On the public citation graph

New Circulin Macrocyclic Polypeptides from Chassalia parvifolia

https://doi.org/10.1021/np990432r
0 signed · 113 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1001/jama.1989.03430100133050openalex-snapshot
AIDS: Etiology, Diagnosis, Treatment, and Prevention
inferredcites →https://doi.org/10.1002/pro.5560031022openalex-snapshot
A common structural motif incorporating a cystine knot and a triple‐stranded β‐sheet in toxic and inhibitory polypeptides
inferredcites →https://doi.org/10.1006/bbrc.1996.1708openalex-snapshot
Analysis of the Disulfide Linkage Pattern in Circulin A and B, HIV-Inhibitory Macrocyclic Peptides
inferredcites →https://doi.org/10.1016/0166-0934(91)90010-wopenalex-snapshot
A semiautomated multiparameter approach for anti-HIV drug screening
inferredcites →https://doi.org/10.1016/0166-3542(94)90092-2openalex-snapshot
Biological and biochemical anti-HIV activity of the benzothiadiazine class of nonnucleoside reverse transcriptase inhibitors
inferredcites →https://doi.org/10.1021/bi00013a002openalex-snapshot
Elucidation of the Primary and Three-Dimensional Structure of the Uterotonic Polypeptide Kalata B1
inferredcites →https://doi.org/10.1021/jo00174a010openalex-snapshot
Molecular structures of the briantheins, new insecticidal diterpenes from Briareum polyanthes
inferredcites →https://doi.org/10.1021/jo00174a011openalex-snapshot
Synthesis of (24R)- and (24S)-5,28-stigmastadien-3.beta.-ol and determination of the stereochemistry of their 24-hydroxy analogs, the saringosterols
inferredcites →https://doi.org/10.1021/np50114a002openalex-snapshot
Cyclopsychotride A, a Biologically Active, 31-Residue Cyclic Peptide Isolated from Psychotria longipes
inferredcites →https://doi.org/10.1021/np970342ropenalex-snapshot
Fractionation Protocol for the Isolation of Polypeptides from Plant Biomass
inferredcites →https://doi.org/10.1021/np9803878openalex-snapshot
Seven Novel Macrocyclic Polypeptides fromViolaarvensis

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.2021.112749zenodo-depositor-declared
Tropical vibes from Sri Lanka - cyclotides from Viola betonicifolia by transcriptome and mass spectrometry analysis
inferred← citeshttps://doi.org/10.1002/9780470054581.eib250openalex-snapshot
Cyclotides
inferred← citeshttps://doi.org/10.1002/9783527620982.ch19openalex-snapshot
Biopharmaceutical Drugs from Natural Sources
inferred← citeshttps://doi.org/10.1002/bip.20451openalex-snapshot
The cyclotide family of circular miniproteins: Nature's combinatorial peptide template
inferred← citeshttps://doi.org/10.1002/bip.20886openalex-snapshot
Cyclotides as natural anti‐HIV agents
inferred← citeshttps://doi.org/10.1002/bip.22284openalex-snapshot
Cyclotides as grafting frameworks for protein engineering and drug design applications
inferred← citeshttps://doi.org/10.1002/bip.22325openalex-snapshot
Cycloviolacin O2 (CyO2) suppresses productive infection and augments the antiviral efficacy of nelfinavir in HIV‐1 infected monocytic cells
inferred← citeshttps://doi.org/10.1002/cbic.201700153openalex-snapshot
Cyclotides: Overview and Biotechnological Applications
inferred← citeshttps://doi.org/10.1002/ijch.201100067openalex-snapshot
Chemical Synthesis of Naturally‐Occurring Cyclic Mini‐Proteins from Plants and Animals
inferred← citeshttps://doi.org/10.1002/psc.2523openalex-snapshot
Joseph Rudinger memorial lecture: Discovery and applications of cyclotides
inferred← citeshttps://doi.org/10.1002/ptr.1629openalex-snapshot
Naturally derived anti‐HIV agents
