Name | Curcumol |
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Synonyms |
6H-3a,6-Epoxyazulen-6-ol, octahydro-3-methyl-8-methylene-5-(1-methylethyl)-, (3S,3aS,5S,8aS)-
(3S,3aS,5S,8aS)-3-methyl-8-methylidene-5-(propan-2-yl)octahydro-6H-3a,6-epoxyazulen-6-ol (3S,3aS,5S,6R,8aS)-Octahydro-3-methyl-8-methylene-5-(1-methylethyl)-6H-3a,6-epoxyazulen-6-ol (1S,2S,5S,9S)-9-Isopropyl-2-methyl-6-methylene-11-oxatricyclo[6.2.1.0]undecan-8-ol |
Description | Curcumol is a sesquiterpene originally isolated from curcuma rhizomes; shows anticancer activities both in vitro and in vivo.IC50 value:Target: Anticancer natural compoundin vitro: Curcumol exhibited time- and concentration-dependent anti-proliferative effects in SPC-A-1 human lung adenocarcinoma cells with cell cycle arrest in the G0/G1 phase while apoptosis-induction was also confirmed with flow cytometry and morphological analyses [1]. Curcumol-induced growth inhibition correlated with apoptosis induction as evidenced by Annexin V staining, and cleavage of caspase-3 and poly (ADP-ribose) polymerase (PARP) in HSC-T6. Suppression of the NF-κB translocation via inhibition of IκB-α phosphorylation by the curcumol led to the inhibition of expression of NF-κB-regulated gene, e.g. Bcl-xL and Bcl-2, in a PI3K-dependent manner, which is upstream of NF-κB activation [2]. Curcumol exhibits an inhibitory effect on receptor activator of nuclear factor kappaB ligand (RANKL)-induced osteoclast differentiation with both bone marrow-derived macrophages and RAW264.7 cells in a dose-dependent manner [3].in vivo: Anti-neoplastic effects of curcumol were also confirmed in tumor bearing mice. Curcumol (60 mg/kg daily) significantly reduced tumor size without causing notable toxicity [1]. |
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Related Catalog | |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 334.5±42.0 °C at 760 mmHg |
Melting Point | 141-142ºC |
Molecular Formula | C15H24O2 |
Molecular Weight | 236.350 |
Flash Point | 134.7±22.1 °C |
Exact Mass | 236.177628 |
PSA | 29.46000 |
LogP | 3.25 |
Vapour Pressure | 0.0±1.6 mmHg at 25°C |
Index of Refraction | 1.526 |
Hazard Codes | Xi |
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RIDADR | NONH for all modes of transport |
HS Code | 29321900 |
~98% 4871-97-0 |
Literature: Li, Xian; Wu, Lijun; Ji, Zhizong; Harigaya, Yoshihiro; Konda, Yaeko; et al. Journal of Heterocyclic Chemistry, 1988 , vol. 25, p. 1403 - 1406 |
Precursor 1 | |
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DownStream 0 |