On the public citation graph

Novel phosphonate analogs of sulforaphane: Synthesis, in vitro and in vivo anticancer activity

https://doi.org/10.1016/j.ejmech.2017.03.028
0 signed · 90 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1006/bbrc.1993.2438openalex-snapshot
A New Method for the Cytofluorometric Analysis of Mitochondrial Membrane Potential Using the J-Aggregate Forming Lipophilic Cation 5,5′,6,6′-Tetrachloro-1,1′,3,3′-tetraethylbenzimidazolcarbocyanine Iodide (JC-1)
inferredcites →https://doi.org/10.1006/bbrc.1995.1106openalex-snapshot
Reversible Conjugation of Isothiocyanates with Glutathione Catalyzed by Human Glutathione Transferases
inferredcites →https://doi.org/10.1007/s10549-010-1299-8openalex-snapshot
Oral administration of benzyl-isothiocyanate inhibits solid tumor growth and lung metastasis of 4T1 murine mammary carcinoma cells in BALB/c mice
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/j.bcp.2010.10.005openalex-snapshot
Anti-angiogenic effects of dietary isothiocyanates: Mechanisms of action and implications for human health
inferredcites →https://doi.org/10.1016/j.bmcl.2011.05.113openalex-snapshot
Synthesis and antiproliferative activity of novel α- and β-dialkoxyphosphoryl isothiocyanates
inferredcites →https://doi.org/10.1016/j.bmcl.2015.11.045openalex-snapshot
Synthesis and biological activity of diisothiocyanate-derived mercapturic acids
inferredcites →https://doi.org/10.1016/j.canlet.2005.02.033openalex-snapshot
Chemoprotection by sulforaphane: Keep one eye beyond Keap1
inferredcites →https://doi.org/10.1016/j.canlet.2008.04.018openalex-snapshot
Multi-targeted prevention of cancer by sulforaphane
inferredcites →https://doi.org/10.1016/j.ejmech.2011.12.003openalex-snapshot
Design, synthesis and biological evaluation of new naphtalene diimides bearing isothiocyanate functionality
inferredcites →https://doi.org/10.1016/j.ejmech.2013.03.045openalex-snapshot
Synthesis and biological evaluation of sulforaphane derivatives as potential antitumor agents
inferredcites →https://doi.org/10.1016/j.ejmech.2014.02.036openalex-snapshot
New enantiomeric fluorine-containing derivatives of sulforaphane: Synthesis, absolute configurations and biological activity
inferredcites →https://doi.org/10.1016/j.ejphar.2010.06.069openalex-snapshot
8-Prenylnaringenin is an inhibitor of multidrug resistance-associated transporters, P-glycoprotein and MRP1
inferredcites →https://doi.org/10.1016/j.jesp.2013.03.013openalex-snapshot
Detecting outliers: Do not use standard deviation around the mean, use absolute deviation around the median
inferredcites →https://doi.org/10.1016/j.reactfunctpolym.2013.06.003openalex-snapshot
A novel click-chemistry approach to flame retardant polyurethanes
inferredcites →https://doi.org/10.1016/j.tet.2006.09.048openalex-snapshot
The aza-Wittig reaction: an efficient tool for the construction of carbon–nitrogen double bonds
inferredcites →https://doi.org/10.1016/j.tetlet.2012.08.037openalex-snapshot
Convenient syntheses of novel 1-isothiocyano-alkylphosphonate diphenyl ester derivatives with potential biological activity
inferredcites →https://doi.org/10.1016/j.yexmp.2006.06.007openalex-snapshot
Murine mammary carcinoma 4T1 induces a leukemoid reaction with splenomegaly: Association with tumor-derived growth factors
inferredcites →https://doi.org/10.1016/s0031-9422(00)00316-2openalex-snapshot
The chemical diversity and distribution of glucosinolates and isothiocyanates among plants
inferredcites →https://doi.org/10.1016/s0040-4039(01)92575-4openalex-snapshot
The facile dealkylation of phosphonic acid dialkyl esters by bromotrimethylsilane
inferredcites →https://doi.org/10.1021/bi00105a020openalex-snapshot
Mitoxantrone resistance in HL-60 leukemia cells: reduced nuclear topoisomerase II catalytic activity and drug-induced DNA cleavage in association with reduced expression of the topoisomerase II .beta. isoform
inferredcites →https://doi.org/10.1021/cr00044a004openalex-snapshot
Michaelis-Arbuzov rearrangement
inferredcites →https://doi.org/10.1021/jm00027a021openalex-snapshot
