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1
Hijacking SARS-CoV-2/ACE2 Receptor Interaction by Natural and Semi-synthetic Steroidal Agents Acting on Functional Pockets on the Receptor Binding Domain
Hijacking SARS-CoV-2/ACE2 Receptor Interaction by Natural and Semi-synthetic Steroidal Agents Acting on Functional Pockets on the Receptor Binding Domain
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Hijacking SARS-CoV-2/ACE2 Receptor Interaction by Natural and Semi-synthetic Steroidal Agents Acting on Functional Pockets on the Receptor Binding Domain

Frontiers in chemistry, 2020-10, Vol.8, p.572885-572885 [Peer Reviewed Journal]

Copyright © 2020 Carino, Moraca, Fiorillo, Marchianò, Sepe, Biagioli, Finamore, Bozza, Francisci, Distrutti, Catalanotti, Zampella and Fiorucci. ;Copyright © 2020 Carino, Moraca, Fiorillo, Marchianò, Sepe, Biagioli, Finamore, Bozza, Francisci, Distrutti, Catalanotti, Zampella and Fiorucci. 2020 Carino, Moraca, Fiorillo, Marchianò, Sepe, Biagioli, Finamore, Bozza, Francisci, Distrutti, Catalanotti, Zampella and Fiorucci ;ISSN: 2296-2646 ;EISSN: 2296-2646 ;DOI: 10.3389/fchem.2020.572885 ;PMID: 33195060

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2
Discovering New G-Quadruplex DNA Catalysts in Enantioselective Sulfoxidation Reaction
Discovering New G-Quadruplex DNA Catalysts in Enantioselective Sulfoxidation Reaction
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Discovering New G-Quadruplex DNA Catalysts in Enantioselective Sulfoxidation Reaction

International journal of molecular sciences, 2022-01, Vol.23 (3), p.1092 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms23031092 ;PMID: 35163018

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3
Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor (FXR) Antagonists/Pregnane X Receptor (PXR) Agonists
Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor (FXR) Antagonists/Pregnane X Receptor (PXR) Agonists
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Expanding the Library of 1,2,4-Oxadiazole Derivatives: Discovery of New Farnesoid X Receptor (FXR) Antagonists/Pregnane X Receptor (PXR) Agonists

Molecules (Basel, Switzerland), 2023-03, Vol.28 (6), p.2840 [Peer Reviewed Journal]

2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules28062840 ;PMID: 36985811

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4
Introduction of Nonacidic Side Chains on 6-Ethylcholane Scaffolds in the Identification of Potent Bile Acid Receptor Agonists with Improved Pharmacokinetic Properties
Introduction of Nonacidic Side Chains on 6-Ethylcholane Scaffolds in the Identification of Potent Bile Acid Receptor Agonists with Improved Pharmacokinetic Properties
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Introduction of Nonacidic Side Chains on 6-Ethylcholane Scaffolds in the Identification of Potent Bile Acid Receptor Agonists with Improved Pharmacokinetic Properties

Molecules (Basel, Switzerland), 2019-03, Vol.24 (6), p.1043 [Peer Reviewed Journal]

2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 by the authors. 2019 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules24061043 ;PMID: 30884797

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5
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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6
The First Total Synthesis of Solomonsterol B, a Marine Pregnane X Receptor Agonist
The First Total Synthesis of Solomonsterol B, a Marine Pregnane X Receptor Agonist
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The First Total Synthesis of Solomonsterol B, a Marine Pregnane X Receptor Agonist

European journal of organic chemistry, 2012-09, Vol.2012 (27), p.5187-5194 [Peer Reviewed Journal]

Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 INIST-CNRS ;Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.201200619

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7
Plakilactones G and H from a marine sponge. Stereochemical determination of highly flexible systems by quantitative NMR-derived interproton distances combined with quantum mechanical calculations of 13C chemical shifts
Plakilactones G and H from a marine sponge. Stereochemical determination of highly flexible systems by quantitative NMR-derived interproton distances combined with quantum mechanical calculations of 13C chemical shifts
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Plakilactones G and H from a marine sponge. Stereochemical determination of highly flexible systems by quantitative NMR-derived interproton distances combined with quantum mechanical calculations of 13C chemical shifts

Beilstein journal of organic chemistry, 2013-12, Vol.9 (1), p.2940-2949 [Peer Reviewed Journal]

Copyright © 2013, Di Micco et al. 2013 Di Micco et al. ;ISSN: 1860-5397 ;EISSN: 1860-5397 ;DOI: 10.3762/bjoc.9.331 ;PMID: 24454574

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8
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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9
New tridecapeptides of the theonellapeptolide family from the Indonesian sponge Theonella swinhoei
New tridecapeptides of the theonellapeptolide family from the Indonesian sponge Theonella swinhoei
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New tridecapeptides of the theonellapeptolide family from the Indonesian sponge Theonella swinhoei

Beilstein journal of organic chemistry, 2013-08, Vol.9 (1), p.1643-1651 [Peer Reviewed Journal]

Copyright © 2013, Sinisi et al. 2013 Sinisi et al. ;ISSN: 1860-5397 ;EISSN: 1860-5397 ;DOI: 10.3762/bjoc.9.188 ;PMID: 24062824

