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Some observations on classical QSAR

https://doi.org/10.1007/bf02174527
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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/ddr.430010403openalex-snapshot
The physicochemical approach to drug design and discovery (QSAR)
inferredcites →https://doi.org/10.1002/jps.2600600643openalex-snapshot
Advances in Drug Research, vol. 5
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Relationship between Lipophilic Character and Anesthetic Activity
inferredcites →https://doi.org/10.1002/jps.2600740828openalex-snapshot
Drug Design: Fact or Fantasy?
inferredcites →https://doi.org/10.1002/jps.2600760902openalex-snapshot
Hydrophobicity and Central Nervous System Agents: On the Principle of Minimal Hydrophobicity in Drug Design
inferredcites →https://doi.org/10.1002/jps.2600800905openalex-snapshot
Relative Lipophilicities, Solubilities, and Structure–Pharmacological Considerations of 3-Hydroxy-3-Methylglutaryl-Coenzyme A (HMG-CoA) Reductase Inhibitors Pravastatin, Lovastatin, Mevastatin, and Simvastatin
inferredcites →https://doi.org/10.1007/bf00500963openalex-snapshot
Lipophilicity and brain disposition of clonidine and structurally related imidazolidines
inferredcites →https://doi.org/10.1016/0076-6879(91)02026-6openalex-snapshot
[24] Quantitative structure-activity relationships and molecular graphics in evaluation of enzyme-ligand interactions
inferredcites →https://doi.org/10.1016/0165-6147(84)90499-1openalex-snapshot
Progress in drug research. Vol. 27
inferredcites →https://doi.org/10.1016/0165-6147(91)90535-zopenalex-snapshot
Comprehensive medicinal chemistry
inferredcites →https://doi.org/10.1016/0223-5234(90)90145-sopenalex-snapshot
Potential antipsychotic agents. 6. Synthesis and antidopaminergic properties of substituted N-(1-benzyl-4-piperidinyl)salicylamides and related compounds. QSAR based design of more active members
inferredcites →https://doi.org/10.1016/b978-0-12-695150-9.50015-5openalex-snapshot
Absorption, Distribution, and Metabolism of Drugs
inferredcites →https://doi.org/10.1016/b978-0-12-695150-9.x5001-6openalex-snapshot
Quantitative Structure–Activity Relationships of Drugs
inferredcites →https://doi.org/10.1021/ar00028a003openalex-snapshot
Quantitative structure-activity relationships and the unnamed science
inferredcites →https://doi.org/10.1021/ar00132a003openalex-snapshot
Molecular graphics and QSAR in the study of enzyme-ligand interactions. On the definition of bioreceptors
inferredcites →https://doi.org/10.1021/bk-1978-0083.ch008openalex-snapshot
1-Aralkyl-2-pyrazolin-5-ones: A New Class of Highly Potent Diuretics with High Ceiling Activity
inferredcites →https://doi.org/10.1021/bk-1980-0118openalex-snapshot
Drugs Affecting the Respiratory System
inferredcites →https://doi.org/10.1021/bk-1980-0118.ch006openalex-snapshot
Antiallergic Purinones: A Successful Application of QSAR
inferredcites →https://doi.org/10.1021/ja01062a035openalex-snapshot
p-σ-π Analysis. A Method for the Correlation of Biological Activity and Chemical Structure
inferredcites →https://doi.org/10.1021/jm00068a002openalex-snapshot
Nonpeptide angiotensin II receptor antagonists. 2. Design, synthesis, and structure-activity relationships of 2-alkyl-4-(1H-pyrrol-l-yl)-1H-imidazole derivatives: profile of…
inferredcites →https://doi.org/10.1021/jm00087a011openalex-snapshot
Rationally designed dipeptoid analogs of cholecystokinin. A Free-Wilson/Fujita-Ban analysis of some .alpha.-methyltryptophan derivatives as cholecystokinin-B antagonists
inferredcites →https://doi.org/10.1021/jm00092a004openalex-snapshot
Comparative molecular field analysis of anticoccidial triazines
