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SKI II

SKI II Structure
CAS No.
312636-16-1
Chemical Name:
SKI II
Synonyms
SphK-I2;CS-1145;SKI II;SKI-II;SKI II - SKI 2;SKI II (SphK-I2);SKI II USP/EP/BP;SKIII(SphK-I2), >98%;Sphingosine Kinase Inhibitor;Sphingosine Kinase Inhibitor 2;SKI II (Sphingosine Kinase Inhibitor)
CBNumber:
CB1498400
Molecular Formula:
C15H11ClN2OS
Molecular Weight:
302.78
MOL File:
312636-16-1.mol
MSDS File:
SDS
Modify Date:
2023/6/30 15:45:59

SKI II Properties

Boiling point 507.1±60.0 °C(Predicted)
Density 1.415±0.06 g/cm3(Predicted)
RTECS SK5900000
storage temp. 2-8°C
solubility DMSO: ≥20 mg/mL
form solid
pka 10.17±0.26(Predicted)
color off-white
Sensitive Air & Light Sensitive
CAS DataBase Reference 312636-16-1

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
WGK Germany  3

SKI II price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S5696 SKI II ≥98% (HPLC), solid 312636-16-1 10MG ₹17568.98 2022-06-14 Buy
Sigma-Aldrich(India) S5696 SKI II ≥98% (HPLC), solid 312636-16-1 50MG ₹78481.25 2022-06-14 Buy
Product number Packaging Price Buy
S5696 10MG ₹17568.98 Buy
S5696 50MG ₹78481.25 Buy

SKI II Chemical Properties,Uses,Production

Uses

SKI II is a nonlipid inhibitor of sphingosine kinase. SKI II s orally bioavailable and has shown significant inhibition of tumor growth in mice.

Biological Activity

Selective non-lipid inhibitor of sphingosine kinase (IC 50 = 0.5 μ M); does not act at ATP-binding site. Displays no inhibition of ERK2, PI 3-kinase, or PKC α at concentrations up to 60 μ M. Reduces levels of sphingosine-1-phosphate in MDA-MB-231 breast cancer cells. Induces apoptosis and inhibits proliferation in several other tumor cell lines in vitro (IC 50 = 0.9-4.6 μ M).

Biochem/physiol Actions

Sphingosine kinase (SK) plays a pivotal role in regulating tumor growth and SK can act as an oncogene. Expression of SK RNA is significantly elevated in a variety of solid tumors, compared with normal tissue from the same patient. A number of novel inhibitors of human SK were identified, and several representative compounds were characterized in detail. These compounds demonstrated activity at sub- to micromolar concentrations, making them more potent than any other reported SK inhibitor, and were selective toward SK compared with a panel of human lipid and protein kinases. Kinetic studies revealed that the compounds were not competitive inhibitors of the ATP-binding site of SK. 4-[4-(4-chloro-phenyl)-thiazol-2-ylamino]-phenol (SKI-II) inhibitor is orally bioavailable, detected in the blood for at least 8 h, and showed a significant inhibition of tumor growth in mice with IC50 = 0.5 μM; SKI II does not act at ATP-binding site. Displays no inhibition of ERK2, PI 3-kinase, or PKCa at concentrations up to 60 μM.SKI II induces apoptosis and inhibits proliferation in several other tumor cell lines in vitro (IC50 = 0.9-4.6 μM).

SKI II Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 114)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
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TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry

SKI II Spectrum

Sphingosine Kinase Inhibitor Sphingosine Kinase Inhibitor 2 SKI II (SphK-I2) SphK-I2 SKI II (Sphingosine Kinase Inhibitor) Phenol, 4-[[4-(4-chlorophenyl)-2-thiazolyl]amino]- 4-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol SKI II 4-(4-(4-chlorophenyl)thiazol-2-ylamino)phenol SKI II;SKI-II SKIII(SphK-I2), >98% SKI II - SKI 2 SPHINGOSINE KINASE INHIBITOR;SPHINGOSINE KINASE INHIBITOR 2;SKI II (SPHK-I2);SPHK-I2;SKI II (SPHINGOSINE KINASE INHIBITOR) CS-1145 4-[[4-(4-chlorophenyl)-1,3-thiazol-2-yl]amino]phenol SKI II USP/EP/BP SKI II,Sphingosine kinase,Apoptosis,SphK,Wnt,Inhibitor,inhibit 4-(4-chlorophenyl)-N-(p-tolyl)thiazol-2-amine 312636-16-1 Inhibitors Lysophospholipid receptor and related