Design and synthesis of bifunctional isothiocyanate analogs of sulforaphane: correlation between structure and potency as inducers of anticarcinogenic detoxication enzymes
inferredcites →https://doi.org/10.1021/jm800993ropenalex-snapshot
Synthesis and Anticancer Activity Comparison of Phenylalkyl Isoselenocyanates with Corresponding Naturally Occurring and Synthetic Isothiocyanates
inferredcites →https://doi.org/10.1034/j.1399-3054.1996.970128.xopenalex-snapshot
The myrosinase-glucosinolate system, its organisation and biochemistry
inferredcites →https://doi.org/10.1039/c0gc00509fopenalex-snapshot
Efficient and ‘green’ microwave-assisted synthesis of haloalkylphosphonates via the Michaelis–Arbuzov reaction
inferredcites →https://doi.org/10.1055/s-0034-1380162openalex-snapshot
A Practical Route for the Preparation of Bis(2,2,2-trifluoroethyl) 2-Oxoalkylphosphonates
inferredcites →https://doi.org/10.1055/s-1982-29877openalex-snapshot
Convenient Improved Syntheses of Isocyanates or Isothiocyanates from Amines
inferredcites →https://doi.org/10.1073/pnas.89.6.2399openalex-snapshot
A major inducer of anticarcinogenic protective enzymes from broccoli: isolation and elucidation of structure.
inferredcites →https://doi.org/10.1074/jbc.m109760200openalex-snapshot
Involvement of the Mitochondrial Death Pathway in Chemopreventive Benzyl Isothiocyanate-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m113.491415openalex-snapshot
Conformational Plasticity and Ligand Binding of Bacterial Monoacylglycerol Lipase
inferredcites →https://doi.org/10.1074/jbc.m802330200openalex-snapshot
Covalent Binding to Tubulin by Isothiocyanates
inferredcites →https://doi.org/10.1080/00397911.2016.1221114openalex-snapshot
Microwave-assisted synthesis of dialkyl ω -azidoalkylphosphonates
inferredcites →https://doi.org/10.1080/00397918708078788openalex-snapshot
Expedient and High-Yield Synthesis of Alkylphos-Phonyl Bichlorides Under Mild, Neutral Conditions: Reaction of Bis(Trimethylsilyl)Alkyl Phosphonates with Oxalyl Chloride/Dimethylformamide
inferredcites →https://doi.org/10.1080/10426509808032465openalex-snapshot
RAPID AND EFFICIENT ARBUZOV REACTION UNDER MICROWAVE IRRADIATION
inferredcites →https://doi.org/10.1083/jcb.66.1.188openalex-snapshot
Rapid flow cytofluorometric analysis of mammalian cell cycle by propidium iodide staining.
inferredcites →https://doi.org/10.1093/carcin/21.5.175openalex-snapshot
Role of glutathione in the accumulation of anticarcinogenic isothiocyanates and their glutathione conjugates by murine hepatoma cells
inferredcites →https://doi.org/10.1093/carcin/bgi301openalex-snapshot
Effects of benzyl and phenethyl isothiocyanate on P450s 2A6 and 2A13: potential for chemoprevention in smokers
inferredcites →https://doi.org/10.1093/carcin/bgl087openalex-snapshot
Phenethyl isothiocyanate-induced apoptosis in PC-3 human prostate cancer cells is mediated by reactive oxygen species-dependent disruption of the mitochondrial membrane potential
inferredcites →https://doi.org/10.1093/carcin/bgq242openalex-snapshot
Isothiocyanates inhibit proteasome activity and proliferation of multiple myeloma cells
inferredcites →https://doi.org/10.1093/carcin/bgr111openalex-snapshot
Proteins as binding targets of isothiocyanates in cancer prevention
inferredcites →https://doi.org/10.1093/jnci/37.5.677openalex-snapshot
Influence of α-Naphthyl-Isothiocyanate on Liver Tumorigenesis in Rats Ingesting Ethionine and N-2-Fluorenylacetamide 2
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.1134/s1070363212120055openalex-snapshot
ω-haloalkylphosphoryl compounds: Synthesis and properties
inferredcites →https://doi.org/10.1155/2013/120305openalex-snapshot
Novel Hematopoietic Target Genes in the NRF2-Mediated Transcriptional Pathway
inferredcites →https://doi.org/10.1158/0008-5472.can-04-1326openalex-snapshot
A Novel Mechanism of Chemoprotection by Sulforaphane
inferredcites →https://doi.org/10.1158/0008-5472.can-07-0340openalex-snapshot
The Role of Protein Binding in Induction of Apoptosis by Phenethyl Isothiocyanate and Sulforaphane in Human Non–Small Lung Cancer Cells
inferredcites →https://doi.org/10.1186/1471-2407-13-294openalex-snapshot
