On the public citation graph
Rare Cembranoids from Chinese Soft Coral Sarcophyton ehrenbergi: Structural and Stereochemical Studies
0 signed · 88 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known work and none has been retracted — and get a dated CiteStamped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 this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbdv.201000016openalex-snapshot
Terpenes from the Soft Corals Litophyton arboreum and Sarcophyton ehrenbergi
inferredcites →https://doi.org/10.1002/cbdv.201200122openalex-snapshot
Terpenes from the Soft Corals of the Genus Sarcophyton: Chemistry and Biological Activities
inferredcites →https://doi.org/10.1002/chir.22138openalex-snapshot
SpecDis: Quantifying the Comparison of Calculated and Experimental Electronic Circular Dichroism Spectra
inferredcites →https://doi.org/10.1016/j.apsb.2018.06.004openalex-snapshot
Cembrane-type diterpenoids from the South China Sea soft coral Sarcophyton mililatensis
inferredcites →https://doi.org/10.1016/j.tet.2010.06.094openalex-snapshot
Steroid and cembranoids from the Dongsha atoll soft coral Lobophytum sarcophytoides
inferredcites →https://doi.org/10.1016/j.tet.2013.06.068openalex-snapshot
Sartrolides A–G and bissartrolide, new cembranolides from the South China Sea soft coral Sarcophyton trocheliophorum Marenzeller
inferredcites →https://doi.org/10.1016/j.tet.2018.02.059openalex-snapshot
Structural, stereochemical, and bioactive studies of cembranoids from Chinese soft coral Sarcophyton trocheliophorum
inferredcites →https://doi.org/10.1016/j.tetlet.2007.05.096openalex-snapshot
Two new biscembranes with unprecedented carbon skeleton and their probable biogenetic precursor from the Hainan soft coral Sarcophyton latum
inferredcites →https://doi.org/10.1016/s0040-4039(02)01266-2openalex-snapshot
Two new cembrane diterpenes from a Madagascan soft coral of the genus Sarcophyton
inferredcites →https://doi.org/10.1017/cbo9780511615412openalex-snapshot
Logit Models from Economics and Other Fields
inferredcites →https://doi.org/10.1021/acs.jafc.6b05238openalex-snapshot
Structural and Stereochemical Studies of Laurokamurols A–C, Uncommon Bis-sesquiterpenoids from the Chinese Red Alga Laurencia okamurai Yamada
inferredcites →https://doi.org/10.1021/acs.jmedchem.8b01430openalex-snapshot
Design and Synthesis of Marine Phidianidine Derivatives as Potential Immunosuppressive Agents
inferredcites →https://doi.org/10.1021/acs.joc.8b01634openalex-snapshot
Unified Total Synthesis, Stereostructural Elucidation, and Biological Evaluation of Sarcophytonolides
inferredcites →https://doi.org/10.1021/acs.orglett.6b00737openalex-snapshot
Total Synthesis of Sarcophytonolide H and Isosarcophytonolide D: Structural Revision of Isosarcophytonolide D and Structure–Antifouling Activity Relationship of Sarcophytonolide H
inferredcites →https://doi.org/10.1021/acs.orglett.7b01716openalex-snapshot
Xishacorenes A–C, Diterpenes with Bicyclo[3.3.1]nonane Nucleus from the Xisha Soft Coral Sinularia polydactyla
inferredcites →https://doi.org/10.1021/acs.orglett.8b00842openalex-snapshot
Sarinfacetamides A and B, Nitrogenous Diterpenoids with Tricyclo[6.3.1.01,5]dodecane Scaffold from the South China Sea Soft Coral Sarcophyton infundibuliforme
inferredcites →https://doi.org/10.1021/jo400069nopenalex-snapshot
Biscembranoids Formed from an α,β-Unsaturated γ-Lactone Ring as a Dienophile: Structure Revision and Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra
inferredcites →https://doi.org/10.1021/jo951400lopenalex-snapshot
Simple Circular Dichroic Method for the Determination of Absolute Configuration of 5-Substituted 2(5H)-Furanones
inferredcites →https://doi.org/10.1021/jo960044jopenalex-snapshot
Sinulariadiolide, a Novel Marine Norditerpenoid from Okinawan Soft Coral of the Genus, Sinularia
inferredcites →https://doi.org/10.1021/np050477uopenalex-snapshot
Sarcophytonolides E−H, Cembranolides from the Hainan Soft Coral Sarcophyton latum
