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Metal-free transesterification catalyzed by tetramethylammonium methyl carbonate

Green chemistry : an international journal and green chemistry resource : GC, 2018, Vol.20 (6), p.1193-1198

2018

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Mechanism of Action of ME1111, a Novel Antifungal Agent for Topical Treatment of Onychomycosis

Antimicrobial agents and chemotherapy, 2016-02, Vol.60 (2), p.873-880

2016

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The phosphodiesterase 4 inhibitor AA6216 suppresses activity of fibrosis-specific macrophages

Biochemistry and biophysics reports, 2021-12, Vol.28, p.101118-101118, Article 101118

2021

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Characterization of Antifungal Activity and Nail Penetration of ME1111, a New Antifungal Agent for Topical Treatment of Onychomycosis

Antimicrobial agents and chemotherapy, 2016-02, Vol.60 (2), p.1035-1039

2016

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Serological survey of equine viral diseases in Mongolia

Microbiology and immunology, 2011-04, Vol.55 (4), p.289-292

2011

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Chiral Macrocyclic Catalysts for the Enantioselective Addition of Lithium Acetylides to Ketones

Journal of the American Chemical Society, 2023-12, Vol.145 (48), p.26238-26248

2023

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Antidermatophyte activity and PK/PD of ME1111 in a guinea pig model of tinea corporis

Journal of antibiotics, 2024-05

2024

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NBRI17671, a new antitumor compound, produced by Acremonium sp. CR17671

Journal of antibiotics, 2010-05, Vol.63 (5), p.237-243

2010

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A novel phosphodiesterase 4 inhibitor, AA6216, reduces macrophage activity and fibrosis in the lung

European journal of pharmacology, 2020-10, Vol.885, p.173508-173508, Article 173508

2020

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Anti-inflammatory effects of a novel phosphodiesterase-4 inhibitor, AA6216, in mouse dermatitis models

European journal of pharmacology, 2021-09, Vol.906, p.174258-174258, Article 174258

2021

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ME3183, a novel phosphodiesterase-4 inhibitor, exhibits potent anti-inflammatory effects and is well tolerated in a non-clinical study

European journal of pharmacology, 2024-01, Vol.962, p.176202-176202, Article 176202

2024

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Pharmacological characterization and feeding-suppressive property of FMS586 [3-(5,6,7,8-tetrahydro-9-isopropyl-carbazol-3-yl)-1-methyl-1-(2-pyridin-4-yl-ethyl)-urea hydrochloride], a novel, selective, and orally active antagonist for neuropeptide Y Y5 receptor

The Journal of pharmacology and experimental therapeutics, 2006-05, Vol.317 (2), p.562

2006

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Metal-free transesterification catalyzed by tetramethylammonium methyl carbonateElectronic supplementary information (ESI) available: Experimental procedure, characterization data, additional control experiments, copies of 1H NMR and 13C NMR spectra of all new compounds. See DOI: 10.1039/c7gc03858e

2018-03

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In Vitro Human Onychopharmacokinetic and Pharmacodynamic Analyses of ME1111, a New Topical Agent for Onychomycosis

Antimicrobial agents and chemotherapy, 2018-01, Vol.62 (1)

2018

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Endocrinological properties of two novel nonsteroidal progesterone receptor modulators, CP8816 and CP8863

The Journal of pharmacology and experimental therapeutics, 2005-05, Vol.313 (2), p.916

2005

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1279. In Vitro Activity of Nacubactam (OP0595) Alone and in Combination with β-Lactams against β-Lactamase-Producing Enterobacterales Isolated in Japan

Open forum infectious diseases, 2020-12, Vol.7 (Supplement_1), p.S655-S655

2020

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PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum: I. Taxonomy of Producing Strain, Fermentation, Isolation and Biological Activities

The Journal of Antibiotics, 1997/04/25, Vol.50(4), pp.304-308

1997

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PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum: II. Physico-chemical Properties and Structure Elucidation

The Journal of Antibiotics, 1997/04/25, Vol.50(4), pp.309-313

1997

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Isolation of a novel substrate-competitive tyrosine kinase inhibitor, desmal, from the plant Desmos chinensis

