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Isolation, Characterization, and Structure–Activity Relationship Analysis of Abietane Diterpenoids fromCallicarpa bodinierias Spleen Tyrosine Kinase Inhibitors

https://doi.org/10.1021/acs.jnatprod.7b01082
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What this work says

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

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SpecDis: Quantifying the Comparison of Calculated and Experimental Electronic Circular Dichroism Spectra
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Accurate conformation‐dependent molecular electrostatic potentials for high‐throughput in silico drug discovery
inferredcites →https://doi.org/10.1007/s10600-009-9279-0openalex-snapshot
Chemical composition of the essential oil from leaves of Callicarpa nudiflora
inferredcites →https://doi.org/10.1007/s10600-011-9846-zopenalex-snapshot
Flavonoids from Callicarpa nudiflora leaves
inferredcites →https://doi.org/10.1007/s11418-007-0135-xopenalex-snapshot
A new phenylethanoid glycoside from the fruits of Callicarpa japonica Thunb. var. luxurians Rehd.
inferredcites →https://doi.org/10.1007/s11418-008-0289-1openalex-snapshot
A new lignan glucoside from the stems of Callicarpa japonica Thunb. var. luxurians Rehd.
inferredcites →https://doi.org/10.1007/s12038-010-0061-zopenalex-snapshot
Antibacterial abietane-type diterpenoid, taxodone from Metasequoia glyptostroboides Miki ex Hu
inferredcites →https://doi.org/10.1016/j.bmc.2010.09.035openalex-snapshot
Biflavonoids from Torreya nucifera displaying SARS-CoV 3CLpro inhibition
inferredcites →https://doi.org/10.1016/j.cclet.2009.03.022openalex-snapshot
A novel phenylpropanoid glycoside from Callicarpa kwangtungensis Chun
inferredcites →https://doi.org/10.1016/j.drudis.2010.05.001openalex-snapshot
Spleen tyrosine kinases: biology, therapeutic targets and drugs
inferredcites →https://doi.org/10.1016/j.ejmech.2009.10.010openalex-snapshot
Synthesis and biological evaluation of dehydroabietic acid derivatives
inferredcites →https://doi.org/10.1016/j.fitote.2012.12.014openalex-snapshot
Phenylethanoid glycosides from the stems of Callicarpa peii (hemostatic drug)
inferredcites →https://doi.org/10.1016/j.jep.2012.12.051openalex-snapshot
The medicinal uses of Callicarpa L. in traditional Chinese medicine: An ethnopharmacological, phytochemical and pharmacological review
inferredcites →https://doi.org/10.1016/s0040-4020(01)88015-7openalex-snapshot
Further acidic constituents and neutral components of pinus massoniana Resin
inferredcites →https://doi.org/10.1016/s0960-894x(03)00658-9openalex-snapshot
Potent small molecule inhibitors of spleen tyrosine kinase (Syk)
inferredcites →https://doi.org/10.1021/acsmedchemlett.6b00353openalex-snapshot
Carboxamide Spleen Tyrosine Kinase (Syk) Inhibitors: Leveraging Ground State Interactions To Accelerate Optimization
inferredcites →https://doi.org/10.1021/ci6005646openalex-snapshot
Generating Conformer Ensembles Using a Multiobjective Genetic Algorithm
inferredcites →https://doi.org/10.1021/np060325eopenalex-snapshot
Fungal Biotransformation Products of Dehydroabietic Acid
inferredcites →https://doi.org/10.1055/s-0029-1185724openalex-snapshot
Naphthalene Aglycones and Glycosides from the Australian Medicinal Plant,Dianella callicarpa
inferredcites →https://doi.org/10.1055/s-0036-1596594openalex-snapshot
Anti-inflammatory diterpenoids from Callicarpa randaiensis
inferredcites →https://doi.org/10.1080/10286020.2014.969246openalex-snapshot
Two new triterpenoids from Callicarpa kwangtungensis
inferredcites →https://doi.org/10.1080/10286020903569434openalex-snapshot
New iridoid glycosides from the twigs and leaves of Callicarpa formosana var. formosana
inferredcites →https://doi.org/10.1139/b89-189openalex-snapshot
Acids from blue-stain diseased lodgepole pine
inferredcites →https://doi.org/10.1177/1934578x1000500221openalex-snapshot
Volatiles of Callicarpa macrophylla: A Rich Source of Selinene Isomers
inferredcites →https://doi.org/10.3390/molecules20059071openalex-snapshot
Four New Triterpenoids from Callicarpa kwangtungensis
inferredcites →https://doi.org/10.3987/com-13-12738openalex-snapshot
ent-3,4-seco-Labdane Diterpenoids from Callicarpa nudiflora Leaves with Anti-inflammatory Activity

