Grundinformationen
- Standard-SMILES
COc1cc(O)c(C(=O)/C=C/c2ccccc2)c(OC)c1- InChIKey
QKQLSQLKXBHUSO-CMDGGOBGSA-N- Summenformel
- C17H16O4
- Durchschnittliche Molmasse
- 284,31 g/mol
- Monoisotopische Masse
- 284,10485899
Überblick
Flavokawain B is a member of the class of chalcones that consists of trans-chalcone substituted by hydroxy group at positions 2' and methoxy groups at positions 4' and 6'. Isolated from Piper methysticum and Piper rusbyi, it exhibits antileishmanial, anti-inflammatory and antineoplastic activities. It has a role as a metabolite, an antineoplastic agent, an anti-inflammatory agent, an apoptosis inducer and an antileishmanial agent. It is a member of chalcones, a member of phenols and a dimethoxybenzene. It is functionally related to a trans-chalcone.
Namen und Bezeichner
- Bevorzugter Name
- Flavokawain B
- IUPAC
- (E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one
- Englischer Name
- 4',6'-Dimethoxy-2'-hydroxychalcone
- Summenformel
- C17H16O4
- Molmasse
- 284.31
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
1775-97-9、76554-24-0- PubChem CID
- 5356121
- DTXSID
DTXSID601028794- ChEMBL
CHEMBL104255- ChEBI
CHEBI:65899- UNII
- R9WC6SM4UQ
- Nikkaji
- J647.133A、J816.775C
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,8
- Polarare Oberfläche (TPSA)
- 55,8 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 5
- Schwere Atome
- 21
- Formalladung
- 0
- Komplexität
- 360
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 85 · 85-87°C
- Siedepunkt
- 500.1 · 500.1±50.0 °C(Predicted)
- Dichte
- 1.203 · 1.203±0.06 g/cm3(Predicted)
- storage temp.
- -20 °C · -20°C Freezer
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly)
- pka
- 6.84 · 6.84±0.40(Predicted)
- Aggregatzustand
- Solid
- Farbe
- Yellow to Dark Yellow
- Major Application
- food and beverages
- InChI
- 1S/C17H16O4/c1-20-13-10-15(19)17(16(11-13)21-2)14(18)9-8-12-6-4-3-5-7-12/h3-11,19H,1-2H3/b9-8+
- InChIKey
- QKQLSQLKXBHUSO-CMDGGOBGSA-N
- SMILES
- O(C)c1c(c(cc(c1)OC)O)C(=O)\C=C\c2ccccc2
- LogP
- 4.206 · 4.206 (est)
- CAS Datenbank
- 1775 · 1775-97-9(CAS DataBase Reference)
Sicherheit und Regulatorisches
Sicherheitsdaten
- wgk
- WGK 3
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Pharmakologische Informationen
Anwendungen
BeschreibungFlavokawain B is a natural chalcone first isolated from extracts of kava roots. It induces apoptosis in androgen receptor-negative, hormone-refractory prostate cancer cell lines (IC50s = 32, 48, 6.2, and 3.9 μM for LAPC4, LNCaP, PC-3, and DU145 cells, respectively, treated for 48 hours), with increased expression of the proapoptotic protein Bim. Flavokawain B increases Bim expression and inhibits growth of DU145 xenografts in mice. It also increases Bim expression, promotes apoptosis, and induces cell cycle arrest in uterine leiomyosarcoma cells. However, flavokawain B is hepatotoxic, triggering oxidative stress, inhibiting NF-κB signaling, and activating MAPK pathways, culminating in HepG2 and L-02 cell death (LD50s = 15 and 32 μM, respectively).
VerwendenFlavokavain B is a secondary metabolite of the kava plant (Piper methysticum Forst. f., Piperaceae, which has anticancer properties and demonstrated oral efficacy in murine cancer models. Futhermore, it also has suspected roles in rare cases of kava-induced hepatotoxicity. In addition, it is a potential candidate for the development of novel antifungal phytotherapic products.
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