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PROADIFEN HYDROCHLORIDE

CAS No.
62-68-0
Chemical Name:
PROADIFEN HYDROCHLORIDE
Synonyms
skf525a;PROADIFEN;SKF-525A, HYDROCHLORIDE;5171rp;U 5446;SU-5446;SKF 525;nsc39690;SKF-525A HCL;PROADIFEN, HCL
CBNumber:
CB5120727
Molecular Formula:
C23H32ClNO2
Molecular Weight:
389.96
MDL Number:
MFCD00055151
MOL File:
62-68-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:02:24
Product description Number Pack Size Price
Proadifen hydrochloride analytical standard, ≥95% P1061 100mg $115
SKF-525A, Hydrochloride - CAS 62-68-0 - Calbiochem Cell permeable. Blocks glibenclamide-sensitive K+ channels. Inhibits neuronal nitric oxide synthase. Also inhibits hepatic drug metabolism by inhibiting the cytochrome P450 system. 567300 1G $391
SKF 525A (hydrochloride) ≥95% 15040 100mg $63
SKF 525A (hydrochloride) ≥95% 15040 250mg $99
SKF 525A (hydrochloride) ≥95% 15040 500mg $183
More product size

PROADIFEN HYDROCHLORIDE Properties

Melting point 122-123°C
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Soluble in DMSO (up to 20 mg/ml)
form White solid
color Lustrous crystals from Me2CO/pet ether
Water Solubility Soluble in methanol or water
Stability Store in Freezer
Major Application forensics and toxicology
pharmaceutical (small molecule)
InChI 1S/C23H31NO2.ClH/c1-4-17-23(20-13-9-7-10-14-20,21-15-11-8-12-16-21)22(25)26-19-18-24(5-2)6-3;/h7-16H,4-6,17-19H2,1-3H3;1H
InChIKey FHIKZROVIDCMJA-UHFFFAOYSA-N
SMILES Cl.CCCC(C(=O)OCCN(CC)CC)(c1ccccc1)c2ccccc2
FDA UNII 30624AA6X2
EPA Substance Registry System Proadifen hydrochloride (62-68-0)
UNSPSC Code 41116107
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312a-P330-P501a
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn
Risk Statements  22
Safety Statements  36-24/25
WGK Germany  3
RTECS  YV7175000
HS Code  29221990
Storage Class 11 - Combustible Solids
Toxicity LD50 oral in rat: 2140mg/kg
NFPA 704
0
2 0

PROADIFEN HYDROCHLORIDE price More Price(54)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P1061 Proadifen hydrochloride analytical standard, ≥95% 62-68-0 100mg $115 2026-04-30 Buy
Sigma-Aldrich 567300 SKF-525A, Hydrochloride - CAS 62-68-0 - Calbiochem Cell permeable. Blocks glibenclamide-sensitive K+ channels. Inhibits neuronal nitric oxide synthase. Also inhibits hepatic drug metabolism by inhibiting the cytochrome P450 system. 62-68-0 1G $391 2026-04-30 Buy
Cayman Chemical 15040 SKF 525A (hydrochloride) ≥95% 62-68-0 100mg $63 2026-04-30 Buy
Cayman Chemical 15040 SKF 525A (hydrochloride) ≥95% 62-68-0 250mg $99 2026-04-30 Buy
Cayman Chemical 15040 SKF 525A (hydrochloride) ≥95% 62-68-0 500mg $183 2026-04-30 Buy
Product number Packaging Price Buy
P1061 100mg $115 Buy
567300 1G $391 Buy
15040 100mg $63 Buy
15040 250mg $99 Buy
15040 500mg $183 Buy

PROADIFEN HYDROCHLORIDE Chemical Properties,Uses,Production

Description

SKF 525A is a widely used, nonspecific cytochrome P (CYP)450 inhibitor that demonstrates 100% inhibition of the various CYP450 isoforms at 1-100 μM. It therefore potentiates the effects of many different drugs by inhibiting their metabolism (IC50 values in the μM range when tested using human liver microsomes). SKF 525A inhibits CYP450-dependent arachidonic acid conversion to active EET metabolites, antagonizing the recovery of functional calcium pools. It also acts as a noncompetitive inhibitor of acetylcholine nicotinic receptors (IC50 = 19 μM in mouse skeletal muscle).

Chemical Properties

Off-White Crystalline Solid

Uses

anti-infective

Uses

An inhibitor of NOS1, AChR, cytochrome P-450, and KIR6.1.

Uses

Cytochrome P-459 inhibitor; blocks glibenclamide-sensitive K+ channels; inhibits neuronal nitric oxide synthetase; stimulates endothelial cell prostacyclin while inhibiting platelet thromboxane synthesis

Uses

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.

Safety Profile

Poison by intraperitoneal, subcutaneous, and intravenous routes. Moderately toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits very toxic fumes of NOx and HCl.

in vitro

previous study found that when incubated with human liver microsomes, skf525a could undergo cyp-dependent oxidative n-deethylation to its secondary amine metabolite skf8742. in addition, skf525a and its metabolite and primary amine analog all inhibited cyp2b6-, cyp2c9-, cyp2c19-, cyp2d6-, as well as cyp3a-selective reactions to various degrees but had little effect on cyp1a2, cyp2a6, and cyp2e1 reactions [1].

in vivo

animal study found that skf 525a at 1.5-9 mg/kg could reduce or abolish the hypertensive effect of mcn-a-343, dmpp and nicotine, but could neither noticeably affect the hypertensive effect of tyramine, adrenaline and noradrenaline, nor the hypotensive effect of acetylcholine and orciprenaline. thus, skf 525a was able to block the rat sympathetic ganglia and the adrenal medulla and such blockade was non-specific. moreover, the blockade might result from the stabilizing effect of skf 525a on postsynaptic membranes of the sympathetic ganglia and the adrenal medulla [2].

