On the public citation graph
Manzamine A, a novel antitumor alkaloid from a sponge
0 signed · 476 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112887zenodo-depositor-declared
Design, synthesis and screening of a drug discovery library based on an Eremophila-derived serrulatane scaffold
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199905)1999:5<959::aid-ejoc959>3.0.co;2-kopenalex-snapshot
Synthesis Mediated by Ring-Closing Metathesis – Applications in the Synthesis of Azasugars and Alkaloids
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981002)110:19<2806::aid-ange2806>3.0.co;2-ropenalex-snapshot
Untersuchungen zur Hypothese der Manzaminalkaloid-Biosynthese
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000103)112:1<46::aid-ange46>3.0.co;2-popenalex-snapshot
Der Stand der Totalsynthese zu Beginn des 21. Jahrhunderts
inferred← citeshttps://doi.org/10.1002/0470052171.ch16openalex-snapshot
Marine Compounds as a New Source for Glycogen Synthase Kinase 3 Inhibitors
inferred← citeshttps://doi.org/10.1002/1521-3757(20020503)114:9<1651::aid-ange1651>3.0.co;2-#openalex-snapshot
Evaluation of Diene Hierarchies for Diels–Alder Reactions En Route to Xestocyclamine A: Elaboration of an Ansa Bridge by B ‐Alkyl Suzuki Macrocyclization
inferred← citeshttps://doi.org/10.1002/1521-3773(20020503)41:9<1581::aid-anie1581>3.0.co;2-fopenalex-snapshot
Evaluation of Diene Hierarchies for Diels-Alder Reactions En Route to Xestocyclamine A: Elaboration of an Ansa Bridge byB-Alkyl Suzuki Macrocyclization
inferred← citeshttps://doi.org/10.1002/9781118342886.ch9openalex-snapshot
Domino Reactions in the Enantioselective Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/9781118356654.ch7openalex-snapshot
USE OF TRANSITION METAL–CATALYZED CASCADE REACTIONS IN NATURAL PRODUCT SYNTHESIS AND DRUG DISCOVERY
inferred← citeshttps://doi.org/10.1002/9781118596784.ssd029openalex-snapshot
Stereoselective Hydrogenation of C C Bonds: Application to Drug and Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/9781119143802.ch107openalex-snapshot
Nanogram and Nanomolar Active Marine Antiplasmodial Antibiotics
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod193openalex-snapshot
Porifera (Sponges)–3
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/9783527634606.ch6openalex-snapshot
Biomimetic Synthesis of Manzamine Alkaloids
inferred← citeshttps://doi.org/10.1002/9783527803781.ch7openalex-snapshot
Marine‐Derived Anti‐Alzheimer's Agents of Promise
inferred← citeshttps://doi.org/10.1002/ange.19961081505openalex-snapshot
Chemie und Biologie der Saragossasäuren/Squalestatine
inferred← citeshttps://doi.org/10.1002/ange.200200534openalex-snapshot
Chemie und Biologie natürlicher Diels‐Alder‐Reaktionen
inferred← citeshttps://doi.org/10.1002/ange.200250642openalex-snapshot
Biogenesis of 3‐Alkylpyridine Alkaloids in the Marine Mollusc Haminoea Orbignyana
inferred← citeshttps://doi.org/10.1002/ange.201001127openalex-snapshot
A Direct Entry to Substituted N‐Methoxyamines from N‐Methoxyamides via N‐Oxyiminium Ions
inferred← citeshttps://doi.org/10.1002/ange.201103937openalex-snapshot
Enantioselective Michael/Mannich Polycyclization Cascade of Indolyl Enones Catalyzed by Quinine‐Derived Primary Amines
inferred← citeshttps://doi.org/10.1002/ange.201302268openalex-snapshot
Neurotrophe Naturstoffe – ihre Chemie und Biologie
inferred← citeshttps://doi.org/10.1002/anie.199616221openalex-snapshot
Chemistry and Biology of the Zaragozic Acids (Squalestatins)
inferred← citeshttps://doi.org/10.1002/anie.200200534openalex-snapshot
Chemistry and Biology of Biosynthetic Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/anie.200250642openalex-snapshot
