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Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent α1-Adrenoceptor Antagonists

Chemical and Pharmaceutical Bulletin, 2011/01/01, Vol.59(1), pp.96-99

2011

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Synthesis and Blocking Activities of a New Class of α1-Adrenoceptor Antagonists

Chemical biology & drug design, 2010-12, Vol.76 (6), p.505-510

2010

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Drug metabolism-based design, synthesis, and bioactivities of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxyphenylethylamino)propane hydrochloride (DDPH) analogs as α₁-adrenoceptors antagonists

Bioorganic & medicinal chemistry, 2011-01, Vol.19 (2), p.783-788

2011

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Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent .ALPHA.1-Adrenoceptor Antagonists

Chemical & pharmaceutical bulletin, 2011, Vol.59 (1), p.96-99

2011

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Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors

Chinese journal of natural medicines, 2010-11, Vol.8 (6), p.441-448

2010

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6-(Methylsulfanyl)-2-phenylthiazolo[5,4- b ]pyridine

Acta crystallographica. Section E, Structure reports online, 2007-02, Vol.63 (2), p.o968-o969

2007

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Synthesis and blocking activities of isoindolinone- and isobenzofuranone-containing phenoxylalkylamines as potent α(1)-adrenoceptor antagonists

Chemical & pharmaceutical bulletin, 2011, Vol.59 (1), p.96-99

2011

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Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent [alpha]1-Adrenoceptor Antagonists

Chemical & pharmaceutical bulletin, 2011-01, Vol.59 (1), p.96

2011

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Design and synthesis of amidino-tyrosine derivatives as non-peptide fibrinogen receptor antagonists

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (14), p.1933-1936

1999

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Drug metabolism-based design, synthesis, and bioactivities of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxyphenylethylamino)propane hydrochloride (DDPH) analogs as alpha sub(1)-adrenoceptors antagonists

Bioorganic & medicinal chemistry, 2011-01, Vol.19 (2), p.783-788

2011

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Drug metabolism-based design, synthesis, and bioactivities of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxyphenylethylamino)propane hydrochloride (DDPH) analogs as α 1-adrenoceptors antagonists

Bioorganic & medicinal chemistry, 2011, Vol.19 (2), p.783-788

2011

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Novel intramolecular rearrangement of 5-carbamoyluraclls into barbituric acids

Tetrahedron, 1990, Vol.46 (10), p.3431-3438

1990

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ChemInform Abstract: Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent α1-Adrenoceptor Antagonists

ChemInform, 2011-08, Vol.42 (32), p.no-no

2011

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Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors: Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors

Chinese Journal of Natural Medicines, 2011-01, Vol.8 (6), p.441-448

2011

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Synthesis and Blocking Activities of a New Class of α 1 ‐Adrenoceptor Antagonists

Chemical biology & drug design, 2010-12, Vol.76 (6), p.505-510

2010

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The Dimroth Rearrangement of 6-Aminouracil Derivatives

Chemical and Pharmaceutical Bulletin, 1992/10/25, Vol.40(10), pp.2839-2841

1992

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Synthesis and anti alpha-adrenoceptor activity in vitro of 4-((4-((2-substitutedphenoxy)ethyl)-1-piperazinyl) methyl)- 1,2-dihydro-quinoline-2-one compounds

Yao hsüeh hsüeh pao, 2002-03, Vol.37 (3), p.181

2002

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ChemInform Abstract: Synthesis and Blocking Activities of Isoindolinone‐ and Isobenzofuranone‐Containing Phenoxylalkylamines as Potent α 1 ‐Adrenoceptor Antagonists

ChemInform, 2011-08, Vol.42 (32)

2011

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Pyrimidines. part LIIX. The Dimroth Rearrangement of 6-Aminouracil Derivatives

Chemical & pharmaceutical bulletin, 1992, Vol.40 (10), p.2839-2841

1992

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Study on the phase II metabolites of phenoprolamine hydrochloride in rat bile by LC/DAD/MSD

