about
Phenylethanoid glycosides in plants: structure and biological activity.Oviposition cues for a specialist butterfly--plant chemistry and sizeA continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis.Cytotoxicity studies of semi-synthetic derivatives of theveside derived from the aqueous extract of leaves of 'suicide tree' Cerbera odollam.Study of Anti Cancer Property of Scrophularia striata Extract on the Human Astrocytoma Cell Line (1321)Asymmetric total synthesis of the iridoid beta-glucoside (+)-geniposide via phosphine organocatalysis.Anatomical study of secondary tuberized roots of Harpagophytum procumbens DC and quantification of harpagoside by high-performance liquid chromatography method.Anti-hepatitis B virus active lactones from the traditional Chinese herb: Swertia mileensis.Analysis of catalpol derivatives by characteristic neutral losses using liquid chromatography combined with electrospray ionization multistage and time-of-flight mass spectrometry.Determination of iridoid glycosides by micellar electrokinetic capillary chromatography-mass spectrometry with use of the partial filling technique.Glycosidic monoterpenes from Linaria capraria.Antioxidant iridoid glucosides from Wendlandia formosana.Minor secoiridoid aglycones from the low-polarity part of the traditional Chinese herb: Swertia mileensis.Iridoidic pattern in endemic Sardinian plants: the case of Galium species.Iridoids and Flavonoids of Four Siberian Gentians: Chemical Profile and Gastric Stimulatory Effect.Inhibitory effect of Aucubin isolated from Eucommia ulmoides against UVB-induced matrix metalloproteinase-1 production in human skin fibroblasts.Stereocontrolled Synthesis of Amino-Substituted Carbocycles by Pd-Catalyzed Alkene Carboamination Reactions.
P2860
Q35812188-04D3E2E7-11B8-4D3B-B650-004B54680648Q36843913-7A431CAA-154C-4688-BD33-8CD11E21D2C2Q38052878-B0457950-100B-40BC-84C0-AF14A190952AQ38997471-2CFC8004-F69C-49EA-8BFA-0777A6F48F77Q39650127-DF801A91-33FE-4E42-834B-65651E6B932DQ40317446-6338334C-3FC8-43DE-BD25-E46F5A4A7B23Q42192827-B8339BC3-7408-40C0-B58E-3844237C9A2AQ42747833-F1F66F93-5705-48DD-8F34-548DB725B635Q42925408-E58234DC-30DE-4194-AF39-DB7C9D4FAF97Q43717921-3498F13A-9ED9-41A2-8793-3A0589C43522Q44896327-DD242930-CB94-4021-9CC5-AE3A5D02D848Q44949870-59E1D962-CA66-4AE9-9D4F-FBF5F18303E1Q46096242-F68D944A-5C3F-4500-8D13-1D0A5FBF9942Q46527278-19C0D8DE-2EB8-4E39-A26A-54C6119B789FQ46648356-91DB7FDD-1C53-477B-9E52-48DBDBF22927Q46818953-032DF1CB-CDF0-4E88-B325-C47A633A6254Q48124386-922945DD-93CC-4F36-8C04-B0B25BCB7B69
P2860
description
1980 nî lūn-bûn
@nan
1980 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1980 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
name
Iridoids. A review.
@ast
Iridoids. A review.
@en
Iridoids. A review.
@nl
type
label
Iridoids. A review.
@ast
Iridoids. A review.
@en
Iridoids. A review.
@nl
prefLabel
Iridoids. A review.
@ast
Iridoids. A review.
@en
Iridoids. A review.
@nl
P356
P1476
Iridoids. A review.
@en
P2093
L J El-Naggar
P304
P356
10.1021/NP50012A001
P577
1980-11-01T00:00:00Z