Biogenesis of 3‐Alkylpyridine Alkaloids in the Marine Mollusc Haminoea Orbignyana
inferred← citeshttps://doi.org/10.1002/anie.201001127openalex-snapshot
A Direct Entry to Substituted N‐Methoxyamines from N‐Methoxyamides via N‐Oxyiminium Ions
inferred← citeshttps://doi.org/10.1002/anie.201103937openalex-snapshot
Enantioselective Michael/Mannich Polycyclization Cascade of Indolyl Enones Catalyzed by Quinine‐Derived Primary Amines
inferred← citeshttps://doi.org/10.1002/anie.201302268openalex-snapshot
Neurotrophic Natural Products: Chemistry and Biology
inferred← citeshttps://doi.org/10.1002/bscb.19880970707openalex-snapshot
2D‐NMR Study of Petrosins: Revised Structure for Petrosin‐A
inferred← citeshttps://doi.org/10.1002/chem.201000142openalex-snapshot
Concise Access to a Model of the Marine Alkaloid Halicyclamine A through Macrocycle‐Forming Addition of a 5‐Aminopenta‐2,4‐dienal onto a 2,3‐Dihydropyridinium Salt
inferred← citeshttps://doi.org/10.1002/chem.201101362openalex-snapshot
Viscosalines B1,2 and E1,2: Challenging New 3‐Alkyl Pyridinium Alkaloids from the Marine Sponge Haliclona viscosa
inferred← citeshttps://doi.org/10.1002/chem.202402082openalex-snapshot
Synthesis of a Library of Terpenoid Alkaloid–Like Compounds Containing Medium‐Sized Rings via Reconstruction of the Humulene Skeleton
inferred← citeshttps://doi.org/10.1002/chin.198706071openalex-snapshot
ChemInform Abstract: Manzamine A, a Novel Antitumor Alkaloid from a Sponge.
inferred← citeshttps://doi.org/10.1002/chin.200014243openalex-snapshot
ChemInform Abstract: Marine Natural Products as Leads to Develop New Drugs and Insecticides
inferred← citeshttps://doi.org/10.1002/chin.200815242openalex-snapshot
ChemInform Abstract: Strategies for the Synthesis of Manzamine Alkaloids
inferred← citeshttps://doi.org/10.1002/cjoc.202000291openalex-snapshot
Catalytic Asymmetric Total Synthesis of Macrocyclic Marine Natural Product (–)‐Haliclonin A†
inferred← citeshttps://doi.org/10.1002/cmdc.202100134openalex-snapshot
An Efficient Synthesis of 3‐Alkylpyridine Alkaloids Enables Their Biological Evaluation
inferred← citeshttps://doi.org/10.1002/ejoc.200400026openalex-snapshot
Two New Haliclamines from the Arctic Sponge Haliclona viscosa
inferred← citeshttps://doi.org/10.1002/ejoc.200400728openalex-snapshot
Synthesis of New Azocine Derivatives and Their Functionalization by Nucleophilic Addition to Their Iminium Salts
inferred← citeshttps://doi.org/10.1002/ejoc.200500208openalex-snapshot
Synthesis and Mass Spectrometric Analysis of CyclostellettaminesH, I, K and L
inferred← citeshttps://doi.org/10.1002/ejoc.200800929openalex-snapshot
New Route to the Synthesis of the Isocryptolepine Alkaloid and Its Related Skeletons Using a Modified Pictet–Spengler Reaction
inferred← citeshttps://doi.org/10.1002/ijch.199700008openalex-snapshot
An Approach to the Synthesis of the Manzamine Alkaloids Via the Vinylogous Amide PHotocycloAddition/Retro‐Mannich Fragmentation/Mannich Closure Cascade (pharM)
inferred← citeshttps://doi.org/10.1002/jccs.199400104openalex-snapshot
Reaction of (η5‐C5H4R)Fe(CO)2l (R = H, Me) with 1,1′‐Bis(diphenylphosphino)ferrocene (Dppf); Crystal Structure of {[(η5‐C5H5)Fe(CO)(η2‐dppf)]+l−}
inferred← citeshttps://doi.org/10.1002/jhet.5570310303openalex-snapshot
Synthetic strategies directed to the antitumour alkaloids sesbanimide A and manzamine A
inferred← citeshttps://doi.org/10.1002/jhet.5570310304openalex-snapshot
Synthesis of bioactive nitrogen heterocycles from marine organisms
inferred← citeshttps://doi.org/10.1002/jhet.5570310308openalex-snapshot
Strategies for the synthesis of heterocyclic natural products
inferred← citeshttps://doi.org/10.1002/jhet.5570370314openalex-snapshot
