1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-phenyl-2-propen-1-one (Q27164253)

1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one (English)

9 October 2016

chemical formula

C₁₇H₁₆O₄

1 reference

1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one (English)

9 October 2016

canonical SMILES

COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O

1 reference

Phytochemical and cytotoxic investigations of Alpinia mutica rhizomes.

1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one (English)

9 October 2016

2 references

Constituents of the rhizomes of two Alpinia species of Malaysia

Alpinia pricei

1 reference

Anti-inflammatory activity of Flavokawain B from Alpinia pricei Hayata

Alpinia rafflesiana

1 reference

Constituents of the rhizomes of two Alpinia species of Malaysia

Cedrelopsis grevei

1 reference

Chalcones from the seed of Cedrelopsis grevei (Ptaeroxylaceae).

Kaempferia parviflora

1 reference

Phenolic glycosides from Kaempferia parviflora

Litsea pedunculata

1 reference

Novel cytotoxic chalcones from Litsea rubescens and Litsea pedunculata.

Piper cubeba

1 reference

Radical scavenging ability of some compounds isolated from Piper cubeba towards free radicals

Piper dilatatum

1 reference

Antifungal benzoic acid derivatives from Piper Dilatatum in honour of Professor G. H. Neil Towers 75th birthday

Piper rusbyi

1 reference

Leishmanicidal Constituents from the Leaves of Piper rusbyi

Renealmia nicolaioides

1 reference

Activity-guided isolation of constituents of Renealmia nicolaioides with the potential to induce the phase II enzyme quinone reductase.

Uvaria mocoli

1 reference

A novel retrodihydrochalcone from the stem bark of Uvaria mocoli

Bryobium erioides

1 reference

Phenolic glycosides from Kaempferia parviflora

Polygonum patulum

1 reference

Antimicrobial, antiviral and cytotoxic activity of extracts and constituents from Polygonum spectabile Mart.

Bryobium eriaeoides

1 reference

Phenolic glycosides from Kaempferia parviflora

Piper methysticum

6 references

Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses

Flavokawain A, a novel chalcone from kava extract, induces apoptosis in bladder cancer cells by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice

Flavokawain B, a kava chalcone, induces apoptosis via up-regulation of death-receptor 5 and Bim expression in androgen receptor negative, hormonal refractory prostate cancer cell lines and reduces tumor growth

In vitro cytotoxicity of nonpolar constituents from different parts of kava plant (Piper methysticum).

Novel compounds from Piper methysticum Forst (Kava Kava) roots and their effect on cyclooxygenase enzyme

Zwei Chalkonpigmente aus Piper Methysticum Forst.

Piper majusculum

6 references

Novel compounds from Piper methysticum Forst (Kava Kava) roots and their effect on cyclooxygenase enzyme

Flavokawain A, a novel chalcone from kava extract, induces apoptosis in bladder cancer cells by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice

Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses

Flavokawain B, a kava chalcone, induces apoptosis via up-regulation of death-receptor 5 and Bim expression in androgen receptor negative, hormonal refractory prostate cancer cell lines and reduces tumor growth

In vitro cytotoxicity of nonpolar constituents from different parts of kava plant (Piper methysticum).

Zwei Chalkonpigmente aus Piper Methysticum Forst.

Persicaria ferruginea

2 references

Detection of antifungal compounds in Polygonum ferrugineum Wedd. extracts by bioassay-guided fractionation. Some evidences of their mode of action.

An unusual homoisoflavanone and a structurally-related dihydrochalcone from Polygonum ferrugineum (Polygonaceae)

Alpinia zerumbet

1 reference

Phenolic compounds from the rhizomes of Alpinia speciosa

Etlingera elatior

1 reference

Phenolic compounds from the rhizomes of Alpinia speciosa

Identifiers

InChI

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

1 reference

1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one (English)

QKQLSQLKXBHUSO-UHFFFAOYSA-N

9 October 2016

InChIKey

2 references

1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one (English)

9 October 2016

ChEBI release 2020-09-01

1 reference

1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-phenyl-2-propen-1-one (English)

9 October 2016

2 references

1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one (English)

matched by identifier from

9 October 2016

InChIKey

QKQLSQLKXBHUSO-UHFFFAOYSA-N

ChEBI ID

92523

mapping relation type

2 references

1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenyl-2-propen-1-one (English)