• Bulletin of the Korean Chemical Society
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• 제16권9호
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• pp.831-834
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• 1995

The nature of hydrogen bonding between thioacetamide and azines has been thoroughly investigated using near IR absorption spectroscopy. The νN-H + amide II combination band in thioacetamide (TA) has been analyzed to determine the thermodynamic constants for the formation of hydrogen bonded 1:1 TA:azine complexes in CCl4 and CHCl3 solutions. The relative stabilities of TA-azine complexes (pyridine->1,2-diazine->1,3-diazine->1,4-diazine-TA) are in good agreement with the relative proton affinities of azines in the gas phase. The results serve as a basis for analyzing the factors which influence the hydrogen bonding formation of TA in nonaqueous solutions.

• 약학회지
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• 제29권2호
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• pp.103-106
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• 1985

Reaction between 2-aminobenzamide and thionylchloride gave benzo-2-this-1,3[2H]-diazine-4-one-2-oxide (I) at room temperature. With other carbonyl derivatives quinazoline-4-one derivatives (II-VIII) were obtained.

• 약학회지
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• 제46권2호
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• pp.89-92
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• 2002

Allylthio group of the sulfur compounds of garlic oil plays an important role for prevention and treatment of hepatic diseases induced by toxic substances or carbon tetrachloride. Thus allylthio group as pharmacologically active group was introduced into pyridazine heterocycle ring. Aryloxyallylthiopyridazine derivatives were synthesized and their hepatoprotective activities were screened in rat. The activities of these compounds were weaker than alkoxyallylthiopyridazine derivatives, which exhibit a superior hepatoprotective effect.

• 약학회지
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• 제46권3호
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• pp.155-160
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• 2002

Through a modification of allicin structure a disagreeable odor and chemical instability of allicin can be improved. 3-Alkoxy-6-allylthiopyridazine derivatives exhibit a superior effect for prevention and treatment of hepatic diseases induced by carbon tetrachloride and aflatoxin B1 and for prevention of human tissues from radiation. These compounds inhibit also efficiently SK-Hep-1 cell proliferation through induction of apoptosis. So another 4,5-mono- or di-substituted 3-alkyloxy-6-allylthiopyridazine derivatives were synthesized on purpose to find out SAR of allylthiopyridazine in hepatoprotective and hepatotherapeutic acitivitis and to develop more effective drug candidate.

• Biomolecules & Therapeutics
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• 제8권1호
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• pp.1-12
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• 2000

Although the first pyridazine was obtained in 1886, this heterocycle was not thoroughly investigated such isomers as pyrimidine and pyrazine especially in the field of drug development because pyridazine derivatives do not occur as natural products. Recently medicinal chemists have an growing interest in the pyridazine derivatives, since many Pyridazine derivatives were found to possess various potential therapeutic activities. In this paper sixty-eight pyridazine derivatives, which are already introduced as medicines or are being developed as drugs were classified according to their pharmacological activities, reviewed since 1955 and the relationship of structure-activities was discussed.

• 약학회지
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• 제44권1호
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• pp.9-15
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• 2000

Four 3-alkoxy-6-allylthiopyridazines and 3-chloro-6-allylthiopyridazine were synthesized and their protective effects against oxidative stress and UV-C irradiation were tested. 3-Methoxy-6-allylthiopyridazine and 3-ethoxy-6-allylthiopyridazine did not show protective effect on the oxidative stress but showed the strongest protective effect on UV-C irradiation among the tested compounds. Especially 500 $\mu\textrm{g}$/$m\ell$ of the two compounds was the most effective concentration.

• 한국잡초학회지
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• 제5권2호
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• pp.164-168
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• 1985

