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Search Results for " jnk1 "

Targets

35

Compounds

5

Natural Products

2

Recombinant Proteins

Cat No. Product Name Synonyms Targets
T33467 MOMIPP PI3K
MOMIPP is a PIKfyve inhibitor and a macropinocytosis inducer. MOMIPP readily penetrates the blood-brain barrier and is moderately effective in suppressing progression of intracerebral glioblastoma xenografts[1][2].
T9688 CC-90001 JNK
CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.
T4646 TA-02 p38 MAPK , Autophagy
TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM.TA-02 especially inhibits TGFBR-2.
T6150 TAK-715 p38 MAPK , Casein Kinase , JNK
TAK-715 is a p38 MAPK inhibitor for p38α.
T3200 DB07268 JNK
DB07268 is a potent and selective JNK1 inhibitor.
T3598 JNK-IN-7 JNK inhibitor JNK
JNK-IN-7 (JNK inhibitor) is a selective JNK1/2/3 inhibitor (IC50: 1.54/1.99/0.75 nM). It can also inhibit phosphorylation of c-Jun, which is a substrate of JNK kinase.
T14895 Tanzisertib CC-930 JNK
Tanzisertib (CC-930) (CC-930) is a potent inhibitor of JNK1/2/3 with IC50s of 61/7/6 nM, respectively, with potential antifibrotic activity.
T2668 JNK-IN-8 JNK Inhibitor XVI JNK , c-Kit
JNK-IN-8 (JNK Inhibitor XVI) is an irreversible JNK1/2/4 inhibitor (IC50: 4.7/18.7/1 nM). The selectivity is higher 10-fold than MNK2, Fms and no inhibition of Met, c-Kit, PDGFRβ in A375 cell line.
T8477 IQ-3 JNK
IQ3 is a selective inhibitor of JNK3(JNK3, JNK1 and JNK2 with Kd of 66 nM, 240 nM and 290 nM, respectively). IQ 3 inhibits NF-κB/AP1 transcriptional activity in THP1-Blue cells with IC50 of 1.4 μM, also inhibits TNF-α an...
T3109 SP600125 1PMV,JNK Inhibitor II,Nsc75890,Pyrazolanthrone Apoptosis , Ferroptosis , Trk receptor , JNK , Aurora Kinase , Autophagy
SP600125 (JNK Inhibitor II) is a JNK inhibitor that inhibits JNK1, JNK2, and JNK3 (IC50=40/40/90 nM) with oral potency, reversibility, and ATP-competitive properties. SP600125 inhibits autophagy and induces apoptosis.
T2675 Bentamapimod AS 602801 JNK
Bentamapimod (AS 602801) is a novel, orally active inhibitor of JNK.
T60534 JNK-IN-11
JNK-IN-11 (compound 1) is a potent inhibitor of JNK with the potential for Alzheimer's and Parkinson's disease research. JNK-IN-11 has IC50 values of 2.2, 21.4, 1.8 μM for JNK1, JNK2, JNK3, respectively.
T6525 GW 5074 GW5074,Raf1 Kinase Inhibitor I Apoptosis , Raf
GW 5074 (Raf1 Kinase Inhibitor I)(IC50=9 nM) is an effective and specific c-Raf inhibitor. It has no effect on the activities of JNK1/2/3, MEK1, MKK6/7, CDK1/2, c-Src, p38 MAP, VEGFR2 or c-Fms.
T6440 CGP 57380 MNK1 Inhibitor Apoptosis , MNK
CGP 57380 (MNK1 Inhibitor) is a potent MNK1 inhibitor with IC50 of 2.2 μM, exhibiting no inhibitory activity on p38, JNK1, ERK1 and -2, PKC, or c-Src-like kinases.
T3627 IQ-1S free acid IQ-1,IQ-1S,IQ-1S (free acid) NF-κB , JNK
IQ-1S free acid (IQ-1S) is an effective and specific c-Jun N-Terminal Kinase Inhibitor. IQ-1S inhibits murine delayed-type hypersensitivity. IQ-1S can reduce inflammation and cartilage loss associated with CIA and can se...
T5094 IRAK inhibitor 1 IRAK , JNK
IRAK inhibitor 1 is an effective IRAK-4 inhibitor (IC50: 216 nM), is poorly active against JNK-1 (IC50: 3.801 μM) and JNK-2 (IC50>10 μM).
T26349 ZG-10 ZG 10,ZG10
ZG-10 is a JNK1 inhibitor targeting JNK and p38 signaling.
TP2145 JTP10-△-R9 TFA JNK
JTP10-△-R9 TFA is a selective inhibitor of JNK2 peptide (IC50: 89 nM), exhibiting 10-fold selectivity for JNK2 over JNK1 and JNK3.
TP2146 JTP10-△-TATi TFA JNK
JTP10-△-TATi TFA is a selective inhibitor of JNK2 peptide (IC50: 92 nM), exhibiting 10-fold selectivity for JNK2 over JNK1 and JNK3.
