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Pyrroloacridine Alkaloids from Plakortis quasiamphiaster: Structures and Bioactivity
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4615-0747-5_1openalex-snapshot
Systema Porifera. A Guide to the Classification of Sponges
inferredcites →https://doi.org/10.1016/s0006-2952(03)00209-0openalex-snapshot
The anti-neoplastic and novel topoisomerase II-mediated cytotoxicity of neoamphimedine, a marine pyridoacridine
inferredcites →https://doi.org/10.1016/s0040-4020(00)01009-7openalex-snapshot
Amphiasterins: a new family of cytotoxic metabolites from the marine sponge Plakortis quasiamphiaster
inferredcites →https://doi.org/10.1016/s0040-4020(01)87960-6openalex-snapshot
Biosynthesis of shermilamine B
inferredcites →https://doi.org/10.1016/s0040-4039(00)82330-8openalex-snapshot
A highly practical synthesis of chiral (E)-1-trimethylsilyl-1-alken-3,4-diols via the sharpless asymmetric epoxidation of 1,5-bis(trimethylsilyl)-1,4-pentadien-3-ol. Formal total synthesis of lipoxin b
inferredcites →https://doi.org/10.1021/ja00157a001openalex-snapshot
Novel marine sponge alkaloids. 1. Plakinidine A and B, anthelmintic active alkaloids from a Plakortis sponge
inferredcites →https://doi.org/10.1021/ja00157a002openalex-snapshot
Principal values of carbon-13 NMR chemical shift tensors for a collection of substituted benzenes
inferredcites →https://doi.org/10.1021/jm00048a017openalex-snapshot
Inhibition of Topoisomerase II Catalytic Activity by Pyridoacridine Alkaloids from a Cystodytes sp. Ascidian: A Mechanism for the Apparent Intercalator-Induced Inhibition of Topoisomerase II
inferredcites →https://doi.org/10.1021/jo010153kopenalex-snapshot
Deoxyamphimedine, a New Pyridoacridine Alkaloid from Two Tropical Xestospongia Sponges
inferredcites →https://doi.org/10.1021/jo026459oopenalex-snapshot
Structures and Cytotoxic Properties of Sponge-Derived Bisannulated Acridines
inferredcites →https://doi.org/10.1021/jo982047xopenalex-snapshot
Neoamphimedine: A New Pyridoacridine Topoisomerase II Inhibitor Which Catenates DNA
inferredcites →https://doi.org/10.1021/np020016yopenalex-snapshot
The Pyridoacridine Family Tree: A Useful Scheme for Designing Synthesis and Predicting Undiscovered Natural Products
inferredcites →https://doi.org/10.1021/np020601zopenalex-snapshot
Probing Biotransformation Relationships among Pyridoacridines by Focusing on Oxygenated Analogues
inferredcites →https://doi.org/10.1021/np040031yopenalex-snapshot
Marine Natural Products and Related Compounds in Clinical and Advanced Preclinical Trials
inferredcites →https://doi.org/10.1021/np970311wopenalex-snapshot
Plakinidine D, a New Pyrroloacridine Alkaloid from Two Ascidians of the Genus Didemnum
inferredcites →https://doi.org/10.1021/np970312oopenalex-snapshot
Plakinidine D, a New Pyrroloacridine Alkaloid from the Ascidian Didemnum rubeum
inferredcites →https://doi.org/10.1021/tx025618wopenalex-snapshot
Mechanism of Ascididemin-Induced Cytotoxicity
inferredcites →https://doi.org/10.1039/b401662aopenalex-snapshot
Biological activities of pyridoacridines
inferredcites →https://doi.org/10.1046/j.1359-4117.2002.01038.xopenalex-snapshot
Discovery and development of anticancer agents from plants
inferredcites →https://doi.org/10.1385/1-59259-329-1:555openalex-snapshot
Novel Approaches to Screen for Anticancer Drugs Using Saccharomyces cerevisiae
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.4466.1.4zenodo-depositor-declared
New sciaphilic plakinids (Porifera, Homoscleromorpha) from the Central-Western Pacific
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod019openalex-snapshot
Porifera (Sponges)–1
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/cbdv.202300561openalex-snapshot
A Review of the Chemistry and Biological Activities of Natural Colorants, Dyes, and Pigments: Challenges, and Opportunities for Food, Cosmetics, and Pharmaceutical Application
inferred← citeshttps://doi.org/10.1002/ejoc.201300227openalex-snapshot
Bisannulation of 2,3‐Dichloro‐1,4‐naphthoquinone with o‐Nitrophenylacetic Acid Derivatives: A Succinct Synthesis of the ABCD Ring System of Alpkinidine
inferred← citeshttps://doi.org/10.1002/slct.201601718openalex-snapshot
An Amino Sugar Promoted Green Protocol: A One‐Pot, Meglumine‐Catalyzed, Multicomponent Strategy for Synthesis of Multifaceted Pyrroloacridin‐1(2H)‐one Derivatives
inferred← citeshttps://doi.org/10.1002/slct.201900357openalex-snapshot
A Concise Approach for the Synthesis of the ABCD Ring System of Alpkinidine
inferred← citeshttps://doi.org/10.1002/tcr.70239openalex-snapshot
Serendipitous Emergence of Pyrrolo[2,3,4‐ kl ]acridin‐1(2 H )‐one Derivatives: From Unexpected Discovery to Synthetic Development
inferred← citeshttps://doi.org/10.1007/s11144-019-01709-3openalex-snapshot
Chemoselective synthesis of drug-like pyrrolo[2,3,4-kl]acridin-1-one using polyoxometalate@lanthanoid catalyst
