On the public citation graph
Pachyelasides A−D, Novel Molluscicidal Triterpene Saponins from Pachyelasma Tessmannii
0 signed · 25 inferred · view as graph
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.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0021-9673(87)80036-5openalex-snapshot
Efficient isolation of insect growth inhibitory macrolide alkaloids using recycle high-performance gel permeation chromatography
inferredcites →https://doi.org/10.1016/0031-9422(94)00551-4openalex-snapshot
A plant growth inhibitory sesquiterpenoid from Heterotheca inuloides
inferredcites →https://doi.org/10.1016/s0031-9422(00)89811-8openalex-snapshot
Molluscicidal saponins from a zimbabwean strain of Phytolacca dodecandra
inferredcites →https://doi.org/10.1016/s0031-9422(02)00112-7openalex-snapshot
Triterpene glycosides of Lupinus angustifolius
inferredcites →https://doi.org/10.1016/s0031-9422(02)00398-9openalex-snapshot
(+)-2,3-Dehydro-10-oxo-α-isosparteine in Uresiphita reversalis larvae fed on Cytisus monspessulanus leaves
inferredcites →https://doi.org/10.1021/jf00072a010openalex-snapshot
Molluscicides from the cashew Anacardium occidentale and their large-scale isolation
inferredcites →https://doi.org/10.1021/jf00072a011openalex-snapshot
Scilliroside and other scilla compounds in red squill
inferredcites →https://doi.org/10.1021/jf010567eopenalex-snapshot
Polyhydroxylated Alkaloids Isolated from Mulberry Trees (Morus alba L.) and Silkworms (Bombyx mori L.)
inferredcites →https://doi.org/10.1021/jf020245qopenalex-snapshot
Insect Antifeedants from Tropical Plants II: Structure of Zumsin
inferredcites →https://doi.org/10.1021/np020400vopenalex-snapshot
Isolation and Structures of Avicins D and G: In Vitro Tumor-Inhibitory Saponins Derived from Acacia victoriae
inferredcites →https://doi.org/10.1021/np990633vopenalex-snapshot
Anti-AIDS Agents 38. Anti-HIV Activity of 3-O-Acyl Ursolic Acid Derivatives
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/phytokeys.240.101716zenodo-depositor-declared
Advances in Legume Systematics 14. Classification of Caesalpinioideae. Part 2: Higher-level classification
inferred← citeshttps://doi.org/10.1002/cbdv.200800070openalex-snapshot
Naturally Occurring Triterpenoid Saponins
inferred← citeshttps://doi.org/10.1007/s00436-021-07288-4openalex-snapshot
Molluscicides against the snail-intermediate host of Schistosoma: a review
inferred← citeshttps://doi.org/10.1007/s11101-022-09836-xopenalex-snapshot
Plant extracts and compounds for combating schistosomiasis
inferred← citeshttps://doi.org/10.1007/s43450-021-00207-9openalex-snapshot
Chemical Profiling of Strongylodon macrobotrys Flowers and its Molluscicidal Activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110643openalex-snapshot
Progress in defense glycosides from plants for the discovery of novel botanical pesticides
inferred← citeshttps://doi.org/10.1016/j.chroma.2006.01.037openalex-snapshot
Chromatographic determination of plant saponins—An update (2002–2005)
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104264openalex-snapshot
Triterpene saponins from the roots of Parkia bicolor A. Chev
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112428openalex-snapshot
Triterpene saponins from the seeds of Erythrophleum fordii and their cytotoxic activities
inferred← citeshttps://doi.org/10.1016/s1572-557x(06)03004-2openalex-snapshot
Chapter 4 New concept to search for alternate insect control agents from plants
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00077openalex-snapshot
Multilevel Residual Complexity Analysis Reveals Origin of Nanomolar Antiviral Bioactives of “Isoquercitrin”
inferred← citeshttps://doi.org/10.1104/pp.112.202747openalex-snapshot
UDP-Glycosyltransferases from the UGT73C Subfamily in Barbarea vulgaris Catalyze Sapogenin 3- O -Glucosylation in Saponin-Mediated Insect Resistance
inferred← citeshttps://doi.org/10.1371/journal.pntd.0003489openalex-snapshot
A Novel Bacterial Pathogen of Biomphalaria glabrata: A Potential Weapon for Schistosomiasis Control?
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.