T79754 JNK-IN-14 JNK
JNK-IN-14 is a potent inhibitor of JNK with IC50 values of 1.81 nM for JNK1, 12.7 nM for JNK2, and 10.5 nM for JNK3. It induces early-stage apoptosis, arrests cell population at the G2/M phase, and moderately inhibits be...
T74850 YL5084
YL5084, a covalent inhibitor selective for JNK2 and JNK3 over JNK1, demonstrates IC50 values of 70 nM and 84 nM for JNK2 and JNK3, respectively, compared to 2173 nM for JNK1. This compound also shows antiproliferative ef...
T72714 JNK3 inhibitor-3 JNK
JNK3 Inhibitor-3 (compound 15g) is a selective, blood-brain barrier permeable, and orally active inhibitor of c-Jun N-terminal kinase 3 (JNK3) with IC50 values of 147.8 nM, 44.0 nM, and 4.1 nM against JNK1, JNK2, and JNK...
T2343 AS601245 JNK
AS601245 is an inhibitor of the c-Jun NH2-terminal kinase (JNK), with neuroprotective properties.
T72956 Darizmetinib HRX215 MAPK
Darizmetinib (HRX215) is an MKK4 inhibitor. Inhibition of MKK4 leads to enhancement of the MKK7 and JNK1 signaling pathways, thereby activating the transcription factors ATF2 and ELK1, promoting cell proliferation and li...
T60805 JNK3 inhibitor-2
JNK3 inhibitor-2 is a potent and selective JNK3 inhibitor. The IC50 values of JNK3 inhibitor-2 for JNK1, JNK2, JNK3 are >100, >100, 0.25 μM, respectively. JNK3 inhibitor-2 also inhibits DDR1 and EGFR (T790M, L858R) [1].
T9138 Indirubin-3′-oxime Indirubin-3'-monoxime GSK-3 , CDK , JNK
Indirubin-3′-oxime is an effective inhibitor of cyclin-dependent protein kinases, and may play an obligate role in neuronal apoptosis in Alzheimer's disease.
T7677 JNK Inhibitor VIII TCS JNK 6o JNK
JNK Inhibitor VIII (TCS JNK 6o) is an ATP-competitive selective inhibitor of c-Jun N-terminal kinase (JNK)(IC50 values of 45 nM and 160 nM for JNK-1 and -2, respectively).
T74817 JNK3 inhibitor-7
JNK3 inhibitor-7, a potent and orally active compound that can cross the blood-brain barrier, acts as a JNK3 inhibitor with IC50 values of 53 nM for JNK3, 973 nM for JNK2, and 1039 nM for JNK1. Demonstrating significant ...
T36260 NR 7h
Potent and selective p38α and p38β degrader (DC50 < 50 nM). Displays no significant degradation of p38γ, p38δ, JNK1/2 or ERK1/2. Inhibits phosphorylation of MK2 in UV-treated cancer cells and LPS-stimulated bone marrow-d...
T8661 AS601245.2TFA (345987-15-7 free base) AS601245.2TFA JNK
AS601245.2TFA (345987-15-7 free base) (AS601245.2TFA) is a cell-permeable Inhibitor of JNK (IC50s of 150, 220, and 70 nM for hJNK1, hJNK2, and hJNK3, respectively).
T74818 JNK3 inhibitor-8
JNK3 Inhibitor-8 is a potent, selective, and orally active inhibitor that can cross the blood-brain barrier, targeting JNK3 with IC50 values of 21 nM for JNK3, 2203 nM for JNK2, and >10000 nM for JNK1. This compound demo...
T72715 JNK3 inhibitor-4
JNK3 Inhibitor-4, a potent 2-aryl-1-pyrimidinyl-1H-imidazole-5-yl acetonitrile derivative, demonstrates a strong inhibitory effect on JNK3 with an IC 50 value of 1.0 nM. It exhibits exceptional selectivity against JNK3 w...
T10298L2 AMG-548 dihydrochloride (864249-60-5 free base) AMG-548 dihydrochloride p38 MAPK
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 against p38γ/p38δ. It is also extremely potent in the inhi...
T10298 AMG-548 hydrochloride (864249-60-5 free base) AMG-548 hydrochloride p38 MAPK
AMG-548 hydrochloride 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 against p38γ/p38δ. It is also extremely potent in the inhibi...
T10298L AMG-548 p38 MAPK
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 p38δ and is also extremely potent in the inhibition of whole b...

