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Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors

Journal of medicinal chemistry, 1995-03, Vol.38 (7), p.1084-1089

1995

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An initial three-component pharmacophore for specific serotonin-3 receptor ligands

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2721-2725

1990

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Aromatic thiazole derivatives: structurally novel and selective serotonin-3 receptor antagonists

Journal of medicinal chemistry, 1990-01, Vol.33 (1), p.13-16

1990

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SYNTHESIS, IN VITRO AND IN VIVO ACTIVITY OF NOVEL 9-DEOXO-9a-AZA-9a-HOMOERYTHROMYCIN A DERIVATIVES; A NEW CLASS OF MACROLIDE ANTIBIOTICS, THE AZALIDES

The Journal of Antibiotics, 1988/08/25, Vol.41(8), pp.1029-1047

1988

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1-Naphthylpiperazine derivatives as potential atypical antipsychotic agents

Journal of medicinal chemistry, 1991-06, Vol.34 (6), p.1860-1866

1991

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Selective cleavage of the mycinose sugar from the macrolide antibiotic tylosin: a unique glycosidic scission

Journal of organic chemistry, 1979-06, Vol.44 (12), p.2050-2052

1979

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Thiazole as a carbonyl bioisostere. A novel class of highly potent and selective 5-HT3 receptor antagonists

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2715-2720

1990

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5,7-Dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H-pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: A Potent and Centrally-Selective Inhibitor of Acetylcholinesterase

Journal of medicinal chemistry, 1995-07, Vol.38 (15), p.2802-2808

1995

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Synthesis, in vitro binding profile, and CNS penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole

Journal of medicinal chemistry, 1990-11, Vol.33 (11), p.3020-3023

1990

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Novel Benzisoxazole Derivatives as Potent and Selective Inhibitors of Acetylcholinesterase

Journal of medicinal chemistry, 1994-08, Vol.37 (17), p.2721-2734

1994

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Macrolide neutral sugar chemistry. Chemical conversion of oleandomycin Y to 3-(2,6-dideoxy-L-.alpha.-allosyl)oleandomycin Y and 3-(2,6-dideoxy-L-.alpha.-galactosyl)oleandomycin Y

Journal of organic chemistry, 1982-11, Vol.47 (24), p.4796-4799

1982

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Macrolide fundamental chemistry: sequential conversion of the 14-membered ring macrolide antibiotic oleandomycin to 12- and 10-membered ring macrocyclic lactone systems

Journal of organic chemistry, 1986-12, Vol.51 (26), p.5397-5400

1986

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2‐Amino‐4‐methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo

British journal of pharmacology, 1996-11, Vol.119 (6), p.1101-1108

1996

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Ring contraction of oleandrose on the macrolide antibiotic oleandomycin with [(methoxycarbonyl)sulfamoyl]triethylammonium hydroxide inner salt

Journal of medicinal chemistry, 1982-07, Vol.25 (7), p.881-884

1982

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5,7-dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H- pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: a potent and centrally-selective inhibitor of acetylcholinesterase with an improved margin of safety

Journal of medicinal chemistry, 1995-07, Vol.38 (15), p.2802

1995

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13C-NMR. Spectroscopy of Naturally Occurring Substances. XXXV. Labdanic diterpenes

Helvetica chimica acta, 1975-07, Vol.58 (6), p.1567-1573

1975

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Novel Serotonin-3 Receptor Antagonists

Synlett, 1991-04, Vol.1991 (4), p.213-221

1991

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Novel in vitro and in vivo inhibitors of prolyl endopeptidase

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (11), p.585-590

1991

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Macrolide antibiotics. Chemistry, biology, and practice

Journal of Pharmaceutical Sciences, 1985, Vol.74 (9), p.1023-1023

Nagel, Arthur A.

1985

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Macrolide antibiotics. Chemistry, biology, and practice. Edited by Satoshi Ōmura. Academic Press, Inc., Orlando, FL 32887. 1984. 635 pp. 16 × 23.5 cm. ISBN 0-12-526450-x. $;89.50

Journal of Pharmaceutical Sciences, 1985, Vol.74 (9), p.1023-1023

Nagel, Arthur A.

