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	题名	作者	年代	出处	被引量
1	Flavonols from Heterotheca inuloides: tyrosinase inhibitory activity and structural criteria 显示文摘	Kubo I Kinsy-Hori I Chaudhuri S K	2000	Bio Org Med Chem2000，，8：	1
2	Structure-ae- tivity relationships in the inhibition of monoamine oxidase B by 1- methyl-3-phenylpyrroles显示文摘	Ogunrombi M O Malan S F Terre'blanche G	2008	Bio Org Med Chem2008，16，5：	1
3	Synthesis and biological evaluation of flavonoids as vasorelaxant agents 显示文摘	Chen Z W Hu Y Z Wu H H	2004	Bio org Med Chem Lett2004，14，15：	1
4	Towards development of selective and reversible pyrazoline based MAO-inhibitors:synthesis,bi- ological evaluation and docking studies显示文摘	Sahoo A Yabanoglu S Sinha B N	2010	Bio Org Med Chem2010，20，1：	1
5	Uhrasound promoted syn- thesis of 2-imidazolines in water: a greener approach toward monoamine oxidase inhibitors显示文摘	Gabriela D S Anna S Machado P	2009	Bio Org Med Chem2009，19，2：	1
6	Synthesis and inhibitory activity against COX-2 catalyzed prostaglandin production of chrysin derivatives显示文摘	Dao T T Chi Y S Kim J	2004	Bio org Med Chem Lett2004，，14：	1
7	Investigations on the 2-thi- azolylhydrazyne scaffold:synthesis and molecular modeling of selective human monoamine oxidase inhibitors显示文摘	Chimenti F Bolasco A Secci D	2010	Bio Org Med Chem2010，18，15：	1
8	Synthesis and activity of C2-subsitituted analogs of influenza neuraminidase inhibitors GS 4071显示文摘	ZHANG L WILLIAMS M A MENDEL D B	1997	Bio Org Med Chem Lett1997，7，14：	1
9	Inhibition of monoamine oxidase B by selected benzimidazole and caffeine analogues 显示文摘	Berg D V Zoellner K R Ogunrombi M O	2007	Bio Org Med Chem2007，15，11：	1
10	Inhibition of monoamine oxidase by 8-benzyloxycaffeine analogues显示文摘	Strydoma B Malan S F JR N C	2010	Bio Org Med Chem2010，18，3：	1
11	A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase-B inhibitors 显示文摘	Chimenti F Fioravanti R Bolasco A	2010	Bio Org Med Chem2010，18，3：	1
12	New lupane triterpenoids from Solidago canadensis that inhibit the lyase activity of DNA polymerase beta显示文摘	Zhou BN Gao Z	2004	Bio org Med Chem2004，12，23：	1
13	Chromone-2-and-3-carboxylic acids inhibit differentlymonoamine oxidases A and B显示文摘	Alcaro S Gaspar A Ortuso F	2010	Bio Org Med Chem2010，20，9：	1
14	Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors显示文摘	Alcaro S Reis J Fonseca A	2011	Bio Org Med Chem2011，21，2：	1
15	New halogenated 3-phenyl- coumarius as potent and selective MAO-B inhibitors显示文摘	Matos M J Vina D Janeiro P	2010	Bio Org Med Chem2010，20，17：	1
16	Synthesis and evaluation of 6- methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors 显示文摘	Matos M J Vina D Picciau C	2009	Bio Org Med Chem2009，19，17：	1
17	Struc- ture-activity relationships of bioisosteric replacement of the carboxylic acid in novel androgen receptor pure antagonists显示文摘	YOSHINO H SATO H TACHIBANA K	2010	Bio Org Med Chem2010，18，9：	1
18	Synthe-sis of3-substituted benzamides and5-substituted isoquinolin-1(2H)-ones and preliminary evaluation as inhibitors of poly(ADP-ribose)polymerase(PARP)显示文摘	Watson CY Whish WJ Threadgill MD	1998	Bio Org Med Chem1998，6，：	1
19	Asymmetric organocatalysis显示文摘	Seayad J List B	2005	Org Bio Chem2005，3，：	1
20	Regulation of stress- induced cytokine production by pyridinylimidazoles: inhibition of CSBP kinase显示文摘	Seibel GL Kassis S	1997	Bio Org Med Chem1997，5，：	1

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