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Platinum complex ion ([PtCl42−) behaves like a molecule with lower polarity due to its large size.
Citronellol, the molecule with lower number of π bonds, is an acyclic terpene less able to interact with SCP-2 and is also the molecule with lower larvicidal activity.
The acetone molecule with lower O Mulliken charge (−0.375 e) exhibited lower response than 1-butylamine, probably due to the structure difference.
The HOMO energy (EHOMO) expresses the intrinsic electron donating tendency to an appropriate acceptor i.e., any molecule with lower HOMO energy and empty molecular orbital; while the energy of LUMO (ELUMO) is directly related to the electron affinity and characterizes the susceptibility of the molecule toward attack by nucleophiles[66, 67, 68].
The radical pair in turn reduces the secondary electron acceptor QA, a single electron-accepting plastoquinone molecule, with lower energy than Phe- resulting in the stabilization of the charge separated state.
A first binding phase in which one chitin molecule was bound with ultra-high affinity (kd = 280 pM; n = 0.99) occurred, followed by binding of an additional molecule with lower affinity (kd = 1.70 µM; n = 1.03).
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Molecules with lower energy of the HOMO and LUMO behave as stronger retarders.
The outer layers of the callus starch granules have larger molecules with lower amylose content and shorter amylopectin chains compared to further inside the callus starch granules.
Nevertheless, due to the increase in bone and muscle loss, impotency and occurrence of high-grade prostate tumours, it is important to seek for other potent and specific molecules with lower side effects.
Also, precise structural information involving these amino acid molecules with lower symmetry exhibiting higher trigonal symmetry in their self-assembly is expected to throw light on the nature and strength of intermolecular interactions and their role in self-assembly of molecular aggregates, which are crucial in developing new or at least supplement existing crystal engineering strategies.
Therefore, the prediction for the molecules with higher pLD50 values are worse than those for the molecules with lower pLD50 values.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com