Nimbolide
CAS No. 25990-37-8
Nimbolide( —— )
Catalog No. M24163 CAS No. 25990-37-8
Nimbolide suppresses CDK4/CDK6 kinase activity. Nimbolide inhibits the NF-κB, Wnt, PI3K-Akt, MAPK, and JAK-STAT signaling pathways.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 205 | In Stock |
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| 10MG | 357 | In Stock |
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| 25MG | 597 | In Stock |
|
| 50MG | 851 | In Stock |
|
| 100MG | 1152 | In Stock |
|
| 500MG | 2313 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameNimbolide
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NoteResearch use only, not for human use.
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Brief DescriptionNimbolide suppresses CDK4/CDK6 kinase activity. Nimbolide inhibits the NF-κB, Wnt, PI3K-Akt, MAPK, and JAK-STAT signaling pathways.
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DescriptionNimbolide suppresses CDK4/CDK6 kinase activity. Nimbolide inhibits the NF-κB, Wnt, PI3K-Akt, MAPK, and JAK-STAT signaling pathways. Nimbolide causes apoptosis through the inactivation of NF-κB. Nimbolide is a triterpene derived from the leaves and flowers of neem (Azadirachta indica L).
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In VitroWestern Blot Analysis Cell Line:U87EGFRvIII cells Concentration:5-20 μg/μL Incubation Time:2-12 h Result:Inhibited CDK4/6 activity in a dose-dependent manner.Western Blot Analysis Cell Line:Breast cancer cell lines (MCF-7/MDA-MB-231) Concentration:2-4 μM for MCF-7 cells, 4-6 μM for MDA-MB-231 cells Incubation Time:24 hResult:Decreased protein levels of IGF-IRβ, IRS-2, PI3K, β-catenin, c-Myc, N-Ras, Raf-1, Mek, pERK1/2, cyclin (A1, B, C, D1 and E1) and PCNA.Increased p38, p21, IGFBP-3 and PTEN protein expression.Cell Viability Assay Cell Line:Breast cancer cell lines (MCF-7/MDA-MB-231)Concentration:2-4 μM for MCF-7 cells, 4-6 μM for MDA-MB-231 cells Incubation Time:24 h Result:Increased the G0/G1-phase population in MCF-7 cells by 68.43 and 62.06% at 2 and 4 μM, in MDA-MB-231 cells by 57.56 and 59.35% at 4 and 6 μM.Increased the dead cells accumulation in MCF-7 cells by 7.62 and 22.91% at 2 and 4 μM, in MDA-MB-231 cells by 6.28 and 7.73% at 4 and 6 μM.Western Blot Analysis Cell Line:Colorectal cancer cells (HCT-116/HT-29) Concentration:0-10 μM Incubation Time:12 h Result:Inhibited the expression of anti-apoptotic proteins (Bcl-2/Bcl-xL/c-IAP-1/survivin) and cell proliferative proteins (cyclin D1/c-Myc).Inhibited the expression of proteins involved in tumor cell invasion, metastasis, and angiogenesis (MMP-9, ICAM-1, CXCR4, and VEGF) in a concentration-dependent manner.
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In VivoAnimal Model:HCT-116-derived xenograft mouseDosage:5 mg/kg, 20 mg/kg Administration:Intraperitoneal injection (i.p.), daily, 10 days Result:Suppressed tumor growth in nude mice at a dose as low as 5 mg/kg.Reduced tumor growth by almost 90% on day 10 at a dose as low as 20 mg/kg.
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Synonyms——
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PathwayApoptosis
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TargetApoptosis
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RecptorApoptosis|CDK4|CDK6|NF-κB
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Research Area——
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Indication——
Chemical Information
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CAS Number25990-37-8
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Formula Weight466.52
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Molecular FormulaC27H30O7
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (107.18 mM)
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SMILESC[C@]12[C@@]3([H])[C@](OC([C@@]3(C=CC2=O)C)=O)([H])[C@]4([H])[C@]([C@@H]1CC(OC)=O)(C5=C(C)[C@@](C6=COC=C6)([H])C[C@@]5([H])O4)C
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Chemical Name——
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.Bodduluru LN, et al. Chemopreventive and therapeutic effects of nimbolide in cancer: the underlying mechanisms. Toxicol In Vitro. 2014 Aug;28(5):1026-35.
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