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Structure property relationships of amino acids and some dipeptides
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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/anie.198608821openalex-snapshot
Geometric and Topological Thinking in Organic Chemistry
inferredcites →https://doi.org/10.1002/jps.2600641214openalex-snapshot
Molecular Connectivity I: Relationship to Nonspecific Local Anesthesia
inferredcites →https://doi.org/10.1002/jps.2600651228openalex-snapshot
Molecular Connectivity VII: Specific Treatment of Heteroatoms
inferredcites →https://doi.org/10.1002/jps.2600700602openalex-snapshot
Derivation and Significance of Valence Molecular Connectivity
inferredcites →https://doi.org/10.1002/jps.2600760325openalex-snapshot
Molecular Connectivity in Structure–activity Analysis
inferredcites →https://doi.org/10.1002/jps.2600810407openalex-snapshot
Molecular Connectivity Model for Determination of Isoelectric Point of Amino Acids
inferredcites →https://doi.org/10.1002/jps.2600811002openalex-snapshot
Molecular Connectivity: Treatment of the Electronic Structure of Amino Acids
inferredcites →https://doi.org/10.1016/0097-8485(93)80008-2openalex-snapshot
Molecular connectivity model for determination of T1 relaxation times of α-carbons of amino acids and cyclic dipeptides
inferredcites →https://doi.org/10.1016/0166-1280(89)85013-4openalex-snapshot
The limits of applicability of topological indices
inferredcites →https://doi.org/10.1021/ci00002a018openalex-snapshot
Resolution of ambiguities in structure-property studies by use of orthogonal descriptors
inferredcites →https://doi.org/10.1021/ci00005a005openalex-snapshot
Comparative study of molecular descriptors derived from the distance matrix
inferredcites →https://doi.org/10.1021/ed065p574openalex-snapshot
Chemical applications of graph theory. Part I. Fundamentals and topological indices
inferredcites →https://doi.org/10.1021/ed069p701openalex-snapshot
A graph-theoretical approach to structure-property relationships
inferredcites →https://doi.org/10.1021/j100127a026openalex-snapshot
Molecular connectivity model for determination of physicochemical properties of .alpha.-amino acids
inferredcites →https://doi.org/10.1021/ja00856a001openalex-snapshot
Characterization of molecular branching
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1097-461x(2000)80:6<1199::aid-qua6>3.0.co;2-mopenalex-snapshot
On characterization of physical properties of amino acids
inferred← citeshttps://doi.org/10.1002/9780470175668.ch3openalex-snapshot
Graph Theoretic Models in Chemistry and Molecular Biology
inferred← citeshttps://doi.org/10.1002/advs.202507768openalex-snapshot
Structure‐Function Relationships of Biomass‐Derived Materials for Zinc Metal Protection
inferred← citeshttps://doi.org/10.1002/jssc.201401427openalex-snapshot
Quantitative structure–retardation factor relationship of protein amino acids in different solvent mixtures for normal‐phase thin‐layer chromatography
inferred← citeshttps://doi.org/10.1002/qsar.200730097openalex-snapshot
Quantitative Structure–Retention Relationship (QSRR) Study for Predicting Gas Chromatographic Retention Times for Some Stationary Phases
inferred← citeshttps://doi.org/10.1007/0-306-46907-3_6openalex-snapshot
On Characterization of 3D Molecular Structure
inferred← citeshttps://doi.org/10.1007/bf00805953openalex-snapshot
Modeling the solubility and activity of amino acids with the LCCI method
inferred← citeshttps://doi.org/10.1007/bf01372590openalex-snapshot
Modeling properties of biochemical compounds with connectivity terms
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Topological estimation of cytotoxic activity of some anti-HIV agents: HEPT analogues
inferred← citeshttps://doi.org/10.1007/s00044-010-9406-2openalex-snapshot
QSAR modeling of the inhibition of reverse transcriptase enzyme with benzimidazolone analogs
inferred← citeshttps://doi.org/10.1007/s00044-010-9499-7openalex-snapshot
QSAR analysis of Mur B inhibitors with antibacterial properties discussing role of physico-chemical parameters
inferred← citeshttps://doi.org/10.1007/s00044-011-9721-2openalex-snapshot
Prediction of antimalarial activity of some cyclic peroxy ketals using physico-chemical and topological indices
