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JAK

JAK

The JAK-STAT signalling pathway is a chain of interactions between proteins in a cell, and is involved in processes such as immunity, cell division, cell death and tumour formation. There are 4 JAK proteins: JAK1, JAK2, JAK3 and TYK2. JAKs contains a FERM domain (approximately 400 residues), an SH2-related domain (approximately 100 residues), a kinase domain (approximately 250 residues) and a pseudokinase domain (approximately 300 residues). The kinase domain is vital for JAK activity, since it allows JAKs to phosphorylate (add phosphate groups to) proteins.
TargetMol
1 2 3 4 5 6 7 8 9
Cat. No. Product Name CAS No. Purity Chemical Structure
T79235 JAK-IN-30
化合物 JAK-IN-30
2891469-99-9 98%
TargetMol Chemical Structure JAK-IN-30
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%
TargetMol Chemical Structure JAK2-IN-9
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%
TargetMol Chemical Structure DPP
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%
TargetMol Chemical Structure STAT3-IN-18
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%
TargetMol Chemical Structure JAK kinase-IN-1
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%
TargetMol Chemical Structure JAK-IN-31
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%
TargetMol Chemical Structure QL-1200186
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%
TargetMol Chemical Structure JAK-IN-34
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%
TargetMol Chemical Structure JAK-IN-33
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%
TargetMol Chemical Structure ABBV-712
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%
TargetMol Chemical Structure JAK3/BTK-IN-1
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%
TargetMol Chemical Structure JAK1-IN-4
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%
TargetMol Chemical Structure Britannilactone diacetate
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%
TargetMol Chemical Structure JDTic dihydrochloride
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%
TargetMol Chemical Structure Physalin A
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%
TargetMol Chemical Structure JAK2-IN-4
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%
TargetMol Chemical Structure Ergosterol peroxide
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%
TargetMol Chemical Structure Momelotinib Mesylate
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%
TargetMol Chemical Structure JBJ-04-125-02
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%
TargetMol Chemical Structure Obovatol
Obovatol has antioxidant, neuroprotective, antiinflammatory, antithrombotic and antitumour effects, it is a potent NF-κB inhibitors for Alzheimer's disease treat...
JAK-IN-30
T79235
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。
JAK2-IN-9
T79581
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。
DPP
T79608
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。
STAT3-IN-18
T79609
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...
JAK kinase-IN-1
T79807
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。
JAK-IN-31
T79882
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。
QL-1200186
T81331
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。
JAK-IN-34
T82017
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。
JAK-IN-33
T82018
JAK-IN-33(化合物3(R))为一种JAK抑制剂。
ABBV-712
T83218
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。
JAK3/BTK-IN-1
T9814
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...
JAK1-IN-4
T15606
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...
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...
JDTic dihydrochloride
T11721L
JDTic is a potent antagonist of kappa-opioid receptors (KOR), blocking the κ-agonist U50, 488-induced antinociception.
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...
JAK2-IN-4
T11708
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.
Ergosterol peroxide
TMA1743
Ergosterol peroxide is an inhibitor of osteoclast differentiation, which has antiviral, trypanocidal, antitumor, and antiangiogenic actions, it can stimulate Fox...
Momelotinib Mesylate
T15037
Momelotinib Mesylate is an ATP-competitive JAK1/JAK2 inhibitor (IC50: 11 nM/18 nM). It has 10-fold selectivity versus JAK3.
JBJ-04-125-02
T11714
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...
Obovatol
TN2002
Obovatol has antioxidant, neuroprotective, antiinflammatory, antithrombotic and antitumour effects, it is a potent NF-κB inhibitors for Alzheimer's disease treat...
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