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NMR Study of the Solution Structure of Curcumin

Journal of natural products (Washington, D.C.), 2007-02, Vol.70 (2), p.143-146

2007

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Eugenol Causes Melanoma Growth Suppression through Inhibition of E2F1 Transcriptional Activity

The Journal of biological chemistry, 2005-02, Vol.280 (7), p.5812-5819

2005

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Corrigendum to “Combination of 2-methoxyestradiol (2-ME2) and eugenol for apoptosis induction synergistically in androgen independent prostate cancer cells” [J. Steroid Biochem. Mol. Biol. 113 (2009) 25–35]

The Journal of steroid biochemistry and molecular biology, 2021-10, Vol.213, p.105962-105962, Article 105962

2021

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Selectivity of Polycyclic Inhibitors for Human Cytochrome P450s 1A1, 1A2, and 1B1

Chemical research in toxicology, 1998-09, Vol.11 (9), p.1048-1056

1998

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4-Hydroxy-3-Methoxybenzoic Acid Methyl Ester: A Curcumin Derivative Targets Akt/NFκB Cell Survival Signaling Pathway: Potential for Prostate Cancer Management

Neoplasia (New York, N.Y.), 2003-05, Vol.5 (3), p.255-266

2003

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Novel reversible inactivation of cytochrome P450 2E1 T303A by tert-butyl acetylene: the role of threonine 303 in proton delivery to the active site of cytochrome P450 2E1

The Journal of pharmacology and experimental therapeutics, 2004-07, Vol.310 (1), p.281-290

2004

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Binding of MCF-7 cell mitochondrial proteins and recombinant human estrogen receptors α and β to human mitochondrial dna estrogen response elements

Journal of cellular biochemistry, 2004-10, Vol.93 (2), p.358-373

2004

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4-Methylcatechol-induced oxidative stress induces intrinsic apoptotic pathway in metastatic melanoma cells

Biochemical pharmacology, 2011-05, Vol.81 (10), p.1211-1218

2011

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Combination of 2-methoxyestradiol (2-ME 2) and eugenol for apoptosis induction synergistically in androgen independent prostate cancer cells

The Journal of steroid biochemistry and molecular biology, 2009, Vol.113 (1), p.25-35

2009

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Interactions of Dietary Estrogens with Human Estrogen Receptors and the Effect on Estrogen Receptor-Estrogen Response Element Complex Formation

Environmental health perspectives, 2000-09, Vol.108 (9), p.867-872

2000

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Effect of 17-alpha-ethynylestradiol on activities of cytochrome P450 2B (P450 2B) enzymes: characterization of inactivation of P450s 2B1 and 2B6 and identification of metabolites

The Journal of pharmacology and experimental therapeutics, 2002-02, Vol.300 (2), p.549-558

2002

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Mechanism-based inactivation of cytochrome P450 2B1 by 2-ethynylnaphthalene: Identification of an active-site peptide

Chemical research in toxicology, 1993-07, Vol.6 (4), p.470-479

1993

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Chemical Inactivation of the Cinnamate 4-Hydroxylase Allows for the Accumulation of Salicylic Acid in Elicited Cells

Plant physiology (Bethesda), 2002-10, Vol.130 (2), p.1022-1031

2002

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Mechanism-Based Inactivation of Cytochromes P450 2E1 and 2E1 T303A by tert-Butyl Acetylenes: Characterization of Reactive Intermediate Adducts to the Heme and Apoprotein

Chemical research in toxicology, 2002-12, Vol.15 (12), p.1561-1571

2002

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Curcumin and derivatives

Acta crystallographica. Section C, Crystal structure communications, 2004-08, Vol.60 (8), p.o608-o610

2004

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Aryl Acetylenes as Mechanism-Based Inhibitors of Cytochrome P450-Dependent Monooxygenase Enzymes

Chemical research in toxicology, 1997-01, Vol.10 (1), p.91-102

1997

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Regulation of Phenobarbital-Mediated Induction of CYP102 (Cytochrome P450BM-3) in Bacillus megaterium by Phytochemicals from Soy and Green Tea

Journal of agricultural and food chemistry, 2001-10, Vol.49 (10), p.4930-4936

2001

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Identification of selective mechanism-based inactivators of cytochromes P-450 2B4 and 2B5, and determination of the molecular basis for differential susceptibility

The Journal of pharmacology and experimental therapeutics, 1999-07, Vol.290 (1), p.445

1999

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Differential expression of CYP102 in Bacillus megaterium by 17-β-estradiol and 4- sec-butylphenol

Biochemical and biophysical research communications, 2003-01, Vol.300 (1), p.102-106

2003

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Inactivation of cytochrome P450s 2B1, 2B4, 2B6, and 2B11 by arylalkynes

