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ent-Pimarane Diterpenoids from Siegesbeckia orientalis and Structure Revision of a Related Compound

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf02973998openalex-snapshot

Suppression of anaphylactic reaction in murine bySiegesbeckia pubescens

inferredcites →https://doi.org/10.1016/0031-9422(79)80045-xopenalex-snapshot

Darutoside, a diterpenoid from Siegesbeckia pubescens and its structure revision

inferredcites →https://doi.org/10.1016/0031-9422(91)84212-bopenalex-snapshot

Sesquiterpene lactones and other constituents from Siegesbeckia orientalis and Guizotia scabra

inferredcites →https://doi.org/10.1016/0031-9422(92)80039-hopenalex-snapshot

Diterpenoids from Siegesbeckia pubescens

inferredcites →https://doi.org/10.1016/j.fitote.2008.09.009openalex-snapshot

Sesquiterpene lactones from Carpesium abrotanoides

inferredcites →https://doi.org/10.1016/j.phytochem.2009.03.007openalex-snapshot

Alstonic acids A and B, unusual 2,3-secofernane triterpenoids from Alstonia scholaris

inferredcites →https://doi.org/10.1016/s0040-4039(01)87630-9openalex-snapshot

Eine neuuntersuchung der inhaltsstoffe von siegesbeckia pubescens makino

inferredcites →https://doi.org/10.1016/s0040-4039(01)88814-6openalex-snapshot

A new diterpenoid with pimarane skeleton

inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

inferredcites →https://doi.org/10.1021/jo01315a036openalex-snapshot

Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. 61. The C(15) configuration of naturally occurring pimarene-15,16-diols

inferredcites →https://doi.org/10.1021/np0400407openalex-snapshot

Novel Diterpenoids and Diterpenoid Glycosides from Siegesbeckia orientalis

inferredcites →https://doi.org/10.1055/s-2006-960129openalex-snapshot

Diterpene ausSiegesbeckia glabrescens

inferredcites →https://doi.org/10.1080/10286020903048975openalex-snapshot

New geranyloxycoumarins fromToddalia asiatica

inferredcites →https://doi.org/10.1248/cpb.53.232openalex-snapshot

ent-Pimarane-Type Diterpenoids from Siegesbeckia orientalis L.

inferredcites →https://doi.org/10.1248/cpb.56.864openalex-snapshot

Sulfonated Guaianolides from Saussurea lappa

inferredcites →https://doi.org/10.1248/cpb.57.525openalex-snapshot

New Terpenoids from Isodon sculponeata

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.2021.112889zenodo-depositor-declared

Guaianolide sesquiterpenes and benzoate esters from the aerial parts of Siegesbeckia orientalis L. and their xanthine oxidase inhibitory activity

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113503zenodo-depositor-declared

Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities

inferred← citeshttps://doi.org/10.1002/cbdv.201900519openalex-snapshot

A New Pimarane Diterpenoid from the Botryotinia fuckeliana Fungus Isolated from Deep‐Sea Water

inferred← citeshttps://doi.org/10.1002/cbdv.202201090openalex-snapshot

ent‐Pimarane Diterpenes from the Aerial Parts of Siegesbeckia pubescens

inferred← citeshttps://doi.org/10.1002/hlca.201100272openalex-snapshot

Three New ent‐Kaurane Diterpenoids from Siegesbeckia pubescens

inferred← citeshttps://doi.org/10.1002/jssc.202300160openalex-snapshot

Rapid identification of chemical compositions from three species of Siegesbeckiae Herba by ultra‐performance liquid chromatography‐electrospray ionization‐quadrupole time of flight‐mass spectrometry in combination with deoxyribonucleic acid barcoding

inferred← citeshttps://doi.org/10.1002/vjch.202300041openalex-snapshot

Investigation on chemical constituents from Sigesbeckia orientalis L.

inferred← citeshttps://doi.org/10.1007/s11101-020-09714-4openalex-snapshot

Botany, traditional use, phytochemistry, pharmacology and toxicology of Sigesbeckiae Herba (Xixiancao): a review

inferred← citeshttps://doi.org/10.1007/s13659-016-0107-5openalex-snapshot

Prenylated Coumarins from Heracleum stenopterum, Peucedanum praeruptorum, Clausena lansium, and Murraya paniculata

inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00007-3openalex-snapshot

Five-Membered Ring Systems: Furans and Benzofurans

inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00009-7openalex-snapshot

Five-Membered Ring Systems

inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103854openalex-snapshot

ent-Pimarane diterpenoids from Siegesbeckia glabrescens with anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104537openalex-snapshot

