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JNK

JNK

JNK signaling pathway is such a death pathway that control cell death. There are two main downstream signaling of JNK pathway: one is activation of death signaling such c-Jun, Fos and apoptosis signaling such as BIM, BAD, BAX protein or active P53 transcription, to promote cell apoptosis; the other is inhibition of the cell survival signaling such as STATs and CREB .
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Cat. No. Product Name CAS No. Purity Chemical Structure
T7008 Vacquinol-1
化合物Vacquinol-1
5428-80-8 98.67%
Vacquinol-1 能够激活 MAPK 通路,是MKK4特异性激活剂。它可以诱导肝细胞癌细胞凋亡,在多形性胶质母细胞瘤小鼠模型中特异性诱导人胶质母细胞瘤细胞死亡、减缓肿瘤进展并延长生存期。
T38665 OVA-E1 peptide TFA
化合物OVA-E1 peptide TFA
1262750-80-0
OVA-E1 peptide TFA 在突变型和野生型胸腺细胞中都能同样地激活 p38 和 JNK 级联。
TN4394 Kobophenol A
化合物 TN4394
124027-58-3 98%
Kobophenol A has antimicrobial, and anti-inflammatory activities, it might be a candidate for treatment of inflammatory bone diseases relevant to osteoblast cell...
TN4938 Samidin
化合物 TN4938
477-33-8 98%
Samidin has anti-inflammatory properties through suppression of NF-κB and AP-1-mediated-genes in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells.
T78829 JNK2-IN-1
化合物 JNK2-IN-1
98%
JNK2-IN-1(Compound J27)是一款具有抗炎活性的JNK2抑制剂,其解离常数为79.2 μM。该化合物能通过阻断NF-κB/MAPK信号通路来降低肿瘤坏死因子α(TNF-α)和白细胞介素6(IL-6)的释放,从而减轻脂多糖(LPS)引起的急性肺损伤(ALI)及脓毒症症状。
T79296 JNK-IN-12
化合物 JNK-IN-12
98%
JNK-IN-12(compound P2)是一种针对线粒体的JNK抑制剂,其IC50为66.3 nM,由线粒体特异性细胞穿透肽与特异性JNK抑制剂SP600125构成。该化合物特异性作用于线粒体JNK不影响核内JNK信号,能够抑制线粒体JNK磷酸化。JNK-IN-12在体内外模型中对帕金森病的改善显示出潜在效果。
T79489 JNK-1-IN-2
化合物 JNK-1-IN-2
98%
JNK-1-IN-2(Compound c6)是一种选择性JNK-1抑制剂,其IC50值为33.5 nM。同时,该化合物对JNK-2和JNK-3也具有抑制作用,其IC50值分别为112.9 nM和33.2 nM。通过抑制c-Jun蛋白的磷酸化,JNK-1-IN-2能够逆转肺部损伤,并且可以被应用于肺纤维化的相关研究。
T79754 JNK-IN-14
化合物 JNK-IN-14
98%
JNK-IN-14是一种激酶(JNK1/2/3)抑制剂,IC50值为1.81、12.7和10.5 nM。它能诱导早期apoptosis,并在G2/M阶段引起细胞周期阻滞。与SP600125相比,在K562白血病细胞中,JNK-IN-14更强有效地抑制了Beclin-1的表达。
T80005 N-Butyl α-D-fructofuranoside
化合物 n-Butyl α-D-fructofuranoside
80971-59-1 98%
n-Butyl α-D-fructofuranoside,分离自Ulmus davidiana var. japonica的根皮,通过激活JNK促进Nrf2活性,并表现出抗炎效应。
T10937 D-JNKI-1
化合物 T10937
1445179-97-4 98%
D-JNKI-1 (AM-111) is a highly effective and cell-permeable peptide inhibitor.
TN4410 Lappaol C
化合物 TN4410
64855-00-1 98%
Lappaol C has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. Lappaol C also ...
TN3587 Capillarisin
化合物 TN3587
56365-38-9 98%
Capillarisin is a novel blocker of STAT3 activation and thus may have a potential in negative regulation of growth, metastasis, and chemoresistance of tumor cell...
TN4877 Quercetin 3,4'-dimethyl ether
化合物 TN4877
33429-83-3 98%
Quercetin 3,4'-dimethyl ether shows anti-lipid peroxidation activity (IC 50 values of 0.3 uM), it also shows anti-inflammatory activity. Quercetin 3,4'-dimethyl ...
TN4263 Isoangustone A
化合物 TN4263
129280-34-8 98%
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation ...
TN4317 Isopedicin
化合物 TN4317
4431-42-9 98%
Isopedicin has anti-inflammatory functions, it inhibits the O(2)(*)(-) production in human neutrophils by an elevation of cellular cAMP and activation of PKA thr...
TN2511 Britannilactone diacetate
化合物 TN2511
1286694-67-4 98%
1,6-O,O-Diacetylbritannilactone(OODBL) has anti-inflammatory activity, it has a potential therapeutic efficacy on inflammatory diseases especially allergic airwa...
TN5011 Shizukaol B
化合物 TN5011
142279-40-1 98%
Shizukaol B exerts anti-inflammatory effects in LPS-activated microglia partly by modulating JNK-AP-1 signaling pathway; it also shows significant anti-neuroinfl...
