中国药学杂志
    
           首页  |  期刊介绍  |  编 委 会  |  投稿指南  |  期刊订阅  |  广告服务  |  会议信息  |  联系我们  | 
�й�ҩѧ��־ 2011, Vol. 46 Issue (2) :102-104    DOI:
���� ����Ŀ¼ | ����Ŀ¼ | ������� | �߼����� << | >>
��ҩ��һζ��ѧ�ɷֵ��о�
�Ű������η�ϼ��������*
����ҽѧ��ѧԺ����ҩ���о��������� 100850
ZHANG Ai-jun��REN Feng-xia��ZHAO Yi-min*
Institute of Pharmacology and Toxicology��Academy of Military Medical Science��Beijing 100850�� China

Download: PDF (292KB)   HTML (0KB)   Export: BibTeX or EndNote (RIS)      Supporting Info
ժҪ Ŀ�� �о���һζ(Lamiophlomis rotate���ϲ��ֵĻ�ѧ�ɷ֡����� ����ɫ�׼������뻯ѧ�ɷ֣������������ʺͲ������ݼ���������ṹ����� ������������λ���������9��������ֱ�Ϊɽ���ռ�����1��6��7-���ǻ��㶹�أ�2�������ᣨ3��3��4-���ǻ������ᣨ4���۲���-7-O-��-D-(-6��-p-�㶹����-�������գ�5�������ᣨ6��ľϬ���أ�7���������� B��8���������գ�9������ ������2~6Ϊ�״δӶ�һζ�з���õ���
Service
�ѱ����Ƽ�������
�����ҵ����
�������ù�����
Email Alert
RSS
�����������
�ؼ����� ��һζ   6   7-���ǻ��㶹��   �۲���-7-O-��-D-(-6��-p-�㶹����-��������   ������   ��ѧ�ɷ�     
Abstract�� OBJECTIVE To study the chemical constituents of the aerial parts of Tibetan folk medicine Lamiophlomis rotate. METHODS Chemical compounds were extracted and isolated by diverse chromatography and identified by spectroscopic analysis. RESULTS Compounds were isolated and identified as shanzhiganin-1-O-��-D-glucopyranoside methyl ester(1��6��7-dihydroxycoumarin(2��caffeic acid(3��3��4-dihydroxyhenzoic acid(4��apigenin-7-O-��-D-(-6��-p-coumaroyl-glucoside(5��syringic acid(6��luteolin(7��forsythoside B(8��verbascoside(9. CONCLUSION Compounds 2-6 were obtained from Lamiophlomis rotate for the first time.
Keywords�� Lamiophlomis rotate,   6,   7-dihydroxycoumarin,   apigenin-7-O-��-D-(-6��-p-coumaroyl-glucoside,   syringic acid,   chemical constituent     
�ո�����: 2011-11-11;
���ñ���:   
.��ҩ��һζ��ѧ�ɷֵ��о�[J]  �й�ҩѧ��־, 2011,V46(2): 102-104
.Study on the Chemical Constituents of Tibetan Folk Medicine Lamiophlomis rotate[J]  Chinese Pharmaceutical Journal, 2011,V46(2): 102-104
��
[1] Yunnan Institute of Botany. Yunnan Flora(����ֲ��־[M]. Vol 1. Beijing�� Science Press��1977�� 619. [2] JIA X R�� WANG J. Investigate mechanism of hematostatic activity of traditional Tibetan herb Lamiophlomis rotate[J]. J Gansu Coll Tradit Chin Med(������ҽѧԺѧ���� 1994�� 11(3�� 44-46. [3] SHENG T�� JIA Z P�� LI M X�� et al. Study on the hemostatic effect of extracts from herb Lamiophlomis rotate and its meckanism[J]. Tradit Chin Drug Res Clin Pharmacol(��ҩ��ҩ���ٴ�ҩ�� 2006�� 17(2�� 93-96. [4] JIA Z P�� LI M X�� ZHANG R X�� et al. Experimental study on the effective hemostatic components of herba Lamiophlomis rotata[J]. Pharm J Chin PLA(��ž�ҩѧѧ���� 2005�� 21(4�� 272-274. [5] LIN T M�� GU Y�� FANG K Q. Analgesic effects of different extraction components from Lamiophlomis rotate(Benth. kudo�� a medicinal plant in XiZang(Tibetin mice[J]. J Fourth Mil Med Univ(���ľ�ҽ��ѧѧ���� 2003�� 29(5�� 444-446. [6] JIA Z P�� LI M X�� ZHANG R X�� et al. Vitro screening of the effective anti-tumor or components of herba Lamiophlomis rotata[J]. Med J Nat Def