inferred← citeshttps://doi.org/10.1007/s00044-012-0385-3openalex-snapshot
Synthesis, antitubercular activity, and QSAR analysis of substituted nitroaryl analogs: chalcone, pyrazole, isoxazole, and pyrimidines
inferred← citeshttps://doi.org/10.1007/s00044-013-0543-2openalex-snapshot
Synthesis, antimicrobial activity, and molecular modeling of novel 4-(3-(4-benzylpiperazin-1-yl)propoxy)-7-methoxy-3-substituted phenyl-2H-chromen-2-one
inferred← citeshttps://doi.org/10.1007/s00044-013-0691-4openalex-snapshot
Molecular modeling of pyridine derivatives for COX-2 inhibitors: quantitative structure–activity relationship study
inferred← citeshttps://doi.org/10.1007/s00044-014-1148-0openalex-snapshot
In silico molecular modeling and prediction of activity of substituted tetrahydropyrans as COX-2 inhibitor
inferred← citeshttps://doi.org/10.1007/s00894-005-0059-xopenalex-snapshot
QSAR for anti-malarial activity of 2-aziridinyl and 2,3-bis(aziridinyl)-1,4-naphthoquinonyl sulfonate and acylate derivatives
inferred← citeshttps://doi.org/10.1007/s00894-018-3593-zopenalex-snapshot
QSPR modeling of optical rotation of amino acids using specific quantum chemical descriptors
inferred← citeshttps://doi.org/10.1007/s12539-012-0135-8openalex-snapshot
SAR studies on β-cell KATP channel openers
inferred← citeshttps://doi.org/10.1016/j.aca.2009.01.041openalex-snapshot
Automatic adjustment of the relative importance of different input variables for optimization of counter-propagation artificial neural networks
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.08.014openalex-snapshot
Topological modeling of benzodiazepine receptor binding
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.08.028openalex-snapshot
QSAR study on bioconcentration factor (BCF) of polyhalogented biphenyls using the PI index
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.09.025openalex-snapshot
QSAR study on 5-lipoxygenase inhibitors using distance-Based topological indices
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.09.037openalex-snapshot
Quantitative structure–Activity relationship study on sulfanilamide schiff's bases: carbonic anhydrase (CA) inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.11.024openalex-snapshot
QSAR study of flavonoid derivatives as p56lck tyrosinkinase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.12.017openalex-snapshot
QSAR Study on 13C NMR chemical shifts on carbinol carbon atoms
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.01.009openalex-snapshot
QSAR study on tadpole narcosis using PI index: a case of heterogenous set of compounds
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.01.049openalex-snapshot
QSAR study on CA inhibitory activity of disulfonamides: effect of halogen substitution
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.02.010openalex-snapshot
QSAR study on phenolic activity: need of positive hydrophobic term (logP) in QSAR
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.07.058openalex-snapshot
QSAR studies of N1-(5-chloro-2-pyridyl)-2-{[4-(alkyl methyl)benzoyl]amino}-5-chlorobenzamide analogs
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.07.004openalex-snapshot
QSAR studies on the activation of the human carbonic anhydrase cytosolic isoforms I and II and secretory isozyme VI with amino acids and amines
inferred← citeshttps://doi.org/10.1016/j.bmcl.2003.12.062openalex-snapshot
Correlations between the benzene character of acenes or helicenes and simple molecular descriptors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.03.099openalex-snapshot
Carbonic anhydrase inhibitors: the first QSAR study on inhibition of tumor-associated isoenzyme IX with aromatic and heterocyclic sulfonamides
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.06.094openalex-snapshot
Topological estimation of electronic absorption bands of arene absorption spectra as a tool for modeling their toxicity and environmental pollution
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.08.051openalex-snapshot
Topological modeling of lipophilicity, diuretic activity, and carbonic inhibition activity of benzene sulfonamides: a molecular connectivity approach
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.10.032openalex-snapshot