inferredcites →https://doi.org/10.1021/np500394dopenalex-snapshot
Prostaglandin Derivatives: Nonaromatic Phosphodiesterase-4 Inhibitors from the Soft Coral Sarcophyton ehrenbergi
inferredcites →https://doi.org/10.1021/np800081popenalex-snapshot
Structural and Stereochemical Studies of α-Methylene-γ-lactone-Bearing Cembrane Diterpenoids from a South China Sea Soft Coral Lobophytum crassum
inferredcites →https://doi.org/10.1021/np800362gopenalex-snapshot
Ceramide and Cerebrosides from the Octocoral Sarcophyton ehrenbergi
inferredcites →https://doi.org/10.1021/ol051513jopenalex-snapshot
Sinulochmodins A−C, Three Novel Terpenoids from the Soft Coral Sinularia lochmodes
inferredcites →https://doi.org/10.1021/ol100567dopenalex-snapshot
Lobophytones A−G, New Isobiscembranoids from the Soft Coral Lobophytum pauciflorum
inferredcites →https://doi.org/10.1021/ol303110dopenalex-snapshot
Unprecedented Diterpenoids as a PTP1B Inhibitor from the Hainan Soft Coral Sarcophyton trocheliophorum Marenzeller
inferredcites →https://doi.org/10.1021/ol400157sopenalex-snapshot
Total Synthesis of Two Possible Diastereomers of (+)-Sarcophytonolide C and Its Structural Elucidation
inferredcites →https://doi.org/10.1021/ol901070eopenalex-snapshot
Lobocrasol, a New Diterpenoid from the Soft Coral Lobophytum crassum
inferredcites →https://doi.org/10.1038/aps.2012.110openalex-snapshot
Bioactive natural products from Chinese marine flora and fauna
inferredcites →https://doi.org/10.1039/c7qo01091eopenalex-snapshot
Racemic trinorsesquiterpenoids from the Beihai sponge Spongia officinalis : structure and biomimetic total synthesis
inferredcites →https://doi.org/10.1039/c8ob01085dopenalex-snapshot
Scope of the 2(5H)-furanone helicity rule: a combined ECD, VCD, and DFT investigation
inferredcites →https://doi.org/10.2174/138527212800672583openalex-snapshot
Cembrane Diterpenes Chemistry and Biological Properties
inferredcites →https://doi.org/10.3390/ijms16036140openalex-snapshot
Polyoxygenated Cembrane Diterpenoids from the Soft Coral Sarcophyton ehrenbergi
inferredcites →https://doi.org/10.3390/md15060192openalex-snapshot
Cembrene Diterpenoids with Ether Linkages from Sarcophyton ehrenbergi: An Anti-Proliferation and Molecular-Docking Assessment
inferredcites →https://doi.org/10.3390/md16100388openalex-snapshot
For a Correct Application of the CD Exciton Chirality Method: The Case of Laucysteinamide A
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.2022.113088zenodo-depositor-declared
Nardosinane-related antimicrobial terpenoids from Lemnalia sp. soft coral
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113549zenodo-depositor-declared
Further undescribed cembranoids from South China Sea soft coral Sarcophyton ehrenbergi: Structural elucidation and biological evaluation
inferred← citeshttps://doi.org/10.1002/cbdv.202000503openalex-snapshot
Chemical Constituents from Citrus changshan‐huyou and Their Anti‐Inflammatory Activities
inferred← citeshttps://doi.org/10.1002/cbdv.202300267openalex-snapshot
Extending the Record of Terpenes from Soft Coral Sarcophyton mililatensis
inferred← citeshttps://doi.org/10.1002/chem.202300559openalex-snapshot
X‐ray Study of Cembranoids with Flexible Rings from Boswellia papyrifera Resins Allowing Structural Revision of Misleading Structures from the Past 70 Years
inferred← citeshttps://doi.org/10.1002/cjoc.202000539openalex-snapshot
Polyoxygenated Cembranoids from Soft Coral Lobophytum Crassum and Their Anti‐tumoral Activities
inferred← citeshttps://doi.org/10.1002/cjoc.202100236openalex-snapshot
Uncommon Polycyclic Merosesquiterpenoids and Asteriscanoids from the Hainan Soft Coral Sinularia humesi†
inferred← citeshttps://doi.org/10.1002/cjoc.202100253openalex-snapshot
Sinucrassins A—K, Casbane‐type Diterpenoids from the South China Sea Soft Coral Sinularia crassa
inferred← citeshttps://doi.org/10.1002/cjoc.202100676openalex-snapshot