inferred← citeshttps://doi.org/10.1016/bs.alkal.2023.06.001openalex-snapshot
Marine pyridoacridine, pyridoacridone and pyrroloacridine alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.044openalex-snapshot
A short route to the synthesis of pyrroloacridines via Ullmann–Goldberg condensation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.098openalex-snapshot
Stereoselective synthesis of amphiasterin B4: assignment of absolute configuration
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.070openalex-snapshot
An unexpected multicomponent reaction leading to 2-arylpyrrolo[2,3,4-kl]acridin-1(2H)-ones
inferred← citeshttps://doi.org/10.1017/s0025315410000743openalex-snapshot
Diversity of Indo-Australian Plakortis (Demospongiae: Plakinidae), with description of four new species
inferred← citeshttps://doi.org/10.1021/acsomega.2c02116openalex-snapshot
Toward the Total Synthesis of Alpkinidine: Synthesis of Haloquinone CE Ring System Synthons and Attempted Nucleophilic Bisannulation
inferred← citeshttps://doi.org/10.1021/jo400539xopenalex-snapshot
Tandem Synthesis of Pyrroloacridones via [3 + 2] Alkyne Annulation/Ring-Opening with Concomitant Intramolecular Aldol Condensation
inferred← citeshttps://doi.org/10.1021/jo8020659openalex-snapshot
A Short Access to 3-Hydroxy-4-hydroxymethyltetrahydrofurans: Application to the Total Synthesis of Amphiasterin B4
inferred← citeshttps://doi.org/10.1021/np070307copenalex-snapshot
Pinpointing Pseurotins from a Marine-DerivedAspergillusas Tools for Chemical Genetics Using a Synthetic Lethality Yeast Screen
inferred← citeshttps://doi.org/10.1021/np800184gopenalex-snapshot
Marine Natural Product Libraries for High-Throughput Screening and Rapid Drug Discovery
inferred← citeshttps://doi.org/10.1021/np900565aopenalex-snapshot
Assessing Pressurized Liquid Extraction for the High-Throughput Extraction of Marine-Sponge-Derived Natural Products
inferred← citeshttps://doi.org/10.1021/ol3022935openalex-snapshot
Palladium-Catalyzed Regioselective [3 + 2] Annulation of Internal Alkynes and Iodo-pyranoquinolines with Concomitant Ring Opening
inferred← citeshttps://doi.org/10.1039/b820693gopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c5gc00156kopenalex-snapshot
Single step incorporation of carboxylic acid groups in the lower rim of calix[4]arenes: a recyclable catalyst towards assembly of diverse five ring fused acridines
inferred← citeshttps://doi.org/10.1039/c5ra11747jopenalex-snapshot
Amidic C–N bond cleavage of isatin: chemoselective synthesis of pyrrolo[2,3,4- kl ]acridin-1-ones using Ag NPs decorated rGO composite as an efficient and recoverable catalyst under microwave irradiation
inferred← citeshttps://doi.org/10.1039/c6gc02144aopenalex-snapshot
The synthesis of new 8-imino-1-one acridine derivatives catalyzed by a calix[4]arene mono-acid core
inferred← citeshttps://doi.org/10.1071/ch09665openalex-snapshot
Polyketide-peroxides from a Species of Jamaican Plakortis (Porifera: Demospongiae)
inferred← citeshttps://doi.org/10.1080/00397911.2016.1204462openalex-snapshot
Synthesis of 2H-pyrrolo[3,4-C]quinoline via an Aldol/Van Leusen/Staudinger/aza-Wittig sequence
inferred← citeshttps://doi.org/10.1101/2020.10.23.353169openalex-snapshot
Identification bioactive compounds from marine microorganism and exploration of structure–activity relationships (SARs)
inferred← citeshttps://doi.org/10.1111/j.1365-2672.2011.05211.xopenalex-snapshot
Diversity and antimicrobial activities of microbes from two Irish marine sponges, Suberites carnosus and Leucosolenia sp.
inferred← citeshttps://doi.org/10.12980/jclm.3.201514b343openalex-snapshot
Bioactive profile of Plakortis nigra, a sea sponge from Mauritius Islands
inferred← citeshttps://doi.org/10.2174/1385272823666190725093517openalex-snapshot
Isolation, Synthesis and Medicinal Significance of Marine Pyridoacridine Alkaloids
inferred← citeshttps://doi.org/10.3390/md13053182openalex-snapshot
Alternative and Efficient Extraction Methods for Marine-Derived Compounds
inferred← citeshttps://doi.org/10.3390/molecules26154534openalex-snapshot
Natural Products from Tongan Marine Organisms
inferred← citeshttps://doi.org/10.4236/ojpm.2014.47068openalex-snapshot
New Developments in the Mechanism of Drug Action and Toxicity of Conjugated Imines and Iminiums, including Related Alkaloids
inferred← citeshttps://doi.org/10.70675/5d09f84fz6ea1z4415z9147z9e3269a4dc5dopenalex-snapshot
Synthèse totale de molécules marines biologiquement actives et d’analogues structuraux par application des réactions de métathèse et de la photochimie
inferred← citeshttps://doi.org/10.70675/e1f90413z5e0dz40c6zbd12zfb9360e627bbopenalex-snapshot
Recherche de molecules naturelles bioactives issues de la biodiversite marine de la zone sud-ouest de l'ocean Indien
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