| 
			
 | 
	
		  | 
	 
 
 
    
         ▣ 천연물에서 분리된 개별유효성분 레코드 등록정보  | 
     
    
         | 
     
    
         | 
     
    
         | 
     
    
        성 분 명   | 
        Aconitine  | 
     
    
         | 
     
    
         | 
     
    
         | 
     
    
    
        함유 천연물   | 
        Aconitum carmichaeli Deb.[오두(烏頭)](부자(附子),흑순편(黑順片),백부편(白附片),염부자(鹽附子)) Aconitum ciliare DC.[선덩굴바꽃(Seon-deong-gul-ba-kkot)](초오(草烏)) Aconitum kusnezoffii Rchb.[이삭바꽃(I-sak-ba-kkot)]() Aconitum proliferum Nakai[싹눈바꽃(Ssang-nun-ba-kkot)]() Aconitum szechenyianum Gay.[-]() Aconitum volubile Pall.[가는줄돌쩌귀(Ga-neun-jul-dol-jjeo-gwi)]()  | 
     
    
         | 
     
    
    
       														 분 자 식   | 
      													   C34H47NO11  | 
   															  
  										   				 
       											 			  | 
   											 				  
    
    
       												 화학족 분류   | 
      												 알칼로이드(alkaloid);  | 
   												  
  										   	 
       												  | 
   											 	  
    
    
       												 분 자 량   | 
      												 645.754  | 
   													  
  										   		 
       												  | 
   											 		  
    
       												 녹 는 점   | 
      												 203-205°C MeOH  | 
   													  
  										   		 
       												  | 
   											 		  
    
    
       												 생리학적효과   | 
      												 Toxic agent implicated in poisoning by Aconitum spp., esp. Aconitum chasmanthum in India, exp. arrhythmia effects. Gastric anaesthetic. Toxicity: Very toxic if swallowed or by skin absorption. Human systemic effects by ingestion. LD50 (mus, orl) 1 mg/kg, LD50 (mus, ivn) 0.175 mg/kg, exp. lethal doses by subcutaneous route reported. LD50 in mice (mg/kg): 0.166 i.v.; 0.328 i.p.; approx 1 orally (Dybing); also reported as LD50 in mice (mg/kg): 1.8 orally, 0.270 s.c.; 0.380 i.p.; 0.12 i.v. (Sato).  | 
   													  
  										   		 
       												  | 
   											 		  
    
       												 굴 절 율   | 
      												 [α]23 D = +19.0° (C 0.12,CHCl3)  | 
   													  
  										   		 
       												  | 
   											 		  
    
    
    
       												 HNMR_CHART   | 
      												  δ:1.15(3H,t,NCH2CH3), 1.44(3H,s,OOCCH3), 3.29, 3.38, 3.42, 3.88(ea.3H,s,OMe), 5.04(1H,d,H14beta), 7.67-8.25(aromatic protons)  | 
   													  
  										   		 
       												  | 
   											 		  
    
       												 CNMR_CHART   | 
      												 (CDCl3,25.0 MHz) δ: 83.4, 36.0, 70.4, 43.2, 46.6, 82.3, 44.8, 92.0, 44.2, 40.8, 49.8, 34.0, 74.0, 78.9, 78.9, 90.1, 61.0, 75.6, 48.8, 46.9, 13.3, 55.7, 57.9, 60.9, 58.9, 172.2, 21.3, 165.9, 129.6, 128.6, 129.8, 133.2, 129.8, 128.6  | 
   													  
  										   		 
       												  | 
   											 		  
    
    
    
       												 참고문헌   | 
      												 · SW. Pelletier et al., J. Am. Chem. Soc., 98, 2626, 1976(pmr,cmr)
· S. Morio, Annalen, 476, 181, 1929
· M. Przybylska et al., Can. J. Chem., 37, 1116, 1843, 1959
· FW. Bachelor et al., Tetrahedron Lett., No. 10, 1, 1960
· KB. Birnbaum et al., Tetrahedron Lett., 867, 1971
· X. Chang et al., Yaoxue Xuebao, 16, 474, 1981; CA, 97, 3590f
· H. Hikino et al., J. Nat. Prod., 46, 178, 1983; 47, 190, 1984
· H. Wang et al., Heterocycles, 23, 803, 1985
· E. Arlandini et al., J. Nat. Prod., 50, 937, 1987
· HK. Desai et al., J. Nat. Prod., 52, 720, 1989
· WJ. Sun et al., Yaoxue Xuebao, 24, 71, 1989; CA, 111, 74778s
· H. Liu et al., J. Nat. Prod., 59, 135, 1996  | 
   													  
  										   		 
       												  | 
   											 		  
    
    
    
    
         | 
     
     
    
           | 
     
    
    
 
 |