Force Northwest Chin(��������ҽѧ��־�� 2005�� 26(3�� 173-175. [7] ZHOU J H. Chinese Pharmaceutical Sciences(��ҩҩ��ѧ[M]. Shanghai�� Science and Technology Press�� 1986�� 213. [8] KOBAYASHI S�� MIMA A�� KIHARA M�� et al. Iridoid glucosides from Lamium amplexicaule[J]. Chem Pharm Bull�� 1986�� 34(2�� 876. [9] PAOLA G�� ANNA M C�� SILVANA C�� et al. Somatic embryogenesis and esculin formation in calli and embryoids from bark explants of Aesculus nippocastanum L[J]. Plant Science�� 1996�� 119(1-2�� 157-162. [10] LI H J�� LUO Y G�� HE Z H�� et al. Chemical constituents from Lonicera saccata[J]. Chin J Appl Environ Biol(Ӧ���뻷������ѧ���� 2007�� 13(2�� 188-191. [11] WANG S J�� PEI Y H. Studies on the chemical constituents of the leaves of Betula platyphylla Suk[J]. J Shenyang Pharm Univ(����ҩ�ƴ�ѧѧ���� 2000�� 17(4��256-257. [12] HIDEJI I�� KEIICHI S�� KOICHI T. Studies on a novel p-Coumaroyl glucoside of apigenin and on other flavonoids isolated from Patchouli(Labiatae[J]. Pharm Soc Jap�� 1981�� 29(1�� 254-256. [13] DONG L�� LI L�� LIAO Z H�� et al. Chemical constituents in root of Rhodiola bupleuroides[J]. Acta Bot Boreal Occident Sin(����ֲ��ѧ���� 2007�� 27(12�� 2564-2567. [14] AGRAWAL P K. Carbon-13-NMR of Flavonoids[M]. New York��Elsevier Scientific Pub Co.�� 1989�� 134. [15] CALIS I�� HOSNY M�� KHALIFA T�� et al. Phenylpropanoid glycosides from Marrubium alysson[J]. Phytochemistry�� 1992�� 31(10�� 3624-3626.
[1] ���Σ���ռ�֣�������������ο��������裬 �����º���������.������Դ���Penicillium sacculum�μ���л������о�[J]. �й�ҩѧ��־, 2012,47(8): 577-580
[2] �ᄃ��������Ǯ��������������̫����������.HZ08�й����ʵ�ɫ��-���׽ṹ����[J]. �й�ҩѧ��־, 2012,47(8): 603-607
[3] ������ ������ ���»� ���¿� ������ ��½.�¼�����ѧ�ɷֵij����о�[J]. �й�ҩѧ��־, 2012,47(7): 500-503
[4] ������ ������ ������ ������ ������ ������ .���ɽ��ԲҶ��ѧ�ɷֵ��о�[J]. �й�ҩѧ��־, 2012,47(4): 261-264
[5] ����� ����Ӿ .NHE-1���ữ��øRSK�������Ƽ����о���չ[J]. �й�ҩѧ��־, 2012,47(4): 241-244
[6] �¸� ���� ���� �۰��� ������ ��ΰ�� .����ӫ��̽���ڶ���ҩת��ͨ·�Ŀ���[J]. �й�ҩѧ��־, 2012,47(4): 279-282
[7] ����� ���� ���ɽ ������ Ԭ��Ȩ ��С��.�������л�ͪ�໯ѧ�ɷֵķ���ͽṹ����[J]. �й�ҩѧ��־, 2012,47(3): 177-
[8] �η�֥ ������ ����Ѹ ������ ����� ������.����ݵ����ͪ�໯ѧ�ɷ��о�[J]. �й�ҩѧ��־, 2012,47(3): 179-
[9] ղ���� ��˼�� Ԭ��ï �ν��� ����� .3��4-��-O-�׻�-1��2��5��6-�������¶�����Թ�״�������������ļ�ȱѪ�ı�������[J]. �й�ҩѧ��־, 2012,47(3): 190-
[10] ����ǿ ������ ����ǿ ���� ������ ����ҫ ���� ��ΰ л��ǿ ������.���������ŵͪC-3(��)�ӻ�������˫��NFDE6����������Ѽ���������������ĺϳ�(��)[J]. �й�ҩѧ��־, 2012,47(1): 72-
[11] ���໢ ������ ����˳.��ҩ�˶�˿�Ļ�ѧ�ɷ��о�[J]. �й�ҩѧ��־, 2012,47(1): 23-25
[12] ֣���� ������.���Ტ������������������Խ�����U251ϸ����������������[J]. �й�ҩѧ��־, 2011,46(9): 671-674
[13] ����˧ ��� ��ұ ��С�� ������ .��֦������������-������ɫ������������ɷ�[J]. �й�ҩѧ��־, 2011,46(9): 661-664
[14] �κ� ��ѧ�� ���ɶ� �촺��.���������ùD 2-6���������Դ�л����[J]. �й�ҩѧ��־, 2011,46(8): 569-575
[15] ������ ������ ���׶� ���� ��־�� ţ���� ���̷� ��Ρ.����ɭ��ģ�ʹ���ѪҺ����״��ϸ����Һ�������ҩ��ѧͬ���о�[J]. �й�ҩѧ��־, 2011,46(8): 610-614
Copyright 2010 by �й�ҩѧ��־