Compounds

MOMIPP
T33467
Synonym:
Target: PI3K
CC-90001
T9688
Synonym:
Target: JNK
TA-02
T4646
Synonym:
Target: p38 MAPK, Autophagy
TAK-715
T6150
Synonym:
Target: p38 MAPK, Casein Kinase, JNK
DB07268
T3200
Synonym:
Target: JNK
JNK-IN-7
T3598
Synonym: JNK inhibitor
Target: JNK
Tanzisertib
T14895
Synonym: CC-930
Target: JNK
JNK-IN-8
T2668
Synonym: JNK Inhibitor XVI
Target: JNK, c-Kit
IQ-3
T8477
Synonym:
Target: JNK
SP600125
T3109
Synonym: 1PMV,JNK Inhibitor II,Nsc75890,Pyrazolanthrone
Target: Apoptosis, Ferroptosis, Trk receptor, JNK, Aurora Kinase, Autophagy
Bentamapimod
T2675
Synonym: AS 602801
Target: JNK
JNK-IN-11
T60534
Synonym:
Target:
GW 5074
T6525
Synonym: GW5074,Raf1 Kinase Inhibitor I
Target: Apoptosis, Raf
CGP 57380
T6440
Synonym: MNK1 Inhibitor
Target: Apoptosis, MNK
IQ-1S free acid
T3627
Synonym: IQ-1,IQ-1S,IQ-1S (free acid)
Target: NF-κB, JNK
IRAK inhibitor 1
T5094
Synonym:
Target: IRAK, JNK
ZG-10
T26349
Synonym: ZG 10,ZG10
Target:
JTP10-△-R9 TFA
TP2145
Synonym:
Target: JNK
JTP10-△-TATi TFA
TP2146
Synonym:
Target: JNK
JNK-IN-14
T79754
Synonym:
Target: JNK
YL5084
T74850
Synonym:
Target:
JNK3 inhibitor-3
T72714
Synonym:
Target: JNK
AS601245
T2343
Synonym:
Target: JNK
Darizmetinib
T72956
Synonym: HRX215
Target: MAPK
JNK3 inhibitor-2
T60805
Synonym:
Target:
Indirubin-3′-oxime
T9138
Synonym: Indirubin-3'-monoxime
Target: GSK-3, CDK, JNK
JNK Inhibitor VIII
T7677
Synonym: TCS JNK 6o
Target: JNK
JNK3 inhibitor-7
T74817
Synonym:
Target:
NR 7h
T36260
Synonym:
Target:
AS601245.2TFA (345987-15-7 free base)
T8661
Synonym: AS601245.2TFA
Target: JNK
JNK3 inhibitor-8
T74818
Synonym:
Target:
JNK3 inhibitor-4
T72715
Synonym:
Target:
AMG-548 dihydrochloride (864249-60-5 free base)
T10298L2
Synonym: AMG-548 dihydrochloride
Target: p38 MAPK
AMG-548 hydrochloride (864249-60-5 free base)
T10298
Synonym: AMG-548 hydrochloride
Target: p38 MAPK
AMG-548
T10298L
Synonym:
Target: p38 MAPK
Cat No. Product Name Synonyms Targets
TN7121 D-Epigalbacin (-)-Zuonin A JNK
d-Epigalbacin ((-)-Zuonin A) is a naturally occurring lignin. d-Epigalbacin is a potent, selective JNKs inhibitor, with IC50s of 1.7 μM, 2.9 μM and 1.74 μM for JNK1, JNK2 and JNK3, respectively.
T2S2382 3'-Hydroxypterostilbene 3'-HPT Apoptosis , Autophagy
3'-Hydroxypterostilbene (3'-HPT), a natural pterostilbene analogue, effectively inhibits the growth of human colon cancer cells with IC50s of 9.0, 40.2, and 70.9 μM for COLO 205, HCT-116, and HT-29 cells, respectively, b...
T6S1371 Isovitexin Homovitexin,Saponaretin,Apigenin-6-C-Glucoside NF-κB , JNK , Glucosidase
1. Isovitexin (Apigenin-6-C-Glucoside) exhibits a potential antioxidant activity. 2. Isovitexin shows a strong antihyperglycemic action, inhibits α-glucosidase in vivo.
T3S1641 Esculentoside H TNF , NF-κB , JNK
Phytolaccaceae has anti-tumor activity, the mechanism may be related to the capacity of Esculentoside H for TNF release.
T4S2326 Cornuside 7-Galloylsecologanol,7-O-Galloylsecologanol,Comuside ERK , p38 MAPK , NF-κB , JNK
1. Cornuside (Comuside) has immunomodulatory activity . 2. Cornuside suppresses expression levels of cytokine-induced proinflammatory and adhesion molecules in the human endothelial cells. 3. Cornuside can treat myocardi...

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPY-04554 JNK1 Protein, Human, Recombinant (GST) Human Baculovirus Insect Cells
Mitogen-activated protein kinase 8 (MAPK8), also known as JNK1, is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals and are involved in a wide variety of cellula...
TMPY-04572 MKK4 Protein, Mouse, Recombinant (His & GST) Mouse Baculovirus Insect Cells
Dual specificity mitogen-activated protein kinase kinase 4, also known as MAP kinase kinase 4, MAPKK4, JNK-activating kinase 1, MAPK/ERK kinase 4, SAPK/ERK kinase 1, c-Jun N-terminal kinase kinase 1, JNKK, and MAP2K4, is...
TargetMol