Vitamin D analogs enhance the anticancer activity of 5-fluorouracil in an in vivomouse colon cancer model
inferredcites →https://doi.org/10.1371/journal.pone.0032597openalex-snapshot
Benzyl Isothiocyanate Causes FoxO1-Mediated Autophagic Death in Human Breast Cancer Cells
inferredcites →https://doi.org/10.1371/journal.pone.0106186openalex-snapshot
Cheburator Software for Automatically Calculating Drug Inhibitory Concentrations from In Vitro Screening Assays
inferredcites →https://doi.org/10.1515/bc.2007.135openalex-snapshot
Glutathione- and thioredoxin-related enzymes are modulated by sulfur-containing chemopreventive agents
inferredcites →https://doi.org/10.2174/138527211797374724openalex-snapshot
Microwave Assisted Phosphorus Organic Chemistry: A Review
inferredcites →https://doi.org/10.2174/1389557514666141106131909openalex-snapshot
Isothiocyanate Synthetic Analogs: Biological Activities, Structure-Activity Relationships and Synthetic Strategies

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.4601855openalex-extracted
inferred← citeshttps://doi.org/10.1002/cbdv.202000733openalex-snapshot
Design and in Vitro Characterization of Tricyclic Benzodiazepine Derivatives as Potent and Selective Antileukemic Agents
inferred← citeshttps://doi.org/10.1002/cbdv.202001004openalex-snapshot
Phosphonic Analogs of Alanine as Acylpeptide Hydrolase Inhibitors
inferred← citeshttps://doi.org/10.1002/cmdc.201700619openalex-snapshot
Design, Synthesis, and Evaluation of ω‐(Isothiocyanato)alkylphosphinates and Phosphine Oxides as Antiproliferative Agents
inferred← citeshttps://doi.org/10.1002/ejoc.201900105openalex-snapshot
Direct, Microwave‐Assisted Synthesis of Isothiocyanates
inferred← citeshttps://doi.org/10.1002/ptr.8419openalex-snapshot
Glucosinolates and Their Hydrolytic Derivatives: Promising Phytochemicals With Anticancer Potential
inferred← citeshttps://doi.org/10.1007/978-3-031-63681-3_5openalex-snapshot
The Anticarcinogenic Properties of Brassica Vegetables
inferred← citeshttps://doi.org/10.1007/s10637-018-0611-zopenalex-snapshot
Discovering simple phenylboronic acid and benzoxaborole derivatives for experimental oncology – phase cycle-specific inducers of apoptosis in A2780 ovarian cancer cells
inferred← citeshttps://doi.org/10.1007/s10637-020-00923-4openalex-snapshot
Structure-based design, synthesis, and evaluation of the biological activity of novel phosphoroorganic small molecule IAP antagonists
inferred← citeshttps://doi.org/10.1007/s11356-019-04502-wopenalex-snapshot
RETRACTED ARTICLE: Sulforaphane potentially attenuates arsenic-induced nephrotoxicity via the PI3K/Akt/Nrf2 pathway in albino Wistar rats
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103454openalex-snapshot
Fluoroaryl analogs of sulforaphane – A group of compounds of anticancer and antimicrobial activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104096openalex-snapshot
Discovery of novel aminophosphonate derivatives containing pyrazole moiety as potential selective COX-2 inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104819openalex-snapshot
Effect of the dichloro-substitution on antiproliferative activity of phthalimide-thiazole derivatives. Rational design, synthesis, elastase, caspase 3/7, and EGFR tyrosine kinase activity and molecular modeling study
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.06.042openalex-snapshot
Phosphorus-containing isothiocyanate-derived mercapturic acids as a useful alternative for parental isothiocyanates in experimental oncology
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.10.033openalex-snapshot
Chemoprevention with isothiocyanates – From bench to bedside
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.05.006openalex-snapshot
Discovery of tropinone-thiazole derivatives as potent caspase 3/7 activators, and noncompetitive tyrosinase inhibitors with high antiproliferative activity: Rational design, one-pot tricomponent synthesis, and lipophilicity determination
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116403openalex-snapshot
