| ²é¿´: 426 | »Ø¸´: 0 | ||
jinhong162ͳæ (ÕýʽдÊÖ)
|
[ÇóÖú]
»·ëÄÀàÉúÎï¼î·Òë
|
|
Joullie and Richard developed a system of nomenclature that classifies peptide alkaloids as: (i) cyclopeptide alkaloids sensu stricto, which exhibit basic properties due to a peptidogenic amino acid with an N-mono-methyl or N,Ndimethylated side-chain; (ii) linear peptide alkaloids; and (iii) neutral cyclopeptides, which do not exhibit a peptidogenic amino acid with an N-mono-methyl or N,N-dimethylated side chain¡£ Currently, only eight compounds representative of the latter category have been isolated and characterized,and three of them are named with the ending ene, as scutianene C (=scutianene D) (Sierra et al., 1974), discarenes C and D(Giacomelli et al., 2001), while the others end in ine, as discarines M and N (Giacomelli et al., 2004), lotusanine B, sanjoinenine (Han et al., 1989; Abu-Zarga et al., 1995), and amaiounine (Oliveira et al.,2009). Therefore, in this work we use the termination ene, featuring a double bond, and not the ending ine, used to denominate cyclopeptide alkaloids sensu stricto. |
» ²ÂÄãϲ»¶
3-äåßÁà¤-4-¼×È©ºÏ³É
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁÏר˶322
ÒѾÓÐ6È˻ظ´
Ò»Ö¾Ô¸ÄϾ©º½¿Õº½Ìì´óѧ ²ÄÁÏÓ뻯¹¤329·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
µ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ14È˻ظ´
²ÄÁÏ334Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
332Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
ÕÒµ½Ò»Ð©Ïà¹ØµÄ¾«»ªÌû×Ó£¬Ï£ÍûÓÐÓÃŶ~
ÎÒÔÚ×ö»ÆÍªÀàºÍÉúÎï¼îµÄÏÔÉ«·´Ó¦£¬Ôõôȥ³ýÒ¶ÂÌËØÄØ£¿´óÏÀ°ï°ïæлл
ÒѾÓÐ8È˻ظ´
ÖвÝÒ©ÉúÎï¼¼Êõ-ÌÆ¿ËÐù
ÒѾÓÐ133È˻ظ´
¡¾ÇóÖú¡¿»·ëÄÀ໯ºÏÎï½á¾§
ÒѾÓÐ22È˻ظ´
¡¾·ÖÏí¡¿¡¼Ãû´Ê½âÊÍ¡½ÉúÎﻯѧÃû´Ê½âÊÍ
ÒѾÓÐ14È˻ظ´
ÉúÎïѧÈí¼þ½éÉܼ°ÆäÏÂÔØµØÖ·¡¾Ñ§ÉúÎïµÄ»áºÜÓÐÓá¿
ÒѾÓÐ24È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎѰÕÒ¶àëÄÉÏÊÐÒ©ÎÓÐÄÄÐ©ÍøÕ¾£¿
ÒѾÓÐ11È˻ظ´
¿ÆÑдÓСľ³æ¿ªÊ¼£¬ÈËÈËΪÎÒ£¬ÎÒΪÈËÈË














»Ø¸´´ËÂ¥
µã»÷ÕâÀïËÑË÷¸ü¶àÏà¹Ø×ÊÔ´