine Purity Limit: &ge 98% (HPLC) CAS No.: 262429-49-2 Molecular Formula: C9H10ClNO2 Molecular Weight: 199.

Application ( R) -Butaprost has been used as a prostanoid receptor (EP)-specific agonist to study its effects on protein kinase A (PKA) regulatory subunits in MCF7 cells. It may be used as EP2 agonist in Madin-Darby canine kidney and mouse cortical

Application ( R) -Butaprost has been used as a prostanoid receptor (EP)-specific agonist to study its effects on protein kinase A (PKA) regulatory subunits in MCF7 cells. It may be used as EP2 agonist in Madin-Darby canine kidney and mouse cortical

(R)-Carvedilol ((R)-BM 14190), the R-enantiomer of Carvedilol, is a non-selective β/α-1 blocker. (R)-Carvedilol exerts protection against the vascular or cardiac toxicity of Doxorubicin (DOX)IC50&amp: Target:β/α-1 adrenergic receptor.

(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a calcium channel blocker .

(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a calcium channel blocker .

(R)-Metoprolol is an (R)-Enantiomer of Metoprolol. (R)-Metoprolol is ananti-hypertensive, anti-anginal, and anti-arrhythmic.

Application ( R )- N -[(1 R ,2 R )-2-(3-(3,5-Bis(trifluoromethyl)phenyl)ureido)cyclohexyl]- tert -butyl-sulfinamide is a sulfinamide-urea based chiral catalyst that can be used to synthesize: Enantioselective homoallylic amines by asymmetric

Application ( R )- N -[(1 R ,2 R )-2-(3-(3,5-Bis(trifluoromethyl)phenyl)ureido)cyclohexyl]- tert -butyl-sulfinamide is a sulfinamide-urea based chiral catalyst that can be used to synthesize: Enantioselective homoallylic amines by asymmetric

A potent, cell-permeable inhibitor of SET7/9 (IC₅₀ = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases.

A potent, cell-permeable inhibitor of SET7/9 (IC₅₀ = 2 nM) that demonstrates greater than 1,000-fold selectivity over a panel of 18 other methyltransferases.