JAK
Janus kinase
JAK Isoform Specific Products
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JAK Inhibitors
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JAK Agonists
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JAK Control
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JAK Substrate
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JAK Ligands
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Janus Kinase 1 (JAK1) Proteins
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JAK Related Products (648)
Related Products (648)
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Recombinant Proteins (4)
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Antibodies (7)
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JAK Isoform Comparison
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Liensinine
0 ImagesLiensinine is a bisbenzylisoquinoline alkaloid. By inhibiting the PI3K/AKT and JNK/p38-MAPK signaling pathways, Liensinine suppresses autophagy and apoptosis, clears Aβ, and exerts anti-inflammatory, antioxidant and neuroprotective effects. Liensinine activates AMPK and inhibits the expression of HIF-1α and VEGF, thereby suppressing angiogenesis. Liensinine exerts anti-tumor effects through ROS-mediated inhibition of the JAK2/STAT3 signaling pathway. Liensinine can be used for the research of diseases such as Alzheimer's disease, hepatocellular carcinoma, osteosarcoma, sepsis-induced organ injury and stroke. -
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- AZD-1480
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- Peficitinib
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Pentadecanoic acid
0 ImagesPentadecylic acid is a saturated fatty acid with a 15-carbon backbone. -
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Ruxolitinib (S enantiomer)
0 ImagesSynonyms: S-Ruxolitinib; S-INCB18424Ruxolitinib (S enantiomer) (S-Ruxolitinib) is the S-enantiomer of Ruxolitinib (HY-50856). Ruxolitinib (S enantiomer) is an orally active, potent JAK inhibitor. -
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Lentinan
0 ImagesCat. No.: HY-N6653CAS No.: 37339-90-5Lentinan is an orally active biocompatible multifunctional polysaccharide with biological activities such as anti-inflammatory, antioxidant, immune regulation, anti-tumor, hypoglycemic, and lipid-lowering[1][4]. -
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Delphinidin chloride
0 ImagesDelphinidin chloride is an anthocyanin isolated from berries and red wine. Delphinidin chloride exhibits endothelium-dependent vasodilation and anticancer activity. Delphinidin chloride also modulates JAK/STAT3 and MAPK signaling, thereby inducing apoptosis in HCT116 cells. Delphinidin chloride is also a potent inhibitor of EGFR (IC50: 1.3 μM), shutting down downstream signaling cascades. -
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- Brepocitinib
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- CHZ868
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- Golidocitinib
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Baricitinib phosphate
0 ImagesSynonyms: LY3009104 phosphate; INCB028050 phosphate -
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Ginsenoside Rk1
0 ImagesGinsenoside Rk1 is a unique component created by processing the ginseng plant (mainly Sung Ginseng, SG) at high temperatures. Ginsenoside Rk1 has anti-inflammatory effect, suppresses the activation of Jak2/Stat3 signaling pathway and NF-κB. Ginsenoside Rk1 has anti-tumor effect, antiplatelet aggregation activities, anti-insulin resistance, nephroprotective effect, antimicrobial effect, cognitive function enhancement, lipid accumulation reduction and prevents osteoporosis. Ginsenoside Rk1 induces cell apoptosis by triggering intracellular reactive oxygen species (ROS) generation and blocking PI3K/Akt pathway. -
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- Cucurbitacin I
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- AT9283
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- Pyridone 6
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Zasocitinib
0 ImagesSynonyms: NDI-034858; TAK-279 -
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N-(3-Aminopropyl)cyclohexylamine
0 ImagesN-(3-Aminopropyl)cyclohexylamine, a cyclohexylamine derivative, acts as a selective and competitive inhibitor of spermine synthase. N-(3-Aminopropyl)cyclohexylamine can be used for the research of neurological diseases. -
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- Cerdulatinib
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Fedratinib hydrochloride hydrate
0 ImagesSynonyms: TG-101348 hydrochloride hydrate; SAR 302503 hydrochloride hydrateFedratinib hydrochloride hydrate (TG-101348 hydrochloride hydrate) is a potent, selective, ATP-competitive and orally active JAK2 inhibitor with IC50s of 3 nM for both JAK2 and JAK2V617F kinase. Fedratinib hydrochloride hydrate shows 35- and 334-fold selectivity over JAK1 and JAK3, respectively. Fedratinib hydrochloride hydrate induces cancer cell apoptosis and has the potential for myeloproliferative disorders research. -
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- Delgocitinib
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Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.