Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T79235 | JAK-IN-30
化合物 JAK-IN-30
|
2891469-99-9 | 98% |
|
JAK-IN-30(化合物31)是一种具有水溶性的JAK抑制剂,对JAK2、JAK1、JAK3及TYK2的IC50值分别为2、15、18及2 nM。该化合物作为研究干眼症(DED)的潜在药物而备受关注。 | ||||
T79581 | JAK2-IN-9
化合物 JAK2-IN-9
|
2568842-26-0 | 98% |
|
JAK2-IN-9(Compound A8)是一款选择性JAK2抑制剂(IC50:5 nM),能够抑制JAK2、STAT3和STAT5的磷酸化,并显示出代谢稳定性。此外,JAK2-IN-9能够诱导细胞凋亡(apoptosis),适用于骨髓增生性肿瘤(MPN)的研究。 | ||||
T79608 | DPP
化合物 DPP
|
2668267-47-6 | 98% |
|
DPP,一种含紫檀芪衍生轴向配体的铂(IV)络合物,能够抑制乳腺癌(BC)细胞的JAK2-STAT3通路并显示出抗增殖特性。它通过激活caspase-3和裂解聚ADP-核糖聚合酶诱导细胞凋亡(apoptosis),同时促进树突状细胞成熟及抗原呈现功能,并已证明体内具有安全性。 | ||||
T79609 | STAT3-IN-18
化合物 STAT3-IN-18
|
2668267-41-0 | 98% |
|
STAT3-IN-18 (compound SPP),一种带紫檀芪衍生轴向配体的铂(IV)络合物,能抑制乳腺癌(BC)细胞的JAK2-STAT3通路,显示出抗增殖活性。它激活caspase-3和裂解聚ADP-核糖聚合酶,诱导apoptosis。此外,STAT3-IN-18可促进树突状细胞成熟与抗原呈递,体现了良好的体内安... | ||||
T79807 | JAK kinase-IN-1
化合物 JAK kinase-IN-1
|
2698389-43-2 | 98% |
|
JAKkinase-IN-1 (Example 1)为一种JAK抑制剂,其对TYK2、JAK1、JAK2和JAK3的抑制IC50值分别为4.2 nM、32 nM、27 nM及3473 nM。 | ||||
T79882 | JAK-IN-31
化合物 JAK-IN-31
|
2597016-88-9 | 98% |
|
JAK-IN-31(实施例 75)作为JAK抑制剂,对JAK1、JAK2、JAK3及Tyk2的IC50值分别为≤0.01µM、≤0.01µM、0.01-0.1µM、≤0.01µM,适用于癌症研究领域。 | ||||
T81331 | QL-1200186
化合物 QL-1200186
|
2848664-42-4 | 98% |
|
QL-1200186为具备口服活性与选择性的TYK2抑制剂。经口服后,该药剂量依赖性抑制因interleukin-12刺激所诱导的interferon-γ产生,并在银屑病模型小鼠中显著改善皮肤病变状况。 | ||||
T82017 | JAK-IN-34
化合物 JAK-IN-34
|
2068766-90-3 | 98% |
|
JAK-IN-34 对JAKs具有有效抑制作用,其IC50值分别针对JAK1、JAK2、JAK3、TYK2为0.40、0.83、2.10、1.95 nM 。此外,JAK-IN-34 能够降低关节肿胀,并展现出良好的安全性。 | ||||
T82018 | JAK-IN-33
化合物 JAK-IN-33
|
98% |
|
|
JAK-IN-33(化合物3(R))为一种JAK抑制剂。 | ||||
T83218 | ABBV-712
化合物 ABBV-712
|
2368945-27-9 | 98% |
|
ABBV-712为选择性酪氨酸激酶 2 (TYK2) 抑制剂,IC50值为0.195 μM,关键作用于自身免疫性疾病。 | ||||
T9814 | JAK3/BTK-IN-1
化合物JAK3/BTK-IN-1
|
2674036-91-8 | 98% |
|
JAK3/BTK- in -1是一种特异性靶向和抑制Janus 激酶3 (JAK3)和布鲁顿酪氨酸激酶(BTK)的JAK3/BTK 双重抑制剂 ,BTK 和 JAK3 是自身免疫性疾病的两个重要靶点。JAK3/BTK- in -1同时抑制 BTK/JAK3 信号通路表现出协同效应。 JAK3/BTK- in -1是治疗免... | ||||
T15606 | JAK1-IN-4
化合物 T15606
|
2091134-35-7 | 98% |
|
JAK1-IN-4 is a selective JAK1 inhibitor (IC50s: 85 nM, 12.8 μM and >30 μM for JAK1, JAK2, and JAK3, respectively). JAK1-IN-4 inhibits STAT3 phosphorylation in NC... | ||||
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... | ||||
T11721L | JDTic dihydrochloride
化合物 T11721L
|
785835-79-2 | 98% |
|
JDTic is a potent antagonist of kappa-opioid receptors (KOR), blocking the κ-agonist U50, 488-induced antinociception. | ||||
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... | ||||
T11708 | JAK2-IN-4
化合物 T11708
|
1438284-00-4 | 98% |
|
JAK2-IN-4 is a selective JAK2/JAK3 inhibitor, with IC50 values of 0.7 nM and 23.2 nM for JAK2 and JAK3, respectively. | ||||
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... | ||||
T15037 | Momelotinib Mesylate
化合物 T15037
|
1056636-07-7 | 98% |
|
Momelotinib Mesylate is an ATP-competitive JAK1/JAK2 inhibitor (IC50: 11 nM/18 nM). It has 10-fold selectivity versus JAK3. | ||||
T11714 | JBJ-04-125-02
化合物 T11714
|
2060610-53-7 | 98% |
|
JBJ-04-125-02 can inhibit cancer cell proliferation and EGFRL858R/T790M/C797S signaling. JBJ-04-125-02 has anti-tumor activities. JBJ-04-125-02 is a potent, muta... | ||||
TN2002 | Obovatol
和厚朴新酚
|
83864-78-2 | 98% |
|
Obovatol has antioxidant, neuroprotective, antiinflammatory, antithrombotic and antitumour effects, it is a potent NF-κB inhibitors for Alzheimer's disease treat... |