inferredcites →https://doi.org/10.1021/jm00094a007openalex-snapshot
Quantitative structure-activity relationships of N2-phenylguanines as inhibitors of Herpes simplex virus thymidine kinases
inferredcites →https://doi.org/10.1021/jm00105a008openalex-snapshot
Optimization of hydrophobic and hydrophilic substituent interactions of 2,4-diamino-5-(substituted-benzyl)pyrimidines with dihydrofolate reductase
inferredcites →https://doi.org/10.1021/jm00105a020openalex-snapshot
Three-dimensional structure-activity relationships and receptor mapping of N1-substituents of quinolone antibacterials
inferredcites →https://doi.org/10.1021/jm00105a067openalex-snapshot
Non-steroidal antiandrogens. Design of novel compounds based on an infrared study of the dominant conformation and hydrogen-bonding properties of a series of anilide antiandrogens
inferredcites →https://doi.org/10.1021/jm00105a072openalex-snapshot
8-(Dicyclopropylmethyl)-1,3-dipropylxanthine: a potent and selective adenosine A1 antagonist with renal protective and diuretic activities
inferredcites →https://doi.org/10.1021/jm00109a006openalex-snapshot
5-Lipoxygenase inhibitors: the synthesis and structure-activity relationships of a series of 1-phenyl-3-pyrazolidinones
inferredcites →https://doi.org/10.1021/jm00111a009openalex-snapshot
Quantitative structure-activity relationships of antitumor guanidinothiazolecarboxamides with survival enhancement for therapy in the 3LL Lewis lung carcinoma model
inferredcites →https://doi.org/10.1021/jm00125a014openalex-snapshot
2,3-Dihydro-5-benzofuranols as antioxidant-based inhibitors of leukotriene biosynthesis
inferredcites →https://doi.org/10.1021/jm00135a001openalex-snapshot
A practitioner's perspective of the role of quantitative structure-activity analysis in medicinal chemistry
inferredcites →https://doi.org/10.1021/jm00135a004openalex-snapshot
Quantitative structure-activity relationships of colchicines against P388 leukemia in mice
inferredcites →https://doi.org/10.1021/jm00139a018openalex-snapshot
Comparison of mutagenic and carcinogenic activities of aniline mustards
inferredcites →https://doi.org/10.1021/jm00146a016openalex-snapshot
Synthesis of xanthines as adenosine antagonists, a practical quantitative structure-activity relationship application
inferredcites →https://doi.org/10.1021/jm00147a001openalex-snapshot
Computer-assisted drug design
inferredcites →https://doi.org/10.1021/jm00165a017openalex-snapshot
Hydroxamic acid inhibitors of 5-lipoxygenase: quantitative structure-activity relationships
inferredcites →https://doi.org/10.1021/jm00169a014openalex-snapshot
Structure-activity relationships of antineoplastic agents in multidrug resistance
inferredcites →https://doi.org/10.1021/jm00171a008openalex-snapshot
Synthesis and quantitative structure-activity relationships of diclofenac analogs
inferredcites →https://doi.org/10.1021/jm00172a021openalex-snapshot
A Free-Wilson/Fujita-Ban analysis and prediction of the analgesic potency of some 3-hydroxy- and 3-methoxy-N-alkylmorphinan-6-one opioids
inferredcites →https://doi.org/10.1021/jm00176a016openalex-snapshot
Rm values and structure-activity relationship of benzodiazepines
inferredcites →https://doi.org/10.1021/jm00180a022openalex-snapshot
Relationship of octanol/water partition coefficient and molecular weight to rat brain capillary permeability
inferredcites →https://doi.org/10.1021/jm00186a014openalex-snapshot
Structure-activity relationships of antibacterial 6,7- and 7,8-disubstituted 1-alkyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acids
inferredcites →https://doi.org/10.1021/jm00192a019openalex-snapshot