Design, synthesis, and biological activity of D-bishomo-1α,25-dihydroxyvitamin D3 analogs and their crystal structures with the vitamin D nuclear receptor
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.01.020openalex-snapshot
New diaryl ω-(isothiocyanato)alkylphosphonates and their mercapturic acids as potential antibacterial agents
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.06.005openalex-snapshot
3,4-dimethoxybenzyl isothiocyanate enhances doxorubicin efficacy in LoVoDX doxorubicin-resistant colon cancer and attenuates its toxicity in vivo
inferred← citeshttps://doi.org/10.11606/d.60.2019.tde-24052019-145414openalex-snapshot
Influência do sulforafano, um inibidor de histonas desacetilases, sobre a instabilidade genômica e mecanismos epigenéticos em linhagens celulares humanas
inferred← citeshttps://doi.org/10.1186/s12935-022-02631-wopenalex-snapshot
Comparison of anti-cancer effects of novel protein disulphide isomerase (PDI) inhibitors in breast cancer cells characterized by high and low PDIA17 expression
inferred← citeshttps://doi.org/10.18632/oncotarget.26125openalex-snapshot
Sulforaphane inhibits growth and blocks Wnt/β-catenin signaling of colorectal cancer cells
inferred← citeshttps://doi.org/10.2147/dddt.s100534openalex-snapshot
Chemopreventive activity of sulforaphane
inferred← citeshttps://doi.org/10.2174/1570163816666191112122047openalex-snapshot
In Silico Drug-designing Studies on Sulforaphane Analogues: Pharmacophore Mapping, Molecular Docking and QSAR Modeling
inferred← citeshttps://doi.org/10.3390/biom16091280openalex-snapshot
Design, Synthesis, and Biological Activity of Isothiocyanate-Triazine Conjugates as AChE and BACE1 Inhibitors
inferred← citeshttps://doi.org/10.3390/biomedicines7030062openalex-snapshot
The Glucosinolates: A Sulphur Glucoside Family of Mustard Anti-Tumour and Antimicrobial Phytochemicals of Potential Therapeutic Application
inferred← citeshttps://doi.org/10.3390/cells10113219openalex-snapshot
The Anti-Tumoral Potential of Phosphonate Analog of Sulforaphane in Zebrafish Xenograft Model
inferred← citeshttps://doi.org/10.3390/ijms22052781openalex-snapshot
Vitamin D Compounds PRI-2191 and PRI-2205 Enhance Anastrozole Activity in Human Breast Cancer Models
inferred← citeshttps://doi.org/10.3390/ijms23158644openalex-snapshot
Isothiocyanates (ITCs) 1-(Isothiocyanatomethyl)-4-phenylbenzene and 1-Isothiocyanato-3,5-bis(trifluoromethyl)benzene—Aldehyde Dehydrogenase (ALDH) Inhibitors, Decreases Cisplatin Tolerance and Migratory Ability of NSCLC
inferred← citeshttps://doi.org/10.3390/ijms241813674openalex-snapshot
Isothiocyanates as Tubulin Polymerization Inhibitors—Synthesis and Structure–Activity Relationship Studies
inferred← citeshttps://doi.org/10.3390/ijms27125620openalex-snapshot
Isothiocyanates as Multi-Target Natural Compounds in Leukemia: Mechanisms, Selectivity, and Therapeutic Potential
inferred← citeshttps://doi.org/10.3390/molecules26092740openalex-snapshot
Synthesis of Isothiocyanates Using DMT/NMM/TsO− as a New Desulfurization Reagent
inferred← citeshttps://doi.org/10.3390/molecules27051750openalex-snapshot
Sulforaphane and Its Bifunctional Analogs: Synthesis and Biological Activity
inferred← citeshttps://doi.org/10.3390/ph19030497openalex-snapshot
NRF2 as a Therapeutic Target in Dermatological Disorders: Mechanisms and Molecules
inferred← citeshttps://doi.org/10.6084/m9.figshare.20110580openalex-snapshot
Additional file 1 of Comparison of anti-cancer effects of novel protein disulphide isomerase (PDI) inhibitors in breast cancer cells characterized by high and low PDIA17 expression
inferred← citeshttps://doi.org/10.6084/m9.figshare.20110583openalex-snapshot
Additional file 2 of Comparison of anti-cancer effects of novel protein disulphide isomerase (PDI) inhibitors in breast cancer cells characterized by high and low PDIA17 expression
inferred← citeshttps://doi.org/10.6084/m9.figshare.20110586openalex-snapshot
Additional file 3 of Comparison of anti-cancer effects of novel protein disulphide isomerase (PDI) inhibitors in breast cancer cells characterized by high and low PDIA17 expression
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.