IC 50

in the μm range when tested using human liver microsomes

References

[1] MICHAEL R FRANKLIN L B H. 2-Diethylaminoethyl-2,2-diphenylvalerate-HCl (SKF525A) revisited: comparative cytochrome P450 inhibition in human liver microsomes by SKF525A, its metabolites, and SKF-acid and SKF-alcohol.[J]. Drug Metabolism and Disposition, 2008, 36 12: 2539-2546. DOI:10.1124/dmd.108.023549
[2] G SUAREZ-KURTZ  C P B. Sites of action of SKF 525-A in nerve and muscle.[J]. Journal of Pharmacology and Experimental Therapeutics, 1970, 172 1: 33-43.
[3] GUILLERMO SPITZMAUL. The local anaesthetics proadifen and adiphenine inhibit nicotinic receptors by different molecular mechanisms[J]. British Journal of Pharmacology, 2009, 157 5: 804-817. DOI:10.1111/j.1476-5381.2009.00214.x
[4] R J PRINCE  S M S. Acetylcholine and epibatidine binding to muscle acetylcholine receptors distinguish between concerted and uncoupled models.[J]. The Journal of Biological Chemistry, 1999, 274 28: 19623-19629. DOI:10.1074/jbc.274.28.19623
[5] HIDENARI SAKUTA  Ikuo Y. Inhibition by SKF 525A and quinacrine of endogenous glibenclamide-sensitive K+ channels in follicle-enclosed Xenopus oocytes[J]. European journal of pharmacology, 1994, 252 1: Pages 117-121. DOI:10.1016/0014-2999(94)90583-5

PROADIFEN HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 139)Suppliers
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ATK CHEMICAL COMPANY LIMITED
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Aceschem Inc.
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Aladdin Scientific
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Amadis Chemical Company Limited
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J & K SCIENTIFIC LTD. 18210857532; 18210857532 jkinfo@jkchemical.com China 96815 76

View Lastest Price from PROADIFEN HYDROCHLORIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Proadifen hydrochloride pictures 2026-05-11 Proadifen hydrochloride
62-68-0
$29.00 99.98% 10g TargetMol Chemicals Inc.

PROADIFEN HYDROCHLORIDE Spectrum

SKF-525A HYDROCHLORIDE >98% (PROADIFEN) ALPHA-PHENYL-ALPHA-PROPYLBENZENEACETIC ACID 2-[DIETHYLAMINO]ETHYL ESTER, HCL ALPHA-PHENYL-ALPHA-PROPYLBENZENEACETIC ACID 2-[DIETHYLAMINO]ETHYL ESTER HYDROCHLORIDE SK AND F 525A HYDROCHLORIDE SKF-525A HCL SKF-525A, HYDROCHLORIDE diethylaminoethanolesterofdiphenylpropylaceticacidhydrochloride nsc39690 pentanoicacid,2,2-diphenyl-,2-(n,n-diethylamino)ethylester,hydrochloride propyladiphenin valericacid,2,2-diphenyl-,2-(diethylamino)ethylester,hydrochloride Proadifen, HCl, a-Phenyl-a-propylbenzeneacetic Acid 2-[Diethylamino]ethyl Ester, HCl Benzeneacetic acid, .alpha.-phenyl-.alpha.-propyl-, 2-(diethylamino)ethyl ester, hydrochloride SU-5446 SKF-525A, Hydrochloride - CAS 62-68-0 - Calbiochem PROADIFEN, HCL PROADIFEN HYDROCHLORIDE ACETICACID,PROPYLDIPHENYL-,2-(DIETHYLAMINO)ETHYLESTER 2’-diethylaminoethyl2,2-diphenylpentanoatehydrochloride 2-diethylaminoethyl2,2-diphenylvaleratehydrochloride 2-diethylaminoethylalpha,alpha-diphenylvaleratehydrochloride 5171rp alpha-phenyl-alpha-propyl-benzeneaceticaci2-(diethylamino)ethylesterh beta-diethylaminoethyldiphenylpropylacetatehydrochloride α-phenyl-α-propylbenzeneacetic acid 2-(diethylamino)ethyl ester Proadifen, HCl, α-Phenyl-α-propylbenzeneacetic Acid 2-[Diethylamino]ethyl Ester, HCl N,N-Diethylaminoethyl 2,2-diphenylvalerate, SKF-525A, α-Phenyl-α-propylbenzeneacetic acid 2-(diethylamino)ethyl ester N,N-Diethylaminoethyl 2,2-diphenylvalerate SKF 525 U 5446 2-(diethylamino)ethyl ester Proadifen hydrochloride (SKF-525A), Cytochrome P450 inhibitor 2,2-diphenylpentanoic acid2,2-diethylaminoethyl esterhydrochloride PROADIFEN skf525a 62-68-0 1302-33-0 C23H32ClNO2 C32H31NO2HCl C23H31NO2HCl Biochemicals and Reagents BioChemical L to O Enzymes, Inhibitors, and Substrates Enzyme Inhibitors Enzyme Inhibitors by Enzyme Nitric Oxide Synthase neuronal Inhibitors All Inhibitors Amines Aromatics CLORINE