about
Methylthio-aspochalasins from a marine-derived fungus Aspergillus sp.Pseudonocardians A-C, new diazaanthraquinone derivatives from a deap-sea actinomycete Pseudonocardia sp. SCSIO 01299.Diketopiperazines from marine organisms.Microindolinone A, a Novel 4,5,6,7-Tetrahydroindole, from the Deep-Sea-Derived Actinomycete Microbacterium sp. MCCC 1A11207.Cladosporone A, a new dimeric tetralone from fungus Cladosporium sp. KcFL6' derived of mangrove plant Kandelia candel.Minor valepotriates from Valeriana jatamansi and their cytotoxicity against metastatic prostate cancer cells.Structure determination of two unusual C25 steroids with bicyclo[4.4.1]A/B rings from Penicillium decumbens by NMR spectroscopy.Chemical constituents of Abies nukiangensis.Differential effects of antofine N-oxide on solid tumor and leukemia cells.Pseudolarenone, an unusual nortriterpenoid lactone with a fused 5/11/5/6/5 ring system featuring an unprecedented bicyclo[8.2.1]tridecane core from Pseudolarix amabilis.Sesquiterpenoids and triterpenoids from Abies holophylla and their bioactivities.Phenolic compounds of Abies nephrolepis and their NO production inhibitory activities.Antiviral Merosesquiterpenoids Produced by the Antarctic Fungus Aspergillus ochraceopetaliformis SCSIO 05702.Strepsesquitriol, a rearranged zizaane-type sesquiterpenoid from the deep-sea-derived actinomycete Streptomyces sp. SCSIO 10355.Systematic phytochemical investigation of Abies spectabilis.Mono- and sesquiterpenoids, flavonoids, lignans, and other miscellaneous compounds of Abies georgei.Polyhydroxy steroids and saponins from China Sea starfish Asterina pectinifera and their biological activities.Abiesatrines A-J: anti-inflammatory and antitumor triterpenoids from Abies georgei Orr.A new 1,4-diazepine from South China Sea marine sponge Callyspongia species.Chemical constituents of Dracocephalum forrestii.Two new spirobiflavonoids from Abies chensiensis with moderate NO production inhibitory activity.Tarennanosides A-H, eight new lignan glucosides from Tarenna attenuata and their protective effect on H2O2-induced impairment in PC12 cells.Chemical constituents of Aeschynanthus bracteatus and their weak anti-inflammatory activities.Anti-inflammatory and anti-tumour effects of Abies georgei extracts.Mass spectrometric profiling of valepotriates possessing various acyloxy groups from Valeriana jatamansi.New N-acyl taurine from the sea urchin Glyptocidaris crenularis.A new flavone C-glycoside from Clematis rehderiana.The hepatoprotective and antifibrotic effects of Saururus chinensis against carbon tetrachloride induced hepatic fibrosis in rats.Acylated iridoids with cytotoxicity from Valeriana jatamansi.Antioxidant lignans from Mananthes patentiflora.Chemical constituents from the stem bark of Trewia nudiflora L. and their antioxidant activities.Inhibitory Activities of Compounds from the Marine Actinomycete Williamsia sp. MCCC 1A11233 Variant on IgE-Mediated Mast Cells and Passive Cutaneous Anaphylaxis.Saccharopolytide A, a new cyclic tetrapeptide with rare 4-hydroxy-proline moieties from the deep-sea derived actinomycete Saccharopolyspora cebuensis MCCC 1A09850.Spirograterpene A, a Tetracyclic Spiro-Diterpene with a Fused 5/5/5/5 Ring System from the Deep-Sea-Derived Fungus Penicillium granulatum MCCC 3A00475.Three minor valepotriate isomers from Valeriana jatamansi and their cytotoxicity.Polyketides from the Deep-Sea-Derived Fungus Graphostroma sp. MCCC 3A00421 Showed Potent Antifood Allergic Activities.New anti-inflammatory guaianes from the Atlantic hydrotherm-derived fungus Graphostroma sp. MCCC 3A00421.A new cyclopeptide metabolite of marine gut fungus from Ligia oceanica.The anti-hyperplasia of mammary gland effect of Thladiantha dubia root ethanol extract in rats reduced by estrogen and progestogen.Roquefortine J, a novel roquefortine alkaloid, from the deep-sea-derived fungus Penicillium granulatum MCCC 3A00475.
