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Record W1963752629 · doi:10.1021/jp0403240

Resolution of Carvedilol's Conformational Surface via Gas and Solvent Phase Density Functional Theory Optimizations and NMR Spectroscopy

2004· article· en· W1963752629 on OpenAlexaff
David R. P. Almeida, Donna M. Gasparro, Tamás A. Martinek, Ferenc Fülöp, Imre G. Csizmadia

Bibliographic record

VenueThe Journal of Physical Chemistry A · 2004
Typearticle
Languageen
FieldChemistry
TopicAdvanced NMR Techniques and Applications
Canadian institutionsUniversity of Toronto
Fundersnot available
KeywordsChemistryConformational isomerismDensity functional theorySolvent effectsNuclear magnetic resonance spectroscopyIntramolecular forceSpectroscopySolventComputational chemistryMoleculeStereochemistryOrganic chemistry

Abstract

fetched live from OpenAlex

The pharmaceutical carvedilol acts as a nonselective β (β 1 /β 2 ) and selective α (α 1 ) adrenoceptor antagonist, cardioprotector, antioxidant, oxidative phosphorylation uncoupler, and amyloid-β (Aβ) antifibrillar agent. Given these diverse pharmacodynamic profiles, the resolution of carvedilol's highly populated conformations are necessary to divulge the basis of its interactions with these molecular targets. However, given carvedilol's sizable conformational hypersurface (11 torsional angles and 3 11 conformational possibilities), this task is preferentially achieved by means of a novel rational molecular fragmentation method to minimize computational and experimental resources. Presently we have isolated and optimized nine low energy carvedilol conformers with high level B3LYP/6-31G(d) density functional theory (DFT with the Becke 3LYP hybrid exchange-correlation functional) molecular orbital computations in the gas phase and in the solvent phase (DMSO and water) with Onsager solvent reaction field calculations as a means to arrive at the uncharacterized low energy structures and solvent effect of carvedilol. Additionally, carvedilol has been analyzed with NMR spectroscopy (in DMSO) to correlate theoretical- and experimental-derived electronic structure. Gas phase results show that seven of the nine conformers possess a novel tetracentric spiro-type conformation composed of intramolecular six- and eight-membered rings. This structural motif is dictated by the necessary stabilization of the positively charged nitrogen group and by the inflexibility of the carbazole aromatic ring. DMSO and water DFT optimizations and NMR spectroscopy closely mirror each other indicating that carvedilol has a subtle energetic and structural solvent effect. ROESY and scalar coupling show further evidence of the rigid rotation about the large carbazole pharmacophore. Given the harmony achieved between theoretical and experimental results, this study suggests the most populated states of carvedilol expected to dominate physical and biological samples and gives credence to the ability of methodically analyzing complex molecular systems by means of theoretical structure−activity fragmentation. Together, this will critically aid the molecular understating of carvedilol's pharmacodynamic mechanisms and structural underpinnings.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.005
Threshold uncertainty score0.009

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0010.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.010
GPT teacher head0.268
Teacher spread0.259 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations7
Published2004
Admission routes1
Has abstractyes

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