
Calphostin C
CAS No. 121263-19-2
Calphostin C( UCN 1028C | PKF115-584 )
Catalog No. M10793 CAS No. 121263-19-2
A potent, selective and photo-dependent inhibitor of PKC with IC50 of 50 nM.
Purity : >98% (HPLC)






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100MG | Get Quote | Get Quote |
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Biological Information
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Product NameCalphostin C
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, selective and photo-dependent inhibitor of PKC with IC50 of 50 nM.
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DescriptionA potent, selective and photo-dependent inhibitor of PKC with IC50 of 50 nM; displays >1,000-fold selectivity over other protein kinases such as cAMP-dependent protein kinase and tyrosine-specific protein kinase; inhibits cell growth and promotes apoptosis in HeLa S3 and MCF-7 cells with IC50 of 0.23 and 0.18 uM, respectively; also inhibits phospholipase D1 and D2 (IC50=100 nM); also blocks β-catenin/Tcf transcriptional activity.Solid Tumors Discontinued.
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In Vitro——
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In Vivo——
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SynonymsUCN 1028C | PKF115-584
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PathwayAngiogenesis
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TargetPKC
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RecptorPKC
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Research AreaCancer
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IndicationSolid Tumors
Chemical Information
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CAS Number121263-19-2
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Formula Weight790.76
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Molecular FormulaC44H38O14
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(CC1=C2C3=C(C(=C(C4=C3C(=C5C2=C(C(=O)C=C5OC)C(=C1OC)O)C(=CC4=O)OC)O)OC)CC(C)OC(=O)OC6=CC=C(C=C6)O)OC(=O)C7=CC=CC=C7
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Chemical Name1-(4,9-dihydroxy-12-(2-(((4-hydroxyphenoxy)carbonyl)oxy)propyl)-2,6,7,11-tetramethoxy-3,10-dioxo-3,10-dihydroperylen-1-yl)propan-2-yl benzoate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference



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Bisindolylmaleimide ...
Bisindolylmaleimide X hydrochloride (BIM-X hydrochloride) is a potent and selective PKC inhibitor and a CDK2 antagonist with an IC50 of 200 nM.
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PKC-theta inhibitor
PKC-theta inhibitor is PKC-θinhibitor with an?IC50?of 12 nM.
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PKC β pseudosubstrat...
Selective cell-permeable peptide inhibitor of protein kinase C (IC50 ~ 0.5 μM). Consists of amino acids 19 - 31 of PKC pseudosubstrate domain linked by a disulphide bridge to a cell permeabilisation Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the inhibitor peptide. Once inside the cell, the disulphide bonds are subjected to reduction in the cytoplasm leading to release of the inhibitor peptide.