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Anti-infective Discorhabdins from a Deep-Water Alaskan Sponge of the Genus Latrunculia
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/s0040-4020(01)86737-5openalex-snapshot
Cytotoxic pigments from new zealand sponges of the genus latrunculia : discorhabdins a, b and c
inferredcites →https://doi.org/10.1021/jo00105a047openalex-snapshot
Natural and Synthetic Derivatives of Discorhabdin C, a Cytotoxic Pigment from the New Zealand Sponge Latrunculia cf. bocagei
inferredcites →https://doi.org/10.1021/jo00376a096openalex-snapshot
Discorhabdin C, a highly cytotoxic pigment from a sponge of the genus Latrunculia
inferredcites →https://doi.org/10.1021/jo00376a097openalex-snapshot
Dramatic effects of oxygen substituents on 1,3-asymmetric induction in additions of allyltriphenylstannane to .beta.-alkoxy aldehydes: a chemical and spectroscopic investigation
inferredcites →https://doi.org/10.1021/jo070302kopenalex-snapshot
Determination of the Absolute Configuration of a Chiral Oxadiazol-3-one Calcium Channel Blocker, Resolved Using Chiral Chromatography, via Concerted Density Functional Theory Calculations of Its Vibrational Circular Dichroism, Electronic Circular Dichroism, and Optical Rotation
inferredcites →https://doi.org/10.1021/jo071134zopenalex-snapshot
Theoretical Calculation of Electronic Circular Dichroism of the Rotationally Restricted 3,8‘ ‘-Biflavonoid Morelloflavone
inferredcites →https://doi.org/10.1021/jo801622nopenalex-snapshot
Enantiomeric Discorhabdin Alkaloids and Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra
inferredcites →https://doi.org/10.1021/jp0275802openalex-snapshot
Systematic Investigation of Modern Quantum Chemical Methods to Predict Electronic Circular Dichroism Spectra
inferredcites →https://doi.org/10.1021/jp075046uopenalex-snapshot
The Current State of Ab Initio Calculations of Optical Rotation and Electronic Circular Dichroism Spectra
inferredcites →https://doi.org/10.1021/np0303761openalex-snapshot
Discorhabdins I and L, Cytotoxic Alkaloids from the Sponge Latrunculia brevis
inferredcites →https://doi.org/10.1021/np034084bopenalex-snapshot
Cytotoxic Pyrroloiminoquinones from Four New Species of South African Latrunculid Sponges
inferredcites →https://doi.org/10.1021/np0601399openalex-snapshot
Manzamine B and E and Ircinal A Related Alkaloids from an Indonesian Acanthostrongylophora Sponge and Their Activity against Infectious, Tropical Parasitic, and Alzheimer's Diseases
inferredcites →https://doi.org/10.1021/np50124a020openalex-snapshot
Discorhabdin Alkaloids from the Antarctic Sponge Latrunculia apicalis
inferredcites →https://doi.org/10.1021/np800146vopenalex-snapshot
Theoretical Calculation of Electronic Circular Dichroism of a Hexahydroxydiphenoyl-Containing Flavanone Glycoside
inferredcites →https://doi.org/10.1021/np8007667openalex-snapshot
Discorhabdins Revisited: Cytotoxic Alkaloids from Southern Australian Marine Sponges of the Genera Higginsia and Spongosorites
inferredcites →https://doi.org/10.1039/b407299popenalex-snapshot
Pyrroloiminoquinone and related metabolites from marine sponges
inferredcites →https://doi.org/10.1039/b515476fopenalex-snapshot
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
inferredcites →https://doi.org/10.1128/aac.41.5.1004openalex-snapshot
Microplate alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium
inferredcites →https://doi.org/10.1128/aac.47.1.244-254.2003openalex-snapshot
Ribonucleoside Analogue That Blocks Replication of Bovine Viral Diarrhea and Hepatitis C Viruses in Culture
inferredcites →https://doi.org/10.1128/aac.48.11.4450-4452.2004openalex-snapshot
Antimicrobial and Antileishmanial Activities of Hypocrellins A and B
inferredcites →https://doi.org/10.11646/zootaxa.1155.1.1openalex-snapshot
New species of Poecilosclerida (Demospongiae, Porifera) from the Aleutian Islands, Alaska, USA
inferredcites →https://doi.org/10.11646/zootaxa.1250.1.1openalex-snapshot
New species of deep-sea demosponges (Porifera) from the Aleutian Islands (Alaska, USA)
inferredcites →https://doi.org/10.11646/zootaxa.371.1.1openalex-snapshot
South African Latrunculiidae (Porifera: Demospongiae: Poecilosclerida): descriptions of new species of Latrunculia du Bocage, Strongylodesma Lévi, and Tsitsikamma Samaai & Kelly
