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p38 MAPK

p38 MAPK

p38 MAPKs (α, β, γ, and δ) are members of the MAPK family that are activated by a variety of environmental stresses and inflammatory cytokines. As with other MAPK cascades, the membrane-proximal component is a MAPKKK, typically a MEKK or a mixed lineage kinase (MLK). The MAPKKK phosphorylates and activates MKK3/6, the p38 MAPK kinases. MKK3/6 can also be activated directly by ASK1, which is stimulated by apoptotic stimuli. p38 MAPK is involved in regulation of HSP27, MAPKAPK-2 (MK2), MAPKAPK-3 (MK3), and several transcription factors including ATF-2, Stat1, the Max/Myc complex, MEF-2, Elk-1, and indirectly CREB via activation of MSK1.
TargetMol
1 2 3 4 5 6 7 8 9
Cat. No. Product Name CAS No. Purity Chemical Structure
TN1211 2-Hydroxy-3-methylanthraquinone
化合物2-Hydroxy-3-methylanthraquinone
17241-40-6 98%
TargetMol Chemical Structure 2-Hydroxy-3-methylanthraquinone
2-Hydroxy-3-methylanthraquinone enhances apoptosis of U937 cells,in part,through activation of p-p38MAPK and downregulation of p-ERK1/2; triggers caspase-3 activ...
T16477 PF-03715455
化合物 T16477
1056164-52-3 98%
TargetMol Chemical Structure PF-03715455
PF-03715455 potently inhibits LPS-induced TNFα production in human whole blood (IC50=1.7 nM). PF-03715455 is an effective inhibitor of inhaled p38 MAPK. PF-03715...
T10298L AMG-548
化合物 T10298L
864249-60-5 98%
TargetMol Chemical Structure AMG-548
AMG-548 is an orally active and selective p38α inhibitor (Ki=0.5 nM), shows slightly selective over p38β (Ki=36 nM) and >1000 fold selective against p38γ and p38...
TN3711 Corylifol C
化合物 TN3711
775351-91-2 98%
TargetMol Chemical Structure Corylifol C
Corylifol C and, to a lesser extent, xanthoangelol are potent protein kinase inhibitors (inhibitory concentration 50% values for epidermal growth factor receptor...
T10298L2 AMG-548 dihydrochloride (864249-60-5 free base)
化合物 T10298L2
T10298L2 98%
TargetMol Chemical Structure AMG-548 dihydrochloride (864249-60-5 free base)
AMG-548 dihydrochloride is an orally active and selective p38α inhibitor (Ki: 0.5 nM) and shows slightly selective over p38β (Ki: 36 nM) and >1000 fold selective...
TL0014 Pinusolide
化合物 TL0014
31685-80-0 98%
TargetMol Chemical Structure Pinusolide
Pinusolide is a platelet activating factor ( PAF) antagonist, it may prove of therapeutic value in the treatment of hypotension, it has antileukemic potential, a...
TN3719 Cristacarpin
化合物 TN3719
74515-47-2 98%
TargetMol Chemical Structure Cristacarpin
Cristacarpin exhibits moderate but selective activity towards DNA repair-deficient yeast mutants. It promotes endoplasmic reticulum (ER) stress, leading to sub-l...
TN5050 Sprengerinin C
化合物 TN5050
88861-91-0 98%
TargetMol Chemical Structure Sprengerinin C
Sprengerinin C exerts anti-tumorigenic effects in hepatocellular carcinoma via inhibition of proliferation and angiogenesis and induction of apoptosis, it can st...
T11327 FR 167653
化合物 T11327
158876-66-5 98%
TargetMol Chemical Structure FR 167653
FR 167653 (FR 167653 sulfate) is effective in treating inflammation, relieving trauma and ischemia-reperfusion injury in vivo. FR 167653 , an orally active and s...
TN3839 Desoxo-narchinol A
化合物 TN3839
53859-06-6 98%
TargetMol Chemical Structure Desoxo-narchinol A
Desoxo-narchinol A exhibits protective effects against LPS-induced endotoxin shock and inflammation through p38 deactivation, it shows inhibitory activity agains...
TN2075 Pimaric acid
海松酸
127-27-5 98%
TargetMol Chemical Structure Pimaric acid
Pimaric acid has potent anti-atherosclerotic activity with inhibitory action on matrix metalloproteinase-9 production and cell migration in TNF-α±-induced human ...
TN4490 Manassantin B
化合物 TN4490
88497-88-5 98%
TargetMol Chemical Structure Manassantin B
Manassantin B is a potent inhibitor of NF-κB activation by the suppression of transciptional activity of RelA/p65 subunit of NF-κB. It also possesses anti-EBV ...
TN1882 Lucidenic acid D
赤芝酸D
98665-16-8 98%
TargetMol Chemical Structure Lucidenic acid D
Lucidenic acid D2 is a nartural product from G. lucidum AF.
T3229 Cytochalasin D
细胞松弛素D
22144-77-0 98%
TargetMol Chemical Structure Cytochalasin D
Cytochalasin D is an actin inhibitor, the removal of actin stress fibers is crucial for the chondrogenic differentiation. It may be an inhibitor of some fertiliz...
TN2039 Panaxydol
人参环氧炔醇
72800-72-7 98%
TargetMol Chemical Structure Panaxydol
Panaxydol has anti-cancer activity, can inhibit the growth and apoptosis of cancer cells, the signaling mechanisms involve a [Ca(2+)](i) increase, JNK and p38 MA...
