166 Results for "

FMS

" in MedChemExpress (MCE) Product Catalog:
Products (166)

166 Results for "FMS" in MCE Product Catalog:

Cat. No.: HY-119942
CAS No.: 1255303-58-2
Purity:  99.47%
Target:  

c-Fms

Research Areas:  

Cancer

c-Fms-IN-8 (compound 4a) is a colony stimulating factor-1 receptor (CSF-1R, c-FMS) Type II inhibitor, with an IC50 of 9.1 nM .
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Cat. No.: HY-10208S
CAS No.: 1219592-01-4
Purity:  ≥98.0%
Synonyms: GW786034-d6
Pazopanib-d6 is the deuterium labeled Pazopanib. Pazopanib (GW786034) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with IC50s of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
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Cat. No.: HY-P991114
CAS No.: 2921564-55-6

Target:  

FLT3

Research Areas:  

Inflammation/Immunology

Adezkibart is a human monoclonal antibody immunosuppressant targeting the human FMS-like tyrosine kinase 3 ligand (FLT3LG). Adezkibart is found in the Chinese hamster ovary cell line CHO-K1, which binds to FLT3LG to block the relevant signaling pathway, inhibits the immune response, and exerts immunosuppressive activity. Adezkibart is promising for research of immune-related diseases .
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Cat. No.: HY-148181
CAS No.: 885704-58-5
Purity:  99.27%
Target:  

c-Fms

Research Areas:  

Inflammation/Immunology

c-Fms-IN-13 (compound 14) is a potent FMS kinase inhibitor with an IC50 value of 17 nM. c-Fms-IN-13 can be used as an anti-inflammatory agent .
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Cat. No.: HY-128571
CAS No.: 2304799-09-3
Purity:  99.73%
Target:  

FLT3

Research Areas:  

Cancer

FLT3-IN-4 is a potent and orally effective Fms-like tyrosine receptor kinase 3 (FLT3; IC50=7 nM) inhibitor for treating acute myelogenous leukemia .
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Cat. No.: HY-18787
CAS No.: 791587-67-2
Target:  

c-Fms

Research Areas:  

Inflammation/Immunology

c-Fms-IN-2 is a FMS kinase inhibitor with an IC50 of 0.024 μM.
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Cat. No.: HY-13075
CAS No.: 885704-21-2
Purity:  99.69%
c-Fms-IN-3 is an orally active c-Fms (CSF1R) kinase inhibitor (IC50 = 0. 8 nM). c-Fms-IN-3 inhibits CSF1R kinase activity and reduces macrophage populations. c-Fms-IN-3 reduces bone erosion, pannus invasion, cartilage damage, and inflammation in collagen (HY-NP003)-induced arthritis mouse model. c-Fms-IN-3 is useful for arthritis research .
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Cat. No.: HY-111948
CAS No.: 1313408-89-7
Target:  

c-Fms

Research Areas:  

Inflammation/Immunology Cancer

c-Fms-IN-7 is a cFMS inhibitor extracted from patent WO2011079076A1, example159, has an IC50 of 18.5 nM .
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Cat. No.: HY-134481
CAS No.: 2088735-51-5
Purity:  98.80%
Target:  

FLT3

Research Areas:  

Cancer

FLT3-IN-10 (compound 7c) is a potent inhibitor of FMS-like tyrosine kinase 3 (FLT3). FLT3-IN-10 has the potential for the research of FLT3-mutated acute myeloid leukemia (AML) .
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Cat. No.: HY-110272
CAS No.: 212142-18-2
Synonyms: PTK787 succinate; ZK-222584 succinate; CGP-79787 succinate
Target:  

VEGFR

Research Areas:  

Cancer

Vatalanib (PTK787) succinate is a potent and orally active VEGFR inhibitor with IC50s of 37 nM, 77 nM, 270 nM, 660 nM, 730 nM, 1400 nM, and 580 nM for KDR, Flt-1, Flk, Flt-4, c-Kit, c-Fms, and PDGFR-β, respectively .
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Cat. No.: HY-12009R
CAS No.: 635702-64-6
Synonyms: GW786034 Hydrochloride (Standard)
Research Areas:  

