464 Results for "

colony

" in MedChemExpress (MCE) Product Catalog:
Products (464)

464 Results for "colony" in MCE Product Catalog:

161
161 Publications Verification
Referencia número: HY-16749A
No. CAS: 2040295-03-0
Synonyms: PLX-3397 hydrochloride
Target:  

c-Fms c-Kit Apoptosis

Áreas de investigación:  

Cancer

Pexidartinib hydrochloride (PLX-3397 hydrochloride) is a potent, orally active, selective, and ATP-competitive colony stimulating factor 1 receptor (CSF1R or M-CSFR) and c-Kit inhibitor, with IC50s of 20 and 10 nM, respectively. Pexidartinib hydrochloride exhibits 10- to 100-fold selectivity for c-Kit and CSF1R over other related kinases. Pexidartinib hydrochloride induces cell apoptosis and has anti-cancer activity .
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161
161 Publications Verification
Referencia número: HY-16749
No. CAS: 1029044-16-3
Synonyms: PLX-3397
Target:  

c-Fms c-Kit Apoptosis

Áreas de investigación:  

Cancer

Pexidartinib (PLX-3397) is a potent, orally active, selective, and ATP-competitive colony stimulating factor 1 receptor (CSF1R or M-CSFR) and c-Kit inhibitor, with IC50s of 20 and 10 nM, respectively. Pexidartinib (PLX-3397) exhibits 10- to 100-fold selectivity for c-Kit and CSF1R over other related kinases. Pexidartinib (PLX-3397) induces cell apoptosis and has anti-tumor activity. Pexidartinib has limited permeability to the blood-brain barrier, primarily through ABCB1 .
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13
13 Cited Publications
Referencia número: HY-10917
No. CAS: 870483-87-7
Pureza:  99.90%
Target:  

c-Fms

Áreas de investigación:  

Inflammation/Immunology Cancer

GW2580 is an orally bioavailable and selective inhibitor of c-Fms kinase which completely inhibits human cFMS kinase in vitro at 0.06 μM. GW2580 acts as a competitive inhibitor of ATP binding to the cFMS kinase and inhibits colony-stimulating-factor-1 signaling .
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10
10 Cited Publications
Referencia número: HY-116282C
No. CAS: 9011-18-1
Synonyms: DSS (MW 35000-45000); DXS (MW 35000-45000)
Target:  

Apoptosis

Áreas de investigación:  

Infection Inflammation/Immunology Cancer

Dextran sulfate sodium salt (DSS) (MW 35000-45000) is a polymer of dehydrated glucose with a molecular weight of approximately 35000-45000. DSS with different molecular weights exhibits different biological activities. Dextran sulfate sodium salt (DSS) (MW 35000-45000) is a potent inducer of colitis. Dextran sulfate sodium salt (DSS) (MW 35000-45000) can be used to induce model acute colitis, chronic colitis, and colitis-related colon cancer. Dextran sulfate sodium salt (DSS) (MW 35000-45000) may be related to macrophage dysfunction, intestinal flora dysbiosis, and is particularly toxic to the colonic epithelium .
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10
10 Cited Publications
Referencia número: HY-12494
No. CAS: 1361030-48-9
Pureza:  99.64%
Target:  

TAM Receptor FLT3

Áreas de investigación:  

Neurological Disease Cancer

LDC1267 is a AXL/TAM/FLT3 inhibitor with IC50 values of 42 nM, 130 nM, and 63 nM against AXL, MERTK, and TYRO3, respectively. LDC1267 blocks GAS6-induced AXL phosphorylation and the downstream AKT/ERK1/2 signaling pathway. LDC1267 inhibits cancer cell proliferation, colony formation, and glioblastoma cell invasion, without causing obvious impairment of cytotoxic autophagic flux. LDC1267 exerts a synergistic effect when used in combination with Imatinib (HY-15463) in chronic myeloid leukemia models. LDC1267 can be widely applied in studies related to glioblastoma and chronic myeloid leukemia .
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7
7 Cited Publications
Referencia número: HY-P70553
Pureza:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Macrophage colony-stimulating factor 1; CSF-1; MCSF; Csf1; Csfm
Species:  
Source:  
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6
6 Cited Publications
Referencia número: HY-100433
No. CAS: 1401089-31-3
Pureza:  99.32%
Target:  

PDI

Áreas de investigación:  

Cancer

PACMA 31 is an irreversible, orally active protein disulfide isomerase (PDI) inhibitor with an IC50 of 10 μM. PACMA 31 forms a covalent bond with the active site cysteines of PDI. PACMA 31 shows tumor targeting ability and significantly suppresses ovarian tumor growth without causing toxicity to normal tissues . PACMA 31 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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5
5 Cited Publications
Referencia número: HY-19832
No. CAS: 871361-88-5
Target:  

MOFs Akt Apoptosis

Áreas de investigación:  

Cancer

SC66 is an Akt inhibitor, reduces cell viability in a dose- and time-dependent manner, inhibits colony formation and induces apoptosis in hepatocellular carcinoma (HCC) cells.
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5
5 Cited Publications
Referencia número: HY-P70353
Pureza:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: rHuNicotinamide phosphoribosyltransferase/NAMPT, His; Pre-B cell-enhancing factor; Nicotinamide phosphoribosyltransferase; NAmPRTase; Nampt; Pre-B-cell colony-enhancing factor 1; Visfatin; NAMPT; PBEF; PBEF1
Species:  
Source:  
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4
4 Cited Publications
Referencia número: HY-P70263A
Pureza:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuMacrophage colony-stimulating factor 1/M-CSF, His; Macrophage colony-stimulating factor 1; CSF-1; MCSF; Csf1; Csfm
Species:  
Source:  
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4
4 Cited Publications
Referencia número: HY-14933
No. CAS: 524684-52-4
Pureza:  98.05%
Synonyms: ERB-041
Áreas de investigación:  

