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PF-543 HCl

CAS No.
1706522-79-3
Chemical Name:
PF-543 HCl
Synonyms
PF 543 HCl;PF-543 hydrochloride ,S7177;WNKWAZFYPZMDGJ-VQIWEWKSSA-N;PF-543 Hydrochloride DISCONTINUED;PF-543 hydrochloride, 10 mM in DMSO;(2R)-1-[[(4-[[3-Methyl-5-[(phenylsulfonyl)methyl]phenoxy]methyl]phenyl]methyl]-2-pyrrolidinemethanol hydrochloride;Nrf-2,PF543 hydrochloride,anti-cancer,sphingosine-competitive,S1P,Sphingosine Kinase 1 Inhibitor II,Apoptosis,inhibit,PF 543,Lysophospholipid Receptor,PAH,necrosis,SphK,Inhibitor,Autophagy,PF543,PF 543 hydrochloride,caspase-3/7,SK1,Sphingosine kinase,LPL Receptor,anti-inflammatory
CBNumber:
CB43355459
Molecular Formula:
C27H32ClNO4S
Molecular Weight:
502.07
MDL Number:
MOL File:
1706522-79-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-17 09:03:53

PF-543 HCl Properties

Melting point 156-158oC (dec.)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO, Methanol
form Solid
color Beige

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

PF-543 HCl price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 17034 PF-543 (hydrochloride) ≥98% 1706522-79-3 1mg $36 2026-04-30 Buy
Cayman Chemical 17034 PF-543 (hydrochloride) ≥98% 1706522-79-3 5mg $110 2026-04-30 Buy
Cayman Chemical 17034 PF-543 (hydrochloride) ≥98% 1706522-79-3 10mg $203 2026-04-30 Buy
Cayman Chemical 17034 PF-543 (hydrochloride) ≥98% 1706522-79-3 25mg $420 2026-04-30 Buy
Axon Medchem Axon4360 PF-543 hydrochloride 99% 1706522-79-3 5mg $99 2026-05-19 Buy
Product number Packaging Price Buy
17034 1mg $36 Buy
17034 5mg $110 Buy
17034 10mg $203 Buy
17034 25mg $420 Buy
Axon4360 5mg $99 Buy

PF-543 HCl Chemical Properties, Uses, Production

Uses

(2R)-1-[[4-[[3-Methyl-5-[(phenylsulfonyl)methyl]phenoxy]methyl]phenyl]methyl]-2-pyrrolidinemethanol, is a novel Sphingonise Kinas 1 (SphK1, SK1) inhibitor.

Enzyme inhibitor

This potent SphK1 inhibitor (FWHCl-Salt = 502.07 g/mol; CAS 1706522-79- 3; Solubility: 10 mM in H2O, with gentle warming; 100 mM in DMSO), also named (2R)-1-[[(4-[[3-methyl-5-[(phenylsulfonyl)methyl]phenoxy] methyl]phenyl]methyl]-2-pyrrolidinemethanol hydrochloride, selectively targets sphingosine kinase 1 (IC50 = 2 nM; Ki = 3.6 nM). The latter phosphorylates sphingosine to form sphingosine-1-phosphate (S1P), a lipid messenger with both intracellular functions (regulating cell proliferation and survival) and extracellular functions (as a ligand for EDG1, or sphingosine-1-phosphate receptor 1). PF-543 also exhibits >100-fold selectivity for Sphk1 over Sphk2 as well as >5000 fold selectivity over S1P1-5 receptors and 48 protein and lipid kinases. P 543 attenuates proliferation and induces necrosis in human colorectal cancer cells in vitro. It also suppresses human colorectal cancer cell line HCT-116 as a tumor xenograft growth in mice

in vivo

PF-543 (1 mg/kg; intraperitoneal injection; every second day; for 21 days; female C57BL/6 J mice) treatment has no effect on vascular remodelling but reduces right ventricular hypertrophy. The protection involves a reduction in the expression of p53 and an increase in the expression of anti-oxidant nuclear factor Nrf-2[2].
Mice are initially dosed (ip) with 10 mg/kg or 30 mg/kg of PF-543 for 24 h and the T1/2 is 1.2 h in blood samples. Administration of 10 mg/kg PF-543 for 24 h to mice induces a decrease in SK1 expression in pulmonary vessels[2].

Animal Model:Female C57BL/6 J mice (7-12 week-old) with hypoxic-induced pulmonary arterial hypertension[2]
Dosage:1 mg/kg
Administration:Intraperitoneal injection; every second day; for 21 days
Result:Reduced right ventricular hypertrophy. The protection involves a reduction in the expression of p53 (that promotes cardiomyocyte death) and an increase in the expression of anti-oxidant nuclear factor Nrf-2.

IC 50

SphK1

storage

Desiccate at RT

PF-543 HCl Preparation Products And Raw materials

Raw materials

Preparation Products

PF-543 HCl Suppliers

Global Suppliers ( 56)
Supplier Tel Email Country ProdList Advantage
ShangHai Caerulum Pharma Discovery Co., Ltd. 18149758185 18149758185 sales-cpd@caerulumpharma.com China 3493 58
Bide Pharmatech Ltd. 400-164-7117 18317119277 product02@bidepharm.com China 40000 60
Shanghai Lollane Biological Technology Co.,Ltd. 021-52996696,15000506266 15000506266 China 4859 55
YouCoChem (Beijing) Chemical Technology Co., Ltd. 18800159827 youcochem@163.com China 163 50
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Shanghai Rechem science Co., Ltd. 021-31433387 15618786686 sales@rechemscience.com China 2968 58
Jinan elephant international trading co., LTD 13006575422@163.com China 6347 58
Shanghai Chaolan Chemical Technology Center QQ:65489617 13301690235 Sales@ATKchemical.com China 9699 58
Beijing Solarbio Science & Tecnology Co., Ltd. 17801761073 18101056239 3193328036@qq.com China 28150 68
Amadis Chemical Company Limited 571-89925085 sales@amadischem.com China 131885 58

View Latest Price from PF-543 HCl manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
PF-543 hydrochloride pictures 2026-07-17 PF-543 hydrochloride
1706522-79-3
$33.00-137.00 98.90% 10g TargetMol Chemicals Inc.

PF-543 HCl Spectrum

WNKWAZFYPZMDGJ-VQIWEWKSSA-N (2R)-1-[[(4-[[3-Methyl-5-[(phenylsulfonyl)methyl]phenoxy]methyl]phenyl]methyl]-2-pyrrolidinemethanol hydrochloride PF 543 HCl PF-543 Hydrochloride DISCONTINUED Nrf-2,PF543 hydrochloride,anti-cancer,sphingosine-competitive,S1P,Sphingosine Kinase 1 Inhibitor II,Apoptosis,inhibit,PF 543,Lysophospholipid Receptor,PAH,necrosis,SphK,Inhibitor,Autophagy,PF543,PF 543 hydrochloride,caspase-3/7,SK1,Sphingosine kinase,LPL Receptor,anti-inflammatory PF-543 hydrochloride, 10 mM in DMSO PF-543 hydrochloride ,S7177 1706522-79-3