Cancer

Pazopanib (Hydrochloride) (Standard) is the analytical standard of Pazopanib (Hydrochloride). This product is intended for research and analytical applications. Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with an IC50 of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
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Cat. No.: HY-10208R
CAS No.: 444731-52-6
Synonyms: GW786034 (Standard)
Research Areas:  

Cancer

Pazopanib (Standard) is the analytical standard of Pazopanib. This product is intended for research and analytical applications. Pazopanib (GW786034) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with IC50s of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
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Cat. No.: HY-W705479
CAS No.: 2469755-67-5
Synonyms: GW786034-d3 hydrochloride
Pazopanib-d3 (hydrochloride) (GW786034-d3 (hydrochloride)) is deuterium labeled Pazopanib (Hydrochloride). Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with an IC50 of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
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Cat. No.: HY-10208S2
CAS No.: 1219591-97-5
Synonyms: GW786034-d3
Pazopanib-d3 (GW786034-d3) is deuterium labeled Pazopanib. Pazopanib (GW786034) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with IC50s of 10, 30, 47, 84, 74, 140 and 146 nM, respectively .
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Cat. No.: HY-12768B
CAS No.: 2222138-40-9
Synonyms: BLZ945 dihydrochloride
Target:  

c-Fms

Research Areas:  

Neurological Disease Cancer

Sotuletinib (BLZ945) dihydrochloride is a potent, selective, orally active and brain-penetrant CSF-1R (c-Fms) inhibitor with an IC50 of 1 nM, showing more than 1,000-fold selectivity against its closest receptor tyrosine kinase homologs. Sotuletinib dihydrochloride can be used for microglia depletion, and for tumor and CNS-related disease research .
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Cat. No.: HY-P99913
CAS No.: 1384099-30-2

Target:  

c-Fms

Research Areas:  

Inflammation/Immunology Cancer

Eflapegrastim is a composite protein consisting of a genetically modified granulocyte-colony stimulating factor (GCSF) molecule linked via a chemical bond to an IgG4 Fc fragment (LAPS-carrier). Eflapegrastim targets to G-CSF receptor (c-Fms). Eflapegrastim stimulates proliferation and differentiation of neutrophil progenitor cells and maintains stable numbers of mature and functional neutrophils. Eflapegrastim also shortens the duration of neutropenia .
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Cat. No.: HY-147864
CAS No.: 2145102-33-4
Target:  

c-Fms c-Kit Apoptosis

Research Areas:  

Cancer

c-Fms-IN-12 (Compound 4g) is an FMS kinase inhibitor. c-Fms-IN-12 can also inhibits c-KIT. c-Fms-IN-12 is a potential broad-spectrum anticancer agent against multiple cancer types. c-Fms-IN-12 induces A549 cell apoptosis .
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Cat. No.: HY-156556
CAS No.: 1898210-99-5
Target:  

c-Fms

Research Areas:  

Inflammation/Immunology Cancer

c-Fms-IN-14 (Example 76) is a c-Fms inhibitor with an IC50 value of 4 nM. c-Fms-IN-14 can be used for research of cancer and autoimmune diseases .
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Cat. No.: HY-128680
CAS No.: 1628574-50-4
Target:  

c-Fms

Research Areas:  

Cancer

c-Fms-IN-9 is a c-FMS inhibitor extracted from patent WO2014145023A1, Compound Example 7. c-Fms-IN-9 inhibits unphosphorylated c-FMS kinase (uFMS) and uKIT with IC50s of <0.01 μM and 0.1-1 μM, respectively .
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Cat. No.: HY-111947
CAS No.: 1628574-81-1
Target:  

c-Fms

Research Areas:  

Inflammation/Immunology

c-Fms-IN-6 is a potent inhibitor of c-FMS, with an IC50 of ≤10 nM for unphosphorylated c-FMS, also weakly inhibits unphosphorylated c-KIT and PDGFR (IC50, > 1 μM). Used in the research of autoimmune diseases .
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