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Merck
CN

SML1003

K145 hydrochloride

≥98% (HPLC)

别名:

3-(2-Amino-ethyl)-5-[3-(4-butoxyl-phenyl)-propylidene]-thiazolidine-2,4-dione hydrochloride

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关于此项目

经验公式(希尔记法):
C18H24N2O3S · HCl
化学文摘社编号:
分子量:
384.92
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
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SMILES string

S1\C(=C/CCc2ccc(cc2)OCCCC)\C(=O)N(C1=O)CCN.Cl

InChI

1S/C18H24N2O3S.ClH/c1-2-3-13-23-15-9-7-14(8-10-15)5-4-6-16-17(21)20(12-11-19)18(22)24-16;/h6-10H,2-5,11-13,19H2,1H3;1H/b16-6-;

InChI key

HADFDMGQKBGVAV-NKBLJONXSA-N

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 20 mg/mL, clear

storage temp.

2-8°C

Quality Level

General description

K145 hydrochloride (3-(2-Amino-ethyl)-5-[3-(4-butoxyl-phenyl)-propylidene]-thiazolidine-2,4-dione) is an analog of sphingosine.

Application

K145 hydrochloride has been used in the analysis of apoptosis.

Biochem/physiol Actions

It has the ability to prevent leukemia cell growth in vitro.
K145 (3-(2-amino-ethyl)-5-[3-(4-butoxyl-phenyl)-propylidene]-thiazolidine-2,4-dione) is a selective inhibitor of sphingosine kinase-2 (SphK2) and an anticancer agent. K145 selectively inhibited SphK2 in a dose-dependent manner with an IC50 of 4.30 +/- 0.06 μM with no inhibition of SphK1 at concentrations up to 10 μM. K145 significantly suppressed the growth of U937 tumors in nude mice and the growth of JC tumor cells in BALB/c mice.
K145 is a selective inhibitor of sphingosine kinase-2 and an anticancer agent.

Features and Benefits

This compound is a featured product for Kinase Phosphatase Biology research. Click here to discover more featured Kinase Phosphatase Biology products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

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Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington?s disease
Di Pardo A, et al.
Scientific Reports, 7(1), 5280-5280 (2017)
Structure?activity relationship studies of the lipophilic tail region of sphingosine kinase 2 inhibitors
Congdon M D, et al.
Bioorganic & Medicinal Chemistry Letters, 25(21), 4956-4960 (2015)

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