FEBS letters, 1993-04, Vol.320 (2), p.169-172

1993

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Nonsteroidal progesterone receptor ligands (II); synthesis and SAR of new tetrahydrobenzindolone derivatives

Bioorganic & medicinal chemistry, 2006-07, Vol.14 (14), p.4862-4878

2006

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Nonsteroidal progesterone receptor ligands (I): Synthesis and SAR of new tetrahydronaphthofuranone derivatives

Bioorganic & medicinal chemistry, 2006-07, Vol.14 (14), p.4850-4861

2006

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BIOSYNTHETIC PREPARATION OF RADIOACTIVELY LABELED ERBSTATIN

The Journal of Antibiotics, 1992/08/25, Vol.45(8), pp.1382-1384

1992

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Estrogen and progesterone receptors as molecular targets for anticancer drug

Drug delivery system, 2003, Vol.18 (4), p.336-342

2003

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CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton

European journal of pharmacology, 2003-02, Vol.461 (1), p.73-78

2003

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Erratum to “CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton” [Eur. J. Pharmacol. 461 (2003) 73–78]

European journal of pharmacology, 2003-04, Vol.465 (3), p.299-299

2003

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Metal-free transesterification catalyzed by tetramethylammonium methyl carbonate

Mechanism of Action of ME1111, a Novel Antifungal Agent for Topical Treatment of Onychomycosis

The phosphodiesterase 4 inhibitor AA6216 suppresses activity of fibrosis-specific macrophages

Characterization of Antifungal Activity and Nail Penetration of ME1111, a New Antifungal Agent for Topical Treatment of Onychomycosis

Serological survey of equine viral diseases in Mongolia

Chiral Macrocyclic Catalysts for the Enantioselective Addition of Lithium Acetylides to Ketones

Antidermatophyte activity and PK/PD of ME1111 in a guinea pig model of tinea corporis

NBRI17671, a new antitumor compound, produced by Acremonium sp. CR17671

A novel phosphodiesterase 4 inhibitor, AA6216, reduces macrophage activity and fibrosis in the lung

Anti-inflammatory effects of a novel phosphodiesterase-4 inhibitor, AA6216, in mouse dermatitis models

ME3183, a novel phosphodiesterase-4 inhibitor, exhibits potent anti-inflammatory effects and is well tolerated in a non-clinical study

Pharmacological characterization and feeding-suppressive property of FMS586 [3-(5,6,7,8-tetrahydro-9-isopropyl-carbazol-3-yl)-1-methyl-1-(2-pyridin-4-yl-ethyl)-urea hydrochloride], a novel, selective, and orally active antagonist for neuropeptide Y Y5 receptor

Metal-free transesterification catalyzed by tetramethylammonium methyl carbonateElectronic supplementary information (ESI) available: Experimental procedure, characterization data, additional control experiments, copies of 1H NMR and 13C NMR spectra of all new compounds. See DOI: 10.1039/c7gc03858e

In Vitro Human Onychopharmacokinetic and Pharmacodynamic Analyses of ME1111, a New Topical Agent for Onychomycosis

Endocrinological properties of two novel nonsteroidal progesterone receptor modulators, CP8816 and CP8863

1279. In Vitro Activity of Nacubactam (OP0595) Alone and in Combination with β-Lactams against β-Lactamase-Producing Enterobacterales Isolated in Japan

PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum: I. Taxonomy of Producing Strain, Fermentation, Isolation and Biological Activities

PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum: II. Physico-chemical Properties and Structure Elucidation

Isolation of a novel substrate-competitive tyrosine kinase inhibitor, desmal, from the plant Desmos chinensis

Nonsteroidal progesterone receptor ligands (II); synthesis and SAR of new tetrahydrobenzindolone derivatives

Nonsteroidal progesterone receptor ligands (I): Synthesis and SAR of new tetrahydronaphthofuranone derivatives

BIOSYNTHETIC PREPARATION OF RADIOACTIVELY LABELED ERBSTATIN

Estrogen and progesterone receptors as molecular targets for anticancer drug

CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton

Erratum to “CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton” [Eur. J. Pharmacol. 461 (2003) 73–78]

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