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A theoretical study of some new analogues of the anti-cancer drug camptothecin

https://doi.org/10.1007/s00894-006-0157-4
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What this work says

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

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Mismatch base pairing of the mutagen 8‐oxoguanine and its derivatives with adenine: A theoretical search for possible antimutagenic agents
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Mapping of molecular electric potentials and fields
inferredcites →https://doi.org/10.1016/0009-2614(96)00349-1openalex-snapshot
Ab initio study of solvated molecules: a new implementation of the polarizable continuum model
inferredcites →https://doi.org/10.1016/0166-1280(94)03904-yopenalex-snapshot
Electric field mapping and structure-activity relationships for some dihydropyridazinone cardiotonics
inferredcites →https://doi.org/10.1016/j.bmc.2004.08.052openalex-snapshot
Synthesis and topoisomerase I inhibitory properties of luotonin A analogues
inferredcites →https://doi.org/10.1016/j.bmc.2004.11.011openalex-snapshot
On the role of E-ring oxygen atoms in the binding of camptothecin to the topoisomerase I–DNA covalent binary complex
inferredcites →https://doi.org/10.1016/j.bmcl.2004.02.069openalex-snapshot
Synthesis and biochemical properties of E-ring modified luotonin A derivatives
inferredcites →https://doi.org/10.1016/s0026-895x(24)23195-3openalex-snapshot
7- and 10-Substituted Camptothecins: Dependence of Topoisomerase I-DNA Cleavable Complex Formation and Stability on the 7- and 10-Substituents
inferredcites →https://doi.org/10.1016/s0166-1280(96)04676-3openalex-snapshot
J. Mol. Struct. (Theochem)
inferredcites →https://doi.org/10.1016/s0960-894x(97)00398-3openalex-snapshot
BN 80245: An E-ring modified camptothecin with potent antiproliferative and topoisomerase I inhibitory activities
inferredcites →https://doi.org/10.1016/s1040-8428(02)00090-2openalex-snapshot
Homocamptothecins: potent topoisomerase I inhibitors and promising anticancer drugs
inferredcites →https://doi.org/10.1021/bi010913lopenalex-snapshot
A Structural Model for the Ternary Cleavable Complex Formed between Human Topoisomerase I, DNA, and Camptothecin
inferredcites →https://doi.org/10.1021/bi011774aopenalex-snapshot
Human Topoisomerase I Inhibition: Docking Camptothecin and Derivatives into a Structure-Based Active Site Model
inferredcites →https://doi.org/10.1021/bi982708kopenalex-snapshot
Role of the 20-Hydroxyl Group in Camptothecin Binding by the Topoisomerase I−DNA Binary Complex
inferredcites →https://doi.org/10.1021/bi990947hopenalex-snapshot
Homocamptothecin, an E-Ring-Modified Camptothecin Analogue, Generates New Topoisomerase I-Mediated DNA Breaks
inferredcites →https://doi.org/10.1021/ja0368857openalex-snapshot
Luotonin A. A Naturally Occurring Human DNA Topoisomerase I Poison
inferredcites →https://doi.org/10.1021/ja0442769openalex-snapshot
14-Azacamptothecin: A Potent Water-Soluble Topoisomerase I Poison
inferredcites →https://doi.org/10.1021/ja052542sopenalex-snapshot
Dynamic Behavior of DNA Base Pairs Containing 8-Oxoguanine
inferredcites →https://doi.org/10.1021/ja052637uopenalex-snapshot
New Hints on the pH-Driven Tautomeric Equilibria of the Topotecan Anticancer Drug in Aqueous Solutions from an Integrated Spectroscopic and Quantum-Mechanical Approach
inferredcites →https://doi.org/10.1021/jm9605445openalex-snapshot
Molecular Modeling Studies of the DNA−Topoisomerase I Ternary Cleavable Complex with Camptothecin
inferredcites →https://doi.org/10.1021/jp050646jopenalex-snapshot
Mechanisms of Formation of 8-Oxoguanine Due To Reactions of One and Two OH• Radicals and the H2O2 Molecule with Guanine: A Quantum Computational Study
inferredcites →https://doi.org/10.1021/ol030119nopenalex-snapshot
Water-Soluble Camptothecin Derivatives that Are Intrinsic Topoisomerase I Poisons
inferredcites →https://doi.org/10.1021/tx950080yopenalex-snapshot
Inhibition of Topoisomerase I Function by Coralyne and 5,6-Dihydrocoralyne
inferredcites →https://doi.org/10.1039/j29680000923openalex-snapshot
The structure of camptothecin: X-ray analysis of camptothecin iodoacetate
inferredcites →https://doi.org/10.1063/1.470829openalex-snapshot
Density-functional thermochemistry. IV. A new dynamical correlation functional and implications for exact-exchange mixing
inferredcites →https://doi.org/10.1073/pnas.192282699openalex-snapshot
8-Oxoguanine rearranges the active site of human topoisomerase I
inferredcites →https://doi.org/10.1073/pnas.242259599openalex-snapshot
The mechanism of topoisomerase I poisoning by a camptothecin analog
inferredcites →https://doi.org/10.1103/physrevb.37.785openalex-snapshot
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
inferredcites →https://doi.org/10.1126/science.279.5356.1504openalex-snapshot
Crystal Structures of Human Topoisomerase I in Covalent and Noncovalent Complexes with DNA
inferredcites →https://doi.org/10.1139/v95-063openalex-snapshot
Family-independent relationships between computed molecular surface quantities and solute hydrogen bond acidity/basicity and solute-induced methanol O–H infrared frequency shifts
inferredcites →https://doi.org/10.1177/001258069211037909openalex-snapshot
Obituary
inferredcites →https://doi.org/10.2174/1568011054222373openalex-snapshot
Camptothecin: Roles of the D and E Rings in Binding to the Topoisomerase I-DNA Covalent Binary Complex