Diverse diterpenoids and sesquiterpenoids from Siegesbeckia pubescens and their activity against RANKL-induced osteoclastogenesis

inferred← citeshttps://doi.org/10.1016/j.bmc.2019.02.032openalex-snapshot

Semisynthesis of epoxy-pimarane diterpenoids from kirenol and their FXa inhibition activities

inferred← citeshttps://doi.org/10.1016/j.bse.2010.10.009openalex-snapshot

Ent-kaurane derivatives from the root cortex of yacon and other three Smallanthus species (Heliantheae, Asteraceae)

inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104870openalex-snapshot

Shanpanootols A-F, diterpenoids from Kaempferia pulchra rhizomes collected in Myanmar and their Vpr inhibitory activities

inferred← citeshttps://doi.org/10.1016/j.fitote.2025.107068openalex-snapshot

Six undescribed diterpenoids from the aerial parts of Siegesbeckia pubescens Makino and their anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107189openalex-snapshot

Three new ent-pimarane diterpenoids from Siegesbeckia pubescens and their anti-vascular endothelial injury activity

inferred← citeshttps://doi.org/10.1016/j.indcrop.2016.08.023openalex-snapshot

Biological activity of extracts and active compounds isolated from Siegesbeckia orientalis L.

inferred← citeshttps://doi.org/10.1016/j.jep.2011.07.016openalex-snapshot

Topical anti-inflammatory and analgesic activity of kirenol isolated from Siegesbeckia orientalis

inferred← citeshttps://doi.org/10.1016/j.jep.2019.112159openalex-snapshot

A selection of eleven plants used as traditional Polynesian cosmetics and their development potential as anti-aging ingredients, hair growth promoters and whitening products

inferred← citeshttps://doi.org/10.1016/j.jep.2021.114117openalex-snapshot

Herba Siegesbeckiae: A review on its traditional uses, chemical constituents, pharmacological activities and clinical studies

inferred← citeshttps://doi.org/10.1016/j.jpba.2011.02.023openalex-snapshot

Simultaneous quantification of eight major constituents in Herba Siegesbeckiae by liquid chromatography coupled with electrospray ionization time-of-flight tandem mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.phytol.2017.07.003openalex-snapshot

New ent -kaurane and ent -pimarane diterpenoids from Siegesbeckia pubescens

inferred← citeshttps://doi.org/10.1016/j.phytol.2018.04.010openalex-snapshot

Two 9,10- syn -pimarane diterpenes from the roots of Lonicera macranthoides

inferred← citeshttps://doi.org/10.1016/j.phytol.2026.104164openalex-snapshot

Two new diterpenoids isolated from Siegesbeckia pubescens and their in vitro anti-inflammatory activities

inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22007-5openalex-snapshot

Five-Membered Ring Systems

inferred← citeshttps://doi.org/10.1016/s1875-5364(12)60002-8openalex-snapshot

A new carbamate with cytotoxic activity from the aerial parts of Siegesbeckia pubecens

inferred← citeshttps://doi.org/10.1016/s1875-5364(25)60827-2openalex-snapshot

Ent-pimarane and ent-kaurane diterpenoids from Siegesbeckia pubescens and their anti-endothelial damage effect in diabetic retinopathy

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00150openalex-snapshot

ent-Strobane andent-Pimarane Diterpenoids fromSiegesbeckia pubescens

inferred← citeshttps://doi.org/10.1021/cr2003344openalex-snapshot

Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents

inferred← citeshttps://doi.org/10.1021/np500125xopenalex-snapshot

Anti-inflammatory Diterpenoids from the Root Bark of Acanthopanax gracilistylus

inferred← citeshttps://doi.org/10.1021/ol1007247openalex-snapshot

Bi-linderone, a Highly Modified Methyl-linderone Dimer from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity in Vitro

inferred← citeshttps://doi.org/10.1021/ol1011289openalex-snapshot

A Pair of Windmill-Shaped Enantiomers from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity

inferred← citeshttps://doi.org/10.1039/c1np90021hopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.1039/d5ra08807kopenalex-snapshot