T12871L Talmapimod hydrochloride
化合物 T12871L
309915-12-6 98%
TargetMol Chemical Structure Talmapimod hydrochloride
Talmapimod hydrochloride is a selective and ATP-competitive p38α inhibitor (IC50: 9 nM). It also shows about 10-fold selectivity over p38β, and at least 2000-fol...
TN3931 Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid
化合物 TN3931
57719-81-0 98%
TargetMol Chemical Structure ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid
Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid has anti-cancer activity, it induces apoptosis of human malignant cancer cells, it also inhibits hepatocellular ...
TN4162 Goshonoside F5
化合物 TN4162
90851-28-8 98%
TargetMol Chemical Structure Goshonoside F5
Goshonoside F5 has anti-inflammatory activity, it significantly inhibits the pro-inflammatory response induced by LPS, both in vitro and in vivo.
T36067 Bongkrekic acid
米酵菌酸
11076-19-0 98%
TargetMol Chemical Structure Bongkrekic acid
Bongkrekic acid (Bongkrekic Acid (ammonium salt)) 是一种由伯克霍尔德菌(Burkholderia gladioli)分泌的线粒体毒素,抑制腺嘌呤核苷酸转位酶 (ANT)。Bongkrekic acid Bongkrekic acid 通过 p38、ERK、PAD4 和 P...
TMA0291 Dehydroglyasperin D
化合物 TMA0291
517885-72-2 98%
TargetMol Chemical Structure Dehydroglyasperin D
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 h...
2-Hydroxy-3-methylanthraquinone
TN1211
2-Hydroxy-3-methylanthraquinone enhances apoptosis of U937 cells,in part,through activation of p-p38MAPK and downregulation of p-ERK1/2; triggers caspase-3 activ...
PF-03715455
T16477
PF-03715455 potently inhibits LPS-induced TNFα production in human whole blood (IC50=1.7 nM). PF-03715455 is an effective inhibitor of inhaled p38 MAPK. PF-03715...
AMG-548
T10298L
AMG-548 is an orally active and selective p38α inhibitor (Ki=0.5 nM), shows slightly selective over p38β (Ki=36 nM) and >1000 fold selective against p38γ and p38...
Corylifol C
TN3711
Corylifol C and, to a lesser extent, xanthoangelol are potent protein kinase inhibitors (inhibitory concentration 50% values for epidermal growth factor receptor...
AMG-548 dihydrochloride (864249-60-5 free base)
T10298L2
AMG-548 dihydrochloride is an orally active and selective p38α inhibitor (Ki: 0.5 nM) and shows slightly selective over p38β (Ki: 36 nM) and >1000 fold selective...
Pinusolide
TL0014
Pinusolide is a platelet activating factor ( PAF) antagonist, it may prove of therapeutic value in the treatment of hypotension, it has antileukemic potential, a...
Cristacarpin
TN3719
Cristacarpin exhibits moderate but selective activity towards DNA repair-deficient yeast mutants. It promotes endoplasmic reticulum (ER) stress, leading to sub-l...
Sprengerinin C
TN5050
Sprengerinin C exerts anti-tumorigenic effects in hepatocellular carcinoma via inhibition of proliferation and angiogenesis and induction of apoptosis, it can st...
FR 167653
T11327
FR 167653 (FR 167653 sulfate) is effective in treating inflammation, relieving trauma and ischemia-reperfusion injury in vivo. FR 167653 , an orally active and s...
Desoxo-narchinol A
TN3839
Desoxo-narchinol A exhibits protective effects against LPS-induced endotoxin shock and inflammation through p38 deactivation, it shows inhibitory activity agains...
Pimaric acid
TN2075
Pimaric acid has potent anti-atherosclerotic activity with inhibitory action on matrix metalloproteinase-9 production and cell migration in TNF-α±-induced human ...
Manassantin B
TN4490
Manassantin B is a potent inhibitor of NF-κB activation by the suppression of transciptional activity of RelA/p65 subunit of NF-κB. It also possesses anti-EBV ...
Lucidenic acid D
TN1882
Lucidenic acid D2 is a nartural product from G. lucidum AF.
Cytochalasin D
T3229
Cytochalasin D is an actin inhibitor, the removal of actin stress fibers is crucial for the chondrogenic differentiation. It may be an inhibitor of some fertiliz...
Panaxydol
TN2039
Panaxydol has anti-cancer activity, can inhibit the growth and apoptosis of cancer cells, the signaling mechanisms involve a [Ca(2+)](i) increase, JNK and p38 MA...
Talmapimod hydrochloride
T12871L
Talmapimod hydrochloride is a selective and ATP-competitive p38α inhibitor (IC50: 9 nM). It also shows about 10-fold selectivity over p38β, and at least 2000-fol...
ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid
TN3931
Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid has anti-cancer activity, it induces apoptosis of human malignant cancer cells, it also inhibits hepatocellular ...
Goshonoside F5
TN4162
Goshonoside F5 has anti-inflammatory activity, it significantly inhibits the pro-inflammatory response induced by LPS, both in vitro and in vivo.
Bongkrekic acid
T36067
Bongkrekic acid (Bongkrekic Acid (ammonium salt)) 是一种由伯克霍尔德菌(Burkholderia gladioli)分泌的线粒体毒素,抑制腺嘌呤核苷酸转位酶 (ANT)。Bongkrekic acid Bongkrekic acid 通过 p38、ERK、PAD4 和 P...
Dehydroglyasperin D
TMA0291
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 h...
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