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Taichunins E–T, Isopimarane Diterpenes and a 20-nor-Isopimarane, from Aspergillus taichungensis (IBT 19404): Structures and Inhibitory Effects on RANKL-Induced Formation of Multinuclear Osteoclasts

https://doi.org/10.1021/acs.jnatprod.1c00486

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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.200604381openalex-snapshot

Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, Aspergillus sp.

inferredcites →https://doi.org/10.1002/anie.200800106openalex-snapshot

Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)‐Stephacidin A and (+)‐Notoamide B from Aspergillus versicolor NRRL 35600

inferredcites →https://doi.org/10.1002/anie.201509462openalex-snapshot

Taichunamides: Prenylated Indole Alkaloids from Aspergillus taichungensis (IBT 19404)

inferredcites →https://doi.org/10.1002/cber.19781110304openalex-snapshot

Natürlich vorkommende Terpen‐Derivate, 117: Neue Sandaracopimardien‐Derivate, Sesquiterpene und Sesquiterpenlactone aus Zexmenia‐Arten

inferredcites →https://doi.org/10.1002/chir.23009openalex-snapshot

Pimarane diterpenes: Natural source, stereochemical configuration, and biological activity

inferredcites →https://doi.org/10.1016/0031-9422(96)00206-3openalex-snapshot

A phytotoxic pimarane diterpene of Sphaeropsis sapinea f. sp. Cupressi, the pathogen of a canker disease of cypress

inferredcites →https://doi.org/10.1016/j.bmcl.2014.09.043openalex-snapshot

Halenaquinone inhibits RANKL-induced osteoclastogenesis

inferredcites →https://doi.org/10.1016/j.bmcl.2017.10.017openalex-snapshot

Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts

inferredcites →https://doi.org/10.1016/j.fitote.2018.05.001openalex-snapshot

New inhibitors of RANKL-induced Osteoclastogenesis from the marine sponge Siphonochalina siphonella

inferredcites →https://doi.org/10.1016/j.tetlet.2016.02.031openalex-snapshot

Carteritins A and B, cyclic heptapeptides from the marine sponge Stylissa carteri

inferredcites →https://doi.org/10.1016/s0031-9422(97)00006-xopenalex-snapshot

Sphaeropsidins B and C, phytotoxic pimarane diterpenes from Sphaeropsis sapinea f. sp. Cupressi and Diplodia mutila

inferredcites →https://doi.org/10.1016/s0140-6736(10)62349-5openalex-snapshot

Osteoporosis: now and the future

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00158openalex-snapshot

Ceylonamides A–F, Nitrogenous Spongian Diterpenes That Inhibit RANKL-Induced Osteoclastogenesis, from the Marine Sponge Spongia ceylonensis

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00725openalex-snapshot

Ceylonins A–F, Spongian Diterpene Derivatives That Inhibit RANKL-Induced Formation of Multinuclear Osteoclasts, from the Marine Sponge Spongia ceylonensis

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00610openalex-snapshot

Lamellodysidines A and B, Sesquiterpenes Isolated from the Marine Sponge Lamellodysidea herbacea

inferredcites →https://doi.org/10.1021/acs.jnatprod.8b01032openalex-snapshot

Taichunins A–D, Norditerpenes from Aspergillus taichungensis (IBT 19404)

inferredcites →https://doi.org/10.1021/np200321sopenalex-snapshot

p-Terphenyl and Diterpenoid Metabolites from Endophytic Aspergillus sp. YXf3

inferredcites →https://doi.org/10.1021/np500258ropenalex-snapshot

Diplopimarane, a 20-nor-ent-Pimarane Produced by the Oak Pathogen Diplodia quercivora

inferredcites →https://doi.org/10.1038/nature01658openalex-snapshot

Osteoclast differentiation and activation

inferredcites →https://doi.org/10.1038/nri2062openalex-snapshot

Osteoimmunology: shared mechanisms and crosstalk between the immune and bone systems

inferredcites →https://doi.org/10.1039/c7np00042aopenalex-snapshot

Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi

inferredcites →https://doi.org/10.1177/0022034513500306openalex-snapshot

Advances in the Regulation of Osteoclasts and Osteoclast Functions

inferredcites →https://doi.org/10.1248/cpb.55.899openalex-snapshot

Facile Discrimination of Aldose Enantiomers by Reversed-Phase HPLC

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.2022.113548zenodo-depositor-declared

Arteperoxides A–C, tris-normonoterpene–sesquiterpene conjugates with peroxide-bridges from Artemisia judaica exhibiting antiosteoclastogenic activity

inferred← citeshttps://doi.org/10.1007/s00018-023-05033-xopenalex-snapshot

Metabolic bone disorders and the promise of marine osteoactive compounds

inferred← citeshttps://doi.org/10.1007/s11418-025-01878-7openalex-snapshot

A new diterpenoid, carneadiol, isolated from Nocardia carnea IFM 12324

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113510openalex-snapshot

Seco- and isopimarane diterpenoids from Kaempferia marginata rhizomes and their NO inhibition activities

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113872openalex-snapshot

Aaptocarbamates A−G, chlorinated terpene carbamates with antiosteoclastogenic activities from the marine sponge Aaptos sp.

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00640openalex-snapshot

Machine Learning Accelerates Screening of Osteoclast Differentiation Inhibitors from Natural Products

inferred← citeshttps://doi.org/10.1038/s41598-025-12456-yopenalex-snapshot

Molecular networking derived from untargeted LC-MS/MS analysis to discover inhibitors of RANKL-induced osteoclastogenesis from Egyptian marine sponge-associated fungi

inferred← citeshttps://doi.org/10.1080/14786419.2024.2426071openalex-snapshot

Pimarane diterpenoids: sources, structures and biological activities

inferred← citeshttps://doi.org/10.3114/sim.2022.102.01openalex-snapshot

A monograph of Aspergillus section Candidi

inferred← citeshttps://doi.org/10.3389/fpls.2023.1257744openalex-snapshot

The novel nematicide chiricanine A suppresses Bursaphelenchus xylophilus pathogenicity in Pinus massoniana by inhibiting Aspergillus and its secondary metabolite, sterigmatocystin

inferred← citeshttps://doi.org/10.3390/ph15101291openalex-snapshot

Pimarane Diterpenes from Fungi

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