Conformational energetics of cationic backbone rearrangements in triterpenoid biosynthesis provide an insight into enzymatic control of product

Medicine & Life Sciences

• 2,3-oxidosqualene 100%
• friedelin 92%
• Triterpenes 64%
• Density Functional Theory 44%
• Pentacyclic Triterpenes 42%
• Static Electricity 30%
• Hydrogen 29%
• Cations 25%
• Carbon 25%
• Acceleration 25%

Chemical Compounds

• Triterpenoid 61%
• Biosynthesis 43%
• Friedelin 41%
• Hartree-Fock Calculation 15%
• Density Functional Theory 7%
• Cation 7%
• Hydrogen 6%
• Carbon Atom 5%

Engineering & Materials Science

• Biosynthesis 81%
• Positive ions 15%
• Discrete Fourier transforms 13%
• Electrostatics 13%
• Hydrogen 10%
• Carbon 9%