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Institution

Roussel Uclaf

About: Roussel Uclaf is a based out in . It is known for research contribution in the topics: Alkyl & Alkoxy group. The organization has 1888 authors who have published 2338 publications receiving 36508 citations.
Topics: Alkyl, Alkoxy group, Aryl, Carbon, Carboxylic acid


Papers
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Journal ArticleDOI
TL;DR: The Active Center of the 3-Oxosteroid Δ1-dehydrogenase from Arthrobacter simplex is represented as a cleft in the protein molecule one side of which is in contact with the α-face of the steroid, the other side being located a few tenths of nanometer above the β-face.
Abstract: The Active Center of the 3-Oxosteroid Δ1-dehydrogenase from Arthrobacter simplex The kinetic parameters of the semi-purified, hydrocortisone induced 3-oxosteroid Δ1-dehydrogenase from Arthrobacter simplex have been determined with twenty different steroids. The values thus obtained with nortestosterone and six of its stereoisomers and with derivatives bearing substituents at positions 10, 13 and 17, show that for the reaction to take place, first the presence of a 3-oxo group, a Δ4-double bond and axial hydrogens at 1α and 2β positions, are necessary, secondly no bulky substituents must be present in the middle part of the α-face and at position 4; thirdly at positions 10β and 13β no substituents with more than two carbon atoms must be present. With steroids bearing a methyl group in position 10, the chirality of this center has to be natural, and with 19-norsteroids, the conformation of the whole molecule has to be almost flat. The active center could be represented as a cleft in the protein molecule one side of which is in contact with the α-face of the steroid, the other side being located a few tenths of nanometer above the β-face, The Δ4-double bond is required for the reaction but not for binding. There is no contact point in the area of carbon atom 17.

12 citations

Journal ArticleDOI
Jean Salmon1, D. Coussediere1, C. Cousty1, V. Delaroff1, Jean-Pierre Raynaud1 
01 Oct 1979-Steroids
TL;DR: Reference compounds for the subsequent identification of the metabolites of the potent estrogen, moxestrol (R 2858) in various species were isolated from the bile of phenobarbital pretreated rats or obtained via enzymatic hydroxylation by microorganisms.

12 citations

Journal ArticleDOI
TL;DR: In this paper, a new preparation of dihydro-γ-pyrones derived from forskolin 1 is reported, in which the cuprates are added in good yield in BF3-Et2O.

12 citations

Patent
02 Jun 1967

12 citations


Authors

Showing all 1888 results

NameH-indexPapersCitations
Fernand Labrie11088548308
Lionel H. Opie8451925964
Alain Bélanger7024416469
Michel J. Tremblay5327310485
Pierre Monsan512168049
Samir Z. Zard5057510739
Alejandro Aruffo4712314084
Samuel S.C. Yen47966865
Dominique Maraninchi471888108
Serge Erlinger461528200
Romain Lefebvre402215269
William B. Motherwell393056357
Jean-Pierre Raynaud381045075
André Lemay381144264
Patrick J. Creaven321023435
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20181
20114
20104
20091
20084
20072