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Sarcomililate A, an Unusual Diterpenoid with Tricyclo[11.3.0.02,16]hexadecane Carbon Skeleton, and Its Potential Biogenetic Precursors from the Hainan Soft Coral Sarcophyton mililatensis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.201705123openalex-snapshot
A Self‐Assembled Oligopeptide as a Versatile NMR Alignment Medium for the Measurement of Residual Dipolar Couplings in Methanol
inferredcites →https://doi.org/10.1002/cbdv.201200122openalex-snapshot
Terpenes from the Soft Corals of the Genus Sarcophyton: Chemistry and Biological Activities
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Relative and Absolute Configuration of Vatiparol (1 mg): A Novel Anti‐inflammatory Polyphenol
inferredcites →https://doi.org/10.1002/ejoc.201200862openalex-snapshot
Absolute Configuration of Highly Flexible Natural Products by the Solid‐State ECD/TDDFT Method: Ximaolides and Sinulaparvalides
inferredcites →https://doi.org/10.1002/ejoc.201301683openalex-snapshot
Sarsolenane and Capnosane Diterpenes from the Hainan Soft Coral Sarcophyton trocheliophorum Marenzeller as PTP1B Inhibitors
inferredcites →https://doi.org/10.1002/hlca.201100278openalex-snapshot
Yalongenes A and B, Two New Cembranoids with Cytoprotective Effects from the Hainan Soft Coral Sarcophyton trocheliophorum Marenzeller
inferredcites →https://doi.org/10.1002/mrc.3905openalex-snapshot
MSpin‐RDC. A program for the use of residual dipolar couplings for structure elucidation of small molecules
inferredcites →https://doi.org/10.1007/s13659-018-0174-xopenalex-snapshot
Residual Dipolar Couplings in Structure Determination of Natural Products
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.jmr.2008.03.009openalex-snapshot
The CLIP/CLAP-HSQC: Pure absorptive spectra for the measurement of one-bond couplings
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/10.1021/acs.jnatprod.7b00926openalex-snapshot
Computer-Assisted 3D Structure Elucidation (CASE-3D) of Natural Products Combining Isotropic and Anisotropic NMR Parameters
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/ja9812610openalex-snapshot
Validation of Protein Structure from Anisotropic Carbonyl Chemical Shifts in a Dilute Liquid Crystalline Phase
inferredcites →https://doi.org/10.1021/jo010136vopenalex-snapshot
Determination of Absolute Configuration of Acyclic 1,2-Diols with Mo2(OAc)4. 1. Snatzke's Method Revisited
inferredcites →https://doi.org/10.1021/jo062445xopenalex-snapshot
Practical Method for the Absolute Configuration Assignment of tert / tert 1,2-Diols Using Their Complexes with Mo 2 (OAc) 4
inferredcites →https://doi.org/10.1021/np300728bopenalex-snapshot
RDC-Based Determination of the Relative Configuration of the Fungicidal Cyclopentenone 4,6-Diacetylhygrophorone A12
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/10.1038/srep46584openalex-snapshot
New Bicyclic Cembranoids from the South China Sea Soft Coral Sarcophyton trocheliophorum
inferredcites →https://doi.org/10.1039/c5ra01151eopenalex-snapshot
Structural diversity of terpenoids in the soft coral Sinularia flexibilis, evidenced by a collection from the South China Sea
inferredcites →https://doi.org/10.1039/c7ra04261bopenalex-snapshot
Discovery of new BTK inhibitors with B cell suppression activity bearing a 4,6-substituted thieno[3,2-d]pyrimidine scaffold
inferredcites →https://doi.org/10.1039/c7sc01996copenalex-snapshot
Unequivocal determination of caulamidines A and B: application and validation of new tools in the structure elucidation tool box
inferredcites →https://doi.org/10.1080/14786419.2012.701211openalex-snapshot
New precursor of tetraterpenoids from the soft coralSarcophyton glaucum
inferredcites →https://doi.org/10.1126/science.aam5349openalex-snapshot
Unequivocal determination of complex molecular structures using anisotropic NMR measurements
inferredcites →https://doi.org/10.1248/cpb.37.631openalex-snapshot
Marine terpenes and terpenoids. VII. Minor cembranoid derivatives, structurally related to the potent anti-tumor-promoter sarcophytol A, from the soft coral Sarcophyton glaucum.