inferred← citeshttps://doi.org/10.1002/slct.202303969openalex-snapshot
Cyclotides, Cyclic Peptides Derived from Clitoria ternatea Linn Mature Pods, Hold Promise as Potential Antimicrobial Agent
inferred← citeshttps://doi.org/10.1002/vjch.70024openalex-snapshot
Cyclotides from Violaceae: Isolation, characterization, and potential applications
inferred← citeshttps://doi.org/10.1007/978-94-007-6464-4_7openalex-snapshot
Cyclotides: Plant Defense Toxins
inferred← citeshttps://doi.org/10.1007/978-94-007-6728-7_7-1openalex-snapshot
Cyclotides: Plant Defense Toxins
inferred← citeshttps://doi.org/10.1007/bf02442584openalex-snapshot
Diversity in the disulfide folding pathways of cystine knot peptides
inferred← citeshttps://doi.org/10.1007/bf02446507openalex-snapshot
Discovery and structures of the cyclotides: novel macrocyclic peptides from plants
inferred← citeshttps://doi.org/10.1007/s00018-021-03759-0openalex-snapshot
Antiviral activities and applications of ribosomally synthesized and post-translationally modified peptides (RiPPs)
inferred← citeshttps://doi.org/10.1007/s00249-011-0672-9openalex-snapshot
NMR and protein structure in drug design: application to cyclotides and conotoxins
inferred← citeshttps://doi.org/10.1007/s10989-004-1722-2openalex-snapshot
Structure of Circulin B and Implications for Antimicrobial Activity of the Cyclotides
inferred← citeshttps://doi.org/10.1007/s10989-022-10437-7openalex-snapshot
The Updated Review on Plant Peptides and Their Applications in Human Health
inferred← citeshttps://doi.org/10.1007/s11030-025-11113-wopenalex-snapshot
Advances in cyclotide research: bioactivity to cyclotide-based therapeutics
inferred← citeshttps://doi.org/10.1007/s11030-026-11480-yopenalex-snapshot
Molecular insights into anti-cancer cyclotides and their interaction with breast cancer targets: an in silico study
inferred← citeshttps://doi.org/10.1007/s11101-020-09682-9openalex-snapshot
Production of bioactive cyclotides: a comprehensive overview
inferred← citeshttps://doi.org/10.1007/s11240-005-9056-0openalex-snapshot
Establishment of in vitro plants, cell and tissue cultures from Oldenlandia affinis for the production of cyclic peptides
inferred← citeshttps://doi.org/10.1007/s11240-017-1223-6openalex-snapshot
Callus and cell suspension culture of Viola odorata as in vitro production platforms of known and novel cyclotides
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00115-5openalex-snapshot
Plant Peptide Toxins from Nonmarine Environments
inferred← citeshttps://doi.org/10.1016/bs.abr.2015.08.004openalex-snapshot
Primary Structural Analysis of Cyclotides
inferred← citeshttps://doi.org/10.1016/bs.abr.2015.09.002openalex-snapshot
Cyclotides in the Rubiaceae
inferred← citeshttps://doi.org/10.1016/bs.abr.2015.10.001openalex-snapshot
Natural Functions and Structure–Activity Relationships of Cyclotides
inferred← citeshttps://doi.org/10.1016/j.addr.2009.05.003openalex-snapshot
Discovery, structure and biological activities of cyclotides☆
inferred← citeshttps://doi.org/10.1016/j.bmc.2017.08.005openalex-snapshot
Ribosomally-synthesised cyclic peptides from plants as drug leads and pharmaceutical scaffolds
inferred← citeshttps://doi.org/10.1016/j.febslet.2004.08.007openalex-snapshot
The role of the cyclic peptide backbone in the anti‐HIV activity of the cyclotide kalata B1
inferred← citeshttps://doi.org/10.1016/j.febslet.2004.10.034openalex-snapshot
Capped acyclic permutants of the circular protein kalata B1
inferred← citeshttps://doi.org/10.1016/j.jhip.2024.06.003openalex-snapshot
