Tetrahydrocurcumin

HCID 124072CAS 36062-04-1

Grundinformationen

Standard-SMILES
COc1cc(CCC(=O)CC(=O)CCc2ccc(O)c(OC)c2)ccc1O
InChIKey
LBTVHXHERHESKG-UHFFFAOYSA-N
Summenformel
C21H24O6
Durchschnittliche Molmasse
372,4 g/mol
Monoisotopische Masse
372,15728849

Überblick

Tetrahydrocurcumin is a beta-diketone that is curcumin in which both of the double bonds have been reduced to single bonds. It has a role as a metabolite. It is a polyphenol, a beta-diketone and a diarylheptanoid. It is functionally related to a curcumin.

Namen und Bezeichner

Bevorzugter Name
Tetrahydrocurcumin
IUPAC
1,7-bis(4-hydroxy-3-methoxyphenyl)heptane-3,5-dione
Englischer Name
Tetrahydrocurcumin
Summenformel
C21H24O6
Molmasse
372.41

Namen und Synonyme

Tetrahydrocurcumin36062-04-11,7-bis(4-hydroxy-3-methoxyphenyl)heptane-3,5-dioneSabiwhiteTetrahydrodiferuloylmethane3,5-Heptanedione, 1,7-bis(4-hydroxy-3-methoxyphenyl)-NSC-687845DTXSID3086580100U0645U03CHEBI:67263RefChem:188657DTXCID40814168
Weitere Namen anzeigen
tetrahydrocurcuminoidsSabiWhite-LGB-TCHAids110028Aids-110028BioaActive THC
609-201-3Tetrahydro Curcumin1,7-Bis(4-hydroxy-3-methoxyphenyl)-3,5-heptanedioneNSC 687845TetrahydrocucuminHZIV 81-2MFCD04152347NSC687845

Datenbank-Bezeichner

CAS
36062-04-1
PubChem CID
124072
DTXSID
DTXSID30865801
ChEMBL
CHEMBL318743
ChEBI
CHEBI:67263
UNII
00U0645U03
EC Number
609-201-3
Nikkaji
J478.221F

Eigenschaften

Berechnete Struktureigenschaften

XLogP
2,8
Polarare Oberfläche (TPSA)
93,1 Ų
H-Brücken-Donoren
2
H-Brücken-Akzeptoren
6
Frei drehbare Bindungen
10
Schwere Atome
27

Experimentelle und physikochemische Eigenschaften

CosmeticsAntioxidant
Endocrine DisruptorsPotential endocrine disrupting compound
Melting Point95 - 97 °C
Physical DescriptionSolid
Collision Cross Section181.2 Ų [M+Na]+ [CCS Type: DT; Buffer gas: N2; Ionization: ESI+; Dataset: TOXCAST; Source Identifier: DTXSID30865801]

Physikochemische Eigenschaften

Schmelzpunkt
95 · 95-97 ºC
Siedepunkt
564.1 · 564.1±45.0 °C(Predicted)
Dichte
1.222 · 1.222
Flammpunkt
196 ℃ · 196℃
storage temp.
Inert atmosphere,Room Temperature
Löslichkeit
DMSO (Slightly), Methanol (Slightly, Heated)

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 3 Einträge

This chemical does not meet GHS hazard criteria for 100% (2 of 2) of all reports.

Not Classified

Aggregated GHS information provided per 2 reports by companies from 1 notifications to the ECHA C&L Inventory.

Gefahrenhinweise

Regulatory Information · 3 Einträge

Chemical: 3,5-Heptanedione, 1,7-bis(4-hydroxy-3-methoxyphenyl)-

Status: Active Update: 18-06-2014 https://echa.europa.eu/registration-dossier/-/registered-dossier/7283

3,5-Heptanedione, 1,7-bis(4-hydroxy-3-methoxyphenyl)-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.

Hazard Classes and CategoriesNot Classified

Sicherheitsdaten

wgk
3
Speicherklasse
11 - Combustible Solids

Chemie und Industrie

Pharmakologische Informationen

Cellular LocationsMembrane

Verwendung und Herstellung

Use ClassificationCosmetics -> Antioxidant
Anwendungen · 2 Einträge

BeschreibungTetrahydrocurcumin (THC), the active metabolite of curcumin, is gaining popularity amongst scientist due to its wide spectrum of pharmacological activities, better stability and colourless nature. Tetrahydrocurcumin has a similar structure to that of curcumin. THC lacks the α, β-unsaturated carbonyl moiety in its chemical structure. It is naturally sourced from the roots of Curcuma zedoaria, Zingiber mioga, and Zingiber officinale and has potent antioxidant activity and depigmentation of the skin. THC is being studied for the treatment of cancer and dementia. THC is also known to epigenetically ameliorate mitochondrial dysfunction in brain vasculature during Ischemic Stroke. Tetrahydrocurcumin (THC) has been used as a neuroprotective agent to study its therapeutic potential in improving mitochondrial dysfunction in the ischemic stroke mice model.

VerwendenTetrahydrocurcumin is an antioxidant and skin-whitening ingredient. It is a major curcuminoid metabolite of curcumin that has been shown to have protective effects against diabetes and vascular dysfunction via alleviation of oxidative stress.The interest in tetrahydrocurcumin research is increasing because it is superior to curcumin in its solubility in water, chemical stability, bioavailability, and anti-oxidative activity. Curcumin metabolizes into tetrahydrocurcumin by bacterial enzyme NADPH-dependent curcumin reductase in the intestine.

Darstellung · 1 Eintrag

synthetischeTetrahydrocurcumin can also be chemically synthesized from curcumin by catalytic hydrogenation using PtO2 or palladium as a catalyst.One gram (1.0 g) of curcumin was dissolved in 20 ml of acetone and placed in a 100-ml glass reactor for reduction, to which was then added 500 mg of activated Raney-nickel catalyst. Subsequently, the atmosphere of the reactor was replaced for hydrogen gas by the routine method. A rubber-made balloon filled with hydrogen gas was arranged on the upper portion of the reactor in order to keep hydrogen gas pressure constant in the reactor by supplying hydrogen gas to make up for the consumed amount of hydrogen gas. The reactor was stirred while maintained at a given temperature in a constant-temperature water bath kept at 30° C. for 2-hour reduction.After completion of the reaction, the Raney-nickel catalyst was removed from the solution by filtering, which was then evaporated and dried by concentration under reduced pressure and was dissolved again in a small amount of acetone.Subsequently, the eluate was concentrated and dried under reduced pressure to obtain 674 mg of tetrahydrocurcumin.Method for making tetrahydrocurcumin and a substance containing the antioxidative substance tetrahydrocurcumin

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Ergänzende Hinweise · 1 Eintrag

DefinitionChEBI: Tetrahydrocurcumin is a beta-diketone that is curcumin in which both of the double bonds have been reduced to single bonds. It has a role as a metabolite. It is a beta-diketone, a polyphenol and a diarylheptanoid. It derives from a curcumin.

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