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Diterpenoid Alkaloids from Delphinium majus

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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

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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/(sici)1098-2299(199610)39:2<147::aid-ddr6>3.0.co;2-popenalex-snapshot
Recent studies on traditional Chinese medicinal plants
inferredcites →https://doi.org/10.1007/978-1-4612-3006-9_3openalex-snapshot
Carbon-13 and Proton NMR Shift Assignments and Physical Constants of Norditerpenoid Alkaloids
inferredcites →https://doi.org/10.1007/bf01386185openalex-snapshot
Search for and study of curaremimetic drugs among the diterpene alkaloids
inferredcites →https://doi.org/10.1007/bf02291540openalex-snapshot
Diterpenoid alkaloids as a new class of antiarrhythmic agents. Structure-activity relationship
inferredcites →https://doi.org/10.1016/j.bmc.2005.07.015openalex-snapshot
8-O-Azeloyl-14-benzoylaconine: A new alkaloid from the roots of Aconitum karacolicum Rapcs and its antiproliferative activities
inferredcites →https://doi.org/10.1016/s0099-9598(02)59008-8openalex-snapshot
C20-diterpenoid alkaloids
inferredcites →https://doi.org/10.1021/ja00411a062openalex-snapshot
Structure revision of 37 lycoctonine-related diterpenoid alkaloids
inferredcites →https://doi.org/10.1021/jm000155hopenalex-snapshot
Medicinal Chemistry of Neuronal Voltage-Gated Sodium Channel Blockers
inferredcites →https://doi.org/10.1021/np0401922openalex-snapshot
C20-Diterpenoid Alkaloids from Delphinium trifoliolatum
inferredcites →https://doi.org/10.1021/np070270wopenalex-snapshot
Inhibitory Effects of Diterpenoid Alkaloids on the Growth of A172 Human Malignant Cells
inferredcites →https://doi.org/10.1021/np50009a011openalex-snapshot
The Diterpenoid Alkaloids of Consolida ambigua
inferredcites →https://doi.org/10.1055/s-2006-957359openalex-snapshot
Cardiac Effects of Lappaconitine andN-Deacetyllappaconitine, Two Diterpenoid Alkaloids from Plants of theAconitumandDelphiniumSpecies
inferredcites →https://doi.org/10.1139/v79-266openalex-snapshot
13C nuclear magnetic resonance spectra of some C19-diterpenoid alkaloids and their derivatives
inferredcites →https://doi.org/10.1358/dof.1999.024.08.858626openalex-snapshot
Alkaloids of Chinese Aconitum plants
inferredcites →https://doi.org/10.3987/com-91-5830openalex-snapshot
Norditerpenoid Alkaloids from Delphinium menziesii DC
inferredcites →https://doi.org/10.3987/r-1983-07-1347openalex-snapshot
The Diterpenoid Alkaloids of Delphinium tatsienense Franch