Cyclotides prediction in Leptopetalum biflorum based on de novo transcriptome assembly and annotation
inferred← citeshttps://doi.org/10.1016/j.jmb.2004.12.030openalex-snapshot
Structures of the Agouti Signaling Protein
inferred← citeshttps://doi.org/10.1016/j.peptides.2007.04.025openalex-snapshot
Plant cyclotides: An unusual class of defense compounds
inferred← citeshttps://doi.org/10.1016/j.peptides.2010.05.004openalex-snapshot
Isolation and characterization of cytotoxic cyclotides from Viola tricolor
inferred← citeshttps://doi.org/10.1016/j.peptides.2020.170430openalex-snapshot
An insight into biological activities of native cyclotides for potential applications in agriculture and pharmaceutics
inferred← citeshttps://doi.org/10.1016/j.peptides.2023.171024openalex-snapshot
A review of the antiviral activity of cationic antimicrobial peptides
inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.09.023openalex-snapshot
Cyclotide proteins and precursors from the genus Gloeospermum: Filling a blank spot in the cyclotide map of Violaceae
inferred← citeshttps://doi.org/10.1016/j.str.2003.11.019openalex-snapshot
Solution Structure of the Cyclotide Palicourein
inferred← citeshttps://doi.org/10.1016/j.toxicon.2010.02.021openalex-snapshot
Discovery and applications of the plant cyclotides
inferred← citeshttps://doi.org/10.1016/j.toxicon.2019.10.244openalex-snapshot
Cyclotides: Disulfide-rich peptide toxins in plants
inferred← citeshttps://doi.org/10.1016/s0003-2697(03)00114-3openalex-snapshot
Expression of Viola cyclotides by liquid chromatography–mass spectrometry and tandem mass spectrometry sequencing of intercysteine loops after introduction of charges and cleavage sites by aminoethylation
inferred← citeshttps://doi.org/10.1016/s0031-9422(01)00173-xopenalex-snapshot
First cyclotide from Hybanthus (Violaceae)
inferred← citeshttps://doi.org/10.1016/s0041-0101(00)00160-4openalex-snapshot
The cystine knot motif in toxins and implications for drug design
inferred← citeshttps://doi.org/10.1016/s0041-0101(01)00129-5openalex-snapshot
Plant cyclotides: circular, knotted peptide toxins
inferred← citeshttps://doi.org/10.1016/s0968-0004(02)02057-1openalex-snapshot
Circular proteins — no end in sight
inferred← citeshttps://doi.org/10.1021/acs.analchem.9b03671openalex-snapshot
Gas-Phase Sequencing of Cyclotides: Introduction of Selective Ring Opening at Dehydroalanine via Ion/Ion Reaction
inferred← citeshttps://doi.org/10.1021/acs.chemrev.9b00402openalex-snapshot
Cyclotides: From Structure to Function
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01004openalex-snapshot
Cyclotides from the Indian Medicinal Plant Viola odorata (Banafsha): Identification and Characterization
inferred← citeshttps://doi.org/10.1021/bi049711qopenalex-snapshot
Thermal, Chemical, and Enzymatic Stability of the Cyclotide Kalata B1: The Importance of the Cyclic Cystine Knot
inferred← citeshttps://doi.org/10.1021/cb100388jopenalex-snapshot
Discovery of Cyclotides in the Fabaceae Plant Family Provides New Insights into the Cyclization, Evolution, and Distribution of Circular Proteins
inferred← citeshttps://doi.org/10.1021/cr040699hopenalex-snapshot
Plant Cyclopeptides
inferred← citeshttps://doi.org/10.1021/ja0123608openalex-snapshot
The Effect of Backbone Cyclization on the Thermodynamics of β-Sheet Unfolding: Stability Optimization of the PIN WW Domain
inferred← citeshttps://doi.org/10.1021/np000372lopenalex-snapshot
A Novel Anti-HIV Macrocyclic Peptide from Palicourea condensata
inferred← citeshttps://doi.org/10.1021/np0103362openalex-snapshot
Biologically Active Proteins from Natural Product Extracts
