p38 MAP Kinase Inhibitor III
- Product Name
- p38 MAP Kinase Inhibitor III
- CAS No.
- 581098-48-8
- Chemical Name
- p38 MAP Kinase Inhibitor III
- Synonyms
- (S)-p38 MAPK Inhibitor III;(S)-p38 MAP Kinase Inhibitor III;p38 MAP Kinase Inhibitor III - CAS 581098-48-8 - Calbiochem;(S)-p-38 MAPK Inhibitor III,(S) p38 MAPK Inhibitor III,(S)p38 MAPK Inhibitor III;4-[5-(4-fluorophenyl)-2-(methylthio)-1H-imidazol-4-yl]-N-[(1S)-1-phenylethyl]-2-pyridinamine;2-Pyridinamine, 4-[5-(4-fluorophenyl)-2-(methylthio)-1H-imidazol-4-yl]-N-[(1S)-1-phenylethyl]-
- CBNumber
- CB53136792
- Molecular Formula
- C23H21FN4S
- Formula Weight
- 404.5
- MOL File
- 581098-48-8.mol
p38 MAP Kinase Inhibitor III Property
- Melting point:
- 117-119 °C
- Boiling point:
- 589.4±60.0 °C(Predicted)
- Density
- 1.30±0.1 g/cm3(Predicted)
- storage temp.
- +2C to +8C
- solubility
- DMF: 20 mg/mL; DMSO: 12 mg/mL; Ethanol: 30 mg/mL; Ethanol:PBS (pH 7.2)(1:2): 0.33 mg/mL
- form
- Yellow solid
- pka
- 9.07±0.10(Predicted)
- color
- White to off-white
N-Bromosuccinimide Price
- Product number
- 506121
- Product name
- p38 MAP Kinase Inhibitor III - CAS 581098-48-8 - Calbiochem
- Packaging
- 1mg
- Price
- $216
- Updated
- 2024/03/01
- Product number
- 19696
- Product name
- (S)-p38 MAPK Inhibitor III
- Purity
- ≥98%
- Packaging
- 500μg
- Price
- $68
- Updated
- 2024/03/01
- Product number
- 19696
- Product name
- (S)-p38 MAPK Inhibitor III
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $130
- Updated
- 2024/03/01
- Product number
- 19696
- Product name
- (S)-p38 MAPK Inhibitor III
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $535
- Updated
- 2024/03/01
- Product number
- 19696
- Product name
- (S)-p38 MAPK Inhibitor III
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $936
- Updated
- 2024/03/01
p38 MAP Kinase Inhibitor III Chemical Properties,Usage,Production
Description
(S)-p38 MAPK inhibitor III is a methylsulfanylimidazole that inhibits p38 MAP kinase (IC50 = 0.90 μM in vitro). It is cell-permeable, potently blocking the release of TNF-α and IL-1β from human peripheral blood mononuclear cells (IC50s = 0.37 and 0.044 μM, respectively).
General Description
A cell-permeable methylsulfanylimidazole compound that acts as a potent, selective, reversible, and ATP-competitive p38 MAP kinase inhibitor (IC50 = 0.38 μM for p38α). Shown to effectively suppresses LPS-induced cytokine release both in vitro (IC50 = 0.16 and 0.039 μM for TNF-α and IL-1β release, respectively, in human PBMC) and in vivo (ED50 = 1.33 mg/kg for TNF-α release in mouse). When compared with SB 203580 (Cat. No. 559389 and 559398), it exhibits reduced inhibitory activity against cytochrome P450-2D6 isoform and, therefore, is better suited for in vivo use. A 10 mM (1 mg/247 μl) solution of p38 MAP Kinase Inhibitor III (Cat. No. 506148) in DMSO is also available.
Biochem/physiol Actions
Cell permeable: yes
p38 MAP Kinase Inhibitor III Preparation Products And Raw materials
Raw materials
Preparation Products
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