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Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20000818)39:16<2812::aid-anie2812>3.0.co;2-#openalex-snapshot
Enzyme Mechanisms for Polycyclic Triterpene Formation
inferredcites →https://doi.org/10.1002/cbic.201300035openalex-snapshot
Identification of Novel Sesterterpene/Triterpene Synthase from Bacillus clausii
inferredcites →https://doi.org/10.1002/chem.201100503openalex-snapshot
The Truth about False Unicorn (Chamaelirium luteum): Total Synthesis of 23R,24S‐Chiograsterol B Defines the Structure and Stereochemistry of the Major Saponins from this Medicinal Herb
inferredcites →https://doi.org/10.1002/jps.3030330605openalex-snapshot
Pharmacological Studies. I. Aletris Farinos**From the Research Laboratories of the Lydia E. Pinkham Medicine Company, Lynn, Mass.
inferredcites →https://doi.org/10.1007/978-1-59259-365-1openalex-snapshot
Medicinal Plants of the World
inferredcites →https://doi.org/10.1016/0301-0104(81)85090-2openalex-snapshot
Electrostatic interaction of a solute with a continuum. A direct utilizaion of AB initio molecular potentials for the prevision of solvent effects
inferredcites →https://doi.org/10.1021/cr200106vopenalex-snapshot
Computational Prediction of 1 H and 13 C Chemical Shifts: A Useful Tool for Natural Product, Mechanistic, and Synthetic Organic Chemistry
inferredcites →https://doi.org/10.1021/ja01867a011openalex-snapshot
Sterols. CVII. Steroidal Sapogenins of Aletris, Asparagus and Lilium*
inferredcites →https://doi.org/10.1021/ja105035ropenalex-snapshot
Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability
inferredcites →https://doi.org/10.1021/ja3089394openalex-snapshot
The Correct Structure of Aquatolide—Experimental Validation of a Theoretically-Predicted Structural Revision
inferredcites →https://doi.org/10.1021/ja4106489openalex-snapshot
Branching Out from the Bisabolyl Cation. Unifying Mechanistic Pathways to Barbatene, Bazzanene, Chamigrene, Chamipinene, Cumacrene, Cuprenene, Dunniene, Isobazzanene, Iso-γ-bisabolene, Isochamigrene, Laurene, Microbiotene, Sesquithujene, Sesquisabinene, Thujopsene, Trichodiene, and Widdradiene…
inferredcites →https://doi.org/10.1021/jo000081hopenalex-snapshot
Mangicols: Structures and Biosynthesis of A New Class of Sesterterpene Polyols from a Marine Fungus of the Genus Fusarium
inferredcites →https://doi.org/10.1021/np200100aopenalex-snapshot
Structure and Absolute Configuration of Helosides A and B, New Saponins from Chamaelirium luteum
inferredcites →https://doi.org/10.1021/np300393yopenalex-snapshot
Structure and Bioactivity of Steroidal Saponins Isolated from the Roots of Chamaelirium luteum (False Unicorn)
inferredcites →https://doi.org/10.1021/np400035nopenalex-snapshot
Structure and Absolute Configuration of Methyl (3R)-Malonyl-(13S)-hydroxycheilanth-17-en-19-oate, a Sesterterpene Derivative from the Roots of Aletris farinosa
inferredcites →https://doi.org/10.1021/ol303408aopenalex-snapshot
Identification of Ophiobolin F Synthase by a Genome Mining Approach: A Sesterterpene Synthase from Aspergillus clavatus
inferredcites →https://doi.org/10.1038/nchem.1843openalex-snapshot
Biosynthetic consequences of multiple sequential post-transition-state bifurcations
inferredcites →https://doi.org/10.1039/c1np00006copenalex-snapshot
Biosynthesis via carbocations: Theoretical studies on terpene formation
inferredcites →https://doi.org/10.1039/c2np20059gopenalex-snapshot
Terpenoid synthase structures: a so far incomplete view of complex catalysis
inferredcites →https://doi.org/10.1039/c3np70028copenalex-snapshot
Walking in the woods with quantum chemistry – applications of quantum chemical calculations in natural products research
inferredcites →https://doi.org/10.1039/c4sc03782kopenalex-snapshot
Modulation of inherent dynamical tendencies of the bisabolyl cation via preorganization in epi-isozizaene synthase
inferredcites →https://doi.org/10.1039/jr9560002419openalex-snapshot
469. Triterpenoids. Part LII. The constitution and stereochemistry of friedelin and cerin
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1063/1.475428openalex-snapshot
Exchange functionals with improved long-range behavior and adiabatic connection methods without adjustable parameters: The mPW and mPW1PW models
inferredcites →https://doi.org/10.1271/bbb.130543openalex-snapshot
Cyclization of All-E- and 2Z-Geranylfarnesols by a Bacterial Triterpene Synthase: Insight into Sesterterpene Biosynthesis inAleuritopterisFerns
inferredcites →https://doi.org/10.5860/choice.37-0939openalex-snapshot
Comprehensive natural products chemistry
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.2021.112780zenodo-depositor-declared
Immunosuppressive gentianellane-type sesterterpenoids from the traditional Uighur medicine Gentianella turkestanorum
inferred← citeshttps://doi.org/10.1002/cbdv.202400549openalex-snapshot
Genomics of Terpene Biosynthesis in Dictyoceratid Sponges (Porifera) – What Do We (Not) Know?
inferred← citeshttps://doi.org/10.1002/chem.201601150openalex-snapshot
Computational Chemistry to the Rescue: Modern Toolboxes for the Assignment of Complex Molecules by GIAO NMR Calculations
inferred← citeshttps://doi.org/10.1002/ece3.72654openalex-snapshot
Integrating Morphology and Chloroplast Genomics: A New East Asian Species of Aletris (Nartheciaceae) With Insights Into Regional Phylogeny and Evolution
inferred← citeshttps://doi.org/10.1002/jemt.23378openalex-snapshot
Pollen morphology of Aletris L. (Nartheciaceae) and its systematic significance
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114305openalex-snapshot
Immunosuppressive leucosceptrane-type sesterterpenoids with antipodal cyclopentenones isolated from Leucosceptrum canum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153869openalex-snapshot
Ancepsone A, a new cheilanthane sesterterpene from Aleuritopteris anceps
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.155972openalex-snapshot
Gentianellin A, an unusual immunosuppressive sesterterpenoid from the traditional Tibetan medicine Gentianella azurea
inferred← citeshttps://doi.org/10.1039/d0np00070aopenalex-snapshot
Sesterterpenoids: chemistry, biology, and biosynthesis
inferred← citeshttps://doi.org/10.1039/d1np00021gopenalex-snapshot
The untapped potential of plant sesterterpenoids: chemistry, biological activities and biosynthesis
inferred← citeshttps://doi.org/10.1039/d1qo00034aopenalex-snapshot
Structural characterisation of natural products by means of quantum chemical calculations of NMR parameters: new insights
inferred← citeshttps://doi.org/10.1039/d4np00041bopenalex-snapshot
Sesterterpenoids: sources, structural diversity, biological activity, and data management
inferred← citeshttps://doi.org/10.1105/tpc.15.00715openalex-snapshot
A Geranylfarnesyl Diphosphate Synthase Provides the Precursor for Sesterterpenoid (C25) Formation in the Glandular Trichomes of the Mint Species Leucosceptrum canum
inferred← citeshttps://doi.org/10.3389/fntpr.2023.1321043openalex-snapshot
Are we still chasing molecules that were never there? The role of quantum chemical simulations of NMR parameters in structural reassignment of natural products
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