Nitrogenous Sesquiterpenoids from the South China Sea Nudibranch Hexabranchus sanguineus and Its Possible Sponge‐Prey Acanthella cavernosa: Chiral Separation, Stereochemistry and Chemical Ecology
inferred← citeshttps://doi.org/10.1007/s13659-021-00303-2openalex-snapshot
Cembranoids of Soft Corals: Recent Updates and Their Biological Activities
inferred← citeshttps://doi.org/10.1007/s42995-019-00021-2openalex-snapshot
Metabolites from marine invertebrates and their symbiotic microorganisms: molecular diversity discovery, mining, and application
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103350openalex-snapshot
Polycyclic furanobutenolide-derived norditerpenoids from the South China Sea soft corals Sinularia scabra and Sinularia polydactyla with immunosuppressive activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103636openalex-snapshot
Uncommon nornardosinane, seconeolemnane and related sesquiterpenoids from Xisha soft coral Litophyton nigrum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103993openalex-snapshot
Further polyoxygenated cembranoids from South China Sea soft coral Sarcophyton ehrenbergi
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104167openalex-snapshot
Uncommon terpenoids with anti-inflammatory activity from the Hainan soft coral Sinularia tumulosa
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104223openalex-snapshot
Rare new bicyclic cembranoid ethers and a novel trihydroxy prenylated guaiane from the Xisha soft coral Lobophytum sp
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104281openalex-snapshot
New cembrane-type diterpenoids from the South China Sea soft coral Sinularia crassa and their α-glucosidase inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104887openalex-snapshot
Diversity-oriented synthesis of cembranoid derivatives as potential anti-inflammatory agents
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105028openalex-snapshot
Unusual polyoxygenated casbane diterpenoids from the South China Sea soft coral Sinularia erecta
inferred← citeshttps://doi.org/10.1016/j.bmc.2021.116139openalex-snapshot
Ximaoglaucumins A − F, new cembranoids with anti-inflammatory activities from the South China Sea soft coral Sarcophyton glaucum
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.11.037openalex-snapshot
Polyoxygenated anti-inflammatory biscembranoids from the soft coral Sarcophyton tortuosum and their stereochemistry
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2025.100287openalex-snapshot
Glaucumolides C-P, cembrane-type diterpenoids from the marine soft coral Sarcophyton glaucum with potential attenuating activities against IgAN nephropathy
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104699openalex-snapshot
Bioactive cembrane diterpenoids from the gum resin of Boswellia carterii
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105299openalex-snapshot
Polyoxygenated cembranoids from the South China Sea soft coral Sarcophyton boettgeri and their stereochemistry
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.09.210openalex-snapshot
New flexible cembrane-type macrocyclic diterpenes as TNF-α inhibitors from the South China Sea soft coral Sarcophyton mililatensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113703openalex-snapshot
Cembrane diterpenoids: Chemistry and pharmacological activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113779openalex-snapshot
Molecular networking-guided isolation of undescribed antifungal odoriferous sesquiterpenoids from a marine mesophotic zone sponge-associated Streptomyces sp. NBU3428
inferred← citeshttps://doi.org/10.1016/j.steroids.2021.108932openalex-snapshot
Polyhydroxylated steroids from the Vietnamese soft coral Sarcophyton ehrenbergi
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132204openalex-snapshot
Polyoxygenated cembranoids from the Hainan soft coral Lobophytum crassum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00630openalex-snapshot
Highly Oxidized Germacranolides from Elephantopus tomentosus and the Configurational Revision of Some Previously Reported Analogues