QSAR study on pKa vis-à-vis physiological activity of sulfonamides: a dominating role of surface tension (inverse steric parameter)
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.10.075openalex-snapshot
Novel estimation of lipophilicity using 13C NMR chemical shifts as molecular descriptor
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.10.076openalex-snapshot
QSAR study on the antibacterial activity of some sulfa drugs: building blockers of Mannich bases
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.12.056openalex-snapshot
QSAR studies on benzene sulfonamide carbonic anhydrase inhibitors: need of hydrophobic parameter for topological modeling of binding constants of sulfonamides to human CA-II
inferred← citeshttps://doi.org/10.1016/j.bmcl.2004.12.057openalex-snapshot
Novel use of chemical shift in NMR as molecular descriptor: a first report on modeling carbonic anhydrase inhibitory activity and related parameters
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.05.136openalex-snapshot
Study on supramolecular complexing ability vis-à-vis estimation of pKa of substituted sulfonamides: Dominating role of Balaban index (J)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2004.03.002openalex-snapshot
QSAR study on carbonic anhydrase inhibitors: aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties, with topical activity as antiglaucoma agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2005.04.006openalex-snapshot
QSAR study on carbonic anhydrase inhibitors: water-soluble sulfonamides incorporating β-alanyl moieties, possessing long lasting-intra ocular pressure lowering properties—a molecular connectivity approach
inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.06.022openalex-snapshot
Exploration of physicochemical properties and molecular modelling studies of 2-sulfonyl-phenyl-3-phenyl-indole analogs as cyclooxygenase-2 inhibitors
inferred← citeshttps://doi.org/10.1016/j.jscs.2009.10.005openalex-snapshot
QSAR studies on anti-apoptotic Bcl-2 protein inhibitors
inferred← citeshttps://doi.org/10.1016/j.jscs.2009.10.006openalex-snapshot
QSAR based modeling of inhibitory activity of alkenyldiarylmethane derivatives
inferred← citeshttps://doi.org/10.1016/j.jscs.2010.02.006openalex-snapshot
Molecular modeling of 8-methoxy quinolone analogues by using quantitative structure activity relationship
inferred← citeshttps://doi.org/10.1016/j.jscs.2010.09.001openalex-snapshot
QSAR based modeling on a series of α-hydroxy amides as a novel class of bradykinin B1 selective antagonists
inferred← citeshttps://doi.org/10.1016/j.jscs.2010.09.007openalex-snapshot
QSAR based modeling of hepatitis C virus NS5B inhibitors
inferred← citeshttps://doi.org/10.1016/j.jscs.2011.02.010openalex-snapshot
QSAR based modeling on a series of lactam fused chroman derivatives as selective 5-HT transporters
inferred← citeshttps://doi.org/10.1016/j.jscs.2013.01.007openalex-snapshot
Quantitative structure–activity relationship based modeling of substituted indole Schiff bases as inhibitor of COX-2
inferred← citeshttps://doi.org/10.1016/s0166-1280(98)00108-0openalex-snapshot
Properties of molecular connectivity terms and physicochemical properties
inferred← citeshttps://doi.org/10.1016/s0960-894x(02)00954-xopenalex-snapshot
Modelling of carbonic anhydrase inhibitory activity of sulfonamides using molecular negentropy
inferred← citeshttps://doi.org/10.1016/s0960-894x(03)00636-xopenalex-snapshot
Topological designing of 4-piperazinylquinazolines as antagonists of PDGFR tyrosine kinase family
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00147-xopenalex-snapshot
QSAR Studies on acylated histamine derivatives
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00211-5openalex-snapshot
QSAR prediction of toxicity of nitrobenzenes
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00241-3openalex-snapshot
QSAR Studies on some antimalarial sulfonamides
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00242-5openalex-snapshot
QSAR study on inhibition of brain 3-hydroxy-anthranilic acid dioxygenase (3-HAO): A molecular connectivity approach
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00375-3openalex-snapshot
QSAR study on toxicity to aqueous organisms using the PI index
