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Results for "

xu 62-320

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    9
    TargetMol | Inhibitors_Agonists
  • Isotope Products
    2
    TargetMol | Isotope_Products
Fluvastatin sodium
XU-62-320, XU 62320 sodium, Fluvastatin sodium salt
T148793957-55-2
Fluvastatin sodium (Fluvastatin sodium salt), a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent.
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Epibestatin Hydrochloride
T71626100992-60-7
Epibestatin Hydrochloride is a stabilizer of 14-3-3 PPIs, as well as a diastereoepimer of aminopeptidase inhibitor bestatin.
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6-8 weeks
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Citalopram hydrobromide
Nitalapram HBr, Lu 10-171, Citalopram HBr, Lu 10-171 HBr, Bonitrile HBr
T148359729-32-7
Citalopram hydrobromide (XU-62-320) , a selective serotonin reuptake inhibitor (SSRI), selectively inhibits the CNS neuronal reuptake of serotonin, thereby potentiating serotonergic activity in the central nervous system (CNS). Citalopram hydrobromide is the orally bioavailable hydrobromide salt of the racemic bicyclic phthalene derivative citalopram with antidepressant activity. This agent has minimal effects on the CNS neuronal reuptake of norepinephrine (NE) and dopamine (DA).
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(3S,5R)-Fluvastatin D6 sodium
(3S,5R)-XU 62-320 D6
T101282249799-35-5
(3S,5R)-Fluvastatin D6 sodium is the deuterium-labeled (3S,5R)-Fluvastatin sodium. Fluvastatin is a first fully synthetic, competitive HMG-CoA reductase inhibitor (IC50: 8 nM).
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(3S,5R)-Fluvastatin sodium
(3S,5R)-XU 62-320
T1012994061-81-1
(3S,5R)-Fluvastatin sodium is the (3S,5R)-enantiomer of Fluvastatin. Fluvastatin is a first fully synthetic, competitive HMG-CoA reductase inhibitor (IC50: 8 nM). Fluvastatin protects vascular smooth muscle cells against oxidative stress through the Nrf2-
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6-8 weeks
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Fluvastatin D6 sodium
XU 62-320 (D6)
T11306
Fluvastatin sodium is a first fully synthetic, competitive HMG-CoA reductase inhibitor with an IC50 of 8 nM.Fluvastatin D6 sodium is deuterium labeled Fluvastatin sodium.
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(3R,5S)-Fluvastatin
(3R,5S)-XU 62-320 free acid, (3R,5S)-Fluvastatin
T39036155229-75-7
(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.
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(3R,5S)-Fluvastatin sodium
(3R,5S)-XU 62-320
T8535994061-80-0
(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].'
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10-14 weeks
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Fluvastatin sodium monohydrate
XU 62-320 monohydrate
T86463201541-53-9
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].
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10-14 weeks
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