Generalized Chemical Block Systems on Chern-Simons φ∘ D∘ r2∘ S∘ r1
Topologies for the generation of the Roccustyrna Holomorphic Ligand.
Abstract
SARS coronavirus 2 (SARS - CoV - 2) in the viral spike (S) encoding a
SARS - COV - 2 SPIKE D614G mutation protein predominate over time in
locales revealing the dynamic aspects of its key viral processes where
it is found, implying that this change enhances viral transmission. In
this paper, we strongly combine topology geometric methods for
generalized formalisms of k - nearest neighbors as a Tipping–Ogilvie
and Machine Learning application within the quantum computing context
targeting the atomistic level of the protein apparatus of the SARS - COV
- 2 viral characteristics. In this effort, we propose computer - aided
rational drug design strategies efficient in computing docking usage,
and powerful enough to achieve very high accuracy levels for this in -
silico effort for the generation of AI - Quantum designed molecules of
GisitorviffirnaTM, Roccustyrna_gs1_TM, and Roccustyrna_fr1_TM
ligands targeting the COVID - 19 - SARS - COV - 2 SPIKE D614G mutation
by unifying Eigenvalue Statements into Shannon entropy quantities as
composed on Tipping–Ogilvie driven Machine Learning potentials for
nonzero Christoffel symbols for Schwarzschild (DFT) ℓneuron (ι) : == ==
φ∘D∘r2∘S∘r102 (1+∑) == == (A∧A’ (p)) • ⋱⋯⊗⋱⋯ •e− ρ (rr) −−¯σ − ¯σσ¯ǫ
−i_+02 (1− ) 2} () ) improver for Chern - Simons Topology Euclidean
Geometrics. I also arrived at a new Zmatter derived finite ‐ dimensional
state integral with a symplectic ω == == (i~)−1 (dx/x) ∧
(dy/y) model for computing the analytically continued “holomorphic
blocks” on an appropriate quantum Hilbert space H that compose physical
Chern ‐ Simons partition function to put pharmacophoric elements back
together.