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.2021.112866zenodo-depositor-declared
Diterpenoid alkaloids from the whole herb of Delphinium grandiflorum L
inferred← citeshttps://doi.org/10.1002/cbdv.202301923openalex-snapshot
Diterpenoid Alkaloids from Delphinium liangshanense
inferred← citeshttps://doi.org/10.1002/chem.201500839openalex-snapshot
Generating Skeletal Diversity from the C19‐Diterpenoid Alkaloid Deltaline: A Ring‐Distortion Approach
inferred← citeshttps://doi.org/10.1002/hlca.200900339openalex-snapshot
Three New C19‐Diterpenoid Alkaloids from Aconitum hemsleyanum var. circinatum
inferred← citeshttps://doi.org/10.1002/hlca.201000322openalex-snapshot
Diterpenoid Alkaloids from Delphinium tatsienense
inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_30openalex-snapshot
Terpenoid Alkaloids Derived by Amination Reaction
inferred← citeshttps://doi.org/10.1007/s00018-010-0452-1openalex-snapshot
The diterpenoid alkaloid noroxoaconitine is a Mapkap kinase 5 (MK5/PRAK) inhibitor
inferred← citeshttps://doi.org/10.1007/s10600-025-04774-4openalex-snapshot
Diterpenoid Alkaloids from Delphinium iliense
inferred← citeshttps://doi.org/10.1007/s13659-021-00302-3openalex-snapshot
Diterpenoid Alkaloids from the Aerial Parts of Aconitum flavum Hand.-Mazz
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.08.001openalex-snapshot
The diterpenoid alkaloids
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.07.035openalex-snapshot
Synthesis of pyrrolomorphinan derivatives as κ opioid agonists
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.04.011openalex-snapshot
Two 2-(quinonylcarboxamino)benzoates from the lateral roots of Aconitum carmichaelii
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106431openalex-snapshot
Five new C19-diterpenoid alkaloids from Delphinium pachycentrum Hemsl. and Delphinium majus Ulbr. as potential acetylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117826openalex-snapshot
Toxicity of Delphinium brunonianum Royle alkaloids against the adults of Diaphorina citri and its mechanism study in insect SF9 cell line
inferred← citeshttps://doi.org/10.1016/j.jfutfo.2023.07.006openalex-snapshot
Chemical constituents and anticoagulant activity from Delphinium brunonianum Royle
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.12.003openalex-snapshot
Five new diterpenoid alkaloids from Aconitum sczukinii Turcz.
inferred← citeshttps://doi.org/10.1016/j.phytol.2024.03.003openalex-snapshot
Two new cytotoxic diterpenoid alkaloids from Delphinium grandiflorum
inferred← citeshttps://doi.org/10.1016/j.tet.2017.10.063openalex-snapshot
Multicomponent Mannich reactions: General aspects, methodologies and applications
inferred← citeshttps://doi.org/10.1016/s1875-5364(11)60011-3openalex-snapshot
Natural Products Chemistry Research 2009's Progress in China
inferred← citeshttps://doi.org/10.1016/s1875-5364(17)30007-9openalex-snapshot
A new diterpenoid alkaloid isolated from Delphinium caeruleum
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00169openalex-snapshot
DU8ML: Machine Learning-Augmented Density Functional Theory Nuclear Magnetic Resonance Computations for High-Throughput In Silico Solution Structure Validation and Revision of Complex Alkaloids
inferred← citeshttps://doi.org/10.1021/jacs.6c03728openalex-snapshot
A Vakognavine-Type Diterpenoid Alkaloid as FoxO1 Inhibitors against Rheumatoid Arthritis
inferred← citeshttps://doi.org/10.1039/c7ra02869eopenalex-snapshot
Grandiflodines A and B, two novel diterpenoid alkaloids from Delphinium grandiflorum
inferred← citeshttps://doi.org/10.1039/d0ra00813copenalex-snapshot
An overview of the chemical constituents from the genus Delphinium reported in the last four decades
inferred← citeshttps://doi.org/10.1080/10286020.2024.2376244openalex-snapshot
Diterpenoid alkaloids from Delphinium sherriffii
inferred← citeshttps://doi.org/10.1080/14786419.2011.603319openalex-snapshot
X-ray structure study of ranaconitine hydrobromide
inferred← citeshttps://doi.org/10.1080/14786419.2014.927463openalex-snapshot
A new C19-diterpenoid alkaloid from the roots of Aconitum duclouxii
inferred← citeshttps://doi.org/10.1155/2020/9375619openalex-snapshot
Review of Compounds and Pharmacological Effects of Delphinium
inferred← citeshttps://doi.org/10.1177/1934578x1501001214openalex-snapshot
Majusine D: A New C 19 -diterpenoid Alkaloid from Delphinium majus
inferred← citeshttps://doi.org/10.3389/fchem.2022.1012874openalex-snapshot
Grandiflolines A–F, new anti-inflammatory diterpenoid alkaloids isolated from Delphinium grandiflorum
inferred← citeshttps://doi.org/10.3390/molecules26134103openalex-snapshot
Classification, Toxicity and Bioactivity of Natural Diterpenoid Alkaloids
inferred← citeshttps://doi.org/10.3390/molecules29030649openalex-snapshot
Chemical Constituents and Bioactivities of the Plant-Derived Fungus Aspergillus fumigatus
inferred← citeshttps://doi.org/10.34172/jhp.2021.56openalex-snapshot
Chemistry, biological activities and toxic effects of alkaloidal constituents of genus Delphinium - A mini review
inferred← citeshttps://doi.org/10.3987/com-23-14867openalex-snapshot
Diterpenoid Alkaloids from Delphinium pachycentrum Hemsl.
inferred← citeshttps://doi.org/10.70675/3a6cf4a1zef65z490ez8ad7z88297b83ec7copenalex-snapshot
Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives
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