Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity.

Lionel Pochet; Caroline Doucet; Marc Schynts; N Thirry; Nicole Boggetto; Bernard Pirotte; KY Jiang; Bernard Masereel; Pascal de Tullio; Jacques Delarge; Michèle Reboud-Ravaux

Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity.

Lionel Pochet, Caroline Doucet, Marc Schynts, N Thirry, Nicole Boggetto, Bernard Pirotte, KY Jiang, Bernard Masereel, Pascal de Tullio, Jacques Delarge, Michèle Reboud-Ravaux

Namur Research Institute for Life Sciences

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	2579-2585
Number of pages	7
Journal	Journal of Medicinal Chemistry
Volume	1996
Publication status	Published - 1996

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Pochet, L., Doucet, C., Schynts, M., Thirry, N., Boggetto, N., Pirotte, B., Jiang, KY., Masereel, B., de Tullio, P., Delarge, J., & Reboud-Ravaux, M. (1996). Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity. Journal of Medicinal Chemistry, 1996, 2579-2585.

Pochet, Lionel ; Doucet, Caroline ; Schynts, Marc ; Thirry, N ; Boggetto, Nicole ; Pirotte, Bernard ; Jiang, KY ; Masereel, Bernard ; de Tullio, Pascal ; Delarge, Jacques ; Reboud-Ravaux, Michèle. / Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity. In: Journal of Medicinal Chemistry. 1996 ; Vol. 1996. pp. 2579-2585.

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title = "Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity.",

author = "Lionel Pochet and Caroline Doucet and Marc Schynts and N Thirry and Nicole Boggetto and Bernard Pirotte and KY Jiang and Bernard Masereel and {de Tullio}, Pascal and Jacques Delarge and Mich{\`e}le Reboud-Ravaux",

year = "1996",

language = "English",

volume = "1996",

pages = "2579--2585",

journal = "J. Med. Chem.",

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publisher = "American Chemical Society",

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Pochet, L, Doucet, C, Schynts, M, Thirry, N, Boggetto, N, Pirotte, B, Jiang, KY, Masereel, B, de Tullio, P, Delarge, J & Reboud-Ravaux, M 1996, 'Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity.', Journal of Medicinal Chemistry, vol. 1996, pp. 2579-2585.

Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity. / Pochet, Lionel; Doucet, Caroline; Schynts, Marc; Thirry, N; Boggetto, Nicole; Pirotte, Bernard; Jiang, KY; Masereel, Bernard; de Tullio, Pascal; Delarge, Jacques; Reboud-Ravaux, Michèle.

In: Journal of Medicinal Chemistry, Vol. 1996, 1996, p. 2579-2585.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: Significance of the «aromatic» nature of the novel ester-type coumarin for strong inhibitory activity.

AU - Pochet, Lionel

AU - Doucet, Caroline

AU - Schynts, Marc

AU - Thirry, N

AU - Boggetto, Nicole

AU - Pirotte, Bernard

AU - Jiang, KY

AU - Masereel, Bernard

AU - de Tullio, Pascal

AU - Delarge, Jacques

AU - Reboud-Ravaux, Michèle

PY - 1996

Y1 - 1996

M3 - Article

VL - 1996

SP - 2579

EP - 2585

JO - J. Med. Chem.

JF - J. Med. Chem.

SN - 0022-2623

ER -