
Sanggenone C
CAS No. 80651-76-9
Sanggenone C( Sanggenone C | Sanggenon C )
Catalog No. M19128 CAS No. 80651-76-9
Sanggenone C inhibits tumor cellular proteasomal activity and cell viability, via induction of cell cycle arrest and cell death , inhibiting the proteasome function.
Purity : >98% (HPLC)






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5MG | 222 | In Stock |
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10MG | 331 | In Stock |
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25MG | 534 | In Stock |
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50MG | 763 | In Stock |
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100MG | 1044 | In Stock |
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Biological Information
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Product NameSanggenone C
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NoteResearch use only, not for human use.
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Brief DescriptionSanggenone C inhibits tumor cellular proteasomal activity and cell viability, via induction of cell cycle arrest and cell death , inhibiting the proteasome function.
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DescriptionSanggenone C inhibits tumor cellular proteasomal activity and cell viability, via induction of cell cycle arrest and cell death , inhibiting the proteasome function. Sanggenone C and O inhibited NO production and iNOS expression by suppressing NF-κB activity and IκBα activation; inhibited TNF-alpha -stimulated PMN-HSC adhesion and expression of VCAM-1 by suppressing the activation of NF-kappaB.
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In VitroCell Proliferation Assay Cell Line:Human GC cell lines HGC-27 and AGS cells Concentration:4-12 μM Incubation Time:24 hResult:Inhibited the proliferation of GC cells in a dose-dependent manner. The IC50 values of were 9.129 μM for HGC-27 and 9.863 μM for AGS.Cell Cycle Analysis Cell Line:Human GC cell lines HGC-27 and AGS cells Concentration:6, 8, 10 μM Incubation Time:24 h Result:The proportions of cells in the G0-G1 phase were increased and the levels of CDK4 and cyclin D1 were decreased. Apoptosis Analysis Cell Line:Human GC cell lines HGC-27 and AGS cells Concentration:6, 8, 10 μM Incubation Time:24 h Result:Exhibited a dose-dependent induction of apoptosis, with the percentage of apoptotic cells increasing from 7.3% to 24.8% and from 4.6% to 15.1% for HGC-27 and AGS cells, respectively.Western Blot Analysis Cell Line:Human GC cell lines HGC-27 and AGS cells Concentration:6, 8, 10 μM Incubation Time:24 h Result:The levels of p-ERK were markedly downregulated.
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In VivoAnimal Model:Male C57/BL6 mice (weight 23.5-27.5 g; age, 8 weeks)Dosage:10, 20 mg/kg Administration:Intraperitoneally; daily; for 3 weeks Result:Prevented the development of ventricular dysfunction, as evidenced by decreased LV end-diastolic diameter, LV end-systolic diameter, and increased LVFS and LVEF.
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SynonymsSanggenone C | Sanggenon C
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorNF-κB
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Research Area——
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Indication——
Chemical Information
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CAS Number80651-76-9
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Formula Weight708.71
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Molecular FormulaC40H36O12
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (141.10 mM)
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SMILESCC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C=C5C(=C4O)C(=O)C6(C(O5)(C7=C(O6)C=C(C=C7)O)CC=C(C)C)O)O
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Chemical Name2-((1S,2R,3S)-2-(2,4-dihydroxybenzoyl)-2',4'-dihydroxy-5-methyl-1,2,3,6-tetrahydro-[1,1'-biphenyl]-3-yl)-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-en-1-yl)-5a,10a-dihydro-11H-benzofuro[3,2-b]chromen-11-one
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
molnova catalog



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