Cancer

Prinaberel (ERB-041) is a potent and selective estrogen receptor (ER) β agonist with IC50s of 5.4, 3.1 and 3.7 nM for human, rat and mouse ERβ, respectively. Prinaberel displays >200-fold selectivity for ERβ over ERα. Prinaberel is a potent skin cancer chemopreventive agent that acts by dampening the WNT/β-catenin signaling pathway. Prinaberel induces ovarian cancer apoptosis .
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4
4 Cited Publications
Referencia número: HY-P70576
Pureza:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Interleukin-3; IL-3; Hematopoietic Growth Factor; Mast Cell Growth Factor; MCGF; Multipotential colony-Stimulating Factor; P-Cell-Stimulating Factor; IL3
Species:  
Source:  
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3
3 Cited Publications
Referencia número: HY-W050026
No. CAS: 28047-15-6
Synonyms: NSC 203800; Phenylacetyl-L-glutamine
Phenylacetylglutamine is a colonic microbial metabolite from amino acid fermentation.
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3
3 Cited Publications
Referencia número: HY-P72629
Pureza:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Granulocyte-Macrophage colony-Stimulating Factor; GM-CSF; CSF; CSF2; GMCSF
Species:  
Rat
Source:  
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3
3 Cited Publications
Referencia número: HY-109086
No. CAS: 1142363-52-7
Pureza:  98.80%
Synonyms: JNJ-40346527; JNJ-527
Target:  

c-Fms

Áreas de investigación:  

Neurological Disease Inflammation/Immunology Cancer

Edicotinib (JNJ-40346527) is a potent, selective, brain penetrant and orally active colony-stimulating factor-1 receptor (CSF-1R) inhibitor with an IC50 of 3.2 nM. Edicotinib exhibits less inhibitory effects on KIT and FLT3 with IC50 values of 20 nM and 190 nM, respectively . Edicotinib limits microglial expansion and attenuates microglial proliferation and neurodegeneration in mice. Edicotinib has the potential for Alzheimer’s disease and rheumatoid arthritis research .
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3
3 Cited Publications
Referencia número: HY-P701314
Pureza:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: rHuNicotinamide phosphoribosyltransferase/NAMPT, His; Pre-B cell-enhancing factor; Nicotinamide phosphoribosyltransferase; NAmPRTase; Nampt; Pre-B-cell colony-enhancing factor 1; Visfatin; NAMPT; PBEF; PBEF1
Species:  
Source:  
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3
3 Cited Publications
Referencia número: HY-P70685
Pureza:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Interleukin-3; IL-3; Hematopoietic growth factor; Multipotential colony-stimulating factor; P-cell-stimulating factor; Il3; Il-3; Mast cell growth factor; MCGF
Species:  
Source:  
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3
3 Cited Publications
Referencia número: HY-113293A
No. CAS: 1240-04-6
Pureza:  99.45%
Estrone sulfate potassium is an inactive endogenous estrogen that can be converted into Estrone (HY-B0234) and Estradiol (HY-B0141). Estrone sulfate potassium is also a substrate of the OATP1B3 transporter. Estrone sulfate potassium can be converted into Estrone and Estradiol in normal mammary parenchymal cells. Estrone sulfate potassium stimulates the growth of nitrosomethylurea-induced mammary tumors in ovariectomized rats and the colony formation of dispersed nitrosomethylurea mammary cells, with conversion into Estrone and Estradiol occurring both in vivo and in vitro during this process. Estrone sulfate potassium is applicable to breast cancer-related research .
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3
3 Cited Publications
Referencia número: HY-113293B
No. CAS: 438-67-5
Pureza:  99.84%
Estrone sulfate sodium is an inactive endogenous estrogen that can be converted into Estrone (HY-B0234) and Estradiol (HY-B0141). Estrone sulfate sodium is also a substrate of the OATP1B3 transporter. Estrone sulfate sodium can be converted into Estrone and Estradiol in normal mammary parenchymal cells. Estrone sulfate sodium stimulates the growth of nitrosomethylurea-induced mammary tumors in ovariectomized rats and the colony formation of dispersed nitrosomethylurea mammary cells, with conversion into Estrone and Estradiol occurring both in vivo and in vitro during this process. Estrone sulfate sodium is applicable to breast cancer-related research .
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3
3 Cited Publications
Referencia número: HY-N0597
No. CAS: 32791-84-7
Panaxatriol is an orally active dammarane-type tetracyclic triterpene sapogenin. Panaxatriol enhances the phosphorylation levels of Akt, insulin receptor and p70S6K in skeletal muscle. Panaxatriol reduces the mRNA expression level of Atrogin1 in skeletal muscle. Panaxatriol induces apoptosis, pre-G1 cell cycle arrest and increased intracellular ROS levels in prostate cancer cells, decreases mitochondrial membrane potential, inhibits cell migration and reduces colony formation. Panaxatriol can be used in research related to insulin resistance, myocardial ischemia/reperfusion injury and prostate cancer [1][2][3].
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