inferred← citeshttps://doi.org/10.1021/np034068eopenalex-snapshot
Variations in Cyclotide Expression in Viola Species
inferred← citeshttps://doi.org/10.1021/np0499719openalex-snapshot
Reversible Antifouling Effect of the Cyclotide Cycloviolacin O2 against Barnacles
inferred← citeshttps://doi.org/10.1021/np0581216openalex-snapshot
Natural Product Extracts of Plant and Marine Origin Having Antileukemia Potential. The NCI Experience
inferred← citeshttps://doi.org/10.1021/np070393gopenalex-snapshot
Anti-HIV Cyclotides from the Chinese Medicinal Herb Viola yedoensis
inferred← citeshttps://doi.org/10.1021/np1000413openalex-snapshot
Isolation, Sequencing, and Structure−Activity Relationships of Cyclotides
inferred← citeshttps://doi.org/10.1021/np9007365openalex-snapshot
Isolation, Characterization, and Bioactivity of Cyclotides from the Micronesian Plant Psychotria leptothyrsa
inferred← citeshttps://doi.org/10.1023/a:1016262020925openalex-snapshot
Discovery and structures of the cyclotides: novel macrocyclic peptides from plants
inferred← citeshttps://doi.org/10.1039/9781847559265-00318openalex-snapshot
Folding Motifs of Cystine-rich Peptides
inferred← citeshttps://doi.org/10.1039/b616856fopenalex-snapshot
NMR as a tool for elucidating the structures of circular and knotted proteins
inferred← citeshttps://doi.org/10.1039/b823020jopenalex-snapshot
Circular proteins from Melicytus (Violaceae) refine the conserved protein and gene architecture of cyclotides
inferred← citeshttps://doi.org/10.1042/bj20051371openalex-snapshot
Kalata B8, a novel antiviral circular protein, exhibits conformational flexibility in the cystine knot motif
inferred← citeshttps://doi.org/10.1074/jbc.m101666200openalex-snapshot
Circular Proteins in Plants
inferred← citeshttps://doi.org/10.1074/jbc.m111.338970openalex-snapshot
Novel Cyclotides and Uncyclotides with Highly Shortened Precursors from Chassalia chartacea and Effects of Methionine Oxidation on Bioactivities
inferred← citeshttps://doi.org/10.1074/jbc.m211147200openalex-snapshot
Twists, Knots, and Rings in Proteins
inferred← citeshttps://doi.org/10.1074/jbc.m308771200openalex-snapshot
Disulfide Mapping of the Cyclotide Kalata B1
inferred← citeshttps://doi.org/10.1074/jbc.m407421200openalex-snapshot
Conserved Structural and Sequence Elements Implicated in the Processing of Gene-encoded Circular Proteins
inferred← citeshttps://doi.org/10.1080/17460441.2016.1245720openalex-snapshot
Discovery and optimization of peptide macrocycles
inferred← citeshttps://doi.org/10.1080/22311866.2012.10719104openalex-snapshot
Naturally Occurring Cyclic Peptides and Their Potential Application in HIV Therapeutics
inferred← citeshttps://doi.org/10.1081/txr-120014405openalex-snapshot
STRUCTURE AND FUNCTION OF PLANT TOXINS (WITH EMPHASIS ON CYSTINE KNOT TOXINS)
inferred← citeshttps://doi.org/10.1093/jxb/erw210openalex-snapshot
Discovery, structure, function, and applications of cyclotides: circular proteins from plants
inferred← citeshttps://doi.org/10.1105/tpc.104.021790openalex-snapshot
Tissue-Specific Expression of Head-to-Tail Cyclized Miniproteins in Violaceae and Structure Determination of the Root CyclotideViola hederacearoot cyclotide1[W]
inferred← citeshttps://doi.org/10.1105/tpc.105.034678openalex-snapshot
A Continent of Plant Defense Peptide Diversity: Cyclotides in AustralianHybanthus(Violaceae)
inferred← citeshttps://doi.org/10.1105/tpc.106.042812openalex-snapshot
Discovery of Cyclotide-Like Protein Sequences in Graminaceous Crop Plants: Ancestral Precursors of Circular Proteins?
