Structure of Curcumol
CAS No.: 4871-97-0
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Curcumol is a sesquiterpene originally isolated from curcuma rhizomes showing anticancer activities both in vitro and in vivo.
Synonyms: (-)-Curcumol
4.5
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
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CAS No. : | 4871-97-0 |
Formula : | C15H24O2 |
M.W : | 236.35 |
SMILES Code : | O[C@@]1(C2)[C@H](C(C)C)C[C@]3(O1)[C@@H](C)CC[C@@]3([H])C2=C |
Synonyms : |
(-)-Curcumol
|
MDL No. : | MFCD00272163 |
InChI Key : | QRMPRVXWPCLVNI-YYFQZIEXSA-N |
Pubchem ID : | 14240392 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Target |
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In Vitro:
Cell Line
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Concentration | Treated Time | Description | References |
LO2 cells | 15, 30, 60 μM | 24 h | Curcumol significantly alleviated PA-induced damage in LO2 cells, reduced lipid accumulation, and inhibited the expression of cellular senescence markers. | PMC8450123 |
primary microglia | 0.1 g/L or 0.3 g/L | 72 h | Curcumol treatment reduced the percentage of CD11b+Iba1+CD16+ and CD11b+Iba1+CD86+ M1 microglia and increased the percentage of CD11b+Iba1+CD163+ and CD11b+Iba1+CD206+ M2 microglia, indicating that Curcumol promoted anti-inflammatory M2 microglial polarization. | PMC11196256 |
C666-1 cells | 100 µg/mL | 24 h | To investigate the inhibitory effect of Curcumol on nasopharyngeal carcinoma cells, the results showed that Curcumol significantly inhibited the invasion and migration of C666-1 cells. | PMC11430640 |
Primary microglia | 0.1 g/L or 0.3 g/L | 72 h | Curcumol induced anti-inflammatory M2 microglial polarization, reduced the production of pro-inflammatory cytokines, and protected neurons from apoptosis. | PMC11196256 |
K7M2 WT cells | 0-500 nM | 72 h | Curcumol inhibited K7M2 WT cell proliferation in a dose-dependent manner | PMC9318016 |
K7M2 WT cells | 100 nM | 48 h | Curcumol combined with CDDP significantly increased apoptosis in K7M2 WT cells | PMC9318016 |
U2OS cells | 37.67 nM | 72 h | Curcumol combined with CDDP significantly inhibited U2OS cell proliferation | PMC9318016 |
MG63 cells | 41.41 nM | 72 h | Curcumol combined with CDDP significantly inhibited MG63 cell proliferation | PMC9318016 |
KHOS cells | 28.3 nM | 72 h | Curcumol combined with CDDP significantly inhibited KHOS cell proliferation | PMC9318016 |
HSC-LX2 cells | 30 μM | 24 h | Curcumol upregulates the phosphorylation levels of RIPK1 and RIPK3, promotes their aggregation to form necrosome in HSCs, and eventually induces HSC necroptosis. | PMC6142373 |
LO2 cells | 15, 30, 60 μM | 24 h | Curcumol was capable of ameliorating ethanol-induced cell damage and effectively suppressed ethanol-induced lipid accumulation and cellular senescence in LO2 cells. | PMC9273900 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
LVG Golden Syrian hamsters | High-fat diet-induced NAFLD model | Oral gavage | 15, 30, 60 mg/kg | Once daily for 4 weeks | Curcumol significantly improved liver injury and steatosis induced by a high-fat diet and inhibited hepatocyte senescence. | PMC8450123 |
Rats | Sprague Dawley (SD) rats | Oral and intravenous | 10, 40, 80 mg/kg (oral), 2.0 mg/kg (intravenous) | Single dose | To investigate the pharmacokinetics, tissue distribution, and plasma protein binding rate of curcumol in rats. Results indicated that curcumol was rapidly absorbed and eliminated in rats, with oral bioavailability ranging from 9.2% to 13.1%. The maximum concentration of curcumol was observed in most organs within 0.5-1.0 hours, with high accumulation in the small intestine, colon, liver, and kidney. The plasma protein binding rate ranged from 85.6% to 93.4%. | PMC9748077 |
C57BL/6 mice | middle cerebral artery occlusion (MCAO) model | intraperitoneal injection | 0.1 g/kg or 0.3 g/kg | once daily for 7 days | Curcumol treatment reduced infarct volume, attenuated neuronal damage and inflammation, and improved motor function recovery in MCAO mice. Curcumol also promoted anti-inflammatory M2 microglial polarization in vivo and reduced local T cell infiltration, impairing the Treg/Th17 balance. | PMC11196256 |
BALB/c nude mice | Nasopharyngeal carcinoma xenograft model | Gavage | 80 mg/kg | Once daily for 2 weeks | To investigate the inhibitory effect of Curcumol on nasopharyngeal carcinoma xenografts in vivo, the results showed that Curcumol significantly inhibited tumor growth and reduced the expression of UBE2C. | PMC11430640 |
C57BL/6 mice | Middle cerebral artery occlusion (MCAO) model | Intraperitoneal injection | 0.1 g/kg or 0.3 g/kg | Once daily for 7 days | Curcumol reduced infarct volume, attenuated neuronal damage and neuroinflammation, and improved motor function recovery in MCAO mice. Additionally, Curcumol promoted anti-inflammatory M2 microglial polarization and modulated Treg/Th17 balance. | PMC11196256 |
BALB/c mice | K7M2 WT orthotopic transplantation model | Curcumol: oral, CDDP: intraperitoneal | 30 mg/kg | Curcumol: daily, CDDP: once per week, for 31 days | Curcumol combined with CDDP significantly inhibited tumor growth and reduced M2-type macrophage recruitment | PMC9318016 |
ICR mice | CCl4-induced liver fibrosis model | Intraperitoneal injection | 15, 30, 60 mg/kg | Every other day for 5-8 weeks | Curcumol ameliorates CCl4-induced liver fibrosis in mice by inducing RIPK1/RIPK3 complex-dependent necroptosis. | PMC6142373 |
C57BL/6J mice | Alcoholic fatty liver disease model | Oral | 30, 45, 60 mg/kg | Once daily for 30 days | Curcumol alleviated ethanol-induced liver injury and lipid deposition, and effectively inhibited hepatocyte senescence. | PMC9273900 |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
4.23mL 0.85mL 0.42mL |
21.16mL 4.23mL 2.12mL |
42.31mL 8.46mL 4.23mL |
Tags: Curcumol | (-)-Curcumol | Apoptosis | sesquiterpenoid |Curcumol | (-)-Curcumol | anticancer | apoptosis | MAPK/ERK | PI3K/Akt | NF-κB | anti-inflammatory| antiviral | anti-inflammatory | 4871-97-0
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