inferred← citeshttps://doi.org/10.1016/s0968-0896(01)00399-6openalex-snapshot
QSAR Studies on Antimalarial Substituted Phenyl Analogues and Their Nω-Oxides
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00123-2openalex-snapshot
QSAR Studies on Carbonic Anhydrase Inhibitors: A Case of Ureido and Thioureido Derivatives of Aromatic/Heterocyclic Sulfonamides
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00158-xopenalex-snapshot
QSAR study on competition binding of rodenticides (PATs) to H1 receptor in rat and guinea pig brain
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00159-1openalex-snapshot
QSAR studies on biological activity of piritrexim analogues against pc DHFR
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00167-0openalex-snapshot
Quantitative structure–Activity relationship studies on 5-phenyl-3-ureido-1,5-benzodiazepine as cholecystokinin-A receptor antagonists
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00226-2openalex-snapshot
Prediction of lipophilicity of polyacenes using quantitative structure–Activity relationships
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00228-6openalex-snapshot
QSAR study on narcotic mechanism of action and toxicity: a molecular connectivity approach to Vibrio fischeri toxicity testing
inferred← citeshttps://doi.org/10.1016/s0968-0896(02)00299-7openalex-snapshot
On the topological evidences for modelling lipophilicity
inferred← citeshttps://doi.org/10.1016/s0968-0896(03)00370-5openalex-snapshot
Topological approach to quantifying molecular lipophilicity of heterogeneous set of organic compounds
inferred← citeshttps://doi.org/10.1016/s0968-0896(03)00446-2openalex-snapshot
QSAR Study on tadpole narcosis
inferred← citeshttps://doi.org/10.1021/ci000106dopenalex-snapshot
Retro-RegressionAnother Important Multivariate Regression Improvement
inferred← citeshttps://doi.org/10.1021/ci300057hopenalex-snapshot
Chirality Measures of α-Amino Acids
inferred← citeshttps://doi.org/10.1021/ci960174topenalex-snapshot
On Characterization of Chemical Structure
inferred← citeshttps://doi.org/10.1080/10629360108039833openalex-snapshot
QSAR Study on Binding Affinity of PATs (Rodenticides) to the [3H]-Mepyramine-Labelled H1Receptor In Rat and Guinea Pig Brain
inferred← citeshttps://doi.org/10.1080/14756360802421094openalex-snapshot
Insights through AM1 calculations into the structural requirement ofN-hydroxythiosemicarbazone analogs as anti-tubercular agents
inferred← citeshttps://doi.org/10.1104/pp.15.00971openalex-snapshot
A Single Amino Acid Substitution in an ORANGE Protein Promotes Carotenoid Overaccumulation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2009.00844.xopenalex-snapshot
QSPR Study on the Estimation of Solubility of Drug‐like Organic Compounds: A Case of Barbiturates
inferred← citeshttps://doi.org/10.1111/j.1747-0285.2010.01034.xopenalex-snapshot
2‐(pyrazin‐2‐yloxy)acetohydrazide Analogs QSAR Study: An Insight into the Structural Basis of Antimycobacterial Activity
inferred← citeshttps://doi.org/10.1155/2013/795621openalex-snapshot
Estimation of Anti-HIV Activity of HEPT Analogues Using MLR, ANN, and SVM Techniques
inferred← citeshttps://doi.org/10.11648/j.mc.20130101.12openalex-snapshot
QSAR, Docking and Invitro Antioxidant Activity Study of Novel Chromone Derivatives
inferred← citeshttps://doi.org/10.1556/amicr.50.2003.4.6openalex-snapshot
QSAR Analysis of Antibacterial Activity of Some 4-aminodiphenylsulfone derivatives
inferred← citeshttps://doi.org/10.2174/1573407210602010019openalex-snapshot
Use of PI Index in Computer-Aided Designing of Bioactive Compounds
inferred← citeshttps://doi.org/10.23880/act-16000276openalex-snapshot
Modelling of the Antibacterial Activity of Some Benzimidazole Derivatives
inferred← citeshttps://doi.org/10.3998/ark.5550190.0007.g01openalex-snapshot
A QSAR study on carbonic anhydrase inhibition: predicting logKi(hCAI) by using (SO2NH2) NMR chemical shift as a molecular descriptor
inferred← citeshttps://doi.org/10.9790/5736-0412633openalex-snapshot
QSAR Studies of Some Bisphosphonates Compounds for their Anticancer Activities
inferred← citeshttps://doi.org/10.9790/5736-0630917openalex-snapshot
Effect of 3D parameters on Antifungal Activities of Some Heterocyclic Compounds
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