Year |
Citation |
Score |
2014 |
Camplo M, Raimundo JM, Navailles L, Grinstaff MW, Barthélémy P. Bioinspired systems in supramolecular chemistry and nanotechnology-introducing the SupraBio themed issue New Journal of Chemistry. 38: 5120-5121. DOI: 10.1039/C4Nj90041C |
0.36 |
|
2012 |
Taib N, Aimé A, Moreau L, Camplo M, Houmadi S, Desbat B, Laguerre M, Grinstaff MW, Bestel I, Barthélémy P. Formation of supramolecular systems via directed Nucleoside-Lipid recognition. Journal of Colloid and Interface Science. 377: 122-30. PMID 22487235 DOI: 10.1016/J.Jcis.2012.03.041 |
0.428 |
|
2012 |
LaManna CM, Lusic H, Camplo M, McIntosh TJ, Barthélémy P, Grinstaff MW. Charge-reversal lipids, peptide-based lipids, and nucleoside-based lipids for gene delivery. Accounts of Chemical Research. 45: 1026-38. PMID 22439686 DOI: 10.1021/Ar200228Y |
0.496 |
|
2011 |
Camplo M, Wathier M, Chow J, Grinstaff MW. A versatile reagent to synthesize diverse ionic liquids ranging from small molecules and dendrimers to functionalized proteins. Chemical Communications (Cambridge, England). 47: 2128-30. PMID 21180737 DOI: 10.1039/C0Cc04459H |
0.442 |
|
2010 |
Ceballos C, Khiati S, Prata CA, Zhang XX, Giorgio S, Marsal P, Grinstaff MW, Barthélémy P, Camplo M. Cationic nucleoside lipids derived from universal bases: A rational approach for siRNA transfection. Bioconjugate Chemistry. 21: 1062-9. PMID 20481514 DOI: 10.1021/Bc100005K |
0.515 |
|
2009 |
Ceballos C, Prata CA, Giorgio S, Garzino F, Payet D, Barthélémy P, Grinstaff MW, Camplo M. Cationic nucleoside lipids based on a 3-nitropyrrole universal base for siRNA delivery. Bioconjugate Chemistry. 20: 193-6. PMID 19159294 DOI: 10.1021/Bc800432N |
0.525 |
|
2008 |
Moreau L, Camplo M, Wathier M, Taib N, Laguerre M, Bestel I, Grinstaff MW, Barthélémy P. Real time imaging of supramolecular assembly formation via programmed nucleolipid recognition. Journal of the American Chemical Society. 130: 14454-5. PMID 18850703 DOI: 10.1021/Ja805974G |
0.412 |
|
2008 |
Gissot A, Camplo M, Grinstaff MW, Barthélémy P. Nucleoside, nucleotide and oligonucleotide based amphiphiles: a successful marriage of nucleic acids with lipids. Organic & Biomolecular Chemistry. 6: 1324-33. PMID 18385837 DOI: 10.1039/B719280K |
0.488 |
|
2006 |
Chabaud P, Camplo M, Payet D, Serin G, Moreau L, Barthélémy P, Grinstaff MW. Cationic nucleoside lipids for gene delivery. Bioconjugate Chemistry. 17: 466-72. PMID 16536479 DOI: 10.1021/Bc050162Q |
0.507 |
|
2006 |
Barral K, Balzarini J, Neyts J, De Clercq E, Hider RC, Camplo M. Synthesis and antiviral evaluation of cyclic and acyclic 2-methyl-3-hydroxy-4-pyridinone nucleoside derivatives. Journal of Medicinal Chemistry. 49: 43-50. PMID 16392791 DOI: 10.1021/Jm0504306 |
0.301 |
|
2000 |
Mourier N, Camplo M, Della Bruna GS, Pellacini F, Ungheri D, Chermann JC, Kraus JL. Synthesis and anti-HIV evaluation of new 2',3'-dideoxy-3'-thiacytidine prodrugs Nucleosides, Nucleotides and Nucleic Acids. 19: 1057-1091. PMID 10999248 DOI: 10.1080/15257770008035031 |
0.402 |
|
1998 |