Application of quantitative structure-activity relationships in the development of the antiallergic pyranenamines
inferredcites →https://doi.org/10.1021/jm00214a001openalex-snapshot
A manual method for applying the Hansch approach to drug design
inferredcites →https://doi.org/10.1021/jm00217a007openalex-snapshot
Cyanoguanidine-thiourea equivalence in the development of the histamine H2-receptor antagonist, cimetidine
inferredcites →https://doi.org/10.1021/jm00223a001openalex-snapshot
Structure of medicinal chemistry
inferredcites →https://doi.org/10.1021/jm00226a007openalex-snapshot
Mode of action and quantitative structure-activity correlations of tuberculostatic drugs of the isonicotinic acid hydrazide type
inferredcites →https://doi.org/10.1021/jm00227a003openalex-snapshot
Quantitative structure-activity relationships. 1. The modified Free-Wilson approach
inferredcites →https://doi.org/10.1021/jm00233a009openalex-snapshot
Use of cluster analysis in the development of structure-activity relations for antitumor triazenes
inferredcites →https://doi.org/10.1021/jm00280a002openalex-snapshot
Utilization of operational schemes for analog synthesis in drug design
inferredcites →https://doi.org/10.1021/jm00284a016openalex-snapshot
Structure-activity relation. 3. Structure-activity study of phenethylamines as substrates of biosynthetic enzymes of sympathetic transmitters
inferredcites →https://doi.org/10.1021/jm00290a001openalex-snapshot
Structure-activity relations in antifungal agents. A survey
inferredcites →https://doi.org/10.1021/jm00307a001openalex-snapshot
Parabolic dependence of drug action upon lipophilic character as revealed by a study of hypnotics
inferredcites →https://doi.org/10.1021/jm00309a004openalex-snapshot
Structure-activity correlations for antibacterial agents on gram-positive and gram-negative cells
inferredcites →https://doi.org/10.1021/jm00311a038openalex-snapshot
Potential antimalarial substances. Antimetabolites of pantothenic acid
inferredcites →https://doi.org/10.1021/jm00334a001openalex-snapshot
A Mathematical Contribution to Structure-Activity Studies
inferredcites →https://doi.org/10.1021/jm00345a015openalex-snapshot
Potential antitumor agents. 36. Quantitative relationships between experimental antitumor activity, toxicity, and structure for the general class of 9-anilinoacridine antitumor agents
inferredcites →https://doi.org/10.1021/jm00398a028openalex-snapshot
Development of a new physicochemical model for brain penetration and its application to the design of centrally acting H2 receptor histamine antagonists
inferredcites →https://doi.org/10.1021/jm00401a013openalex-snapshot
Linear free energy relationship studies of enzyme active site binding: thymidylate synthase
inferredcites →https://doi.org/10.1039/cs9740300273openalex-snapshot
Quantitative drug design
inferredcites →https://doi.org/10.1146/annurev.pa.21.040181.000335openalex-snapshot
Structure-Activity Relationships and Drug Disposition
inferredcites →https://doi.org/10.1177/009286158401800202openalex-snapshot
On the State of QSAR
inferredcites →https://doi.org/10.1201/9781420071009openalex-snapshot
Quantitative Drug Design
inferredcites →https://doi.org/10.1248/cpb.39.1426openalex-snapshot
Quantitative Structure-Activity Relationship Analysis of Phencyclidine Derivatives. I.
inferredcites →https://doi.org/10.1515/9783112706992openalex-snapshot
Theoretical Drug Design Methods
inferredcites →https://doi.org/10.2533/chimia.1992.299openalex-snapshot
Hydrogen-Bonding Capacity and Brain Penetration

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Conformational analysis and QSAR modeling of 14-membered macrolide analogues against mycobacterium tuberculosis
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