TN4774 Physalin A
化合物 TN4774
23027-91-0 98%
Physalin A exerts anti-tumor activity in non-small cell lung cancer cell lines by suppressing JAK/STAT3 signaling, it inhibits androgen-independent prostate canc...
TN1775 Isocryptotanshinone
异隐丹参酮
22550-15-8 98%
Isocryptotanshinone inhibits protein tyrosine phosphatase 1B (PTP1B) activity with 50% inhibitory concentration values of 56.1±6.3 μM, PTP1B acts as a negative r...
TMA1743 Ergosterol peroxide
过氧麦角甾醇
2061-64-5 98%
Ergosterol peroxide is an inhibitor of osteoclast differentiation, which has antiviral, trypanocidal, antitumor, and antiangiogenic actions, it can stimulate Fox...
Vacquinol-1
T7008
Vacquinol-1 能够激活 MAPK 通路,是MKK4特异性激活剂。它可以诱导肝细胞癌细胞凋亡,在多形性胶质母细胞瘤小鼠模型中特异性诱导人胶质母细胞瘤细胞死亡、减缓肿瘤进展并延长生存期。
OVA-E1 peptide TFA
T38665
OVA-E1 peptide TFA 在突变型和野生型胸腺细胞中都能同样地激活 p38 和 JNK 级联。
Kobophenol A
TN4394
Kobophenol A has antimicrobial, and anti-inflammatory activities, it might be a candidate for treatment of inflammatory bone diseases relevant to osteoblast cell...
Samidin
TN4938
Samidin has anti-inflammatory properties through suppression of NF-κB and AP-1-mediated-genes in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells.
JNK2-IN-1
T78829
JNK2-IN-1(Compound J27)是一款具有抗炎活性的JNK2抑制剂,其解离常数为79.2 μM。该化合物能通过阻断NF-κB/MAPK信号通路来降低肿瘤坏死因子α(TNF-α)和白细胞介素6(IL-6)的释放,从而减轻脂多糖(LPS)引起的急性肺损伤(ALI)及脓毒症症状。
JNK-IN-12
T79296
JNK-IN-12(compound P2)是一种针对线粒体的JNK抑制剂,其IC50为66.3 nM,由线粒体特异性细胞穿透肽与特异性JNK抑制剂SP600125构成。该化合物特异性作用于线粒体JNK不影响核内JNK信号,能够抑制线粒体JNK磷酸化。JNK-IN-12在体内外模型中对帕金森病的改善显示出潜在效果。
JNK-1-IN-2
T79489
JNK-1-IN-2(Compound c6)是一种选择性JNK-1抑制剂,其IC50值为33.5 nM。同时,该化合物对JNK-2和JNK-3也具有抑制作用,其IC50值分别为112.9 nM和33.2 nM。通过抑制c-Jun蛋白的磷酸化,JNK-1-IN-2能够逆转肺部损伤,并且可以被应用于肺纤维化的相关研究。
JNK-IN-14
T79754
JNK-IN-14是一种激酶(JNK1/2/3)抑制剂,IC50值为1.81、12.7和10.5 nM。它能诱导早期apoptosis,并在G2/M阶段引起细胞周期阻滞。与SP600125相比,在K562白血病细胞中,JNK-IN-14更强有效地抑制了Beclin-1的表达。
n-Butyl α-D-fructofuranoside
T80005
n-Butyl α-D-fructofuranoside,分离自Ulmus davidiana var. japonica的根皮,通过激活JNK促进Nrf2活性,并表现出抗炎效应。
D-JNKI-1
T10937
D-JNKI-1 (AM-111) is a highly effective and cell-permeable peptide inhibitor.
Lappaol C
TN4410
Lappaol C has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. Lappaol C also ...
Capillarisin
TN3587
Capillarisin is a novel blocker of STAT3 activation and thus may have a potential in negative regulation of growth, metastasis, and chemoresistance of tumor cell...
Quercetin 3,4'-dimethyl ether
TN4877
Quercetin 3,4'-dimethyl ether shows anti-lipid peroxidation activity (IC 50 values of 0.3 uM), it also shows anti-inflammatory activity. Quercetin 3,4'-dimethyl ...
Isoangustone A
TN4263
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation ...
Isopedicin
TN4317
Isopedicin has anti-inflammatory functions, it inhibits the O(2)(*)(-) production in human neutrophils by an elevation of cellular cAMP and activation of PKA thr...
Britannilactone diacetate
TN2511
1,6-O,O-Diacetylbritannilactone(OODBL) has anti-inflammatory activity, it has a potential therapeutic efficacy on inflammatory diseases especially allergic airwa...
Shizukaol B
TN5011
Shizukaol B exerts anti-inflammatory effects in LPS-activated microglia partly by modulating JNK-AP-1 signaling pathway; it also shows significant anti-neuroinfl...
Physalin A
TN4774
Physalin A exerts anti-tumor activity in non-small cell lung cancer cell lines by suppressing JAK/STAT3 signaling, it inhibits androgen-independent prostate canc...
Isocryptotanshinone
TN1775
Isocryptotanshinone inhibits protein tyrosine phosphatase 1B (PTP1B) activity with 50% inhibitory concentration values of 56.1±6.3 μM, PTP1B acts as a negative r...
Ergosterol peroxide
TMA1743
Ergosterol peroxide is an inhibitor of osteoclast differentiation, which has antiviral, trypanocidal, antitumor, and antiangiogenic actions, it can stimulate Fox...
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