inferredcites →https://doi.org/10.13018/bmr6457openalex-snapshot
Validation of Protein Structure from Anisotropic Carbonyl Chemical Shifts in a Dilute Liquid Crystalline Phase
inferredcites →https://doi.org/10.2174/1385272803666220131193916openalex-snapshot
Transition Metal Complexes as Auxiliary Chromophores in Chiroptical Studies on Carbohydrates
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.2022.113578zenodo-depositor-declared
Sarcoelegans A–H, eight undescribed cembranes with anti-inflammatory and anti-thrombotic activities from the South China Sea soft coral Sarcophyton elegans
inferred← citeshttps://doi.org/10.1002/9781119802280.ch13openalex-snapshot
NMR for Stereochemical Elucidation
inferred← citeshttps://doi.org/10.1002/ange.202007243openalex-snapshot
Measurement of Residual Dipolar Couplings of Organic Molecules in Multiple Solvent Systems Using a Liquid‐Crystalline‐Based Medium
inferred← citeshttps://doi.org/10.1002/anie.202007243openalex-snapshot
Measurement of Residual Dipolar Couplings of Organic Molecules in Multiple Solvent Systems Using a Liquid‐Crystalline‐Based Medium
inferred← citeshttps://doi.org/10.1002/cbdv.202000214openalex-snapshot
New Steroids from the South China Sea Soft Coral Lobophytum sp.
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.202203487openalex-snapshot
Guided Isolation of An Uncommon Cembranoid Orthoester, Sarcotortin A, and Three Skeletal Diverse Terpenoids from the Hainan Soft Coral Sarcophyton tortuosum Based on Molecular Networking Strategy
inferred← citeshttps://doi.org/10.1002/cjoc.202100597openalex-snapshot
New Cembrane‐Type Diterpenoids from the South China Sea Soft Coral Sinularia nanolobata
inferred← citeshttps://doi.org/10.1002/cjoc.202200129openalex-snapshot
Structural and Biological Insights into the Hot‐Spot Marine Natural Products Reported from 2012 to 2021
inferred← citeshttps://doi.org/10.1002/cjoc.202300275openalex-snapshot
Natural Sesquiterpenoids, Diterpenoids, Sesterterpenoids, and Triterpenoids with Intriguing Structures from 2017 to 2022
inferred← citeshttps://doi.org/10.1002/marc.202100898openalex-snapshot
Self‐Assembly of Helical Polymers and Oligomers to Create Liquid Crystalline Alignment for Anisotropic NMR Parameters
inferred← citeshttps://doi.org/10.1002/marc.202401002openalex-snapshot
Halogen‐Bearing Peptide Liquid Crystals to Elicit Molecular Alignments for Residual Dipolar Coupling Measurement
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/10.1016/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.2020.104223openalex-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.2021.104888openalex-snapshot
Granatripodins A–B, limonoids featuring a Tricyclo[3.3.1.02,8]nonane motif: Absolute configuration and agonistic effects on human pregnane–X–receptor
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.2019.06.030openalex-snapshot
Highly diverse cembranoids from the South China Sea soft coral Sinularia scabra as a new class of potential immunosuppressive agents
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.fitote.2019.03.018openalex-snapshot
Two new cembrane-type diterpenoids from the xisha soft coral Lemnalia flava
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104902openalex-snapshot
Further new cembranoids from the South China Sea soft coral Sarcophyton trocheliophorum
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.mrl.2024.200171openalex-snapshot
An amphiphilic peptide with unnatural amino acids as an alignment medium for RDC measurements
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113703openalex-snapshot
Cembrane diterpenoids: Chemistry and pharmacological activities
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132204openalex-snapshot
Polyoxygenated cembranoids from the Hainan soft coral Lobophytum crassum
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133301openalex-snapshot
