Rapid evaluation of synthetic and molecular complexity for in silico chemistry. Academic Article uri icon

start page

  • 1237

end page

  • 1243

abstract

  • Methods that rapidly evaluate molecular complexity and synthetic feasibility are becoming increasingly important for in silico chemistry. We propose a new metric based on relative atomic electronegativities and bond parameters that evaluate both synthetic and molecular complexity (SMCM) starting from chemical structures. Against molecular weight, SMCM has the lowest fraction of adjusted variance (R2=0.535) on a series of 261,048 diverse compounds, when compared to the complexity metric of Baron and Chanon (R2=0.777; J. Chem. Inf. Comput. Sci. 2001, 41, 269-272) and Rücker (R2=0.895 for log complexity values; J. Chem. Inf. Comput. Sci. 2004, 44, 378-386), respectively. These metrics are in general agreement when the metabolic synthesis of cholesterol from S-3-hydroxy-3-methyl-glutaryl coenzyme A is monitored, indicating that SMCM can be useful in discerning increases in complexity. Because the presence of substructure patterns can be directly incorporated into this scheme, SMCM is relatively straightforward and can be easily tailored to rapidly evaluate virtual (combinatorial) libraries and high throughput screening hits.

Digital Object Identifier (DOI)

  • 10.1021/ci0501387

PubMed Identifier

  • 16180900

volume

  • 45

number

  • 5

keywords

  • Acyl Coenzyme A
  • Animals
  • Cholesterol
  • Drug Design
  • Drug Evaluation, Preclinical
  • Molecular Structure
  • Molecular Weight
  • Software