
Rottlerin
CAS No. 82-08-6
Rottlerin( Mallotoxin | NSC 94525 )
Catalog No. M16052 CAS No. 82-08-6
Rottlerin (Mallotoxin;NSC 94525) is a polyphenol natural product, cell-permeable and reversible PKC inhibitor that exhibits greater selectivity for PKCδ (IC50=3-6 uM) and PKCθ.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 32 | In Stock |
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10MG | 50 | In Stock |
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25MG | 106 | In Stock |
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100MG | Get Quote | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameRottlerin
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NoteResearch use only, not for human use.
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Brief DescriptionRottlerin (Mallotoxin;NSC 94525) is a polyphenol natural product, cell-permeable and reversible PKC inhibitor that exhibits greater selectivity for PKCδ (IC50=3-6 uM) and PKCθ.
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DescriptionRottlerin (Mallotoxin;NSC 94525) is a polyphenol natural product, cell-permeable and reversible PKC inhibitor that exhibits greater selectivity for PKCδ (IC50=3-6 uM) and PKCθ, with significantly reduced potency (IC50=30-42 uM) for PKCα, PKCβ, and PKCγ; also inhibits CaMK III, suppresses eEF-2 phosphorylation with IC50 of 5.3 uM; also remarkably inhibits MACC1 promoter activity and expression, reduces cell motility in CRC cells.
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In VitroRottlerin (20 μM, 2/6/24 hours) dramatically decreases the cyclin D-1 mRNA levels in a time-dependent manner in primary HMVEC.Rottlerin (20 μM) exhibits cell proliferation in HMVEC. Western Blot Analysis Cell Line:Primary HMVEC (Human Microvascular Endothelial Cell).Concentration:20 μM.Incubation Time:2, 6, 24 hours.Result:Dramatically decreased the cyclin D-1 mRNA levels in a time-dependent manner. After 2 h of treatment, the mRNA level was reduced to 50% of the control, to circa 40% after 6 h, and to 20% after 24 h. Consistently, a similar trend was observed in the protein levels, where the decrease was circa 50% after 2 h, 80% after 6 h, and to almost undetectable levels after 24 h.Cell Proliferation Assay Cell Line:Primary HMVEC (Human Microvascular Endothelial Cell).Concentration:20 μM.Incubation Time:24/48 hours.Result:Exhibited a strong growth inhibition, with a reduction in thymidine incorporation respect to the control cells (DMSO 0.1%) of circa 75% and 80%, respectively.
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In VivoRottlerin (20 mg/kg, gavage 5 days per week, once daily, for 6 weeks) inhibits AsPC-1 pancreatic tumor growth in Balb C nude mice with no toxicity.Rottlerin inhibits tumor cell proliferation, and induces apoptosis through activation of caspase-3 and cleavage of poly(ADP-ribose) polymerase (PARP). Animal Model:Balb C nude mice (4-6 weeks old) with AsPC-1 cells (2×106 cells mixed with Matrigel, 50:50 ratio) injection.Dosage:0 or 20 mg/kg.Administration:Gavage 5 days per week, once daily, for 6 weeks.Result:Inhibited AsPC-1 pancreatic tumor growth in Balb C nude mice and had no effect
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SynonymsMallotoxin | NSC 94525
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PathwayAngiogenesis
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TargetPKC
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RecptorPKC
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Research AreaOther Indications
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Indication——
Chemical Information
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CAS Number82-08-6
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Formula Weight516.54
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Molecular FormulaC30H28O8
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Purity>98% (HPLC)
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SolubilityDMSO : 2 mg/mL 3.87 mM;H2O : < 0.1 mg/mL
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SMILESCC1(C)C=CC2=C(O)C(CC3=C(C(C)=C(C(C(C)=O)=C3O)O)O)=C(O)C(C(/C=C/C4=CC=CC=C4)=O)=C2O1
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Chemical Name(2E)-1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl]-3-phenyl-2-propen-1-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
1. Villalba M, et al. J Immunol. 1999 Dec 1;163(11):5813-9.
2. Gschwendt M, et al. FEBS Lett. 1994 Jan 24;338(1):85-8.
3. Juneja M, et al. PLoS Biol. 2017 Jun 1;15(6):e2000784.
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