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SB242235

CAS No.
193746-75-7
Chemical Name:
SB242235
Synonyms
CS-668;SB242235;SB242235 ≥95%;SB-242235; SB242235;inhibit,SB 242235,Autophagy,Inhibitor,p38 MAPK;4-[4-(4-Fluorophenyl)-1-(4-piperidinyl)-1H-imidazol-5-yl]-2-methoxypyrimidine;4-(4-(4-Fluorophenyl)-1-(piperidin-4-yl)-1H-iMidazol-5-yl)-2-MethoxypyriMidine;Pyrimidine, 4-[4-(4-fluorophenyl)-1-(4-piperidinyl)-1H-imidazol-5-yl]-2-methoxy-
CBNumber:
CB12621150
Molecular Formula:
C19H20FN5O
Molecular Weight:
353.39
MDL Number:
MFCD08690575
MOL File:
193746-75-7.mol
MSDS File:
SDS
Last updated:2023-05-18 11:31:18

SB242235 Properties

Boiling point 568.4±60.0 °C(Predicted)
Density 1.34
storage temp. 2-8°C(protect from light)
solubility DMF: 25 mg/ml; DMSO: 20 mg/ml; Ethanol: 30 mg/ml
form Powder
pka 9.91±0.10(Predicted)

SAFETY

Risk and Safety Statements

HS Code  2924297099

SB242235 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Usbiological 474182 SB 242235 193746-75-7 100mg $1848 2021-12-16 Buy
Biorbyt Ltd orb180841 SB242235 >98% 193746-75-7 1000mg $2395.3 2021-12-16 Buy
Matrix Scientific 132624 4-(4-(4-Fluorophenyl)-1-(piperidin-4-yl)-1H-imidazol-5-yl)-2-methoxypyrimidine 97% 193746-75-7 5g $3960 2021-12-16 Buy
AK Scientific 3254AH 4-(4-(4-Fluorophenyl)-1-(piperidin-4-yl)-1H-imidazol-5-yl)-2-methoxypyrimidine 193746-75-7 5g $5396 2021-12-16 Buy
Matrix Scientific 132624 4-(4-(4-Fluorophenyl)-1-(piperidin-4-yl)-1H-imidazol-5-yl)-2-methoxypyrimidine 97% 193746-75-7 10g $6480 2021-12-16 Buy
Product number Packaging Price Buy
474182 100mg $1848 Buy
orb180841 1000mg $2395.3 Buy
132624 5g $3960 Buy
3254AH 5g $5396 Buy
132624 10g $6480 Buy

SB242235 Chemical Properties,Uses,Production

Biological Activity

SB-242235 is a potent and selective p38 MAP kinase inhibitor with IC50 of 1.0 μM in human chondrocytes.

in vitro

SB 242235 (0-10 μM) dose-dependently inhibits the activation of MAPKAP K2 with an IC 50 of 1.0 μM in human chondrocytes stimulated with IL-1β.
SB 242235 inhibits intracellular p38 activity, MAPKAP K2 was then isolated from these cells and assayed using HSP27 as a substrate.

Western Blot Analysis

< td class="col2"> 15 minutes
Cell Line: Human chondrocytes
Concentration: 0 μM, 0.01 μM, 0.1 μM, 1 μM, 10 μM
Incubation Time:
Result: Dose-dependently inhibited the activation of MAPKAP K2 with an IC 50 of 1.0 μM.

target

IC50: 1.0 μM (p38 MAPK, primary human chondrocytes)

SB242235 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 64)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
InvivoChem
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TargetMol Chemicals Inc.
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Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8474 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2923 55
Haoyuan Chemexpress Co., Ltd. 021-58950125 info@chemexpress.com China 7553 61
SYN|thesis med chem P/L +86-021-50720296 service@synkinase.com China 266 58
SB242235 4-[4-(4-Fluorophenyl)-1-(4-piperidinyl)-1H-imidazol-5-yl]-2-methoxypyrimidine 4-(4-(4-Fluorophenyl)-1-(piperidin-4-yl)-1H-iMidazol-5-yl)-2-MethoxypyriMidine SB-242235; SB242235 CS-668 SB242235 ≥95% Pyrimidine, 4-[4-(4-fluorophenyl)-1-(4-piperidinyl)-1H-imidazol-5-yl]-2-methoxy- inhibit,SB 242235,Autophagy,Inhibitor,p38 MAPK 193746-75-7