Stereochemical investigation of flexible macrocyclic cembranes depending on residual dipolar couplings method
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151308openalex-snapshot
Sinuhirtins A and B, two uncommon norhumulene-type terpenoids from the South China Sea soft coral Sinularia hirta
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152008openalex-snapshot
Absolute configurations of new cembrane-type diterpenoids from the Hainan soft coral Sarcophyton crassocaule
inferred← citeshttps://doi.org/10.1016/s1875-5364(20)60025-5openalex-snapshot
New lobane-type diterpenoids from the Xisha soft coral Sinularia polydactyla
inferred← citeshttps://doi.org/10.1021/accountsmr.3c00181openalex-snapshot
Weak Alignment Liquid Crystal Media from Colloidal Dispersion and Self-assembled Oligopeptide for Anisotropic NMR
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00257openalex-snapshot
Weizhouochrones: Gorgonian-Derived Symmetric Dimers and Their Structure Elucidation Using Anisotropic NMR Combined with DP4+ Probability and CASE-3D
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.joc.0c02397openalex-snapshot
Sinueretone A, a Diterpenoid with Unprecedented Tricyclo[12.1.0.05,9]pentadecane Carbon Scaffold from the South China Sea Soft Coral Sinularia erecta
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.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/10.1021/jacs.9b10961openalex-snapshot
Stereochemical Elucidation of Natural Products from Residual Chemical Shift Anisotropies in a Liquid Crystalline Phase
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/bk9781839167898-00252openalex-snapshot
Structure Determination of Organic Molecules Using RDCs (and RCSAs)
inferred← citeshttps://doi.org/10.1039/bk9781839167898-00306openalex-snapshot
Anisotropic NMR Methods: Orthogonal Verification of Novel and Complex Natural Product Structures
inferred← citeshttps://doi.org/10.1039/d2sc01057gopenalex-snapshot
Programmable alignment media from self-assembled oligopeptide amphiphiles for the measurement of independent sets of residual dipolar couplings in organic solvents
inferred← citeshttps://doi.org/10.1039/d3nr00204gopenalex-snapshot
Weakly aligned Ti 3 C 2 T x MXene liquid crystals: measuring residual dipolar coupling in multiple co-solvent systems
inferred← citeshttps://doi.org/10.1080/10286020.2020.1844675openalex-snapshot
Survey of natural products reported by Asian research groups in 2019
inferred← citeshttps://doi.org/10.1246/bcsj.20210393openalex-snapshot
An Unprecedented Cembranoid with a Novel Tricyclo[9.3.0.02,12]tetradecane Skeleton and Related Diterpenes from the Soft Coral Sarcophyton cinereum
inferred← citeshttps://doi.org/10.3390/ijms24031979openalex-snapshot
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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/md20090566openalex-snapshot
Mililatensols A–C, New Records of Sarsolenane and Capnosane Diterpenes from Soft Coral Sarcophyton mililatensis
inferred← citeshttps://doi.org/10.3390/md20090574openalex-snapshot
Sarcoeleganolides C–G, Five New Cembranes from the South China Sea Soft Coral Sarcophyton elegans
inferred← citeshttps://doi.org/10.3390/md20100602openalex-snapshot
Uncommon Capnosane Diterpenes with Neuroprotective Potential from South China Sea Soft Coral Sarcophyton boettgeri
inferred← citeshttps://doi.org/10.3390/md21020069openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md21060362openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md22120536openalex-snapshot
Cembranoid Diterpenes from South China Sea Soft Coral Sarcophyton crassocaule
inferred← citeshttps://doi.org/10.3390/md23020072openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules29102359openalex-snapshot
Research Progress of Natural Active Substances with Immunosuppressive Activity
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