Catalog |
name |
Description |
price |
R-R-2288 |
Momelotinib sulfate CAS No.1056636-06-6 |
Momelotinib sulfate (CYT387 sulfate salt)/CAS No.1056636-06-6 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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R-R-2289 |
VVD-118313 CAS No.2875046-27-6 |
VVD-118313 (compound 5a)/CAS No.2875046-27-6 is a potent, selective JAK1 inhibitor. VVD-118313 targets an isoform-restricted allosteric cysteine to block JAK1-dependent trans-phosphorylation and cytokine signaling. VVD-118313 can be used for research of cancer. VVD-118313 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. |
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R-R-2290 |
BD750 CAS No.892686-59-8 |
BD750/CAS No.892686-59-8, an effective immunosuppressant and a JAK3/STAT5 inhibitor, inhibits IL-2-induced JAK3/STAT5-dependent T cell proliferation, with IC50 values of 1.5 μM and 1.1 μM in mouse and human T cells, respectively. |
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R-R-2291 |
Povorcitinib CAS No.1637677-22-5 |
Povorcitinib (INCB54707)/CAS No.1637677-22-5 is a potent and selective JAK1 inhibitor that effectively reduces abscesses and inflammatory nodules. Povorcitinib is used to study cutaneous lupus erythematosus (CLE) and lichen planus (LP) (information extracted from patent WO2021076124A1). |
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R-R-2292 |
JAK2-IN-6 CAS No.353512-04-6 |
JAK2-IN-6/CAS No.353512-04-6, a multiple-substituted aminothiazole derivative, is a potent and selective JAK2 inhibitor with an IC50 of 22.86 μg/mL. JAK2-IN-6 shows no activity against JAK1 and JAK3. JAK2-IN-6 has anti-proliferative effect against cancer cells. |
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R-R-2293 |
Broussonin E CAS No.90902-21-9 |
Broussonin E/CAS No.90902-21-9 is a phenolic compound and shows anti-inflammatory activity. Broussonin E can suppress inflammation by modulating macrophages activation statevia inhibiting the ERK and p38 MAPK and enhancing JAK2-STAT3 signaling pathway. Broussonin E can be used for the research of inflammation-related diseases such as atherosclerosis. |
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R-R-2294 |
Itacnosertib CAS No.1628870-27-8 |
Itacnosertib (TP-0184)/CAS No.1628870-27-8 is both inhibitor to JAK2, ACVR1 (ALK2) and ALK5 as described in WO2014151871. |
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R-C-595 |
TG101348 cas:936091-26-8 |
Fedratinib(SAR302503,TG101348)is a selective inhibitor of JAK2 with IC50 of 3 nM in cell-free assays,35-and 334-fold more selective for JAK2 versus JAK1 and JAK3.Fedratinib also inhibits FMS-like tyrosine kinase 3(FLT3)and RET (c-RET)with IC50 of 15 nM and 48 nM,respectively. Fedratinib has potential antineoplastic activity.Fedratinib inhibits proliferation and induces apoptosis. |
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R-R-2295 |
TyK2-IN-2 CAS No.2098466-94-3 |
TyK2-IN-2 (Compoud 18)/CAS No.2098466-94-3 is a TYK2 inhibitor that is potent and selective with IC50s of 7 nM, 0.1 μM, and 0.05 μM for TYK2 JH2, IL-23, and IFNα, respectively. TyK2-IN-2 also inhibits phosphodiesterase 4 (PDE4) with an IC50 of 62 nM. TyK2-IN-2 can be used for research of inflammatory and autoimmune diseases. |
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R-R-2296 |
SJ10542 CAS No.2789678-92-6 |
SJ10542/CAS No.2789678-92-6 is a potent and selective JAK2/3 directing phenyl glutarimide (PG)-PROTAC with DC50s of 14, 11, and 24 nM for JAK2, JAK3, and JAK2-fusion ALL, respectively. SJ10542 utilizes a PG ligand as the cereblon (CRBN) recruiter. |
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