Enantioselective total synthesis of marine alkaloids, manzamine A and related compounds
inferred← citeshttps://doi.org/10.1002/med.21703openalex-snapshot
Biologically active isoquinoline alkaloids covering 2014–2018
inferred← citeshttps://doi.org/10.1002/med.70072openalex-snapshot
Advances in Structural Diversity, Pharmacological Activities, and Drug Development of β‐Carboline Alkaloids
inferred← citeshttps://doi.org/10.1002/mrc.1260261214openalex-snapshot
13C NMR spectra of substituted carbazoles and azacarbazoles (β‐carbolines)
inferred← citeshttps://doi.org/10.1002/open.202300306openalex-snapshot
Relevant Developments in the Use of Three‐Component Reactions for the Total Synthesis of Natural Products. The last 15 Years
inferred← citeshttps://doi.org/10.1002/slct.201800183openalex-snapshot
Recent Developments on the Total Synthesis of Nakadomarin A
inferred← citeshttps://doi.org/10.1002/slct.201804029openalex-snapshot
Reductive Heck Reaction: An Emerging Alternative in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/slct.201902441openalex-snapshot
A Versatile Pre and Post Ugi Modification for the Synthesis of Natural Product Inspired Fused Peptide‐Carboline Scaffolds as Potential Anti‐Leishmanial Agents
inferred← citeshttps://doi.org/10.1002/tcr.200900001openalex-snapshot
Antimalarial natural products of marine and freshwater origin
inferred← citeshttps://doi.org/10.1007/7081_033openalex-snapshot
Strategies for the Synthesis of Manzamine Alkaloids
inferred← citeshttps://doi.org/10.1007/7081_2020_42openalex-snapshot
Manzamines: Marine Bioactive Heterocycles
inferred← citeshttps://doi.org/10.1007/7081_2021_51openalex-snapshot
Total Synthesis of Manzamine Alkaloids
inferred← citeshttps://doi.org/10.1007/978-1-4614-1247-2_7openalex-snapshot
Medicinal Chemistry and Ligand Profiling for Evaluation of Promising Marine Bioactive Molecules
inferred← citeshttps://doi.org/10.1007/978-1-4615-0135-0_70openalex-snapshot
Recent Developments in Marine Indole Alkaloid Synthesis
inferred← citeshttps://doi.org/10.1007/978-1-4899-2391-2_7openalex-snapshot
Antitumor and Cytotoxic Compounds from Marine Organisms
inferred← citeshttps://doi.org/10.1007/978-3-030-89873-1_1openalex-snapshot
Antimalarial Natural Products
inferred← citeshttps://doi.org/10.1007/978-3-032-01098-8_10openalex-snapshot
Impact of Papua New Guinean Marine Biodiversity on the Discovery and Development of New Pharmaceuticals
inferred← citeshttps://doi.org/10.1007/978-3-032-01098-8_2openalex-snapshot
Chemical Evolution of Indonesian Marine Natural Products
inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot
The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/978-3-319-07145-9_34openalex-snapshot
Marine Sponge Derived Actinomycetes and Their Anticancer Compounds
inferred← citeshttps://doi.org/10.1007/978-3-319-92387-1_4openalex-snapshot
Bioactive Compounds and Pharmaceutical Excipients Derived from Animals, Marine Organisms, Microorganisms, Minerals, Synthesized Compounds, and Pharmaceutical Drugs
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_10openalex-snapshot
Bioactive Potential of Sponge Secondary Metabolites
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_11openalex-snapshot
Typification of Chemical Compounds of Marine Sponge Metabolites
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_6openalex-snapshot
Novel Insights on the Symbiotic Interactions of Marine Sponge-Associated Microorganisms: Marine Microbial Biotechnology Perspective
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_9openalex-snapshot
Biologically Active Metabolites from Sponges and Their Activities
