• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.137-137
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• 2013

The most stable adsorption structures and their corresponding energies of 4-pyridone, 4-hydroxypyridine, 2-pyridone and 2-hydroxypyridine have been investigated by Density Functional Theory (DFT) calculation method and high-resolution photoemission spectroscopy (HRPES). We confirmed that between the two reaction centers of 4- and 2-pyridone, only O atom of carbonyl functional group can act as a Lewis base and thus, O dative bonding structure is the most stable. On the other hand, we clarified that both the two reaction centers (the cyclic N atom and the O atom of hydroxyl functional group) of 4- and 2-hydroxypyridine (tautomers of 4- and 2-pyridone) can successfully function as a Lewis base. Through the interpretation of the N 1s and O 1s core level spectra obtained using HRPES, we could confirm the electronic structures and bonding configurations of these molecules with a coverage dependence on the Ge(100) surface.

• 약학회지
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• 제37권1호
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• pp.36-40
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• 1993

The 4-(2'-(N-(l-methyl-3'-carbamylphenyl)-n-propyl))aminoethyl)-l- hydroxy-2-pyridone which has isoelectronic and isosteric structural similarity with dobutamine without having the Catechol-O- Methyltransferase(COMT) vulnerable m-hydroxy group was synthesized via 12 synthetic steps.

• Bulletin of the Korean Chemical Society
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• 제35권2호
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• pp.581-586
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• 2014

The most stable adsorption structures and their corresponding energies of 4-pyridone, 4-hydroxypyridine, 2-pyridone and 2-hydroxypyridine have been investigated by Density Functional Theory (DFT) calculation and high-resolution photoemission spectroscopy (HRPES). We confirmed that between the two reaction centers of 4- and 2-pyridone, only O atom of carbonyl functional group can act as a Lewis base while both the two reaction centers of 4- and 2-hydroxypyridine (tautomers of 4- and 2-pyridone) can successfully function as a Lewis base. On the other hand, owing to their molecular structures, there is a remarkable difference between the adsorption structures of 4- and 2-hydroxypyridine. Through the analysis of the N 1s and O 1s core level spectra obtained using HRPES, we also could corroborate that two different adducts coexist on the surface at room temperature due to their activation energy investigating the coverage dependent variation of bonding configurations when these molecules are adsorbed on the Ge(100) surface.

• Bulletin of the Korean Chemical Society
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• 제35권8호
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• pp.2547-2550
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• 2014

• 생약학회지
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• 제48권4호
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• pp.268-272
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• 2017

Three tricyclic pyridone alkaloids, (-)-4,6'-anhydrooxysporidinone (1), (-)-6-deoxyoxysporidinoCne (2), and (-)-sambutoxin (3) were isolated from cultures of Fusarium lateritium SSF2 derived from the fruits of Cornus officinalis. Chemical structures of the isolated compounds were determined by spectroscopic method and comparisons with reported data values. The compounds 1-3 were isolated for the first time from this fungal strain.

• 한국식품과학회지
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• 제34권1호
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• pp.8-12
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• 2002

수목에 스트레스를 가하여 정유를 증수할 목적으로 화학적 스트레스 자극제 5종과 생물적 스트레스 자극제 4종을 선발하여 실험을 실시하였다. 우선 정상적인 수목의 정유함량은 편백 2% 전후, 화백 1.6%, 소나무 0.4%, 잣나무 0.7%였으며, 상기 수종들은 모두 7월에 최대의 정유함량을 기록하였다. 또한 9종의 스트레스 자극제 처리 6개월 후 잎의 정유함량을 측정한 결과, 스트레스 자극제 처리에 의해 대체로 정류함량은 높아지는 경향을 보이고 있으나 자극제의 종류에 따라 변화가 없거나 또는 감소하는 경우도 있었다. 정유 증수효과에 영향을 미치는 수종별 최적 스트레스 자극제로 소나무는 치마버섯(SCC), 잣나무는 과산화수소수, 편백은 치마버섯(SCC), 화백은 ${\beta}-pyridone$이 선발되었으며, 특히 과산화수소와 ${\beta}-pyridone$은 공시한 4수종에 광범위하게 효과를 나타내는 스트레스 자극제였다. 그러나 뽕나무버섯(ARM)과 소나무잔나비버섯(FOP)의 잣나무 처리군 및 치마버섯(SCC)의 화백 처리군에서는 오히려 정유함량을 감소시켰다.

• Journal of Pharmaceutical Investigation
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• 제22권3호spc1호
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• pp.49-63
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• 1992

Two different types of chemical manipulations of dobutamine were investigated in order to develop novel, improved cardiotonic drugs. Three new analogues of carbostyril, in which the m-hydroxy group of dobutamine was isosterically modified with an amide type carbostyril system, were synthesized from, ${\rho}-methoxyphenethylamine$ via multi-steps. Two analogues of (2'-aminoethyl)-1-hydroxy-2-pyridone system which has isosteric structural similarity with dopamine without having the COMT vulnerable m-hydroxy group were synthesized via 12 synthetic steps. Their biological stabilities in various media and inotropic activities were evaluated.

• Bulletin of the Korean Chemical Society
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• 제29권11호
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• pp.2277-2280
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• 2008

• Bulletin of the Korean Chemical Society
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• 제20권7호
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• pp.857-859
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• 1999

• Bulletin of the Korean Chemical Society
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• 제35권10호
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• pp.3021-3024
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• 2014

The potential energy surface (PES) for the dissociation of the 2-hydroxypyridine (2-HP) radical cation was determined from G3//B3LYP calculations, including the loss of CO, HCN, and HNC. The formation of the 1H-pyrrole radical cation by decarbonylation through a more stable tautomer, the 2-pyridone (2-PY) radical cation, was the most favorable dissociation pathway. Kinetic analysis by the Rice-Ramsperger-Kassel-Marcus model calculations was carried out based on the obtained PES. It is proposed that the dissociation occurs after a rapid tautomerization to 2-$PY^{{\cdot}+}$, and that most of the ions generated by ionization of 2-HP have the structure of 2-$PY^{{\cdot}+}$ at equilibrium above the tautomerization barrier.