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4121.1.1zenodo-depositor-declared
New taxa and arrangements within the family Latrunculiidae (Demospongiae, Poecilosclerida)
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod192openalex-snapshot
Porifera (Sponges)–2
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/9783527634606.ch5openalex-snapshot
Biomimetic Synthesis of Alkaloids with a Modified Indole Nucleus
inferred← citeshttps://doi.org/10.1002/9783527694082.ch3openalex-snapshot
Contribution of Natural Products to Drug Discovery in Tropical Diseases
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On the Discorhabdins Leading to the Aleutianamine Ring System: A One‐Step in Situ Transformation Characterized Through Computational and Experimental Studies and Its Implications on Biosynthesis, Synthesis, and Pharmacology
inferred← citeshttps://doi.org/10.1002/anie.7864883openalex-snapshot
On the Discorhabdins Leading to the Aleutianamine Ring System: A One‐Step in Situ Transformation Characterized Through Computational and Experimental Studies and Its Implications on Biosynthesis, Synthesis, and Pharmacology
inferred← citeshttps://doi.org/10.1002/jhet.2115openalex-snapshot
Synthesis of 2,3,3a,4,5,6‐Hexahydrobenzo[b]thiophene‐3a‐carbaldehydes via a Tandem Reaction of Cyclic β‐Thiocyanatoenals with Electron‐Deficient Alkenes Triggered by Fluoride
inferred← citeshttps://doi.org/10.1007/128_2011_134openalex-snapshot
Marine Pyrroloiminoquinone Alkaloids
inferred← citeshttps://doi.org/10.1007/978-3-031-26629-4_1openalex-snapshot
Naturally Occurring Organohalogen Compounds—A Comprehensive Review
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Marine Pyrroloiminoquinone Alkaloids, Makaluvamines and Discorhabdins, and Marine Pyrrole-Imidazole Alkaloids
inferred← citeshttps://doi.org/10.1007/978-981-97-1619-7_5openalex-snapshot
The Asymmetric Total Synthesis of Discorhabdin B, H, K, and Aleutianamine
inferred← citeshttps://doi.org/10.1007/s00300-015-1722-zopenalex-snapshot
Fatty acid composition and antioxidant activity of Antarctic marine sponges of the genus Latrunculia
inferred← citeshttps://doi.org/10.1007/s10126-023-10268-7openalex-snapshot
Profiling Prokaryotic Communities and Aaptamines of Sponge Aaptos suberitoides from Tulamben, Bali
inferred← citeshttps://doi.org/10.1007/s12526-012-0132-5openalex-snapshot
A new species of Latrunculia (Biannulata) (Porifera: Demospongiae) from Rio de Janeiro, south-eastern Brazil
inferred← citeshttps://doi.org/10.1016/b978-0-12-398282-7.00001-1openalex-snapshot
Occurrence of Halogenated Alkaloids
inferred← citeshttps://doi.org/10.1016/b978-0-12-416002-6.00029-8openalex-snapshot
Biotechnological Exploitation of Marine Animals
inferred← citeshttps://doi.org/10.1016/b978-0-12-811710-1.00027-6openalex-snapshot
Marine resources and animals in modern biotechnology
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Marine natural products as strategic prototypes in the development of a new generation of antimalarial agents
inferred← citeshttps://doi.org/10.1016/b978-0-444-63602-7.00008-4openalex-snapshot
Recent Developments in Natural Product-Based Drug Discovery in Tropical Diseases
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.105011openalex-snapshot
Chemical diversity and biological activities of marine-derived sulphur containing alkaloids: A comprehensive update
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.06.008openalex-snapshot
Synthetic studies towards atkamine
inferred← citeshttps://doi.org/10.1016/j.copbio.2010.09.015openalex-snapshot
The structural diversity and promise of antiparasitic marine invertebrate-derived small molecules
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.115006openalex-snapshot
Prenylated flavonoids with significant anti-hepatoma activity from Daphne giraldii and effects on Fibroblast Growth Factor Receptor 1 (FGFR1)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116287openalex-snapshot
Biological properties of pyrroloquinoline and pyrroloisoquinoline derivatives
inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.08.068openalex-snapshot
Promising antiparasitic agents from marine sponges
inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.057openalex-snapshot