Drug metabolism and disposition, 1997-11, Vol.25 (11), p.1242

1997

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Chemical Inactivation of the Cinnamate 4-Hydroxylase Allows for the Accumulation of Salicylic Acid in Elicited Cells1

Plant physiology (Bethesda), 2002-10, Vol.130 (2), p.1022-1031

2002

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Inhibition of Cytochrome P450 6D1 by Alkynylarenes, Methylenedioxyarenes, and Other Substituted Aromatics

Pesticide biochemistry and physiology, 2000-05, Vol.67 (1), p.63-71

2000

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Catalytic properties of an expressed cytochrome P450 2B1 from a Wistar-Kyoto rat liver cDNA library

Drug metabolism and disposition, 1998-10, Vol.26 (10), p.1026

1998

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Modification of cytochrome P450 1A2 enzymes by the mechanism-based inactivator 2-ethynylnaphthalene and the photoaffinity label 4-azidobiphenyl

Biochemistry (Easton), 1992-11, Vol.31 (43), p.10556-10563

1992

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2-Ethynylnaphthalene as a mechanism-based inactivator of the cytochrome P-450 catalyzed N-oxidation of 2-naphthylamine

Chemical research in toxicology, 1989-11, Vol.2 (6), p.367-374

1989

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NMR Study of the Solution Structure of Curcumin

Eugenol Causes Melanoma Growth Suppression through Inhibition of E2F1 Transcriptional Activity

Corrigendum to “Combination of 2-methoxyestradiol (2-ME2) and eugenol for apoptosis induction synergistically in androgen independent prostate cancer cells” [J. Steroid Biochem. Mol. Biol. 113 (2009) 25–35]

Selectivity of Polycyclic Inhibitors for Human Cytochrome P450s 1A1, 1A2, and 1B1

4-Hydroxy-3-Methoxybenzoic Acid Methyl Ester: A Curcumin Derivative Targets Akt/NFκB Cell Survival Signaling Pathway: Potential for Prostate Cancer Management

Novel reversible inactivation of cytochrome P450 2E1 T303A by tert-butyl acetylene: the role of threonine 303 in proton delivery to the active site of cytochrome P450 2E1

Binding of MCF-7 cell mitochondrial proteins and recombinant human estrogen receptors α and β to human mitochondrial dna estrogen response elements

4-Methylcatechol-induced oxidative stress induces intrinsic apoptotic pathway in metastatic melanoma cells

Combination of 2-methoxyestradiol (2-ME 2) and eugenol for apoptosis induction synergistically in androgen independent prostate cancer cells

Interactions of Dietary Estrogens with Human Estrogen Receptors and the Effect on Estrogen Receptor-Estrogen Response Element Complex Formation

Effect of 17-alpha-ethynylestradiol on activities of cytochrome P450 2B (P450 2B) enzymes: characterization of inactivation of P450s 2B1 and 2B6 and identification of metabolites

Mechanism-based inactivation of cytochrome P450 2B1 by 2-ethynylnaphthalene: Identification of an active-site peptide

Chemical Inactivation of the Cinnamate 4-Hydroxylase Allows for the Accumulation of Salicylic Acid in Elicited Cells

Mechanism-Based Inactivation of Cytochromes P450 2E1 and 2E1 T303A by tert-Butyl Acetylenes: Characterization of Reactive Intermediate Adducts to the Heme and Apoprotein

Curcumin and derivatives

Aryl Acetylenes as Mechanism-Based Inhibitors of Cytochrome P450-Dependent Monooxygenase Enzymes

Regulation of Phenobarbital-Mediated Induction of CYP102 (Cytochrome P450BM-3) in Bacillus megaterium by Phytochemicals from Soy and Green Tea

Identification of selective mechanism-based inactivators of cytochromes P-450 2B4 and 2B5, and determination of the molecular basis for differential susceptibility

Differential expression of CYP102 in Bacillus megaterium by 17-β-estradiol and 4- sec-butylphenol

Inactivation of cytochrome P450s 2B1, 2B4, 2B6, and 2B11 by arylalkynes

Chemical Inactivation of the Cinnamate 4-Hydroxylase Allows for the Accumulation of Salicylic Acid in Elicited Cells1

Inhibition of Cytochrome P450 6D1 by Alkynylarenes, Methylenedioxyarenes, and Other Substituted Aromatics

Catalytic properties of an expressed cytochrome P450 2B1 from a Wistar-Kyoto rat liver cDNA library

Modification of cytochrome P450 1A2 enzymes by the mechanism-based inactivator 2-ethynylnaphthalene and the photoaffinity label 4-azidobiphenyl

2-Ethynylnaphthalene as a mechanism-based inactivator of the cytochrome P-450 catalyzed N-oxidation of 2-naphthylamine

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