NVP-BGT226
CAS No. 1245537-68-1
NVP-BGT226 ( BGT226;NVP-BGT 226;BGT-226 )
Catalog No. M10992 CAS No. 1245537-68-1
NVP-BGT226 (BGT226) is a potent, dual PI3K/mTOR inhibitor with a preference for PI3Kα and mTOR.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 104 | In Stock |
|
10MG | 174 | In Stock |
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25MG | 383 | In Stock |
|
50MG | 566 | In Stock |
|
100MG | 808 | In Stock |
|
500MG | 1638 | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameNVP-BGT226
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NoteResearch use only, not for human use.
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Brief DescriptionNVP-BGT226 (BGT226) is a potent, dual PI3K/mTOR inhibitor with a preference for PI3Kα and mTOR.
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DescriptionNVP-BGT226 (BGT226) is a potent, dual PI3K/mTOR inhibitor with a preference for PI3Kα (wild type and mutated) and mTOR ( PI3Kα, PI3Kβ and PI3Kγ, IC50=4, 63 and 38 nM); displays potent antiproliferative activity against various human head and neck cancer cell lines in vitro (IC50=7.4-30.1 nM), downregulates the expression levels of the downstream proteins p-p70S6K and p-4E-BP1 in cells, induces cell-cycle arrest at the G0-G1 phase at 60 nM; BGT226 significantly delays tumor growth in a dose-dependent manner, along with suppressed cytoplasmic expression of p-p70S6K and the presence of autophagosome formation in xenografted animal modes.Solid Tumors Discontinued
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SynonymsBGT226;NVP-BGT 226;BGT-226
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PathwayPI3K/Akt/mTOR signaling
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TargetPI3K
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RecptorPI3Kα;PI3Kβ;PI3Kγ
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Research AreaCancer
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IndicationSolid Tumors
Chemical Information
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CAS Number1245537-68-1
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Formula Weight650.60
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Molecular FormulaC32H29F3N6O6
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESOC(=O)\C=C/C(O)=O.COC1=CC=C(C=N1)C1=CC=C2N=CC3=C(N(C(=O)N3C)C3=CC=C(N4CCNCC4)C(=C3)C(F)(F)F)C2=C1 |c:11,13,20,41,49,t:9,16,18,22,30,32|
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Chemical Name8-(6-methoxypyridin-3-yl)-3-methyl-1-(4-(piperazin-1-yl)-3-(trifluoromethyl)phenyl)-1H-imidazo[4,5-c]quinolin-2(3H)-one with maleic acid
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Baumann P, et al. Anticancer Drugs. 2012 Jan;23(1):131-8.
2. Chang KY, et al. Clin Cancer Res. 2011 Nov 15;17(22):7116-26.
3. Sanchez CG, et al. Breast Cancer Res. 2011 Mar 1;13(2):R21.
4. Glienke W, et al. Tumour Biol. 2012 Jun;33(3):757-65.
2. Chang KY, et al. Clin Cancer Res. 2011 Nov 15;17(22):7116-26.
3. Sanchez CG, et al. Breast Cancer Res. 2011 Mar 1;13(2):R21.
4. Glienke W, et al. Tumour Biol. 2012 Jun;33(3):757-65.
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