Exploration of the influence of spiro-dienone moiety on biological activity of the cytotoxic marine alkaloid discorhabdin P
inferred← citeshttps://doi.org/10.1016/j.tet.2019.05.009openalex-snapshot
A convenient C–H functionalization platform for pyrroloiminoquinone alkaloid synthesis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00875openalex-snapshot
Informatics and Computational Approaches for the Discovery and Optimization of Natural Product-Inspired Inhibitors of the SARS-CoV-2 2′-O-Methyltransferase
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c01097openalex-snapshot
Manzamine-A Alters In Vitro Calvarial Osteoclast Function
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00549openalex-snapshot
Semisynthetic Studies Establish a Role for Conjugate Halide Exchange in the Formation of Chlorinated Pyrroloiminoquinones and Related Alkaloids
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c01094openalex-snapshot
Aleutianamine B, A Novel Chiral Sulfoxide Isolated from Latrunculia spp. and Generated via Semi-Synthesis, Exhibits Selectivity for Ovarian Cancer Cells
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00830openalex-snapshot
Evolution of Strategies Toward the Total Synthesis of Aleutianamine
inferred← citeshttps://doi.org/10.1021/acsomega.5c11024openalex-snapshot
Fragment-Based Online OzESI-MS, NMR, and Computational DP4+/DFT Approaches to the Characterization of the Putative Biosynthetic Lipid Precursor of Atkamine from Alaskan Latrunculia Sponges
inferred← citeshttps://doi.org/10.1021/cr100435gopenalex-snapshot
Discorhabdins and Pyrroloiminoquinone-Related Alkaloids
inferred← citeshttps://doi.org/10.1021/cr4006318openalex-snapshot
Role of Marine Natural Products in the Genesis of Antiviral Agents
inferred← citeshttps://doi.org/10.1021/jacs.3c06578openalex-snapshot
Unified Divergent Total Synthesis of Discorhabdin B, H, K, and Aleutianamine via the Late-Stage Oxidative N,S-Acetal Formation
inferred← citeshttps://doi.org/10.1021/jacs.4c11897openalex-snapshot
A Divergent Synthesis of Numerous Pyrroloiminoquinone Alkaloids Identifies Promising Antiprotozoal Agents
inferred← citeshttps://doi.org/10.1021/jacs.6c06599openalex-snapshot
Optimized Biomimetic Syntheses of Discorhabdin B and Aleutianamine Drives a Deeper Exploration of Their Anticancer Potential
inferred← citeshttps://doi.org/10.1021/np100443copenalex-snapshot
Isolation and Characterization of Diastereomers of Discorhabdins H and K and Assignment of Absolute Configuration to Discorhabdins D, N, Q, S, T, and U
inferred← citeshttps://doi.org/10.1021/ol400294vopenalex-snapshot
Atkamine: A New Pyrroloiminoquinone Scaffold from the Cold Water Aleutian Islands Latrunculia Sponge
inferred← citeshttps://doi.org/10.1039/c2ob07090aopenalex-snapshot
Investigation of the electrophilic reactivity of the cytotoxic marine alkaloid discorhabdin B
inferred← citeshttps://doi.org/10.1039/c3np20118jopenalex-snapshot
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
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Recent advances in deep-sea natural products
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Solvent effect and fluorescence response of the 7-tert-butylpyrene-dipicolylamine linkage for the selective and sensitive response toward Zn( ii ) and Cd( ii ) ions
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Cold-water marine natural products, 2006 to 2016
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Hepatitis C Virus NS3 Protease and Helicase Inhibitors from Red Sea Sponge (Amphimedon) Species in Green Synthesized Silver Nanoparticles Assisted by in Silico Modeling and Metabolic Profiling
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Structural and Bioactive Studies of Halogenated Constituents from Sponges
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Targeted Isolation of Tsitsikammamines from the Antarctic Deep-Sea Sponge Latrunculia biformis by Molecular Networking and Anticancer Activity
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Exploration of the Electrophilic Reactivity of the Cytotoxic Marine Alkaloid Discorhabdin C and Subsequent Discovery of a New Dimeric C-1/N-13-Linked Discorhabdin Natural Product
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