inferred← citeshttps://doi.org/10.1007/978-90-481-3834-0_21openalex-snapshot
Marine Natural Products Active Against Protozoan Parasites
inferred← citeshttps://doi.org/10.1007/978-90-481-3834-0_4openalex-snapshot
The Chemistry of Marine Sponges∗
inferred← citeshttps://doi.org/10.1007/978-981-10-5708-3_11openalex-snapshot
Marine Sponge-Associated Microbiome: Reservoir of Novel Bioactive Compounds
inferred← citeshttps://doi.org/10.1007/978-981-19-3696-8_8openalex-snapshot
Novel Insights into Environmental Niche Adaptations and Secondary Metabolite Biosynthesis Potential of Marine Sponge Microbiome
inferred← citeshttps://doi.org/10.1007/978-981-99-6770-4_14openalex-snapshot
Neuroactive Peptides and Neuroprotective Molecules from Marine Sponges and Associated Bacteria: An Untapped Resource for Systemic Drug Development
inferred← citeshttps://doi.org/10.1007/b135824openalex-snapshot
Marine Pharmacology: Potentialities in the Treatment of Infectious Diseases, Osteoporosis and Alzheimer's Disease
inferred← citeshttps://doi.org/10.1007/bf01320227openalex-snapshot
Influence of sponges on invertebrate recruitment: A field test of allelopathy
inferred← citeshttps://doi.org/10.1007/s00044-020-02691-5openalex-snapshot
Tuberculosis: current scenario, drug targets, and future prospects
inferred← citeshttps://doi.org/10.1007/s00436-011-2757-xopenalex-snapshot
In vitro antiplasmodial activity of bacterium RJAUTHB 14 associated with marine sponge Haliclona Grant against Plasmodium falciparum
inferred← citeshttps://doi.org/10.1007/s10126-001-0082-6openalex-snapshot
Isolation of Haliclonamides: New Peptides as Antifouling Substances from a Marine Sponge Species, Haliclona
inferred← citeshttps://doi.org/10.1007/s10126-008-9154-1openalex-snapshot
Isolation and Analysis of Bacteria with Antimicrobial Activities from the Marine Sponge Haliclona simulans Collected from Irish Waters
inferred← citeshttps://doi.org/10.1007/s10126-012-9430-yopenalex-snapshot
Diversity of Bacterial Communities Associated with the Indian Ocean Sponge Tsitsikamma favus That Contains the Bioactive Pyrroloiminoquinones, Tsitsikammamine A and B
inferred← citeshttps://doi.org/10.1007/s10637-008-9134-3openalex-snapshot
Brazilian marine sponge Polymastia janeirensis induces apoptotic cell death in human U138MG glioma cell line, but not in a normal cell culture
inferred← citeshttps://doi.org/10.1007/s10637-008-9198-0openalex-snapshot
Extracts of marine sponge Polymastia janeirensis induce oxidative cell death through a caspase-9 apoptotic pathway in human U138MG glioma cell line
inferred← citeshttps://doi.org/10.1007/s11030-021-10194-7openalex-snapshot
Fukuyama reduction, Fukuyama coupling and Fukuyama–Mitsunobu alkylation: recent developments and synthetic applications
inferred← citeshttps://doi.org/10.1007/s11101-012-9249-1openalex-snapshot
The Arctic sponge Haliclona viscosa as a source of a wide array of 3-alkyl pyridine alkaloids
inferred← citeshttps://doi.org/10.1007/s11172-010-0344-4openalex-snapshot
Interaction of manzamine A with glycogen synthase kinase 3β: a molecular dynamics study
inferred← citeshttps://doi.org/10.1007/s12272-014-0503-5openalex-snapshot
Natural products from marine organisms with neuroprotective activity in the experimental models of Alzheimer’s disease, Parkinson’s disease and ischemic brain stroke: their molecular targets and action mechanisms
inferred← citeshttps://doi.org/10.1007/s44371-025-00088-0openalex-snapshot
Exploring some marine-derived manzamine compounds for uterine fibroid treatment: molecular docking and dynamics studies
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00761-vopenalex-snapshot
Rottnestol, a new hemiketal from the sponge Haliclona sp.
