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Refinado por: Nome da Publicação: Journal Of Medicinal Chemistry remover
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1
Aldosterone antagonists. II: New 7α-(acetylthio)-15,16-methylene spirolactones
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Aldosterone antagonists. II: New 7α-(acetylthio)-15,16-methylene spirolactones

NICKISCH, K ; BITTLER, D ; LAURENT, H ; LOSERT, W ; CASALS-STENZEL, J ; NISHINO, Y ; SCHILLINGER, E ; WIECHERT, R

Journal of medicinal chemistry, 1987, Vol.30 (8), p.1403-1409 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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2
Aldosterone antagonists. 2. New 7 alpha-(acetylthio)-15,16-methylene spirolactones
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Aldosterone antagonists. 2. New 7 alpha-(acetylthio)-15,16-methylene spirolactones

Nickisch, K ; Bittler, D ; Laurent, H ; Losert, W ; Casals-Stenzel, J ; Nishino, Y ; Schillinger, E ; Wiechert, R

Journal of medicinal chemistry, 1987-08, Vol.30 (8), p.1403-1409 [Periódico revisado por pares]

United States

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3
Aldosterone antagonists. III: Synthesis and activities of steroidal 7α-(alkoxycarbonyl)-15,16-methylene spiroldactones
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Artigo
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Aldosterone antagonists. III: Synthesis and activities of steroidal 7α-(alkoxycarbonyl)-15,16-methylene spiroldactones

NICKISCH, K ; BITTLER, D ; LAURENT, H ; LOSERT, W ; NISHINO, Y ; SCHILLINGER, E ; WIECHERT, R

Journal of medicinal chemistry, 1990, Vol.33 (2), p.509-513 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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4
Aldosterone antagonists. 3. Synthesis and activities of steroidal 7 alpha-(alkoxycarbonyl)-15,16-methylene spirolactones
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Artigo
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Aldosterone antagonists. 3. Synthesis and activities of steroidal 7 alpha-(alkoxycarbonyl)-15,16-methylene spirolactones

Nickisch, K ; Bittler, D ; Laurent, H ; Losert, W ; Nishino, Y ; Schillinger, E ; Wiechert, R

Journal of medicinal chemistry, 1990-02, Vol.33 (2), p.509-513 [Periódico revisado por pares]

United States

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5
Aldosterone antagonists. IV, Synthesis and activities of steroidal 6,6-ethylene-15,16-methylene 17-spirolactones
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Artigo
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Aldosterone antagonists. IV, Synthesis and activities of steroidal 6,6-ethylene-15,16-methylene 17-spirolactones

NICKISCH, K ; BEIER, S ; BITTLER, D ; ELGER, W ; LAURENT, H ; LOSERT, W ; NISHINO, Y ; SCHILLINGER, E ; WIECHERT, R

Journal of medicinal chemistry, 1991, Vol.34 (8), p.2464-2468 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
Aldosterone antagonists. 4. Synthesis and activities of steroidal 6,6-ethylene-15,16-methylene 17-spirolactones
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Aldosterone antagonists. 4. Synthesis and activities of steroidal 6,6-ethylene-15,16-methylene 17-spirolactones

Nickisch, Klaus ; Beier, Sybille ; Bittler, Dieter ; Elger, Walter ; Laurent, Henry ; Losert, Wolfgang ; Nishino, Yukishige ; Schillinger, Ekkehard ; Wiechert, Rudolf

Journal of medicinal chemistry, 1991-08, Vol.34 (8), p.2464-2468 [Periódico revisado por pares]

United States: American Chemical Society

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7
Synthesis and antibronchospastic activity of 8-alkoxy- and 8-(alkylamino)imidazo[1,2-a]pyrazines
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Synthesis and antibronchospastic activity of 8-alkoxy- and 8-(alkylamino)imidazo[1,2-a]pyrazines

Bonnet, Pierre A ; Michel, Alain ; Laurent, Florence ; Sablayrolles, Claire ; Rechencq, Eliane ; Mani, Jean C ; Boucard, Maurice ; Chapat, Jean P

Journal of medicinal chemistry, 1992-09, Vol.35 (18), p.3353-3358 [Periódico revisado por pares]

WASHINGTON: American Chemical Society

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8
Active site-directed synthetic thrombin inhibitors: synthesis, in vitro and in vivo activity profile of BMY 44621 and analogs. An examination of the role of the amino group in the D-Phe-Pro-Arg-H series
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Active site-directed synthetic thrombin inhibitors: synthesis, in vitro and in vivo activity profile of BMY 44621 and analogs. An examination of the role of the amino group in the D-Phe-Pro-Arg-H series

Balasubramanian, N ; St. Laurent, D. R ; Federici, M. E ; Meanwell, N. A ; Wright, J. J ; Schumacher, W. A ; Seiler, S. M

Journal of medicinal chemistry, 1993, Vol.36 (2), p.300-303 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
Synthetic Routes to 4-Amino-3-carboxy-.beta.-carboline Derivatives: Incidental Formation of Novel Furo[3,4-c]-.beta.-carbolin-2-ones Displaying High Affinities for the Benzodiazepine Receptor
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Synthetic Routes to 4-Amino-3-carboxy-.beta.-carboline Derivatives: Incidental Formation of Novel Furo[3,4-c]-.beta.-carbolin-2-ones Displaying High Affinities for the Benzodiazepine Receptor

Dorey, Gilbert ; Dubois, Laurent ; Prado de Carvalho, Lia Prdo ; Potier, Pierre ; Dodd, Robert H

Journal of medicinal chemistry, 1995-01, Vol.38 (1), p.189-198 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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10
Paullones, a Series of Cyclin-Dependent Kinase Inhibitors:  Synthesis, Evaluation of CDK1/Cyclin B Inhibition, and in Vitro Antitumor Activity
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Paullones, a Series of Cyclin-Dependent Kinase Inhibitors:  Synthesis, Evaluation of CDK1/Cyclin B Inhibition, and in Vitro Antitumor Activity

Schultz, Christiane ; Link, Andreas ; Leost, Maryse ; Zaharevitz, Daniel W ; Gussio, Rick ; Sausville, Edward A ; Meijer, Laurent ; Kunick, Conrad

Journal of medicinal chemistry, 1999-07, Vol.42 (15), p.2909-2919 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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