Home > Compound List > Product Information
SB 203580_Molecular_structure_CAS_152121-47-6)
Click picture or here to close

SB 203580

Catalog No. S8307 Name Sigma Aldrich
CAS Number 152121-47-6 Website http://www.sigmaaldrich.com
M. F. C21H16FN3OS Telephone 1-800-521-8956
M. W. 377.4346432 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 72493

SYNONYMS

IUPAC name
4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-1H-imidazol-5-yl]pyridine
IUPAC Traditional name
4-[5-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-3H-imidazol-4-yl]pyridine
Synonyms
4-(4-Fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)-1H-imidazole

DATABASE IDS

MDL Number MFCD00922198
CAS Number 152121-47-6
PubChem SID 24899788

PROPERTIES

Empirical Formula (Hill Notation) C21H16FN3OS
Purity ≥98% (HPLC)
Gene Information human ... CYP1A2(1544), CYP2C19(1557), CYP2C9(1559), CYP2D6(1565), CYP3A4(1576), IL1B(3553), MAPK14(1432), MAPK8IP2(23542), RAF1(5894), TNF(7124)
Apperance white to off-white solid
Solubility DMSO: ≥20 mg/mL
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Signal Word Danger
GHS Hazard statements H302-H318
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P280-P305 + P351 + P338
Risk Statements 22-41
Safety Statements 26-39
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
SB 203580 is a pyridinyl imidazole that suppresses the activation of MAPKAP kinase-2 and inhibits the phosphorylation of heat shock protein (HSP) 27 in response to IL-1, cellular stresses and bacterial endotoxin in vivo. It does not inhibit JNK or p42 MAP kinase and therefore, is useful for studying the physiological roles and targets of p38 MAPK and MAPKAP kinase-2. It has been shown to induce the activation of the serine/threonine kinase Raf-1 and has been reported to inhibit cytokine production.
Description (简体中文)
Biochem/physiol Actions
SB 203580 is a pyridinyl imidazole that suppresses the activation of MAPKAP kinase-2 and inhibits the phosphorylation of heat shock protein (HSP) 27 in response to IL-1, cellular stresses and bacterial endotoxin in vivo. It does not inhibit JNK or p42 MAP kinase and therefore, is useful for studying the physiological roles and targets of p38 MAPK and MAPKAP kinase-2. It has been shown to induce the activation of the serine/threonine kinase Raf-1 and has been reported to inhibit cytokine production.

REFERENCES