Bigg DC[au] - Search Results

Year	Number of Results
1976	1
1993	1
1995	1
1998	2
1999	3
2000	4
2001	4
2002	1
2004	1
2008	2
2023	0

1

Homocamptothecins: E-ring modified CPT analogues.

Lavergne O, Demarquay D, Kasprzyk PG, Bigg DC. Lavergne O, et al. Among authors: bigg dc. Ann N Y Acad Sci. 2000;922:100-11. doi: 10.1111/j.1749-6632.2000.tb07029.x. Ann N Y Acad Sci. 2000. PMID: 11193885 Review.

2

Synthesis and bioevaluation of 22-hydroxyacuminatine analogs.

Grillet F, Baumlová B, Prévost G, Constant JF, Chaumeron S, Bigg DC, Greene AE, Kanazawa A. Grillet F, et al. Among authors: bigg dc. Bioorg Med Chem Lett. 2008 Mar 15;18(6):2143-6. doi: 10.1016/j.bmcl.2008.01.082. Epub 2008 Jan 30. Bioorg Med Chem Lett. 2008. PMID: 18276141

3

[The other camptothecins: recent advances with camptothecin analogues other than irinotecan and topotecan].

Lavergne O, Bigg DC. Lavergne O, et al. Among authors: bigg dc. Bull Cancer. 1998 Dec;Spec No:51-8. Bull Cancer. 1998. PMID: 9932086 Review. French.

4

New method of synthesis of Vinca alkaloid derivatives.

Fahy J, Thillaye du Boullay V, Bigg DC. Fahy J, et al. Among authors: bigg dc. Bioorg Med Chem Lett. 2002 Feb 11;12(3):505-7. doi: 10.1016/s0960-894x(01)00784-3. Bioorg Med Chem Lett. 2002. PMID: 11814829

5

Topoisomerase I-mediated antiproliferative activity of enantiomerically pure fluorinated homocamptothecins.

Lavergne O, Demarquay D, Bailly C, Lanco C, Rolland A, Huchet M, Coulomb H, Muller N, Baroggi N, Camara J, Le Breton C, Manginot E, Cazaux JB, Bigg DC. Lavergne O, et al. Among authors: bigg dc. J Med Chem. 2000 Jun 1;43(11):2285-9. doi: 10.1021/jm000129j. J Med Chem. 2000. PMID: 10841808

6

Flexible 1-[(2-aminoethoxy)alkyl]-3-ar(o)yl(thio)ureas as novel acetylcholinesterase inhibitors. Synthesis and biochemical evaluation.

Vidaluc JL, Calmel F, Bigg DC, Carilla E, Briley M. Vidaluc JL, et al. Among authors: bigg dc. J Med Chem. 1995 Jul 21;38(15):2969-73. doi: 10.1021/jm00015a020. J Med Chem. 1995. PMID: 7636858

7

Apoptosis induced by the homocamptothecin anticancer drug BN80915 in HL-60 cells.

Lansiaux A, Facompré M, Wattez N, Hildebrand MP, Bal C, Demarquay D, Lavergne O, Bigg DC, Bailly C. Lansiaux A, et al. Among authors: bigg dc. Mol Pharmacol. 2001 Sep;60(3):450-61. Mol Pharmacol. 2001. PMID: 11502875

8

Homocamptothecins: synthesis and antitumor activity of novel E-ring-modified camptothecin analogues.

Lavergne O, Lesueur-Ginot L, Pla Rodas F, Kasprzyk PG, Pommier J, Demarquay D, Prévost G, Ulibarri G, Rolland A, Schiano-Liberatore AM, Harnett J, Pons D, Camara J, Bigg DC. Lavergne O, et al. Among authors: bigg dc. J Med Chem. 1998 Dec 31;41(27):5410-9. doi: 10.1021/jm980400l. J Med Chem. 1998. PMID: 9876111

9

The homocamptothecin BN 80915 is a highly potent orally active topoisomerase I poison.

Demarquay D, Huchet M, Coulomb H, Lesueur-Ginot L, Lavergne O, Kasprzyk PG, Bailly C, Camara J, Bigg DC. Demarquay D, et al. Among authors: bigg dc. Anticancer Drugs. 2001 Jan;12(1):9-19. doi: 10.1097/00001813-200101000-00003. Anticancer Drugs. 2001. PMID: 11272292

10

Binding of antipsychotic drugs at alpha 1A- and alpha 1B-adrenoceptors: risperidone is selective for the alpha 1B-adrenoceptors.

Sleight AJ, Koek W, Bigg DC. Sleight AJ, et al. Among authors: bigg dc. Eur J Pharmacol. 1993 Jul 20;238(2-3):407-10. doi: 10.1016/0014-2999(93)90876-j. Eur J Pharmacol. 1993. PMID: 7691623

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