• Title/Summary/Keyword: polyhydroxy

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Synthesis and Antimicrobial Activities of a New Tetrayneol Compounds (새로운 Tetrayneol계 화합물의 합성과 항균활성)

  • Sung, Nack-Do;Park, Hyeon-Joo
    • Applied Biological Chemistry
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    • v.41 no.3
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    • pp.258-263
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    • 1998
  • This is the first systematically research which investigates structure-activity relationships(SAR) of antibiotics of polyyne. In this paper, it is reported that tetrayne compounds composed of hydrophilic unit and tetrayne unit has possibility of strong antimicrobial activity. Based on the above results, the possibility of development as an antibiotic medicine was examined to synthesise the more improved antibiotic compounds with synthesized polyhydroxy novel sugar analog possessing the part of tetrayneol moiety.

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식물체내 sapogenin의 계절적변화

  • 백근제
    • YAKHAK HOEJI
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    • v.1 no.1
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    • pp.19-22
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    • 1948
  • Yucca schotti, Samuela carnerosana, Agave strita 각부분에 있어 결실전후의 steroidal sapogenin 분포상태를 연구하여 결실후에는 monohydroxy steroid는 존재치 않고 단지복합 polyhydroxy steroid만이 존재함을 증명하였다.

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Development of Whitenin Agents by Synthesis of Polyhydroxy Aromatic Compounds

  • Hyun-Ho Lee;You
    • Journal of the Society of Cosmetic Scientists of Korea
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    • v.23 no.3
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    • pp.86-91
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    • 1997
  • Some natural polyhydroxy aromatic compounds have inhibitory activity against tyrosinase, key enzyme for formation of melanin pigment. We examined the structure-activity relationship of the natural polyhydrowy aromatic compounds and synthesized a number of new derivetives through various methods. Skin lightening effects of these compounds were examined through inhibition of mushroom tyrosinase and inhibitory of melanogenesis on B-16 melanoma cells. These new compounds showed strong inhibitory activity against tyrosinase. Good lightening effects sue to inhibition of melanogenesis were observed from several resorcinol and pyrogallol derivatives. In toxicological tests such as skin primary irritation and sensitization, the above compounds were sufficiently safe for cosmetic use.

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The Nature of Acid-Catalyzed Acetalization Reaction of 1,2-Propylene Glycol and Acetaldehyde

  • Cheng, Chen;Chen, Hui;Li, Xia;Hu, Jianli;Liang, Baochen
    • Korean Chemical Engineering Research
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    • v.53 no.4
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    • pp.463-467
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    • 2015
  • We investigated catalytic activity of ion-exchange resins in acetalization of 1,2-propylene glycol with acetaldehyde. The impacts of reaction variables, such as temperature, reaction time, catalyst loading and feedstock composition, on the conversion of 1,2-propylene glycol were measured. The life of the catalyst was also studied. Furthermore, the reaction kinetics of 1,2-propylene glycol acetalization was studied. It was found that reaction rate followed the first-order kinetics to acetaldehyde and 1,2-propylene glycol, respectively. Therefore, overall acetalization reaction should follow the second-order reaction kinetics, expressed as. Key words: 1,2-propylene Glycol, 2,4-dimethyl-1,3-dioxolane, Ion-exchange Resin, Polyhydroxy Compounds, Acetalization $r=kC^{nA}_AC^{nB}_B=19.74e^{\frac{-6650}{T}}C^1_AC^1_B$.

Regioselective Benzylic Thioether Formation from Polybydroxy Stilbene

  • Koh, Dongsoo;Park, Jongmin;Lim, Yoongho
    • Journal of Applied Biological Chemistry
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    • v.44 no.1
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    • pp.20-22
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    • 2001
  • We have attempted to synthesize polyhydroxy stilbene compounds through the benzyl thioether moiety. During synthesis, we unexpectedly observed that demethylation of the compound under $AlCl_3$ in ethanethiol resulted in a regioselective addition of thiol to the double bond as well as complete demethylation. We report on the regioselective short synthesis for general structure and its structural identification.

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Synthesis of Polyhydroxy Azasugar via Chiral Epoxyaldehyde

  • Shin, Kye-Jung;Kim, Dong-Jin
    • Proceedings of the PSK Conference
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    • 2001.04a
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    • pp.70-71
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    • 2001
  • Naturally occurring azasugar and homologous compounds have been the object of numerous synthetic efforts because these classes of compounds have interesting bioloical activities and the flexibility for the synthesis of chiral alkaloid comounds. As part of a program directed toward the preparation of glycosidase inhibitors, we prepared bicyclic perhydrooxazino- and oxazolopyridine from aminoalcohols and epoxyaldehyde as a common synthetic intermediate.

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