New diterpenoids and sesquiterpenoids from Siegesbeckia pubescens Makino and their anti-inflammatory activity

inferred← citeshttps://doi.org/10.1039/d5ra09664bopenalex-snapshot

ent -Pimarane diterpenoids from the aerial parts of Sigesbeckia pubescens and their myocardial protective activity

inferred← citeshttps://doi.org/10.1080/10286020.2017.1367923openalex-snapshot

Diterpenoids from the roots of Euphorbia fischeriana and their inhibitory effects on α-glucosidase

inferred← citeshttps://doi.org/10.1080/10286020.2021.1915994openalex-snapshot

A novel ent-pimarane-type diterpenoid from Sigesbeckia glabrescens with anti-inflammatory activity

inferred← citeshttps://doi.org/10.1080/10286020903569434openalex-snapshot

New iridoid glycosides from the twigs and leaves of Callicarpa formosana var. formosana

inferred← citeshttps://doi.org/10.1080/13880209.2017.1280061openalex-snapshot

An unprecedented antioxidative isopimarane norditerpenoid from bivalve clam,Paphia malabaricawith anti-cyclooxygenase and lipoxygenase potential

inferred← citeshttps://doi.org/10.1080/14786419.2020.1871342openalex-snapshot

Sigesbeckia K and L, two new diterpenoids from Sigesbeckia glabrescens with anti-inflammatory activity

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

Pimarane diterpenoids: sources, structures and biological activities

inferred← citeshttps://doi.org/10.1155/2019/8957245openalex-snapshot

Study on the Multitarget Mechanism and Key Active Ingredients of Herba Siegesbeckiae and Volatile Oil against Rheumatoid Arthritis Based on Network Pharmacology

inferred← citeshttps://doi.org/10.1177/1934578x1601100314openalex-snapshot

Diterpenoids from Leaves of Rubus Chingii

inferred← citeshttps://doi.org/10.1177/1934578x211056140openalex-snapshot

Four New Acyclic Diterpenes From Siegesbeckia orientalis

inferred← citeshttps://doi.org/10.1186/s12906-017-1698-zopenalex-snapshot

Anti-Hyperuricemic, Anti-Inflammatory and Analgesic Effects of Siegesbeckia orientalis L. Resulting from the Fraction with High Phenolic Content

inferred← citeshttps://doi.org/10.1186/s13020-025-01308-6openalex-snapshot

44-year journey (1980–2024): scientometric insights into Sigesbeckiae herba and update on its medicinal properties and phytochemicals profile

inferred← citeshttps://doi.org/10.1248/cpb.58.1267openalex-snapshot

Scutebarbatines W-Z, New neo-Clerodane Diterpenoids from Scutellaria barbata and Structure Revision of a Series of 13-Spiro neo-Clerodanes

inferred← citeshttps://doi.org/10.18311/jnr/2026/45208openalex-snapshot

Phytochemical Screening and Microbicidal Activity of Siegesbeckia orientalis Against Human Bacterial Pathogens

inferred← citeshttps://doi.org/10.2174/0113862073289977240216075724openalex-snapshot

Pharmacological Mechanisms of Kirenol against Ovarian Carcinoma: A Network Pharmacology and Experimental Validation Study In Vitro

inferred← citeshttps://doi.org/10.3390/molecules191219980openalex-snapshot

Anti-Proliferative Effects of Siegesbeckia orientalis Ethanol Extract on Human Endometrial RL-95 Cancer Cells

inferred← citeshttps://doi.org/10.3390/molecules21081021openalex-snapshot

Siegesbeckia orientalis Extract Inhibits TGFβ1-Induced Migration and Invasion of Endometrial Cancer Cells

inferred← citeshttps://doi.org/10.3390/molecules23092185openalex-snapshot

Comparative Analysis of Chemical Composition, Anti-Inflammatory Activity and Antitumor Activity in Essential Oils from Siegesbeckia orientalis, S. glabrescens and S. pubescens with an ITS Sequence Analysis

inferred← citeshttps://doi.org/10.3390/molecules29194631openalex-snapshot

Three New Ent-Kaurane Diterpenes with Antibacterial Activity from Sigesbeckia orientalis

inferred← citeshttps://doi.org/10.3724/sp.j.1009.2012.00013openalex-snapshot

A new carbamate with cytotoxic activity from the aerial parts of Siegesbeckia pubecens

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