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Homophymine A, an Anti-HIV Cyclodepsipeptide from the Sponge Homophymia sp
Homophymine A, an Anti-HIV Cyclodepsipeptide from the Sponge Homophymia sp
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Homophymine A, an Anti-HIV Cyclodepsipeptide from the Sponge Homophymia sp

Journal of organic chemistry, 2008-07, Vol.73 (14), p.5319-5327 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo800583b ;PMID: 18563935 ;CODEN: JOCEAH

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2
Homophymines B-E and A1-E1, a family of bioactive cyclodepsipeptides from the sponge Homophymia sp
Homophymines B-E and A1-E1, a family of bioactive cyclodepsipeptides from the sponge Homophymia sp
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Homophymines B-E and A1-E1, a family of bioactive cyclodepsipeptides from the sponge Homophymia sp

Organic & biomolecular chemistry, 2009-01, Vol.7 (19), p.4037-44 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/b910015f ;PMID: 19763308

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3
Structures of Microfilament Destabilizing Toxins Bound to Actin Provide Insight into Toxin Design and Activity
Structures of Microfilament Destabilizing Toxins Bound to Actin Provide Insight into Toxin Design and Activity
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Structures of Microfilament Destabilizing Toxins Bound to Actin Provide Insight into Toxin Design and Activity

Proceedings of the National Academy of Sciences - PNAS, 2005-10, Vol.102 (41), p.14527-14532 [Peer Reviewed Journal]

Copyright 2005 National Academy of Sciences of the United States of America ;Copyright National Academy of Sciences Oct 11, 2005 ;Copyright © 2005, The National Academy of Sciences 2005 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.0502089102 ;PMID: 16192358

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4
Toward the Synthesis of Reidispongiolide A: An Improved Stereocontrolled Synthesis of the C23-C35 Fragment of Reidispongiolide A
Toward the Synthesis of Reidispongiolide A: An Improved Stereocontrolled Synthesis of the C23-C35 Fragment of Reidispongiolide A
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Toward the Synthesis of Reidispongiolide A: An Improved Stereocontrolled Synthesis of the C23-C35 Fragment of Reidispongiolide A

Letters in organic chemistry, 2004-10, Vol.1 (4), p.308-312 [Peer Reviewed Journal]

ISSN: 1570-1786 ;EISSN: 1875-6255 ;DOI: 10.2174/1570178043400523

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5
Quantum Mechanical Calculation of Coupling Constants in the Configurational Analysis of Flexible Systems: Determination of the Configuration of Callipeltin A
Quantum Mechanical Calculation of Coupling Constants in the Configurational Analysis of Flexible Systems: Determination of the Configuration of Callipeltin A
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Quantum Mechanical Calculation of Coupling Constants in the Configurational Analysis of Flexible Systems: Determination of the Configuration of Callipeltin A

European Journal of Organic Chemistry, 2006-02, Vol.2006 (3), p.604-609 [Peer Reviewed Journal]

Copyright © 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.200500740

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6
Synthesis, Pharmacological Evaluation, and Molecular Modeling Studies of Novel Peptidic CAAX Analogues as Farnesyl-Protein-Transferase Inhibitors
Synthesis, Pharmacological Evaluation, and Molecular Modeling Studies of Novel Peptidic CAAX Analogues as Farnesyl-Protein-Transferase Inhibitors
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Synthesis, Pharmacological Evaluation, and Molecular Modeling Studies of Novel Peptidic CAAX Analogues as Farnesyl-Protein-Transferase Inhibitors

Journal of medicinal chemistry, 2006-03, Vol.49 (6), p.1882-1890 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm0506165 ;PMID: 16539374 ;CODEN: JMCMAR

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7
Isolation of Plakinamine I: A New Steroidal Alkaloid from the Marine Sponge Corticium sp. and Synthesis of an Analogue Model Compound
Isolation of Plakinamine I: A New Steroidal Alkaloid from the Marine Sponge Corticium sp. and Synthesis of an Analogue Model Compound
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Isolation of Plakinamine I: A New Steroidal Alkaloid from the Marine Sponge Corticium sp. and Synthesis of an Analogue Model Compound