Bouygues M, Medou M, Quéléver G, Chermann JC, Camplo M, Kraus JL. Syntheses of new modified Phe-Pro peptides. Use of proline replacements in potential HIV inhibitors Bioorganic and Medicinal Chemistry Letters. 8: 277-280. PMID 9871669 DOI: 10.1016/S0960-894X(98)00006-7 |
0.406 |
|
1998 |
Dessolin J, Vlieghe P, Bouygues M, Medou M, Quéléver G, Camplo M, Chermann JC, Kraus JL. Tri-N-Boc-tetraazamacrocycle-nucleoside conjugates: Synthesis and anti- HIV activities Nucleosides and Nucleotides. 17: 957-968. PMID 9708333 DOI: 10.1080/07328319808003466 |
0.418 |
|
1998 |
Trabaud C, Dessolin J, Camplo M, Kraus LJ. Synthesis of New Tetrakis N-Substituted Tetra-Azamacrocycles Synthetic Communications. 28: 311-317. DOI: 10.1080/00397919808005724 |
0.338 |
|
1998 |
Bouygues M, Medou M, Chermann JC, Camplo M, Kraus JL. Short and unexpectedly potent 3-pyrrolidinone type inhibitors of HIV-1 replication European Journal of Medicinal Chemistry. 33: 445-450. DOI: 10.1016/S0223-5234(98)80045-7 |
0.352 |
|
1998 |
Medou M, Priem G, Quélever G, Camplo M, Kraus JL. Synthesis of new 7-membered α-phenylthio cyclic oxamides: HIV inhibitors Tetrahedron Letters. 39: 4021-4024. DOI: 10.1016/S0040-4039(98)00680-7 |
0.362 |
|
1998 |
Dessolin J, Quéléver G, Camplo M, Kraus JL. Syntheses of new unsymmetrical bispolyazamacrocycles Tetrahedron Letters. 39: 853-856. DOI: 10.1016/S0040-4039(97)10748-1 |
0.338 |
|
1997 |
Hantz O, Borel C, Trabaud C, Zoulim F, Dessolin J, Camplo M, Vlieghe P, Bouygues M, Trepo C, Kraus JL. Selective inhibition of the duck hepatitis B virus by a new class of tetraazamacrocycles. Antimicrobial Agents and Chemotherapy. 41: 2579-81. PMID 9371374 DOI: 10.1128/Aac.41.11.2579 |
0.301 |
|
1997 |
Sondhi SM, Verma RP, Sharma VK, Singhal N, Kraus JL, Camplo M, Chermann J. SYNTHESIS AND ANTI-HIV SCREENING OF SOME HETEROCYCLIC COMPOUNDS Phosphorus, Sulfur, and Silicon and the Related Elements. 122: 215-225. DOI: 10.1080/10426509708043511 |
0.365 |
|
1997 |
Trabaud C, Dessolin J, Vlieghe P, Bouygues M, Chermann JC, Camplo M, Kraus JL. Modelisation, synthesis and anti-HIV activities of N,N,N',N',N'-pentakis-tetraazamacrocycles salts derivatives Bioorganic and Medicinal Chemistry Letters. 7: 1353-1358. DOI: 10.1016/S0960-894X(97)00222-9 |
0.374 |
|
1997 |
Niddam V, Medou M, Dessolin J, Trabaud C, Camplo M, Kraus J. Urea cyclisation reaction studies Journal of Heterocyclic Chemistry. 34: 829-833. DOI: 10.1002/Jhet.5570340320 |
0.34 |
|
1996 |
Mourier N, Trabaud C, Niddam V, Graciet J, Camplo M, Chermann J, Kraus J. Synthesis and Anti-HIV Evaluation of New 5-Substituted-2′,3′-Dideoxy-3′-thiauridine Nucleosides Nucleosides, Nucleotides & Nucleic Acids. 15: 1397-1409. DOI: 10.1080/07328319608002439 |
0.42 |
|
1996 |
Graciet JC, Niddam V, Gamberoni M, Trabaud C, Dessolin J, Medou M, Mourier N, Zoulim F, Borel C, Hantz O, Camplo M, Chermann JC, Kraus JL. Modelisation, synthesis and antiviral evaluation of new 2,3-disubstituted thiazolidinone nucleoside analogues Bioorganic and Medicinal Chemistry Letters. 6: 1775-1780. DOI: 10.1016/0960-894X(96)00316-2 |
0.395 |
|
1996 |
Niddam V, Camplo M, Le Nguyen D, Chermann JC, Kraus JL. Thiophenoxy peptides : A new class of HIV replication inhibitors Bioorganic and Medicinal Chemistry Letters. 6: 609-614. DOI: 10.1016/0960-894X(96)00085-6 |