Yao hsüeh hsüeh pao, 2001-06, Vol.36 (6), p.440

2001

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6‐(Methylsulfanyl)‐2‐phenylthiazolo[5,4‐b]pyridine

Acta crystallographica. Section E, Structure reports online, 2007-02, Vol.63 (2), p.o968-o969

2007

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Mutagenicity evaluation to UV filters of benzophenone-6, benzophenone-8, and 4-methylbenzylidene camphor by Ames test

PloS one, 2021-09, Vol.16 (9), p.e0255504

2021

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Novel intramolecular rearrangement of 5-carbamoyluracils into barbituric acids

Tetrahedron, 1990, Vol.46 (10), p.3431-3438

1990

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Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors: Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors

Chinese Journal of Natural Medicines, 2011-01, Vol.8 (6), p.436-440

2011

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Genetic aetiology of primary adrenal insufficiency in Chinese children

BMC medical genomics, 2021-06, Vol.14 (1), p.172-14, Article 172

2021

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Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent α1-Adrenoceptor Antagonists

Synthesis and Blocking Activities of a New Class of α1-Adrenoceptor Antagonists

Drug metabolism-based design, synthesis, and bioactivities of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxyphenylethylamino)propane hydrochloride (DDPH) analogs as α₁-adrenoceptors antagonists

Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent .ALPHA.1-Adrenoceptor Antagonists

Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors

6-(Methylsulfanyl)-2-phenylthiazolo[5,4- b ]pyridine

Synthesis and blocking activities of isoindolinone- and isobenzofuranone-containing phenoxylalkylamines as potent α(1)-adrenoceptor antagonists

Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent [alpha]1-Adrenoceptor Antagonists

Design and synthesis of amidino-tyrosine derivatives as non-peptide fibrinogen receptor antagonists

Drug metabolism-based design, synthesis, and bioactivities of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxyphenylethylamino)propane hydrochloride (DDPH) analogs as alpha sub(1)-adrenoceptors antagonists

Drug metabolism-based design, synthesis, and bioactivities of 1-(2,6-dimethylphenoxy)-2-(3,4-dimethoxyphenylethylamino)propane hydrochloride (DDPH) analogs as α 1-adrenoceptors antagonists

Novel intramolecular rearrangement of 5-carbamoyluraclls into barbituric acids

ChemInform Abstract: Synthesis and Blocking Activities of Isoindolinone- and Isobenzofuranone-Containing Phenoxylalkylamines as Potent α1-Adrenoceptor Antagonists

Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors: Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors

Synthesis and Blocking Activities of a New Class of α 1 ‐Adrenoceptor Antagonists

The Dimroth Rearrangement of 6-Aminouracil Derivatives

Synthesis and anti alpha-adrenoceptor activity in vitro of 4-((4-((2-substitutedphenoxy)ethyl)-1-piperazinyl) methyl)- 1,2-dihydro-quinoline-2-one compounds

ChemInform Abstract: Synthesis and Blocking Activities of Isoindolinone‐ and Isobenzofuranone‐Containing Phenoxylalkylamines as Potent α 1 ‐Adrenoceptor Antagonists

Pyrimidines. part LIIX. The Dimroth Rearrangement of 6-Aminouracil Derivatives

Study on the phase II metabolites of phenoprolamine hydrochloride in rat bile by LC/DAD/MSD

6‐(Methylsulfanyl)‐2‐phenylthiazolo[5,4‐b]pyridine

Mutagenicity evaluation to UV filters of benzophenone-6, benzophenone-8, and 4-methylbenzylidene camphor by Ames test

Novel intramolecular rearrangement of 5-carbamoyluracils into barbituric acids

Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors: Synthesis and Biological Evaluation of Arjunolic Acid, Bayogenin, Hederagonic Acid and 4-Epi-hederagonic Acid as Glycogen Phosphorylase Inhibitors

Genetic aetiology of primary adrenal insufficiency in Chinese children

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