inferred← citeshttps://doi.org/10.1016/0040-4020(95)01057-2openalex-snapshot
Chiral resolution of (±)-keramaphidin B and isolation of manzamine L, a new β-carboline alkaloid from a sponge Amphimedon sp.
inferred← citeshttps://doi.org/10.1016/0040-4020(95)95723-9openalex-snapshot
Four new β-carboline alkaloids isolated from two Okinawan marine sponges of Xestospongia sp. and Haliclona sp.)
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00249-9openalex-snapshot
Ring-closing olefin meta thesis for the synthesis of fused nitrogen heterocycles
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00393-6openalex-snapshot
Structural and stereochemical studies of saraines: Macrocyclic alkaloids of the sponge Reniera sarai
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00436-xopenalex-snapshot
Haliclonacyclamines A and B, cytotoxic alkaloids from the tropical marine sponge Haliclona sp
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00607-2openalex-snapshot
Synthesis of a tetracyclic substructure of manzamine A via the Diels-Alder reaction of dihydropyridinones
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00908-8openalex-snapshot
Further studies of alkaloids from Reniera sarai: Structures of saraine-3 and isosaraine-3; absolute stereochemistry of saraine-1 and saraine-2
inferred← citeshttps://doi.org/10.1016/0040-4039(88)85091-3openalex-snapshot
New manzamine alkaloids from a sponge of the genus xestospongia
inferred← citeshttps://doi.org/10.1016/0040-4039(91)80198-fopenalex-snapshot
Construction of the tricyclic ABC ring subunit of manzamine A via a novel intramolecular Diels-Alder reaction
inferred← citeshttps://doi.org/10.1016/0040-4039(92)88141-qopenalex-snapshot
On the Biosynthesis of Manzamines
inferred← citeshttps://doi.org/10.1016/0040-4039(93)88081-sopenalex-snapshot
Dihydropyridinone approach to manzamines: An expedient construction of the tetracyclic core of manzamine A
inferred← citeshttps://doi.org/10.1016/0040-4039(93)88091-vopenalex-snapshot
A highly stereoselective approach to the synthesis of the manzamine alkaloids via the intramolecular vinylogous amide photocycloaddition
inferred← citeshttps://doi.org/10.1016/0040-4039(94)80129-0openalex-snapshot
A biomimetic approach to the manzamine alkaloids; model studies
inferred← citeshttps://doi.org/10.1016/0040-4039(94)88060-3openalex-snapshot
Novel route to fused nitrogen heterocycles by olefin metathesis
inferred← citeshttps://doi.org/10.1016/0040-4039(94)88286-xopenalex-snapshot
Synthetic studies on manzamine A: construction of a key bicyclic AD ring subunit I
inferred← citeshttps://doi.org/10.1016/0040-4039(94)88308-4openalex-snapshot
Ingenamine, a novel pentacyclic alkaloid from the marine sponge Xestospongia ingens
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00296-oopenalex-snapshot
An enantioselective synthesis of the CE ring system of the alkaloids manzamine A, E and F, and ircinal a
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01754-6openalex-snapshot
Selective methylation and stereoselective reduction of a β-carboline to a N(2)-methyl-1,2,3,4-tetrahydro-β-carboline.
