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Design of molecules from quantitative structure-activity relationship models. 3. Role of higher order path counts: Path 3

https://doi.org/10.1021/ci00014a012
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inferred← citeshttps://doi.org/10.1002/0471266949.bmc002openalex-snapshot
Recent Trends in Quantitative Structure‐Activity Relationships
inferred← citeshttps://doi.org/10.1002/9783527613106.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/9783527628766.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/aic.14112openalex-snapshot
Optimization‐based framework for computer‐aided molecular design
inferred← citeshttps://doi.org/10.1002/chin.199347333openalex-snapshot
ChemInform Abstract: Design of Molecules from Quantitative Structure‐Activity Relationship Models. Part 3. Role of Higher Order Path Counts: Path 3.
inferred← citeshttps://doi.org/10.1002/jcc.20931openalex-snapshot
Computational modeling of tetrahydroimidazo‐[4,5,1‐jk][1,4]‐benzodiazepinone derivatives: An atomistic drug design approach using Kier‐Hall electrotopological state (E‐state) indices
inferred← citeshttps://doi.org/10.1002/minf.201700030openalex-snapshot
Finding Chemical Structures Corresponding to a Set of Coordinates in Chemical Descriptor Space
inferred← citeshttps://doi.org/10.1002/minf.201900087openalex-snapshot
Inverse‐QSPR for de novo Design: A Review
inferred← citeshttps://doi.org/10.1002/qsar.19930120406openalex-snapshot
The Generation of Molecular Structures from a Graph‐Based QSAR Equation
inferred← citeshttps://doi.org/10.1002/qua.560560707openalex-snapshot
On characterization of the conformations of nine-membered rings
inferred← citeshttps://doi.org/10.1007/978-3-319-56850-8_2openalex-snapshot
The Use of Topological Indices in QSAR and QSPR Modeling
inferred← citeshttps://doi.org/10.1007/978-3-642-13136-3_18openalex-snapshot
Balanced Multi-process Parallel Algorithm for Chemical Compound Inference with Given Path Frequencies
inferred← citeshttps://doi.org/10.1007/978-3-642-14553-7_13openalex-snapshot
Constant Time Generation of Biconnected Rooted Plane Graphs
inferred← citeshttps://doi.org/10.1007/978-3-642-17461-2_28openalex-snapshot
Listing Triconnected Rooted Plane Graphs
inferred← citeshttps://doi.org/10.1007/s10822-005-9007-1openalex-snapshot
Reverse engineering chemical structures from molecular descriptors: how many solutions?
inferred← citeshttps://doi.org/10.1007/s10822-005-9010-6openalex-snapshot
Can topological indices transmit information on properties but not on structures?
inferred← citeshttps://doi.org/10.1007/s12039-007-0078-5openalex-snapshot
Molecular modelling studies on 2-amino 6-aryl-sulphonylbenzonitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1: A QSPR approach
inferred← citeshttps://doi.org/10.1016/j.cherd.2016.10.014openalex-snapshot
Computer-aided molecular design: An introduction and review of tools, applications, and solution techniques
inferred← citeshttps://doi.org/10.1016/j.ijggc.2014.08.023openalex-snapshot
In silico design of solvents for carbon capture with simultaneous optimisation of operating conditions
inferred← citeshttps://doi.org/10.1016/j.jmgm.2003.10.002openalex-snapshot
The signature molecular descriptor
inferred← citeshttps://doi.org/10.1016/s0045-6535(98)00469-xopenalex-snapshot
SAR/QSAR approaches to solubility, partitioning and sorption of phthalates
inferred← citeshttps://doi.org/10.1016/s0098-1354(97)00257-3openalex-snapshot
Optimization in product design with properties correlated with topological indices
inferred← citeshttps://doi.org/10.1016/s1093-3263(01)00097-3openalex-snapshot
Issues in representation of molecular structure
inferred← citeshttps://doi.org/10.1021/ci020346oopenalex-snapshot
The Signature Molecular Descriptor. 2. Enumerating Molecules from Their Extended Valence Sequences
inferred← citeshttps://doi.org/10.1021/ci700385aopenalex-snapshot
Enumerating Treelike Chemical Graphs with Given Path Frequency
inferred← citeshttps://doi.org/10.1021/ci900318copenalex-snapshot
Prediction of Partial Molar Volumes of Amino Acids and Small Peptides: Counting Atoms versus Topological Indices
inferred← citeshttps://doi.org/10.1021/ci900447zopenalex-snapshot
Branch-and-Bound Algorithms for Enumerating Treelike Chemical Graphs with Given Path Frequency Using Detachment-Cut
inferred← citeshttps://doi.org/10.1023/b:pham.0000012154.09631.26openalex-snapshot
Bioavailability Prediction Based on Molecular Structure for a Diverse Series of Drugs
inferred← citeshttps://doi.org/10.1080/10629369908039111openalex-snapshot
On Characterization of the CC Double Bond in Alkenes
inferred← citeshttps://doi.org/10.1145/3180382.3180384openalex-snapshot
Enumerating Chemical Mono-Block 3-Augmented Trees with Two Junctions
inferred← citeshttps://doi.org/10.1186/1471-2105-12-s14-s3openalex-snapshot
Enumerating tree-like chemical graphs with given upper and lower bounds on path frequencies
inferred← citeshttps://doi.org/10.1186/1758-2946-1-4openalex-snapshot
A constructive approach for discovering new drug leads: Using a kernel methodology for the inverse-QSAR problem
inferred← citeshttps://doi.org/10.1186/1758-2946-6-31openalex-snapshot
Efficient enumeration of monocyclic chemical graphs with given path frequencies
inferred← citeshttps://doi.org/10.3390/i8200456openalex-snapshot
Internal Test Sets Studies in a Group of Antimalarials
inferred← citeshttps://doi.org/10.3797/scipharm.0804-12openalex-snapshot
Chemical Structure Indices in In Silico Molecular Design
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