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20

Compounds

Cat No. Product Name Synonyms Targets
T41277 PACMA 31 Others
PACMA 31 is an irreversible and covalent inhibitor of protein disulfide isomerase (PDI) with an IC50 of 10 μM. PACMA 31 significantly suppresses ovarian tumor growth and exhibits tumor targeting ability.
T5586 CFMS Receptor Inhibitor II c-Fms
cFMS Receptor Inhibitor II is a CSF1R kinase inhibitor
T4335 GNE-617 GNE617 NAMPT
GNE-617, a specific NAMPT inhibitor(IC50=5 nM), shows potency in xenograft models of cancer.
T10894 CSF1R-IN-1 c-Fms
CSF1R-IN-1 is a CSF1R inhibitor with IC50 of 0.5 nM.
T14380 AZD7507 CSF-1R , HER , Sodium Channel
AZD7507 is a CSF-1R inhibitor with an IC50 of 32 nM. AZD7507 has antitumor activity.
T12171 Nampt-IN-5 P450 , NAMPT
Nampt-IN-5 is a potent and orally active inhibitor of nicotinamide phosphoribosyltransferase (NAMPT) .
T22089 HPI 1 Hedgehog/Smoothened
HPI 1 is a hedgehog (Hh) signaling inhibitor. Inhibits Sonic hedgehog (Shh)-, SAG- and Gli-induced Hh pathway activation in Shh-LIGHT2 cells (IC50 values are 1.5, 1.5, 4, and 6 μM for Shh-, SAG-, Gli2- and Gli1-induced a...
T6682 STF-118804 STF 118804,STF118804 Apoptosis , NAMPT
STF-118804 is a highly specific NAMPT inhibitor; reduces the viability of most B-ALL cell lines with IC50 <10 nM.
T6119 Sotuletinib BLZ945 c-Fms , CSF-1R
Sotuletinib (BLZ945) is an orally active, effective and specific CSF-1R inhibitor (IC50: 1 nM), >1000-fold selective against its closest receptor tyrosine kinase homologs.
T13194 CSF1R-IN-2 c-Fms , c-Met/HGFR , Src
CSF1R-IN-2 is an oral-active SRC, MET and c-FMS inhibitor (IC50s: 0.12 nM, 0.14 nM and 0.76 nM for SRC, MET and c-FMS respectively).
TQ0015 PRN1371 c-Fms , FGFR , CSF-1R
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).
T4376 Nampt-IN-1 LSN3154567 c-Fms , NAMPT , CSF-1R
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.
T10652 Vimseltinib DCC-3014 c-Fms , CSF-1R , c-Kit
Vimseltinib (DCC-3014) is a c-FMS (CSF-IR) and c-Kit dual inhibitor (IC50s: <0.01 μM and 0.1-1 μM).
T7100 PLX5622 PLX-5622 c-Fms , CSF-1R
PLX5622 is a highly selective brain penetrant and oral active CSF1R inhibitor.
T2115 Pexidartinib PLX-3397 Apoptosis , c-Fms , FLT , CSF-1R , c-Kit
Pexidartinib (PLX-3397) is a capsule formulation containing a small-molecule receptor tyrosine kinase (RTK) inhibitor of KIT, CSF1R and FLT3 with potential antineoplastic activity.
T2659 GW2580 GW 2580,SC-203877 c-Fms
GW2580 (SC-203877) is a specific, oral-bioavailable CSF-1R inhibitor for c-FMS.
T1998 CHS-828 CHS 828,GMX1778 Apoptosis , NAMPT
CHS-828 (GMX1778), a pyridyl cyanoguanidine, is an effective inhibitor of NAD+ biosynthesis enzyme NAMPT (IC50 <25 nM).
T12854 SBI-797812 NAMPT
SBI-797812 is structurally similar to active-site directed inhibitor of NAMPT(NAMPT with EC50 of 0.37 μM).
T2624 OSI-930 OSI 930 Apoptosis , c-Fms , Raf , VEGFR , FLT , CSF-1R , Src , c-Kit
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 growth (angiogenesis) in tumors.
T15199 Edicotinib JNJ-527,JNJ-40346527 c-Fms , FLT , CSF-1R , c-Kit
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 effects on KIT and FLT3 (IC50: 20 nM and 190 nM). It has the pote...
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TargetMol