Rahier A - Search Results

1

Inhibition of 2,3-oxidosqualene: beta-amyrin-cyclase, S-adenosyl-L-methionine: cycloartenol C-24-methyltransferase and cycloeucalenol: obtusifoliol isomerase by rationally designed molecules containing a tertiary amine function.

Rahier A, Bouvier P, Cattel L, Narula A, Benveniste P. Rahier A, et al. Biochem Soc Trans. 1983 Oct;11(5):537-43. doi: 10.1042/bst0110537. Biochem Soc Trans. 1983. PMID: 6642064

2

Inhibition of 2,3-oxidosqualene cyclases.

Taton M, Benveniste P, Rahier A, Johnson WS, Liu HT, Sudhakar AR. Taton M, et al. Among authors: rahier a. Biochemistry. 1992 Sep 1;31(34):7892-8. doi: 10.1021/bi00149a021. Biochemistry. 1992. PMID: 1510977

3

Inhibition of sterol biosynthesis enzymes in vitro by analogues of high-energy carbocationic intermediates.

Rahier A, Taton M, Benveniste P. Rahier A, et al. Biochem Soc Trans. 1990 Feb;18(1):48-52. doi: 10.1042/bst0180048. Biochem Soc Trans. 1990. PMID: 2185086 Review. No abstract available.

4

Cycloeucalenol-obtusifoliol isomerase. Structural requirements for transformation or binding of substrates and inhibitors.

Rahier A, Taton M, Benveniste P. Rahier A, et al. Eur J Biochem. 1989 May 15;181(3):615-26. doi: 10.1111/j.1432-1033.1989.tb14768.x. Eur J Biochem. 1989. PMID: 2731540 Free article.

5

Potent inhibition of cholesterol biosynthesis in 3T3 fibroblasts by N-[(1,5,9)-trimethyldecyl]-4 alpha,10-dimethyl-8-aza-trans-decal-3 beta-ol, a new 2,3-oxidosqualene cyclase inhibitor.

Gerst N, Duriatti A, Schuber F, Taton M, Benveniste P, Rahier A. Gerst N, et al. Among authors: rahier a. Biochem Pharmacol. 1988 May 15;37(10):1955-64. doi: 10.1016/0006-2952(88)90542-4. Biochem Pharmacol. 1988. PMID: 3377803

6

N-[(1,5,9)-trimethyl-decyl]-4 alpha,10-dimethyl-8-aza-trans-decal-3 beta-ol a novel potent inhibitor of 2,3-oxidosqualene cycloartenol and lanosterol cyclases.

Taton M, Benveniste P, Rahier A. Taton M, et al. Among authors: rahier a. Biochem Biophys Res Commun. 1986 Jul 31;138(2):764-70. doi: 10.1016/s0006-291x(86)80562-9. Biochem Biophys Res Commun. 1986. PMID: 3741433

7

Inhibition of S-adenosyl-L-methionine sterol-C-24-methyltransferase by analogues of a carbocationic ion high-energy intermediate. Structure activity relationships for C-25 heteroatoms (N, As, S) substituted triterpenoid derivatives.

Rahier A, Génot JC, Schuber F, Benveniste P, Narula AS. Rahier A, et al. J Biol Chem. 1984 Dec 25;259(24):15215-23. J Biol Chem. 1984. PMID: 6511791 Free article.

S., Rahier, A., Benveniste, P., and Schuber, F. (1981) J. Am. Chem. Soc. 103, 2408-2409). ...The positive charge leading to inhibition may be conferred by a protonated amine, a quaternary ammonium group, as well as by a sulfonium or an arsonium …

S., Rahier, A., Benveniste, P., and Schuber, F. (1981) J. Am. Chem. Soc. 103, 2408-2409). ...The positive charge leading to in …

8

25-Azacycloartanol, a potent inhibitor of S-adenosyl-L-methionine-sterol-C-24 and C-28 methyltransferases in higher plant cells.

Rahier A, Narula AS, Benveniste P, Schmitt P. Rahier A, et al. Biochem Biophys Res Commun. 1980 Jan 15;92(1):20-5. doi: 10.1016/0006-291x(80)91513-2. Biochem Biophys Res Commun. 1980. PMID: 7356453 No abstract available.

9

Microsomal delta 8,14-sterol delta 14-reductase in higher plants. Characterization and inhibition by analogues of a presumptive carbocationic intermediate of the reduction reaction.

Taton M, Benveniste P, Rahier A. Taton M, et al. Among authors: rahier a. Eur J Biochem. 1989 Nov 20;185(3):605-14. doi: 10.1111/j.1432-1033.1989.tb15156.x. Eur J Biochem. 1989. PMID: 2591378 Free article.

10

Biochemistry and site-directed mutational analysis of Delta7-sterol-C5(6)-desaturase.

Rahier A, Benveniste P, Husselstein T, Taton M. Rahier A, et al. Biochem Soc Trans. 2000 Dec;28(6):799-803. Biochem Soc Trans. 2000. PMID: 11171213

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