inferred← citeshttps://doi.org/10.1016/0040-4039(95)02071-3openalex-snapshot
Stereoselective synthesis of the tricyclic core of manzamine a: The bradsher cycloaddition route
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01516-xopenalex-snapshot
A biomimetic approach to the manzamine alkaloids
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01540-7openalex-snapshot
Preparation and use of chiral (Z)-enol ethers in asymmetric bradsher cycloaddition
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01657-7openalex-snapshot
Synthetic studies on manzamine A: Construction of the tricyclic ABC ring subunit I
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01861-8openalex-snapshot
Absolute stereochemistry of keramaphidin B
inferred← citeshttps://doi.org/10.1016/0305-0491(90)90035-ropenalex-snapshot
Bryozoan secondary metabolites: A chemotaxonomical challenge
inferred← citeshttps://doi.org/10.1016/0960-894x(96)00460-xopenalex-snapshot
Manzamine C congeners with modified azacyclic rings: Synthesis and biological evaluation
inferred← citeshttps://doi.org/10.1016/b978-0-08-091283-7.00015-1openalex-snapshot
The Diels–Alder Reaction in Biosynthesis of Polyketide Phytotoxins
inferred← citeshttps://doi.org/10.1016/b978-0-08-091283-7.00055-2openalex-snapshot
Marine Natural Products and Marine Chemical Ecology
inferred← citeshttps://doi.org/10.1016/b978-0-12-394283-8.00004-7openalex-snapshot
Sponge Chemical Diversity
inferred← citeshttps://doi.org/10.1016/b978-0-12-803959-5.50015-5openalex-snapshot
Targets and Small Molecules Against Tauopathies. Part 1: From Genes to Soluble, Aggregation-Prone Tau Proteins
inferred← citeshttps://doi.org/10.1016/b978-0-12-815723-7.00002-xopenalex-snapshot
Marine natural products as strategic prototypes in the development of a new generation of antimalarial agents
inferred← citeshttps://doi.org/10.1016/b978-0-12-817890-4.00017-2openalex-snapshot
Antimicrobial lead compounds from marine plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-819210-8.00004-7openalex-snapshot
Eight-Membered Ring Heterocycles
inferred← citeshttps://doi.org/10.1016/b978-0-12-824021-2.00001-7openalex-snapshot
Applications of Pauson–Khand reaction in the total synthesis of alkaloids
inferred← citeshttps://doi.org/10.1016/b978-0-323-91942-5.00019-7openalex-snapshot
Marine organisms as natural drug leads in combating vector-borne diseases
inferred← citeshttps://doi.org/10.1016/b978-0-443-15269-6.00008-0openalex-snapshot
Semisynthesis of alkaloids
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00043-5openalex-snapshot
Marine Invertebrates: Sponges
inferred← citeshttps://doi.org/10.1016/bs.acr.2019.05.003openalex-snapshot
Marine natural products in the discovery and development of potential pancreatic cancer therapeutics
inferred← citeshttps://doi.org/10.1016/j.bbagen.2004.03.007openalex-snapshot
Characterization of the cytotoxic mechanism of Mana-Hox, an analog of manzamine alkaloids
inferred← citeshttps://doi.org/10.1016/j.bbapap.2015.03.013openalex-snapshot
Selective inhibitors of Plasmodium falciparum glycogen synthase-3 (PfGSK-3): New antimalarial agents?
