94061-81-1

(3S,5R)-Fluvastatin sodium is the enantiomerically pure form of Fluvastatin, a fully synthetic and competitive HMG-CoA reductase inhibitor with nanomolar potency, (3S,5R)-Fluvastatin sodium additionally protects vascular smooth muscle cells from oxidative stress through activation of the Nrf2-dependent antioxidant pathway, supporting cardiovascular and redox biology research.

3S,5R-Fluvastatin-D6 is a deuterated compound of 3S,5R-Fluvastatin. 3S,5R-Fluvastatin (T10129) has a CAS number of 94061-81-1.

Fluvastatin (XU-62320) is a potent and competitive HMG-CoA reductase inhibitor (IC50: 8 nM) that inhibits oxidative stress in vascular smooth muscle cells through an Nrf2-dependent pathway, and is used for the reduction of plasma cholesterol levels and the prevention of cardiovascular disease.

(3R,5S)-Fluvastatin, the 3R,5S-isomer of Fluvastatin (XU 62-320 free acid), stands as the inaugural fully synthetic, competitive inhibitor of HMG-CoA reductase, exhibiting an IC50 value of 8 nM. It safeguards vascular smooth muscle cells from oxidative stress by activating the Nrf2-dependent antioxidant pathway.

Fluvastatin sodium (Standard) is the standard substance of Fluvastatin sodium, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Fluvastatin sodium (Fluvastatin sodium salt), a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent.

Fluvastatin (XU 62-320) sodium monohydrate, a fully synthetic competitive HMG-CoA reductase inhibitor, features an IC 50 of 8 nM. This compound also safeguards vascular smooth muscle cells from oxidative stress via the Nrf2-dependent antioxidant pathway [1] [2].

Fluvastatin-[D6] Sodium Salt (Standard) is a reference standard of Fluvastatin-[D6] Sodium Salt intended for quantitative analysis, quality control, and related biochemical research applications.

Fluvastatin-D6 sodium is the deuterium-labeled analogue of Fluvastatin sodium. Fluvastatin sodium (T1487) (XU 62320) is the first fully synthetic and competitive HMG-CoA reductase inhibitor, with an IC50 of 8 nM.

Fluvastatin-D6 sodium is a first fully synthetic, competitive HMG-CoA reductase inhibitor with an IC50 of 8 nM. Fluvastatin sodium (TMSM-1236) is deuterium labeled Fluvastatin sodium.

Fluvastatin-D6 Sodium Salt is a deuterated compound of Fluvastatin Sodium Salt. Fluvastatin Sodium Salt (T1487) has a CAS number of 93957-55-2. Fluvastatin sodium, a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent.

(3R,5S)-Fluvastatin ((3R,5S)-XU 62-320) sodium, a specific isomer of Fluvastatin, functions as a fully synthetic, competitive inhibitor of HMG-CoA reductase, exhibiting an IC50 of 8 nM. It is notable for its efficacy in shielding vascular smooth muscle cells from oxidative stress via the Nrf2-dependent antioxidant pathway [1] [2] [3].'

Fluvastatin sodium (Fluvastatin sodium salt), a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent.

Fluvastatin belongs to a class of medications called statins and is used to reduce plasma cholesterol levels and prevent cardiovascular disease. It is also the first entirely synthetic HMG-CoA reductase inhibitor and is structurally distinct from the fungal derivatives of this therapeutic class.