369 Results for "

jak2

" in MedChemExpress (MCE) Product Catalog:
Products (369)

369 Results for "jak2" in MCE Product Catalog:

  • Isoforms Recommended:
  • Targets Recommended:
  • Recombinant Proteins Recommended:
171
171 Publications Verification
製品番号: HY-12000
CAS 番号: 133550-30-8
純度:  99.86%
別名: Tyrphostin AG490; Tyrphostin B42
Target:  

EGFR STAT JAK Autophagy

研究分野:  

Cancer

AG490 (Tyrphostin AG490) is a tyrosine kinase inhibitor that inhibits EGFR, Stat-3 and JAK2/3.
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80
80 Cited Publications
製品番号: HY-15315A
CAS 番号: 1187595-84-1
純度:  99.97%
別名: LY3009104 phosphate; INCB028050 phosphate
Target:  

JAK

研究分野:  

Inflammation/Immunology

Baricitinib phosphate (LY3009104 phosphate; INCB028050 phosphate) is a selective orally bioavailable JAK1/JAK2 inhibitor with IC50 of 5.9 nM and 5.7 nM, respectively.
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80
80 Cited Publications
製品番号: HY-15315
CAS 番号: 1187594-09-7
純度:  99.93%
別名: LY3009104; INCB028050
Target:  

JAK

研究分野:  

Inflammation/Immunology

Baricitinib (LY3009104; INCB028050) is a selective and orally bioavailable JAK1 and JAK2 inhibitor with IC50s of 5.9 nM and 5.7 nM, respectively.
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54
54 Cited Publications
製品番号: HY-10409
CAS 番号: 936091-26-8
純度:  99.83%
別名: TG-101348; SAR 302503
Target:  

JAK Apoptosis

研究分野:  

Cancer

Fedratinib (TG-101348) is a potent, selective, ATP-competitive and orally active JAK2 inhibitor with IC50s of 3 nM for both JAK2 and JAK2V617F kinase. Fedratinib shows 35- and 334-fold selectivity over JAK1 and JAK3, respectively. Fedratinib induces cancer cell apoptosis and has the potential for myeloproliferative disorders research [2].
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54
54 Cited Publications
製品番号: HY-10409A
CAS 番号: 1374744-69-0
純度:  99.92%
別名: TG-101348 hydrochloride hydrate; SAR 302503 hydrochloride hydrate
Target:  

JAK Apoptosis

研究分野:  

Cancer

Fedratinib 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 [2].
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41
41 Cited Publications
製品番号: HY-15312
CAS 番号: 857064-38-1
純度:  99.77%
Target:  

STAT JAK Apoptosis

研究分野:  

Cancer

WP1066 is an inhibitor of JAK2 and STAT3, and also shows effect on STAT5 and ERK1/2, without affecting JAK1 and JAK3. WP1066 can cross the blood-brain barrier[1][2][3][4].
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29
29 Cited Publications
製品番号: HY-N7452
CAS 番号: 4434-05-3
Coumermycin A1 is a JAK2 signal activator. Coumermycin A1 inhibits DNA Gyrase which thereby inhibits cell division in bacteria. Coumermycin A1 shows anti-orthopoxvirus activity.
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28
28 Cited Publications
製品番号: HY-18300
CAS 番号: 1206161-97-8
別名: GLPG0634
Target:  

JAK HIV

研究分野:  

Cancer

Filgotinib (GLPG0634) is a selective, orally available JAK1 inhibitor with anti-inflammatory and antiviral activities. Filgotinib can effectively inhibit the activities of JAK1, JAK2, JAK3 and TYK2 with IC50 values of 10 nM, 28 nM, 810 nM and 116 nM, respectively. Filgotinib also inhibits HIV-1 driven gene transcription and reduces proliferation of HIV-1 infected cells. Filgotinib can be used in the study of rheumatoid arthritis and inflammatory bowel disease [2] .
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28
28 Cited Publications
製品番号: HY-18300A
CAS 番号: 1802998-75-9
別名: GLPG0634 maleate
Target:  

JAK HIV

研究分野:  

Inflammation/Immunology

Filgotinib maleate (GLPG0634 maleate) is a selective, orally available JAK1 inhibitor with anti-inflammatory and antiviral activities. Filgotinib maleate can effectively inhibit the activities of JAK1, JAK2, JAK3 and TYK2 with IC50 values ​​of 10 nM, 28 nM, 810 nM and 116 nM, respectively. Filgotinib maleate also inhibits HIV-1 driven gene transcription and reduces proliferation of HIV-1 infected cells. Filgotinib maleate can be used in the study of rheumatoid arthritis and inflammatory bowel disease [2] .
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27
27 Cited Publications
製品番号: HY-19569
CAS 番号: 1310726-60-3
別名: ABT-494
Target:  