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4135623openalex-extracted
Callicarpnoids A-C, Structurally Intriguing Ent -Clerodane Diterpenoid Dimers with Cytotoxicity Against MCF-7 And HCT-116 Cell Lines From Callicarpa Arborea
inferred← citeshttps://doi.org/10.1002/cbdv.202000552openalex-snapshot
Bioactive Constituents from the Bryophyta Hypnum plumaeforme
inferred← citeshttps://doi.org/10.1002/cbdv.202000798openalex-snapshot
Rubellawus A–D, Four New Diterpenoids Isolated from Callicarpa rubella and Their Anti‐NLRP3 Inflammasome Effects
inferred← citeshttps://doi.org/10.1002/cbdv.202200985openalex-snapshot
Callicarpanes A–L, Twelve New Clerodane Diterpenoids with NLRP3 Inflammasome Inhibitory Activity from Callicarpa integerrima
inferred← citeshttps://doi.org/10.1002/pca.3534openalex-snapshot
New Diterpenoids With Anti‐Inflammatory Activity From Callicarpa rubella Collected in Vietnam
inferred← citeshttps://doi.org/10.1007/s11101-025-10138-1openalex-snapshot
Phytochemistry, pharmacology and bibliometrics insight of the genus Callicarpa L.: an extensive review encompassing the years from approximately 2010 to 2024
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106022openalex-snapshot
The discovery of potentially active diterpenoids to inhibit the pyroptosis from Callicarpa arborea
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106111openalex-snapshot
Callicarpnoids A–C, structurally intriguing ent-Clerodane diterpenoid dimers with cytotoxicity against MCF-7 and HCT-116 cell lines from Callicarpa arborea Roxb
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.09.020openalex-snapshot
Anti-NLRP3 inflammasome abietane diterpenoids from Callicarpa bodinieri and their structure elucidation
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106690openalex-snapshot
Bioactive diterpenoids from the leaves of Callicarpa formosana Rolfe
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.12.009openalex-snapshot
Tyrosine kinase inhibitors and their unique therapeutic potentialities to combat cancer
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113748openalex-snapshot
Diverse diterpenoids from Callicarpa rubella Lindl. as natural inhibitors of macrophage foam cell formation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113825openalex-snapshot
Abietane diterpenoids with anti-inflammatory activities from Callicarpa bodinieri
inferred← citeshttps://doi.org/10.1016/j.phytol.2024.04.010openalex-snapshot
Annamiacids A and B: Two dissymmetric bis-diterpenes containing a rare ketal-γ-lactone motif from Podocarpus annamiensis and their inhibitory effects on ATP-citrate lyase
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154133openalex-snapshot
Recent advances in abietane/icetexane synthesis
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30118-9openalex-snapshot
Clerodane diterpenoids with potential anti-inflammatory activity from the leaves and twigs of Callicarpa cathayana
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00288openalex-snapshot
Callicarpins, Two Classes of Rearranged ent-Clerodane Diterpenoids from Callicarpa Plants Blocking NLRP3 Inflammasome-Induced Pyroptosis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00568openalex-snapshot
Callintegers A and B, Unusual Tricyclo[4.4.0.09,10]tetradecane Clerodane Diterpenoids from Callicarpa integerrima with Inhibitory Effects on NLRP3 Inflammasome Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00266openalex-snapshot
A Highly Rearranged Nor-Abietane Diterpenoid with an Unusual 6/6/6/5/4 Pentacyclic System and Three Other Diterpenoids from Lycopus lucidus var. hirtus and Antineuroinflammatory Activities
inferred← citeshttps://doi.org/10.1021/acsomega.8b01401openalex-snapshot
Catalytic, Tunable, One-Step Bismuth(III) Triflate Reaction with Alcohols: Dehydration Versus Dimerization
inferred← citeshttps://doi.org/10.1039/d0ra02711aopenalex-snapshot
Synthesis of bodinieric acids A and B, both C-18 and C-19-functionalized abietane diterpenoids: DFT study of the key aldol reaction
inferred← citeshttps://doi.org/10.1080/14786419.2022.2102628openalex-snapshot
Systematic characterisation of the effective components of five Callicarpa species with UPLC-Q-TOF-MS and evaluation of their anti-hyperuricaemic activity
inferred← citeshttps://doi.org/10.1093/jimb/kuaf003openalex-snapshot
Biocatalytic diversification of abietic acid in Streptomyces
inferred← citeshttps://doi.org/10.1097/st9.0000000000000135openalex-snapshot
Multicomponent tracking and targeting strategy based on ion identity molecular networking for in vivo characterization of Weifuchun constituents
inferred← citeshttps://doi.org/10.2139/ssrn.5393858openalex-snapshot
Discovery of Clerodane Diterpenoids with Potential as Nlrp3 Inflammasome Inhibitors from Callicarpa Integerrima
inferred← citeshttps://doi.org/10.3390/antiox8100421openalex-snapshot
Alpha-Glucosidase and Alpha-Amylase Inhibitory Activities of Novel Abietane Diterpenes from Salvia africana-lutea
inferred← citeshttps://doi.org/10.3390/foods13182993openalex-snapshot
Qualitative Profiling, Antioxidant and Antimicrobial Activities of Polar and Nonpolar Basil Extracts
inferred← citeshttps://doi.org/10.3390/molecules25184129openalex-snapshot
Glucose-Uptake Activity and Cytotoxicity of Diterpenes and Triterpenes Isolated from Lamiaceae Plant Species
inferred← citeshttps://doi.org/10.3390/plants9010113openalex-snapshot
Callicarpa Species from Central Vietnam: Essential Oil Compositions and Mosquito Larvicidal Activities
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