European Journal of Organic Chemistry, 2005-10, Vol.2005 (20), p.4359-4363 [Peer Reviewed Journal]

Copyright © 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.200500364

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8
ChemInform Abstract: Total Synthesis of Natural Products (2005)
ChemInform Abstract: Total Synthesis of Natural Products (2005)
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ChemInform Abstract: Total Synthesis of Natural Products (2005)

ChemInform, 2008-01, Vol.39 (2), p.no-no

Copyright © 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0931-7597 ;EISSN: 1522-2667 ;DOI: 10.1002/chin.200802266

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9
ChemInform Abstract: Jaspamides M-P: New Tryptophan Modified Jaspamide Derivatives from the Sponge Jaspis splendans
ChemInform Abstract: Jaspamides M-P: New Tryptophan Modified Jaspamide Derivatives from the Sponge Jaspis splendans
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ChemInform Abstract: Jaspamides M-P: New Tryptophan Modified Jaspamide Derivatives from the Sponge Jaspis splendans

ChemInform, 2009-05, Vol.40 (19), p.no-no

Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0931-7597 ;EISSN: 1522-2667 ;DOI: 10.1002/chin.200919179

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10
Isolation and Structural Elucidation of Callipeltins J-M: Antifungal Peptides from the Marine Sponge Latrunculia sp
Isolation and Structural Elucidation of Callipeltins J-M: Antifungal Peptides from the Marine Sponge Latrunculia sp
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Isolation and Structural Elucidation of Callipeltins J-M: Antifungal Peptides from the Marine Sponge Latrunculia sp

ChemInform, 2007-04, Vol.38 (15), p.no-no

Copyright © 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0931-7597 ;EISSN: 1522-2667 ;DOI: 10.1002/chin.200715184

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11
New Jaspamide Derivatives with Antimicrofilament Activity from the Sponge Jaspis splendans
New Jaspamide Derivatives with Antimicrofilament Activity from the Sponge Jaspis splendans
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New Jaspamide Derivatives with Antimicrofilament Activity from the Sponge Jaspis splendans

ChemInform, 2007-09, Vol.38 (38), p.no-no

Copyright © 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0931-7597 ;EISSN: 1522-2667 ;DOI: 10.1002/chin.200738182

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12
ChemInform Abstract: Coscinolactams A and B: New Nitrogen-Containing Sesterterpenoids from the Marine Sponge Coscinoderma mathewsi Exerting Antiinflammatory Properties
ChemInform Abstract: Coscinolactams A and B: New Nitrogen-Containing Sesterterpenoids from the Marine Sponge Coscinoderma mathewsi Exerting Antiinflammatory Properties
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ChemInform Abstract: Coscinolactams A and B: New Nitrogen-Containing Sesterterpenoids from the Marine Sponge Coscinoderma mathewsi Exerting Antiinflammatory Properties

ChemInform, 2009-08, Vol.40 (33), p.no-no

Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0931-7597 ;EISSN: 1522-2667 ;DOI: 10.1002/chin.200933190

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13
Callipeltins F-I: New Antifungal Peptides from the Marine Sponge Latrunculia sp
Callipeltins F-I: New Antifungal Peptides from the Marine Sponge Latrunculia sp
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Callipeltins F-I: New Antifungal Peptides from the Marine Sponge Latrunculia sp

ChemInform, 2006-05, Vol.37 (20), p.no-no

Copyright © 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0931-7597 ;EISSN: 1522-2667 ;DOI: 10.1002/chin.200620197

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14
Isolation of Plakinamine I: A New Steroidal Alkaloid from the Marine Sponge Corticium sp. and Synthesis of an Analogue Model Compound
Isolation of Plakinamine I: A New Steroidal Alkaloid from the Marine Sponge Corticium sp. and Synthesis of an Analogue Model Compound
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Isolation of Plakinamine I: A New Steroidal Alkaloid from the Marine Sponge Corticium sp. and Synthesis of an Analogue Model Compound

ChemInform, 2006-03, Vol.37 (10), p.no-no

Copyright © 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0931-7597 ;EISSN: 1522-2667 ;DOI: 10.1002/chin.200610197

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