1985

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13 C‐NMR. Spectroscopy of Naturally Occurring Substances. XXXV. Labdanic diterpenes

Helvetica chimica acta, 1975-07, Vol.58 (6), p.1567-1573

1975

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ChemInform Abstract: (13)C‐NMR SPECTROSCOPY OF NATURALLY OCCURRING SUBSTANCES PART 35, LABDANIC DITERPENES

Chemischer Informationsdienst, 1975-12, Vol.6 (49)

1975

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Risk-Adjusted Returns of Private Equity Funds: A New Approach

The Review of financial studies, 2024-10

2024

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Risk-Adjusting the Returns to Venture Capital

The Journal of finance (New York), 2016-06, Vol.71 (3), p.1437-1470

2016

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Long term exposure to low level air pollution and mortality in eight European cohorts within the ELAPSE project: pooled analysis

BMJ (Online), 2021-09, Vol.374, p.n1904

2021

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Design and Synthesis of 1-Heteroaryl-3-(1-benzyl-4-piperidinyl)propan-1-one Derivatives as Potent, Selective Acetylcholinesterase Inhibitors

An initial three-component pharmacophore for specific serotonin-3 receptor ligands

Aromatic thiazole derivatives: structurally novel and selective serotonin-3 receptor antagonists

SYNTHESIS, IN VITRO AND IN VIVO ACTIVITY OF NOVEL 9-DEOXO-9a-AZA-9a-HOMOERYTHROMYCIN A DERIVATIVES; A NEW CLASS OF MACROLIDE ANTIBIOTICS, THE AZALIDES

1-Naphthylpiperazine derivatives as potential atypical antipsychotic agents

Selective cleavage of the mycinose sugar from the macrolide antibiotic tylosin: a unique glycosidic scission

Thiazole as a carbonyl bioisostere. A novel class of highly potent and selective 5-HT3 receptor antagonists

5,7-Dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H-pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: A Potent and Centrally-Selective Inhibitor of Acetylcholinesterase

Synthesis, in vitro binding profile, and CNS penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole

Novel Benzisoxazole Derivatives as Potent and Selective Inhibitors of Acetylcholinesterase

Macrolide neutral sugar chemistry. Chemical conversion of oleandomycin Y to 3-(2,6-dideoxy-L-.alpha.-allosyl)oleandomycin Y and 3-(2,6-dideoxy-L-.alpha.-galactosyl)oleandomycin Y

Macrolide fundamental chemistry: sequential conversion of the 14-membered ring macrolide antibiotic oleandomycin to 12- and 10-membered ring macrocyclic lactone systems

2‐Amino‐4‐methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo

Ring contraction of oleandrose on the macrolide antibiotic oleandomycin with [(methoxycarbonyl)sulfamoyl]triethylammonium hydroxide inner salt

5,7-dihydro-3-[2-[1-(phenylmethyl)-4-piperidinyl]ethyl]-6H- pyrrolo[3,2-f]-1,2-benzisoxazol-6-one: a potent and centrally-selective inhibitor of acetylcholinesterase with an improved margin of safety

13C-NMR. Spectroscopy of Naturally Occurring Substances. XXXV. Labdanic diterpenes

Novel Serotonin-3 Receptor Antagonists

Novel in vitro and in vivo inhibitors of prolyl endopeptidase

Macrolide antibiotics. Chemistry, biology, and practice

Macrolide antibiotics. Chemistry, biology, and practice. Edited by Satoshi Ōmura. Academic Press, Inc., Orlando, FL 32887. 1984. 635 pp. 16 × 23.5 cm. ISBN 0-12-526450-x. $;89.50

13 C‐NMR. Spectroscopy of Naturally Occurring Substances. XXXV. Labdanic diterpenes

ChemInform Abstract: (13)C‐NMR SPECTROSCOPY OF NATURALLY OCCURRING SUBSTANCES PART 35, LABDANIC DITERPENES

Risk-Adjusted Returns of Private Equity Funds: A New Approach

Risk-Adjusting the Returns to Venture Capital

Long term exposure to low level air pollution and mortality in eight European cohorts within the ELAPSE project: pooled analysis

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