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00463openalex-snapshot
Unusual Diterpenoids from the South China Sea Soft Coral Sarcophyton ehrenbergi
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01128openalex-snapshot
Cryptic Species Account for the Seemingly Idiosyncratic Secondary Metabolism ofSarcophyton glaucumSpecimens Collected in Palau
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02742openalex-snapshot
Uncommon Diterpenoids from the South China Sea Soft Coral Sinularia humilis and Their Stereochemistry
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01155openalex-snapshot
Quantum Mechanical–NMR-Aided Configuration and Conformation of Two Unreported Macrocycles Isolated from the Soft Coral Lobophytum sp.: Energy Calculations versus Coupling Constants
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01998openalex-snapshot
Klyflaccilides A and B, Diterpenoids with 6/5/8/3 Fused Tetracyclic Carbon Skeleton from the Hainan Soft Coral Klyxum flaccidum
inferred← citeshttps://doi.org/10.1038/s41401-022-00980-wopenalex-snapshot
Chemistry and bioactivity of secondary metabolites from South China Sea marine fauna and flora: recent research advances and perspective
inferred← citeshttps://doi.org/10.1039/d2np00023gopenalex-snapshot
Pitfalls in the structural elucidation of small molecules. A critical analysis of a decade of structural misassignments of marine natural products
inferred← citeshttps://doi.org/10.1080/14786419.2021.2018587openalex-snapshot
Cembranoids from the Vietnamese soft coral Sarcophyton ehrenbergi
inferred← citeshttps://doi.org/10.1080/14786419.2022.2130915openalex-snapshot
A new cembranoid from the Red Sea soft coral Sarcophyton acutum
inferred← citeshttps://doi.org/10.1186/s12934-021-01523-4openalex-snapshot
Synthesis of cembratriene-ol and cembratriene-diol in yeast via the MVA pathway
inferred← citeshttps://doi.org/10.3389/fntpr.2022.1086897openalex-snapshot
Computational methods and points for attention in absolute configuration determination
inferred← citeshttps://doi.org/10.3390/agronomy13030845openalex-snapshot
Manipulation of CBTS1 Expression Alters Tobacco Resistance to Spodoptera frugiperda and Phytophthora nicotianae
inferred← citeshttps://doi.org/10.3390/md18010041openalex-snapshot
Chemical Diversity in Species Belonging to Soft Coral Genus Sacrophyton and Its Impact on Biological Activity: A Review
inferred← citeshttps://doi.org/10.3390/md18090452openalex-snapshot
New Biscembranoids Sardigitolides A–D and Known Cembranoid-Related Compounds from Sarcophyton digitatum: Isolation, Structure Elucidation, and Bioactivities
inferred← citeshttps://doi.org/10.3390/md19050260openalex-snapshot
Cherbonolides M and N from a Formosan Soft Coral Sarcophyton cherbonnieri
inferred← citeshttps://doi.org/10.3390/md19060294openalex-snapshot
Antimicrobial Terpenoids from South China Sea Soft Coral Lemnalia sp.
inferred← citeshttps://doi.org/10.3390/md19060339openalex-snapshot
Six New Diterpene Glycosides from the Soft Coral Lemnaliabournei
inferred← citeshttps://doi.org/10.3390/md20090566openalex-snapshot
Mililatensols A–C, New Records of Sarsolenane and Capnosane Diterpenes from Soft Coral Sarcophyton mililatensis
inferred← citeshttps://doi.org/10.3390/md21020063openalex-snapshot
Marine Natural Products from the Beibu Gulf: Sources, Chemistry, and Bioactivities
inferred← citeshttps://doi.org/10.3390/md23060241openalex-snapshot
Catechol Siderophores from a Mangrove-Derived Bacteria Serratia marcescens F2-2 and Their Cytotoxic Activity
inferred← citeshttps://doi.org/10.3762/bjoc.18.180openalex-snapshot
New cembrane-type diterpenoids with anti-inflammatory activity from the South China Sea soft coral Sinularia sp.
inferred← citeshttps://doi.org/10.6084/m9.figshare.13698312openalex-snapshot
Additional file 1 of Synthesis of cembratriene-ol and cembratriene-diol in yeast via the MVA pathway
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.