0.332 |
|
1996 |
Camplo M, Charvet-Faury AS, Borel C, Turin F, Hantz O, Trabaud C, Niddam V, Mourier N, Graciet JC, Chermann JC, Kraus JL. Synthesis and antiviral activity of N-4'-dihydropyridinyl and dihydroquinolinylcarbonyl-2-hydroxymethyl-5-[cytosin-1'-yl]-1, 3-oxathiolane derivatives against human immunodeficiency virus and duck hepatitis B virus European Journal of Medicinal Chemistry. 31: 539-546. DOI: 10.1016/0223-5234(96)89550-X |
0.338 |
|
1995 |
Mourier N, Trabaud C, Graciet JC, Simon V, Niddam V, Faury P, Charvet AS, Camplo M, Chermann J, Kraus JL. Peptide-Nucleoside Conjugates: Synthesis and Anti-HIV Activities Nucleosides, Nucleotides & Nucleic Acids. 14: 1393-1402. DOI: 10.1080/15257779508010699 |
0.403 |
|
1995 |
Graciet JC, Faury P, Camplo M, Charvet AS, Mourier N, Trabaud C, Niddam V, Simon V, Kraus JL. Synthesis of New Thiazolidinone Nucleoside Analogues Nucleosides, Nucleotides & Nucleic Acids. 14: 1379-1392. DOI: 10.1080/15257779508010698 |
0.327 |
|
1995 |
Camplo M, Niddam V, Barthélémy P, Faury P, Mourier N, Simon V, Charvet AS, Trabaud C, Graciet JC, Chermann JC, Kraus JL. Synthesis and anti-human immunodeficiency virus type 1 activities of new peptido-nucleoside analogues European Journal of Medicinal Chemistry. 30: 789-800. DOI: 10.1016/0223-5234(96)88298-5 |
0.409 |
|
1994 |
Charvet AS, Camplo M, Faury P, Graciet JC, Mourier N, Chermann JC, Kraus JL. Inhibition of human immunodeficiency virus type 1 replication by phosphonoformate- and phosphonoacetate-2′,3′-dideoxy-3′-thiacytidine conjugates Journal of Medicinal Chemistry. 37: 2216-2223. PMID 8035429 DOI: 10.1021/Jm00040A014 |
0.397 |
|
1994 |
Charvet AS, Turin F, Faury P, Hantz O, Camplo M, Mourier N, Berthillon P, Graciet JC, Chermann JC, Trépo C, Kraus JL. Synthesis and antiviral activity of new carbonylphosphonate 2′,3′-dideoxy-3′-thiacytidine conjugates Antiviral Research. 25: 161-168. PMID 7847877 DOI: 10.1016/0166-3542(94)90104-X |
0.395 |
|
1994 |
Camplo M, Faury P, Charvet A, Graciet J, Chermann J, Kraus J. Synthesis and comparative anti-HIV activities of new acetylated 2′,3′-dideoxy-3′-thiacytidine analogues European Journal of Medicinal Chemistry. 29: 357-362. DOI: 10.1016/0223-5234(94)90060-4 |
0.384 |
|
1994 |
Faury P, Camplo M, Charvet A, Mourier N, Barthelemy P, Graciet J, Kraus J. Approaches toward the synthesis of 2,5-disubstituted-1,3-thiazolidines Journal of Heterocyclic Chemistry. 31: 1465-1471. DOI: 10.1002/Jhet.5570310630 |
0.335 |
|
1993 |
Camplo M, Faury P, Charvet AS, Lederer F, Chermann JC, Kraus JL. Synthesis and biological evaluation of a new N4-(N-formyl peptide)- 2',3'-dideoxy-3'-thiacytidine as anti-HIV prodrug Nucleosides and Nucleotides. 12: 631-641. DOI: 10.1080/07328319308019017 |
0.409 |
|
1992 |
Faury P, Camplo M, Charvet A, Chermann J, Kraus J. Synthesis of tetrazole oxathiolane nucleoside analogues and their evaluation as HIV-1 antiviral agents Nucleosides, Nucleotides & Nucleic Acids. 11: 1481-1488. DOI: 10.1080/07328319208021190 |
0.387 |
|
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