inferred← citeshttps://doi.org/10.1016/j.bioorg.2016.11.013openalex-snapshot
Synthesis and in-vitro anti-leishmanial activity of (4-arylpiperazin-1-yl)(1-(thiophen-2-yl)-9 H -pyrido[3,4- b ]indol-3-yl)methanone derivatives
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.05.079openalex-snapshot
2-N-Methyl modifications and SAR studies of manzamine A
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.072openalex-snapshot
Synthetic medicinal chemistry of selected antimalarial natural products
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.09.026openalex-snapshot
Structure–activity relationship studies of manzamine A: Amidation of positions 6 and 8 of the β-carboline moiety
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.04.025openalex-snapshot
Manzamine A, a marine-derived alkaloid, inhibits accumulation of cholesterol ester in macrophages and suppresses hyperlipidemia and atherosclerosis in vivo
inferred← citeshttps://doi.org/10.1016/j.bmc.2018.10.040openalex-snapshot
Butenolides from a marine-derived fungus Aspergillus terreus with antitumor activities against pancreatic ductal adenocarcinoma cells
inferred← citeshttps://doi.org/10.1016/j.bmc.2021.116560openalex-snapshot
Isolation and biological activity of azocine and azocane alkaloids
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.09.036openalex-snapshot
Synthesis and biological studies of 1-amino β-carbolines
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.06.077openalex-snapshot
Design and synthesis of Pictet–Spengler condensation products that exhibit oncogenic-RAS synthetic lethality and induce non-apoptotic cell death
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.01.058openalex-snapshot
Design, synthesis of new β-carboline derivatives and their selective anti-HIV-2 activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.07.039openalex-snapshot
Synthesis of antimalarial amide analogues based on the plant serrulatane diterpenoid 3,7,8-trihydroxyserrulat-14-en-19-oic acid
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.11.028openalex-snapshot
Tetradehydrohalicyclamine B, a new proteasome inhibitor from the marine sponge Acanthostrongylophora ingens
inferred← citeshttps://doi.org/10.1016/j.crbiot.2025.100300openalex-snapshot
Marine-derived secondary metabolites in oncology: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.drudis.2014.06.010openalex-snapshot
Manzamine alkaloids: isolation, cytotoxicity, antimalarial activity and SAR studies
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2026.100330openalex-snapshot
Comprehensive review of β-carbolines from microbes and their biosynthesis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2010.02.001openalex-snapshot
Synthesis and cytotoxicity evaluation of (tetrahydro-β-carboline)-1,3,5-triazine hybrids as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.03.018openalex-snapshot
Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.07.006openalex-snapshot
Manzamine alkaloids as antileishmanial agents: A review
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.10.024openalex-snapshot
Design, synthesis and evaluation of diarylpiperazine derivatives as potent anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.08.014openalex-snapshot
Synthesis and anti-leishmanial evaluation of 1-phenyl-2,3,4,9-tetrahydro-1 H -β-carboline derivatives against Leishmania infantum
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.08.027openalex-snapshot
β-Carboline alkaloid monomers and dimers: Occurrence, structural diversity, and biological activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.026openalex-snapshot
Marine natural products as potential anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112945openalex-snapshot
Tryptophan derived natural marine alkaloids and synthetic derivatives as promising antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113321openalex-snapshot
β-Carbolines as potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113536openalex-snapshot
Structure activity relationship in β-carboline derived anti-malarial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113688openalex-snapshot
A comprehensive overview of β-carbolines and its derivatives as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116850openalex-snapshot
Anticancer potential of active alkaloids and synthetic analogs derived from marine invertebrates
inferred← citeshttps://doi.org/10.1016/j.ejphar.2025.177295openalex-snapshot
Manzamine A: A promising marine-derived cancer therapeutic for multi-targeted interactions with E2F8, SIX1, AR, GSK-3β, and V-ATPase - A systematic review
inferred← citeshttps://doi.org/10.1016/j.exppara.2012.01.009openalex-snapshot
Antifilarial activity of marine sponge Haliclona oculata against experimental Brugia malayi infection
inferred← citeshttps://doi.org/10.1016/j.fitote.2009.01.002openalex-snapshot
Alkaloids as potential anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106326openalex-snapshot
Resource distribution, pharmacological activity, toxicology and clinical drugs of β-Carboline alkaloids: An updated and systematic review
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e04916openalex-snapshot
Recent evolution on synthesis strategies and anti-leishmanial activity of β-carboline derivatives – An update
inferred← citeshttps://doi.org/10.1016/j.mencom.2014.04.011openalex-snapshot
Synthesis of nitrogen-containing benzoannulated eight- and nine-membered heterocycles from methyl 4-amino-3-iodobenzoate
inferred← citeshttps://doi.org/10.1016/j.molcata.2011.04.002openalex-snapshot
A fascinating Suzuki homo-coupling reaction over anchored gold Schiff base complexes on mesoporous host
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146925openalex-snapshot
Tetrahydro-β-carboline alkaloids: recent advances in structural modification toward anticancer applications
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2026.108982openalex-snapshot
A dive into the untapped potential of marine compounds in counteracting neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.phrs.2019.104373openalex-snapshot
Advances in exploring the therapeutic potential of marine natural products
inferred← citeshttps://doi.org/10.1016/j.redox.2023.102861openalex-snapshot
Oxidative stress mediates the inhibitory effects of Manzamine A on uterine leiomyoma cell proliferation and extracellular matrix deposition via SOAT inhibition
inferred← citeshttps://doi.org/10.1016/j.tchem.2022.100025openalex-snapshot
Madangamine alkaloids: Madness and tranquility
inferred← citeshttps://doi.org/10.1016/j.tet.2009.01.032openalex-snapshot
Zamamidine C, 3,4-dihydro-6-hydroxy-10,11-epoxymanzamine A, and 3,4-dihydromanzamine J N-oxide, new manzamine alkaloids from sponge Amphimedon sp.
