Proadifen hydrochloride, Thermo Scientific Chemicals
Proadifen hydrochloride, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Proadifen hydrochloride, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
500 mg
1 g
Catalog number J63833.ME
also known as J63833-ME
Price (USD)/ Each
217.00
-
Add to cart
Quantity:
500 mg
Request bulk or custom format
Price (USD)/ Each
217.00
Add to cart
Proadifen hydrochloride, Thermo Scientific Chemicals
Catalog numberJ63833.ME
Price (USD)/ Each
217.00
-
Add to cart
Chemical Identifiers
CAS62-68-0
IUPAC Namehydrogen 2-(diethylamino)ethyl 2,2-diphenylpentanoate chloride
Molecular FormulaC23H32ClNO2
InChI KeyFHIKZROVIDCMJA-UHFFFAOYSA-N
SMILES[H+].[Cl-].CCCC(C(=O)OCCN(CC)CC)(C1=CC=CC=C1)C1=CC=CC=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Assay (unspecified)> 95%
Proadifen hydrochloride is an inhibitor of NOS1, AChR, cytochrome P-450, and KIR6. Proadifen hydrochloride bind to the protein moiety of P-450, also reduced the hypoxic response. of Proadifen hydrochloride have good antiarrhythmic effects. SKF-525A substantially reduced the depletion of cardiac norepinephrine.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Proadifen hydrochloride is an inhibitor of NOS1, AChR, cytochrome P-450, and KIR6. Proadifen hydrochloride bind to the protein moiety of P-450, also reduced the hypoxic response. of Proadifen hydrochloride have good antiarrhythmic effects. SKF-525A substantially reduced the depletion of cardiac norepinephrine.

Solubility
Soluble in methanol or water

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, heat.
RUO – Research Use Only

General References:

  1. James E. Gibson§ andBernard A. Becker.Effect of phenobarbital and SKF 525-A on the teratogenicity of cyclophosphamide in mice. Teratology. 1968, 1(4), pg no.
  2. M K Buening,; M R Franklin.SKF 525-A inhibition, induction, and 452-nm complex formation.. Drusg metabolism and Deposition. 1976, 4 (3), 244-255.