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.3982275openalex-extracted
DFT Studies of Camptothecins Cytotoxicity II. Protonated Lactone Forms of Camptothecin
inferred← citeshttps://doi.org/10.2139/ssrn.4019267openalex-extracted
Dft Studies of Camptothecins Cytotoxicity Ii. Protonated Lactone Forms of Camptothecin
inferred← citeshttps://doi.org/10.2139/ssrn.4052377openalex-extracted
Comparative Dft Studies of Cytotoxicity of Camptothecin, Irinotecan and Sn-38
inferred← citeshttps://doi.org/10.1002/bip.21714openalex-snapshot
Structure and properties of camptothecin derivatives, their protonated forms, and model interaction with the topoisomerase I–DNA complex
inferred← citeshttps://doi.org/10.1002/jssc.202100491openalex-snapshot
A validated HPLC‐MS/MS method for determination of simmitecan and its metabolite chimmitecan in human plasma and its application to a pharmacokinetic study in Chinese patients with advanced solid tumor
inferred← citeshttps://doi.org/10.1002/slct.201600609openalex-snapshot
Application of Physicochemical and DFT Based Descriptors for QSAR Study of Camptothecin Derivatives
inferred← citeshttps://doi.org/10.1002/wcms.1735openalex-snapshot
Unveiling Drug Discovery Insights Through Molecular Electrostatic Potential Analysis
inferred← citeshttps://doi.org/10.1007/s00894-009-0501-6openalex-snapshot
Quinoline alkaloids as intercalative topoisomerase inhibitors
inferred← citeshttps://doi.org/10.1007/s00894-009-0627-6openalex-snapshot
Theoretical study on the molecular and electronic properties of some substances used for diabetes mellitus treatment
inferred← citeshttps://doi.org/10.1007/s10822-013-9681-3openalex-snapshot
Ab initio study on the noncovalent adsorption of camptothecin anticancer drug onto graphene, defect modified graphene and graphene oxide
inferred← citeshttps://doi.org/10.1016/j.comptc.2022.113677openalex-snapshot
DFT studies of camptothecins cytotoxicity II. Protonated lactone forms of camptothecin
inferred← citeshttps://doi.org/10.1016/j.cplett.2013.07.001openalex-snapshot
On UV–Vis spectra and structure of the anticancer drug camptothecin in solutions
inferred← citeshttps://doi.org/10.1016/j.jmgm.2013.03.004openalex-snapshot
A theoretical study on mechanism of the anticancer drug camptothecin's E-ring-opening
inferred← citeshttps://doi.org/10.1016/j.jmgm.2018.04.006openalex-snapshot
Quantum chemical calculation of free radical substitution reaction mechanism of camptothecin
inferred← citeshttps://doi.org/10.1016/j.molliq.2021.117804openalex-snapshot
Theoretical analysis of lactone and carboxylate forms of camptothecin in aqueous solution: Electronic states, absorption spectra, and hydration
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.12.097openalex-snapshot
Time dependent-density functional theory (TD-DFT) and experimental studies of UV–Visible spectra and cyclic voltammetry for Cu(II) complex with Et2DTC
inferred← citeshttps://doi.org/10.1016/j.saa.2010.12.049openalex-snapshot
Experimental and theoretical investigation of the molecular and electronic structure of anticancer drug camptothecin
inferred← citeshttps://doi.org/10.1016/j.tet.2010.06.003openalex-snapshot
Total synthesis of (±)-17-norcamptothecin, a novel E-ring modified camptothecin
inferred← citeshttps://doi.org/10.1021/cr0780210openalex-snapshot
Camptothecins: A SAR/QSAR Study
inferred← citeshttps://doi.org/10.1021/jp201749uopenalex-snapshot
Structural Photodynamics of Camptothecin, an Anticancer Drug in Aqueous Solutions
inferred← citeshttps://doi.org/10.2478/acs-2022-0009openalex-snapshot
DFT studies of camptothecins cytotoxicity III: camptothecin, irinotecan and SN-38
inferred← citeshttps://doi.org/10.3390/books978-3-0365-8738-7openalex-snapshot
2D Materials for Biomedical Applications
inferred← citeshttps://doi.org/10.3390/molecules27196742openalex-snapshot
Theoretical Study on the Aggregation and Adsorption Behaviors of Anticancer Drug Molecules on Graphene/Graphene Oxide Surface
inferred← citeshttps://doi.org/10.70675/f125a0ddze248z4199zabf3z49c87a1d29b3openalex-snapshot
Synthèse totale de deux nouveaux analogues de la camptothécine modifiés sur le cycle E
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