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PF 543

PF 543 Structure
CAS No.
1415562-82-1
Chemical Name:
PF 543
Synonyms
PF543;CS-745;PF 543;PF-543;PF543/PF-543;PF-543(freebase);PF 543 USP/EP/BP;Sphingosine Kinase 1 Inhibitor II;PF-543,anovelcell-permeantinhibitorofSPHK1;Sphingosine Kinase 1 Inhibitor II, PF-543 - CAS 1415562-82-1 - Calbiochem
CBNumber:
CB92645150
Molecular Formula:
C27H31NO4S
Molecular Weight:
465.6
MOL File:
1415562-82-1.mol
MSDS File:
SDS
Modify Date:
2023/5/18 11:30:59

PF 543 Properties

Boiling point 666.0±55.0 °C(Predicted)
Density 1.224±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility ≥23.3 mg/mL in DMSO; insoluble in H2O; ≥51 mg/mL in EtOH with gentle warming and ultrasonic
pka 14.77±0.10(Predicted)
form powder
color white to light brown

SAFETY

Risk and Safety Statements

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

PF 543 price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) PZ0234 PF-543 hydrochloride ≥98% (HPLC) 1415562-82-1 5MG ₹11528.63 2022-06-14 Buy
Sigma-Aldrich(India) PZ0234 PF-543 hydrochloride ≥98% (HPLC) 1415562-82-1 25MG ₹46515.03 2022-06-14 Buy
Sigma-Aldrich(India) 567741 Sphingosine Kinase 1 Inhibitor II, PF-543 - CAS 1415562-82-1 - Calbiochem The Sphingosine Kinase 1 Inhibitor II, PF-543 controls the biological activity of Sphingosine Kinase 1. This small molecule/inhibitor is primarily use 1415562-82-1 5MG ₹21980 2022-06-14 Buy
Product number Packaging Price Buy
PZ0234 5MG ₹11528.63 Buy
PZ0234 25MG ₹46515.03 Buy
567741 5MG ₹21980 Buy

PF 543 Chemical Properties,Uses,Production

General Description

A cell-permeable hydroxymethylpyrrolidine compound that acts as a high affinity (Kd = 5 nM, kofft1/2 = 8.5 min), but poor, sphingosine kinase-1/SphK1 substrate (1/1,500 of sphingosine processivity) and potently inhibits against SphK1-catalyzed sphingosine-to-S1P conversion (IC50 = 2.0 nM; [sphingosine] = 3 μM) in a reversible, sphingosine-, but not ATP-, competitive manner (Ki = 3.6 nM), exhibiting 132-fold selectivity over SphK2, no affinity toward S1P receptors (S1P1, S1P2, S1P3, S1P5), and much reduced or no inhibitory activity against a panel of 46 other lipid and protein kinases (IC50 >10 μM), including the structurally related diacylglyerol kinase α/DAGKα (3.7% inhibition at 10 μM). PF-543 exposure in 1483 squamous cultures is reported to result in intracellular S1P depletion (by 90% upon 1 h 200 nM or 7 d 1 μM drug exposure) with concomitant elevation of sphingosine level and no detectable cytotoxicity (1 μM for 7 to 9 d in 1483, A549, Jurkat, LN229, MCF7, or U937 cultures). Also active in human whole blood assays in the presence human & bovine serum proteins (IC50 = 26.7 nM against cellular C17-S1P formation from exogenously added 20 μM C17-sphingosine in 10 min with 30 min drug preincubation).

Biochem/physiol Actions

PF-543 hydrochloride is a novel, cell-permeable, potent and selective inhibitor of sphingosine kinase-1 (SphK1). PF-543 inhibits SphK1 with a Ki of 3.6 nM, is sphingosine competitive and is more than 100-fold selective for SphK1 over the SphK2 isoform. PF-543 decreased the level of endogenous S1P by 10-fold with proportional increase of the level of sphingosine.

PF 543 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 82)Suppliers
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ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32836 60 Inquiry
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TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry
ShenZhen Trendseen Biological Technology Co.,Ltd. 13417589054 China 11681 58 Inquiry
Wuhan Topule Biopharmaceutical Co., Ltd +8618327326525 China 8474 58 Inquiry

PF 543 Spectrum

PF 543 PF543 PF-543 PF543/PF-543 (2R)-1-[[4-[[3-Methyl-5-[(phenylsulfonyl)Methyl]phenoxy]Methyl]phenyl]Methyl]-2-pyrrolidineMethanol 2-PyrrolidineMethanol, 1-[[4-[[3-Methyl-5-[(phenylsulfonyl)Methyl]phenoxy]Methyl]phenyl]Methyl]-, (2R)- CS-745 PF-543(freebase) Sphingosine Kinase 1 Inhibitor II, PF-543 - CAS 1415562-82-1 - Calbiochem [(2R)-1-[[4-[[3-(benzenesulfonylmethyl)-5-methylphenoxy]methyl]phenyl]methyl]pyrrolidin-2-yl]methanol {1-[4-({3-Methyl-5-[(phenylsulfonyl)methyl]phenoxy}methyl)benzyl]-2-pyrrolidinyl}methanol Sphingosine Kinase 1 Inhibitor II PF 543 USP/EP/BP PF-543,anovelcell-permeantinhibitorofSPHK1 1415562-82-1 Inhibitors