1. Cell Cycle/DNA Damage Epigenetics PI3K/Akt/mTOR Stem Cell/Wnt TGF-beta/Smad Apoptosis Immunology/Inflammation NF-κB Metabolic Enzyme/Protease
  2. Sirtuin Aurora Kinase Akt GSK-3 β-catenin TGF-β Receptor Apoptosis Reactive Oxygen Species (ROS) Wnt NF-κB TNF Receptor Interleukin Related IKK
  3. Butrin

Butrin is a compound found in Butea monosperma flowers. Butrin reduces expression of SIRT1, AURKB, cyclin D1, pAKT, GSK-3β, β-catenin, and TGF-3β expression, enhances apoptosis and ROS production in cancer cells. Butrin downregulates Wnt and NF-κB signaling, mitigates oxidative stress, reduces proinflammatory cytokine (TNF-α, IL-6 and IL-8) production and suppresses neuroinflammation. Butrin inhibits IKK enzyme activity. Butrin can be used for the researches of colorectal cancer, Alzheimer’s disease, and rheumatoid arthritis.

For research use only. We do not sell to patients.

Butrin

Butrin Chemical Structure

CAS No. : 492-13-7

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Description

Butrin is a compound found in Butea monosperma flowers. Butrin reduces expression of SIRT1, AURKB, cyclin D1, pAKT, GSK-3β, β-catenin, and TGF-3β expression, enhances apoptosis and ROS production in cancer cells. Butrin downregulates Wnt and NF-κB signaling, mitigates oxidative stress, reduces proinflammatory cytokine (TNF-α, IL-6 and IL-8) production and suppresses neuroinflammation. Butrin inhibits IKK enzyme activity. Butrin can be used for the researches of colorectal cancer, Alzheimer’s disease, and rheumatoid arthritis[1][2][3].

IC50 & Target[1]

SIRT1

 

Aurora B

 

IL-6

 

IL-8

 

In Vitro

Butrin (10-120 μM; 24-48 h) inhibits SW480 human colorectal cancer cell proliferation with an IC50 of 40 μM, while sparing IHH human hepatocyte cells[1].
Butrin (40 μM; 48 h) induces both early and late apoptosis in SW480 human colorectal cancer cells with nuclear condensation and fragmentation[1].
Butrin (40 μM; 48 h) disrupts mitochondrial membrane potential and increases intracellular ROS production in SW480 human colorectal cancer cells[1].
Butrin (40 μM; 48 h) upregulates pro-apoptotic gene expression and downregulates cell cycle and Wnt pathway gene expression in SW480 human colorectal cancer cells[1].
Butrin (40 μM; 48 h) upregulates pro-apoptotic and tumor suppressor protein expression and downregulates anti-apoptotic, cell cycle, and Wnt pathway protein expression in SW480 human colorectal cancer cells[1].
Butrin (1-10 µg/mL; 2-hour pretreatment) inhibits PMACI-induced TNF-α, IL-6 and IL-8 levels and inhibits NF-κB p65 activation in HMC-1 human mast cells[3].
Butrin (5-1000 ng/mL) inhibits recombinant human IKK kinase activity in a concentration-dependent manner[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: SW480 human primary adenocarcinoma colorectal cancer cells; IHH immortalized human hepatocyte cells
Concentration: 10, 20, 40, 60,120 μM
Incubation Time: 24 h; 48 h
Result: Inhibited SW480 cell proliferation, with an IC50 value of 40 μM against SW480 cells.
Did not induce major cell death in IHH cells.

Apoptosis Analysis[1]

Cell Line: SW480 human primary adenocarcinoma colorectal cancer cells
Concentration: 40 μM
Incubation Time: 48 h
Result: Induced fragmented green nuclei (early apoptosis) and reddish/orange staining (late apoptosis) in treated cells, whereas control cells had uniformly green viable nuclei.
Induced chromatin condensation and nuclear fragmentation in treated cells, whereas control cells had weak, homogeneous blue-stained nuclei without fragmentation.
Showed nuclear condensation and fragmentation.

RT-PCR[1]

Cell Line: SW480 human primary adenocarcinoma colorectal cancer cells
Concentration: 40 μM
Incubation Time: 48 h
Result: Increased mRNA expression of apoptotic genes miR-34a, p53, p21, BAX, caspase 3, and caspase 7.
Decreased mRNA expression of cell cycle/Wnt pathway genes cyclin D1, SIRT1, Aurora B kinase (AURKB), Mdm2, and GSK-3β.

Western Blot Analysis[1]

Cell Line: SW480 human primary adenocarcinoma colorectal cancer cells
Concentration: 40 μM
Incubation Time: 48 h
Result: Increased protein expression of cytochrome c, p53, and p21.
Decreased protein expression of procaspase 3, cyclin D1, Cdk4, GSK-3β, β-catenin, pAKT, TGF-3β, SIRT1, and AURKB.
Molecular Weight

596.53

Formula

C27H32O15

CAS No.
SMILES

O[C@H]1[C@H](OC2=CC3=C(C=C2)C(C[C@@H](C4=CC(O[C@H]5[C@@H]([C@H]([C@@H]([C@@H](CO)O5)O)O)O)=C(O)C=C4)O3)=O)O[C@H](CO)[C@@H](O)[C@@H]1O

Structure Classification
Initial Source
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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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