Cat. No. | 製品名 | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T35333 | ARRY-382 | 1313407-95-2 | 98% |
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ARRY-382 is a highly selective oral inhibitor of CSF-1R with an IC50 of 9 nM. | ||||
T77125 | Otilimab | 1638332-55-4 | 98% |
Otilimab
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Otilimab (GSK 3196165) is a humanized monoclonal antibody against granulocyt-macrophage colony-stimulating factor (GM-CSF). Otilimab has anti-inflammatory activi... | ||||
T76690 | Mavrilimumab | 1085337-57-0 | 98% |
Mavrilimumab
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Mavrilimumab (CAM 3001) is a monoclonal antibody with antiviral activity that has an affinity for the α subunit of the granulocytic-macrophage colony-stimulating... | ||||
T4315 | Ki20227 | 623142-96-1 |
|
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Ki-20227 is a specific c-Fms tyrosine kinase(CSF1R) inhibitor (IC50: 2 nM). It also has certain inhibitory against VEGFR2(IC50: 12 nM) and c-Kit/PDGFRβ(IC50: 451... | ||||
T1667 | Tandutinib | 387867-13-2 |
|
|
Tandutinib (CT53518) (MLN518, CT53518), an effective FLT3 antagonist (IC50: 0.22 μM), can also inhibit c-Kit and PDGFR, 15-20 fold higher potency for FLT3 versus... | ||||
T64066 | CSF1R-IN-3 | 2760584-90-3 | 97.31% |
|
CSF1R-IN-3 is an orally effective CSF-1R inhibitor with an IC50 value of 2.1 nM. CSF1R-IN-3 has anti-proliferative activity against colorectal cancer cells. CSF1... | ||||
T6119 | Sotuletinib | 953769-46-5 | 97.43% |
|
Sotuletinib (BLZ945) is an orally active, effective and specific CSF-1R inhibitor (IC50: 1 nM), >1000-fold selective against its closest receptor tyrosine kinase... | ||||
T2514 | Linifanib | 796967-16-3 | 98% |
|
Linifanib (AL-39324) (ABT-869) is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR (IC50: 4 nM), CSF-1R (IC50: 3 nM), Flt-1/3 (IC50: 3/4 nM) and PDG... | ||||
T14380 | AZD7507 | 1041852-85-0 | 98.01% |
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AZD7507 is a CSF-1R inhibitor with an IC50 of 32 nM. AZD7507 has antitumor activity. | ||||
T15199 | Edicotinib | 1142363-52-7 | 98.58% |
|
Edicotinib (JNJ-527) is a brain penetrant and orally active inhibitor of the colony-stimulating factor-1 receptor (IC50: 3.2 nM). It shows less inhibitory effect... | ||||
T10652 | Vimseltinib | 1628606-05-2 | 98.98% |
|
Vimseltinib (DCC-3014) is a c-FMS (CSF-IR) and c-Kit dual inhibitor (IC50s: <0.01 μM and 0.1-1 μM). | ||||
T4376 | Nampt-IN-1 | 1698878-14-6 | 99.4% |
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Nampt-IN-1 (LSN3154567) (LSN3154567) is a potent and selective NAMPT inhibitor. Nampt-IN-1 inhibits purified NAMPT with an IC50 of 3.1 nM. | ||||
T2115 | Pexidartinib | 1029044-16-3 | 99.66% |
|
Pexidartinib (PLX-3397) is a capsule formulation containing a small-molecule receptor tyrosine kinase (RTK) inhibitor of KIT, CSF1R and FLT3 with potential antin... | ||||
TQ0015 | PRN1371 | 1802929-43-6 | 99.72% |
|
PRN1371 is a specific and potent FGFR1-4 and CSF1R inhibitor (IC50s: 0.6/1.3/4.1/19.3/8.1 nM for FGFR1/2/3/4 and CSF1R). | ||||
T2624 | OSI-930 | 728033-96-3 | 99.76% |
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OSI-930, an orally active inhibitor of c-Kit and the vascular endothelial growth factor receptor-2 (VEGFR-2), targets cancer cell proliferation and blood vessel ... | ||||
T7100 | PLX5622 | 1303420-67-8 | 99.89% |
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PLX5622 is a highly selective brain penetrant and oral active CSF1R inhibitor. | ||||
T10647 | C-Fms-IN-8 | 1255303-58-2 | 98% |
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c-Fms-IN-8 is a colony-stimulating factor-1 receptor (CSF-1R, c-FMS) Type II inhibitor (IC50: 9.1 nM). It is compound 4a in the reference. | ||||
T11390 | GENZ-882706 | 2070864-35-4 | 98% |
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GENZ-882706 is a potent colony stimulating factor-1 receptor (CSF-1R) Inhibitor. |