T12997 |
SR-318
|
|
TNF
,
p38 MAPK
|
|
SR-318 is a potent and highly selective inhibitor of p38 MAPK(IC50s of 5 nM, 32 nM and 6.11 μM for p38α, p38β and p38α/β... |
T39823L |
Apelin-12 acetate
|
|
Apelin receptor
,
p38 MAPK
,
JNK
|
|
Apelin-12 acetate possesses a high affinity to orphan receptor APJ receptor. Apelin-12 acetate inhibits the JNK and p38 ... |
T5S1058 |
Triptonide
|
PG 492 , NSC 165677 |
Apoptosis
,
Wnt/beta-catenin
,
Autophagy
|
|
1. Triptonide is effective in the treatment of autoimmune diseases and has potent antileukemic and antitumor activities.... |
T6429 |
Caffeic Acid Phenethyl Ester
|
CAPE , Phenylethyl Caffeate |
NF-κB
,
Apoptosis
|
|
Caffeic Acid Phenethyl Ester (CAPE) inhibits the activation of nuclear transcription factor NF-kappa B and may suppress ... |
T7661 |
SD-169
|
SD 169 |
p38 MAPK
|
|
SD 169 is a selective and ATP competitive the MAP kinases p38α and p38β inhibitor. |
TL0004 |
FERULIC ACID METHYL ESTER
|
Methyl ferulate , Methyl 4'-hydroxy-3'-methoxycinnamate |
p38 MAPK
,
Autophagy
|
|
Ferulic acid is a hydroxycinnamic acid that is abundant in plants and originally derived from giant fennel (F. communis)... |
T61803 |
p38 MAPK-IN-3
|
|
|
|
p38 MAPK-IN-3 (Compound 2c) is a p38α MAPK inhibitor. p38 MAPK-IN-3 has antitumor activities and induces apoptosis and R... |
T22710 |
DBM 1285 dihydrochloride
|
|
Others
|
|
p38 MAPK inhibitor |
TN4635 |
Neoechinulin A
|
|
p38 MAPK
,
NOS
,
TNF
,
NF-κB
,
NADPH-oxidase
,
Beta Amyloid
,
IκB/IKK
,
ASK
,
COX
,
Prostaglandin Receptor
|
|
Neoechinulin A has anti-inflammatory effect against LPS-stimulated RAW264.7 macrophages through inhibition of the NF-κB... |
T12667 |
(Rac)-Hesperetin
|
|
Others
|
|
(Rac)-Hesperetin is the racemate of Hesperetin.Hesperetin induces apoptosis via p38 MAPK activation. Hesperetin is a na... |
T61755 |
E6201
|
|
|
|
E6201 (ER-806201) is an ATP-competitive dual kinase inhibitor of MEK1 and FLT3. E6201 inhibits MEK1- induced ERK2 phosph... |
TN5174 |
Trichosanatine
|
|
LDL
,
p38 MAPK
,
Lipoxygenase
,
ROS
,
MMP
|
|
Trichosanatine and squamosamide, as potential candidates as lead compounds for further study in drug development process... |
T41240 |
Verrucarin A
|
|
|
|
Verrucarin A (Muconomycin A), a Type D macrocyclic mycotoxin derived from the pathogen fungus Myrothecium verrucaria, is... |
T38048 |
Globotetraosylceramides (porcine RBC)
|
|
|
|
Globotetraosylceramides are bioactive neutral glycosphingolipids. They are the major glycolipids in human erythrocytes. ... |
T35536 |
Tpl2 Kinase Inhibitor (hydrochloride)
|
|
|
|
Tpl2 kinase inhibitor is an inhibitor of tumor progression locus 2 (Tpl2; IC50= 0.05 μM).1It is selective for Tpl2 over ... |
T37581 |
SCIO 469 hydrochloride
|
|
|
|
Selective, ATP-competitive p38 inhibitor (IC50 = 9 nM for p38α in vitro). Displays approximately 10-fold selectivity for... |
T38665 |
OVA-E1 peptide TFA
|
|
p38 MAPK
,
JNK
|
|
OVA-E1 peptide TFA activates the p38 and JNK cascades similarly in mutant and wild-type thymocytes. |
T35463 |
(±)14(15)-EET
|
(±)14,15-EpETrE , (±)14,15-EET |
|
|
(±)14(15)-EET is a metabolite of arachidonic acid that is formed via epoxidation of arachidonic acid by cytochrome P450.... |
T36010 |
p38 MAPK Inhibitor
|
|
p38 MAPK
|
|
p38 MAPK inhibitor is a potent inhibitor of p38 MAP kinase (IC50 = 35 nM). It inhibits senescence induced by the oncogen... |
T35420 |
(S)-p38 MAPK Inhibitor III
|
|
|
|
(S)-p38 MAPK inhibitor III is a methylsulfanylimidazole that inhibits p38 MAP kinase (IC50 = 0.90 μM in vitro). It is ce... |