Amide 계(系) 제초제(除草劑)와 Diazine계(系) 제초제(除草劑)의 혼합처리(混合處理)에 의한 살초증진효과(殺草增進效果)를 조사(調査)하기 위하여 너도방동산이를 대상으로 0, 3엽기(葉期)에 pretilachlor/pyrazoxyfene와 butachlor/pyrazolate을 각각 8수준(水準)으로 조합(組合)하여 혼합처리(混合處理)한 결과(結果) 얻은 살초효과(殺草效果)를 등효과선법(等效果線法)에 의하여 상호작용(相互作用)을 분석(分析)하였다. 1. Pretilachlor와 pyrazoxyfene을 너도방동산이 0, 3엽기(葉期)에 혼합처리(混合處理)할 때 상호작용지수(相互作用指數)는 2.64와 2.07로서 상승효과(相承效果)가 인정되었으며, pretilachlor와 pyrazoxyfene의 혼합비율(混合比率)이 각각 0.7:1.3g ai/a와 9.0:20.5g ai/a에서 최고(最高)의 상승효과(相乘效果)를 나타냈다. 2. 너도방동산이의 0엽기(葉期)에 혼합처리(混合處理)한 butachlor와 pyrazolate 간의 상호작용지수(相互作用指數)는 1.57로서 너도방동산이 방제에 상승효과(相乘效果)를 나타냈고, butachlor와 pyrazolate의 혼합비율(混合比率) 48.0:20.9g ai/a에서 최고(最高)의 상승효과(相乘效果)를 보였다.

• 농업과학연구
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• 제4권2호
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• pp.229-238
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• 1977

유기인계(有機燐系) 농약(農藥)의 잔류소장(殘留消長)을 파악(把握)하여 작물(作物)에 대(對)한 농약(農藥)의 사용(使用)을 기(期)하고저 배추, 오이, 토마토, 포도, 복숭아에 대(對)해 Diazine에 EPN, Parathion, Malathion, Diazinon, Sumithion의 경전잔류(經前殘留)를 조사(調査)한 결과(結果) 1. 배추에 대(對)한 Diazinone의 잔류소장(殘留消長)은 약제살포(藥劑撒布) 21일후(日後)에 0.25~0.38p.p.m이 EPN은 1 회(回) 살포시(撒布時)는 7일후(日後)에 1.39~2.69p.p.m이 2살(撒) 포시(布時) 14 0.96~2.34p.p.m 검출(檢出)되었다. 2. 포되에 대(對)한 EPN의 잔류소장(殘留消長)은 약제살포(藥劑撒布) 7일후(日後) 1.09~1.80p.p.m이 Sumithion은 14일후(日後) 0.17~0.53p.p.m이 검출(檢出)되었다. 3. 복숭아에 대(對)한 Parathion의 잔류소장(殘留消長)은 약제살포(藥劑撒布) 14일후(日後)에 0.40~0.61p.p.m이 검출(檢出)되었다. 4. 토마토에 대(對)한 Dimethoate의 잔류소장(殘留消長)은 약제살포(藥劑撒布) 7일후(日後)에 0.141p.p.m이 검출(檢出)되었다. 5. 오이에 대(對)한 EPN의 잔류소장(殘留消長)은 약제살포(藥劑撒布) 3일후(日後)에 2.11~2.14p.p.m이 검출(檢出)되었고 Malathion은 약제살포당일(藥劑撒布當日)에 0.46p.p.m 3일후(日後)에 0.062~0.025p.p.m이 검출(檢出)되었다. 6. 과실(果實)및 채소류(菜蔬類)에 대(對)한 약제간(藥劑間) 경시분해도(經時分解度)가 반감기간(半減期間)에는 역(逆)의 관계(關係)가 성립(成立)되었다. 7. 배추 포도 오이에 대(對)한 EPN의 수확전(收穫前) 사용금지기간(使用禁止期間)은 배추는 1회(回) 살포기(撒布期) 7일간(日間), 2회살포기(回撒布期) 14일간(日間), 오이는 3일간(日間), 포도는 7일간(日間)이고 8. 복숭아에 대(對)한 Parathion의 수확전(收穫前) 사용금지기간(使用禁止期間)은 14일간(日間) 9. 토마토에 대(對)한 Dimethoate의 수확전(收穫前) 사용금지기간(使用禁止期間)은 7일간(日間) 10. 오이에 대(對)한 Malathion의 수확전(收穫前) 사용금지(使用禁止) 기간(期間)은 0~3일간(日間) 11. 포도에 대(對)한 Sumithion의 수확전(收穫前) 사용금지(使用禁止) 기간(期間)은 21일간(日間) 12. 배추에 대(對)한 Diazinon의 수확전(收穫前) 사용금지(使用禁止) 기간(期間)은 21일간(日間)으로 정(定)하여 농약(農藥)을 사용(使用)함이 농산물(農産物)의 안전유통(安全流通)을 위(爲)해 좋은 것으로 사료(思料)된다.