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10
Amphiasterins: a new family of cytotoxic metabolites from the marine sponge Plakortis quasiamphiaster
Amphiasterins: a new family of cytotoxic metabolites from the marine sponge Plakortis quasiamphiaster
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Amphiasterins: a new family of cytotoxic metabolites from the marine sponge Plakortis quasiamphiaster

Tetrahedron, 2001-01, Vol.57 (1), p.257-263 [Peer Reviewed Journal]

ISSN: 0040-4020 ;EISSN: 1464-5416 ;DOI: 10.1016/S0040-4020(00)01009-7

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11
Callipeltins B and C; bioactive peptides from a marine Lithistida sponge Callipelta sp
Callipeltins B and C; bioactive peptides from a marine Lithistida sponge Callipelta sp
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Callipeltins B and C; bioactive peptides from a marine Lithistida sponge Callipelta sp

Tetrahedron, 1996-07, Vol.52 (28), p.9589-9596 [Peer Reviewed Journal]

1996 ;ISSN: 0040-4020 ;EISSN: 1464-5416 ;DOI: 10.1016/0040-4020(96)00496-6

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12
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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13
Isolation and structural elucidation of the crellastatins I-M: cytotoxic bis-steroid derivatives from the vanuatu marine sponge Crella sp
Isolation and structural elucidation of the crellastatins I-M: cytotoxic bis-steroid derivatives from the vanuatu marine sponge Crella sp
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Isolation and structural elucidation of the crellastatins I-M: cytotoxic bis-steroid derivatives from the vanuatu marine sponge Crella sp

Tetrahedron, 1999-11, Vol.55 (48), p.13749-13756 [Peer Reviewed Journal]

1999 ;ISSN: 0040-4020 ;EISSN: 1464-5416 ;DOI: 10.1016/S0040-4020(99)00858-3

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14
Discovery of a Novel Class of Dual GPBAR1 Agonists–RORγt Inverse Agonists for the Treatment of IL-17-Mediated Disorders
Discovery of a Novel Class of Dual GPBAR1 Agonists–RORγt Inverse Agonists for the Treatment of IL-17-Mediated Disorders
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Discovery of a Novel Class of Dual GPBAR1 Agonists–RORγt Inverse Agonists for the Treatment of IL-17-Mediated Disorders

ACS omega, 2023-02, Vol.8 (6), p.5983-5994 [Peer Reviewed Journal]

2023 The Authors. Published by American Chemical Society ;2023 The Authors. Published by American Chemical Society. ;2023 The Authors. Published by American Chemical Society 2023 The Authors ;ISSN: 2470-1343 ;EISSN: 2470-1343 ;DOI: 10.1021/acsomega.2c07907 ;PMID: 36816679

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15
Epoxide functionalization on cholane side chains in the identification of G-protein coupled bile acid receptor (GPBAR1) selective agonists
Epoxide functionalization on cholane side chains in the identification of G-protein coupled bile acid receptor (GPBAR1) selective agonists
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Epoxide functionalization on cholane side chains in the identification of G-protein coupled bile acid receptor (GPBAR1) selective agonists

RSC advances, 2017-01, Vol.7 (52), p.32877-32885 [Peer Reviewed Journal]

ISSN: 2046-2069 ;EISSN: 2046-2069 ;DOI: 10.1039/C7RA04922F

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16
Callipeltoside A:  A Cytotoxic Aminodeoxy Sugar-Containing Macrolide of a New Type from the Marine Lithistida Sponge Callipelta sp
Callipeltoside A:  A Cytotoxic Aminodeoxy Sugar-Containing Macrolide of a New Type from the Marine Lithistida Sponge Callipelta sp
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Callipeltoside A:  A Cytotoxic Aminodeoxy Sugar-Containing Macrolide of a New Type from the Marine Lithistida Sponge Callipelta sp

Journal of the American Chemical Society, 1996-11, Vol.118 (45), p.11085-11088 [Peer Reviewed Journal]

Copyright © 1996 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja9621004

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17
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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18
Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp
Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp
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Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp

Journal of the American Chemical Society, 1996-07, Vol.118 (26), p.6202-6209 [Peer Reviewed Journal]

Copyright © 1996 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja954287p

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19
Callipeltosides B and C, two novel cytotoxic glycoside macrolides from a marine lithistida sponge Callipelta sp
Callipeltosides B and C, two novel cytotoxic glycoside macrolides from a marine lithistida sponge Callipelta sp
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Callipeltosides B and C, two novel cytotoxic glycoside macrolides from a marine lithistida sponge Callipelta sp

Tetrahedron, 1997-03, Vol.53 (9), p.3243-3248 [Peer Reviewed Journal]

1997 ;ISSN: 0040-4020 ;EISSN: 1464-5416 ;DOI: 10.1016/S0040-4020(97)00035-5

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20
Stereochemical Studies on Sphinxolide: Advances in the J-Based NMR Determination of the Relative Configuration of Flexible Systems
Stereochemical Studies on Sphinxolide: Advances in the J-Based NMR Determination of the Relative Configuration of Flexible Systems
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Stereochemical Studies on Sphinxolide: Advances in the J-Based NMR Determination of the Relative Configuration of Flexible Systems

European journal of organic chemistry, 2001-01, Vol.2001 (1), p.39-44 [Peer Reviewed Journal]

2001 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/1099-0690(200101)2001:1<39::AID-EJOC39>3.0.CO;2-9

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