inferred← citeshttps://doi.org/10.1016/j.tet.2016.07.067openalex-snapshot
Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients
inferred← citeshttps://doi.org/10.1016/j.tet.2017.11.029openalex-snapshot
The potential of achiral sponge-derived and synthetic bromoindoles as selective cytotoxins against PANC-1 tumor cells
inferred← citeshttps://doi.org/10.1016/j.tet.2018.05.004openalex-snapshot
Generation of all carbon quaternary stereocenters at the C-3 carbon of piperidinones and pyrrolidinones and its application in natural product total synthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130569openalex-snapshot
Efficient access to β- and γ-carbolines from a common starting material by sequential site-selective Pd-catalyzed C–C, C–N coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.12.029openalex-snapshot
Synthetic study of manzamine B: synthesis of the tricyclic central core by an asymmetric Diels–Alder and RCM strategy
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.07.128openalex-snapshot
Facile synthesis of medium-sized cyclic amines based on Friedel–Crafts reaction via iminium cation by use of acetylene dicobalt complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.04.061openalex-snapshot
Reductive amidation of nitroarenes: a practical approach for the amidation of natural products
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.084openalex-snapshot
Palladium-mediated reductive Mizoroki–Heck cyclization strategy for the regioselective formation of dibenzoazocinone framework
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.11.136openalex-snapshot
Expected and unexpected reactions of 1,3-benzothiazine derivatives, II. Formation of isomeric 5,6-dihydro-1,5-benzothiazocines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.07.093openalex-snapshot
Synthetic study on efficient stereoselective construction of tricyclic core skeleton of manzamine A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.09.016openalex-snapshot
Total synthesis of (−)-nakadomarin A: alkyne ring-closing metathesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.03.002openalex-snapshot
Tandem Michael addition–Fries rearrangement of sorbylanilides: a convenient one pot synthesis of novel benzo[b]azocin-6-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.08.140openalex-snapshot
Acantholactone, a new manzamine related alkaloid with an unprecedented δ-lactone and ε-lactam ring system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.09.065openalex-snapshot
On the stereochemistry of the olefinic double bond in 13-membered heterocyclic rings accessible by ring-closing metathesis reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.111openalex-snapshot
An expedient stereoselective route to the ACE tricyclic core of manzamine A via a palladium-catalysed arylative allene spirocyclisation cascade
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153748openalex-snapshot
Discovering manzamine-related alkaloids from sponge Neopetrosia proxima
inferred← citeshttps://doi.org/10.1016/j.toxicon.2004.03.017openalex-snapshot
Extracts from two marine sponges lower cyclin B1 levels, cause a G2/M cell cycle block and trigger apoptosis in SW-13 human adrenal carcinoma cells
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)00758-4openalex-snapshot
New Triterpene-Ketides (Merotriterpenes), Haliclotriol A and B, from an Indo–Pacific Haliclona Sponge
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)80635-9openalex-snapshot
Ingamines A and B, new cytotoxic alkaloids from the marine sponge Xestospongia ingens
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)85280-7openalex-snapshot
Ircinols A and B, first antipodes of manzamine-related alkaloids from an Okinawan marine sponge
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)85671-4openalex-snapshot
1,2,3,4-tetrahydro-8-hydroxymanzamines, alkaloids from two different haplosclerid sponges
showing the first 200 of 476 · page through all 476
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.