Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
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... | ||||
T72714 | JNK3 inhibitor-3
化合物 JNK3 inhibitor-3
|
2873465-25-7 | 98% |
|
JNK3inhibitor-3(compound 15g)是一种选择性的c-Jun N-terminal kinase3(JNK3)抑制剂,具有良好的血脑屏障穿透性和口服生物利用度。其对JNK1、JNK2和JNK3的IC50分别为147.8 nM、44.0 nM和4.1 nM。在小鼠痴呆模型中,JNK3inhibitor... |