JAK

Upadacitinib (ABT-494) is a potent, orally active and selective Janus kinase 1 (JAK1) inhibitor (IC50=43 nM). Upadacitinib (ABT-494) displays approximately 74 fold selective for JAK1 over JAK2 (200 nM) in cellular assays dependent on specific, relevant cytokines. Upadacitinib (ABT-494) can be used for several autoimmune disorders research [2].
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21
21 Cited Publications
製品番号: HY-10193
CAS 番号: 935666-88-9
純度:  99.91%
Target:  

JAK

研究分野:  

Cancer

AZD-1480 is an ATP-competitive inhibitor of JAK1 and JAK2 with IC50s of 1.3 nM and <0.4 nM, respectively .
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21
21 Cited Publications
製品番号: HY-N0484
CAS 番号: 2586-96-1
Liensinine is a bisbenzylisoquinoline alkaloid. By inhibiting the PI3K/AKT and JNK/p38-MAPK signaling pathways, Liensinine suppresses autophagy and apoptosis, clears , 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 [2] .
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21
21 Cited Publications
製品番号: HY-13264
CAS 番号: 856243-80-6
純度:  99.70%
別名: WP1130
研究分野:  

Cancer

Degrasyn (WP1130) is a cell-permeable deubiquitinase (DUB) inhibitor, directly inhibiting DUB activity of USP9x, USP5, USP14, and UCH37. Degrasyn has been shown to downregulate the antiapoptotic proteins Bcr-Abl and JAK2.
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21
21 Cited Publications
製品番号: HY-N5014
CAS 番号: 2385-63-9
Liensinine perchlorate is a bisbenzylisoquinoline alkaloid. By inhibiting the PI3K/AKT and JNK/p38-MAPK signaling pathways, Liensinine perchlorate suppresses autophagy and apoptosis, clears , and exerts anti-inflammatory, antioxidant and neuroprotective effects. Liensinine perchlorate activates AMPK and inhibits the expression of HIF-1α and VEGF, thereby suppressing angiogenesis. Liensinine perchlorate exerts anti-tumor effects through ROS-mediated inhibition of the JAK2/STAT3 signaling pathway. Liensinine perchlorate can be used for the research of diseases such as Alzheimer's disease, hepatocellular carcinoma, osteosarcoma, sepsis-induced organ injury and stroke [2] .
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19
19 Cited Publications
製品番号: HY-16379
CAS 番号: 937272-79-2
別名: SB1518
Target:  

JAK FLT3

研究分野:  

Cancer

Pacritinib (SB1518) is a potent inhibitor of both wild-type JAK2 (IC50=23 nM) and JAK2 V617F mutant (IC50=19 nM). Pacritinib also inhibits FLT3 (IC50=22 nM) and its mutant FLT3 D835Y (IC50=6 nM).
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19
19 Cited Publications
製品番号: HY-16379B
CAS 番号: 1228923-42-9
別名: SB1518 citrate
Target:  

JAK FLT3

研究分野:  

Cancer

Pacritinib (SB1518) citrate is a potent inhibitor of both wild-type JAK2 (IC50=23 nM) and JAK2 V617F mutant (IC50=19 nM). Pacritinib citrate also inhibits FLT3 (IC50=22 nM) and its mutant FLT3 D835Y (IC50=6 nM). Pacritinib citrate can be used for the research of acute myeloid leukemia (AML) and myelofibrosis (MF) [2] .
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18
18 Cited Publications
製品番号: HY-10961
CAS 番号: 1056634-68-4
純度:  99.37%
別名: CYT387
Target:  

JAK Autophagy Apoptosis

研究分野:  

Cancer

Momelotinib (CYT387) is an ATP-competitive inhibitor of JAK1/JAK2 with IC50a of 11 nM and 18 nM,respectively. CYT387 shows much less activity against JAK3.
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18
18 Cited Publications
製品番号: HY-10962
CAS 番号: 1056636-06-6
純度:  98.06%
別名: CYT387 sulfate salt
Target:  

JAK Autophagy Apoptosis

研究分野:  

Cancer

Momelotinib sulfate (CYT387 sulfate salt) is an ATP-competitive inhibitor of JAK1/JAK2 with IC50 of 11 nM/18 nM, 10-fold selectivity versus JAK3 (IC50=155 nM).
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17
17 Cited Publications
製品番号: HY-102084
CAS 番号: 1239600-18-0
純度:  98.93%
Target:  

Interleukin Related

研究分野:  

Inflammation/Immunology

LMT-28 is an orally active and the first synthetic IL-6 inhibitor that functions through direct binding to gp130. LMT-28 shows low toxicity and selectively inhibits IL-6-induced phosphorylation of STAT3, JAK2, and gp130 .
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13
13 Cited Publications
製品番号: HY-N1405
CAS 番号: 2222-07-3
別名: Elatericin B; JSI-124; NSC-521777
Cucurbitacin I is a natural selective inhibitor of JAK2/STAT3, with potent anti-cancer activity.
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