P50
Q34411510-FFA2CFEA-028F-4DB1-85A6-FE73533EB554Q35188283-A3658FAD-C188-4967-97FF-31D2A8559E15Q37821421-DD759B57-8F0E-4B54-A4D6-14EE60479CCFQ38654921-E203C8E0-12F8-4B97-9D30-E52FC5DEF2D1Q38864166-8D27DF17-9C94-4727-8685-914E2865DCF9Q38932666-11BF9C39-3443-4A17-A783-DF369FD0B60FQ38952154-FAD86CC7-251A-4B8F-AF94-1BB33C129369Q38969816-311B02C9-B5E0-4FD0-9B45-B92B77A1587CQ38981585-F4D55BBE-09B1-43A9-ABCA-CB882C1C392DQ39217631-0E062D2A-9BAE-457F-B2CA-3064074DE003Q39428713-B371DB0E-CA4B-4C6A-B8A9-05C705F60A32Q39429371-98CF16F0-0A48-49EC-80DB-D9CEE0297112Q39573945-5761E86E-8ACB-4E95-99A8-87F314BEBBEAQ39613725-39F91FEE-AA57-425F-A37A-8BEE7312B242Q39622723-9F81EF51-00C3-47A9-8430-C1FEB11535C1Q39628231-43636718-8922-4E17-8231-113AA9CAB912Q39696799-0DDF4F68-8AC6-4DA9-8548-BC65BCAAA7BCQ39718032-815D4351-FE4A-4F07-85A3-7C80B7223319Q39723256-04946487-E9FA-41A8-A57C-5253E814F63FQ39828853-4B1E60D5-E3F9-46B4-96AB-BD020DA8C59BQ39842360-B4CE039F-91AE-4B2B-8CA3-04EA58906E6BQ39862949-449D2AA7-3039-475C-AC82-AB4F03D45D46Q39966818-A2C8DE70-A560-4477-A737-CE73311521A9Q39972943-D7A7F720-03BC-499B-A355-1030B7FF2389Q40387926-F9E0E3E3-89B8-4BB0-B8C8-0C32BFCA05E8Q42164559-66B1959F-058E-40F2-A965-CD04CB36B336Q43119506-603FC4B8-CC37-4FBF-8A52-54186334C19DQ43275253-2498AB22-D098-4DD3-9CA9-9F6EE1F41E73Q43528961-DFD50793-4C7F-464D-BCC0-50ADF9C0B268Q46120937-D68A8080-400D-4C09-9ACA-35229C4C3C05Q46592299-C40EBC8D-8EF2-40E8-8D07-D6CBDBC2A61CQ47338085-13411A9F-B8F8-4804-9A2F-605B79A6749AQ47727819-21E88AA3-8A74-40F0-905B-37F34282A6B6Q47942294-23C0391B-790B-4333-A45E-A8EA2A0E71CEQ48025412-904172DA-B7F9-401E-A8DC-9CA74BBC190FQ48199195-798A8093-1A09-4FCC-A4F5-8922312A570AQ48263027-451592E3-3A3B-4A22-B5AD-9E4AF9BE6ABBQ51435607-B03C0817-338E-4C5B-8DBD-99A0C3690979Q51529754-E5362A0C-970E-42FE-AC08-6E7F823A1375Q52606379-6AF2FF57-D61D-4E7D-A4F2-A3475A2FC375
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Xianwen Yang
@ast
Xianwen Yang
@en
Xianwen Yang
@es
Xianwen Yang
@nl
type
label
Xianwen Yang
@ast
Xianwen Yang
@en
Xianwen Yang
@es
Xianwen Yang
@nl
prefLabel
Xianwen Yang
@ast
Xianwen Yang
@en
Xianwen Yang
@es
Xianwen Yang
@nl
P106
P1153
8846397200
P31
P496
0000-0002-4967-0844