inferred← citeshttps://doi.org/10.1105/tpc.108.062331openalex-snapshot
Distribution and Evolution of Circular Miniproteins in Flowering Plants
inferred← citeshttps://doi.org/10.1128/aac.49.8.3387-3395.2005openalex-snapshot
Human Lactoferricin Is Partially Folded in Aqueous Solution and Is Better Stabilized in a Membrane Mimetic Solvent
inferred← citeshttps://doi.org/10.1134/s1068162011010158openalex-snapshot
The search for and identification of peptides from the moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1177/2156587211428077openalex-snapshot
Cyclotides
inferred← citeshttps://doi.org/10.14218/jerp.2022.00029openalex-snapshot
Structures, Functions and Therapeutic Potential of Cyclotides
inferred← citeshttps://doi.org/10.1517/13543776.2011.620606openalex-snapshot
Cyclotides: a patent review
inferred← citeshttps://doi.org/10.1517/13543784.16.5.595openalex-snapshot
Potential therapeutic applications of the cyclotides and related cystine knot mini-proteins
inferred← citeshttps://doi.org/10.1517/17460441.2012.661554openalex-snapshot
Cyclotides as a basis for drug design
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2577101/v1openalex-snapshot
WITHDRAWN: Quest for Novel Plant based Therapeutic Options Against Dengue Virus NS2B-NS3 protease: An integrative computational methodology
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2577101/v2openalex-snapshot
WITHDRAWN: Quest for Novel Plant based Therapeutic Options Against Dengue Virus NS2B-NS3 protease: An integrative computational methodology
inferred← citeshttps://doi.org/10.2139/ssrn.4844142openalex-snapshot
Redefining Vaccines: Nucleic Acid Vaccines Encoding Short Therapeutic Peptides
inferred← citeshttps://doi.org/10.2174/138161211798999438openalex-snapshot
Cyclotides, a Novel Ultrastable Polypeptide Scaffold for Drug Discovery
inferred← citeshttps://doi.org/10.2174/1389203720666191119095624openalex-snapshot
Therapeutic Potential of Medicinal Plant Proteins: Present Status and Future Perspectives
inferred← citeshttps://doi.org/10.3390/plants11233271openalex-snapshot
Nutritional and Pharmaceutical Applications of Under-Explored Knottin Peptide-Rich Phytomedicines
inferred← citeshttps://doi.org/10.3390/toxins4020139openalex-snapshot
Host-Defense Activities of Cyclotides
inferred← citeshttps://doi.org/10.3410/f.739484140.793583073openalex-snapshot
Faculty Opinions recommendation of Antiviral activities and applications of ribosomally synthesized and post-translationally modified peptides (RiPPs).
inferred← citeshttps://doi.org/10.34133/2022/9898241openalex-snapshot
An Overview of Antiviral Peptides and Rational Biodesign Considerations
inferred← citeshttps://doi.org/10.4049/jimmunol.170.9.4708openalex-snapshot
Retrocyclin, an Antiretroviral θ-Defensin, Is a Lectin
inferred← citeshttps://doi.org/10.4103/2229-5186.99559openalex-snapshot
The bountiful biological activities of cyclotides
inferred← citeshttps://doi.org/10.4155/fmc.09.129openalex-snapshot
Design and Therapeutic Applications of Cyclotides
inferred← citeshttps://doi.org/10.47499/revistaaccb.v1i34.264openalex-snapshot
Análisis in silico de la inmunogenicidad e interacción molecular de péptidos de plantas aromáticas con SARS-CoV-2
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.