about
Further cytotoxic sesquiterpene lactones from Elephantopus mollis KUNTH.Alpha-glucosidase inhibitory constituents from Duranta repens.Structure determination of bioactive galloyl derivatives by NMR spectroscopy.Alpha-glucosidase inhibitors from Millettia conraui.Alpha-glucosidase inhibitors ellagic acid derivatives with immunoinhibitory properties from Terminalia superba.Alpha-glucosidase inhibitory anthranols, kenganthranols A-C, from the stem bark of Harungana madagascariensis.Microbial transformation of oleanolic acid by Fusarium lini and alpha-glucosidase inhibitory activity of its transformed products.Bioactive aristolactams from Piper umbellatum.alpha-Glucosidase inhibitory activity of triterpenoids from Cichorium intybus.Kaurane-type diterpenoids from Chromoleana odorata, their X-ray diffraction studies and potent α-glucosidase inhibition of 16-kauren-19-oic acid.Synthesis, spectroscopy, and biological properties of vanadium(IV)-hydrazide complexes.Alpha-glucosidase inhibitory and antioxidant acridone alkaloids from the stem bark of Oriciopsis glaberrima ENGL. (Rutaceae).HIV-1 Tat interactions with cellular 7SK and viral TAR RNAs identifies dual structural mimicrySyntheses and biological activities of chalcone and 1,5-benzothiazepine derivatives: promising new free-radical scavengers, and esterase, urease, and alpha-glucosidase inhibitorsalpha-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae)Duboscic acid: a potent α-glucosidase inhibitor with an unprecedented triterpenoidal carbon skeleton from Duboscia macrocarpaStudies on α-glucosidase inhibition and anti-glycation potential of Iris loczyi and Iris unguicularisFungal transformation of cedryl acetate and α-glucosidase inhibition assay, quantum mechanical calculations and molecular docking studies of its metabolites
P50
Q40018207-4D55B615-9B1D-4138-BBDD-25085F1FB60AQ44980983-BBC740E1-80C0-4E0E-BF32-F94E4A76AD84Q46385355-82DBAC91-3EFE-4B8E-88C6-193EE98C2871Q46474289-47777EBA-62DE-426F-BBA1-3948626684DEQ46562332-EEF4CC8B-5D69-4321-BF3E-03FED5AE5D6BQ46623331-1BB24AF0-5805-4689-B0F7-DFB80FC23DCDQ46642147-E213C675-0CB5-4DE5-9124-259FF73343ADQ46654575-25ABF836-F676-47CD-91AA-0544507176AAQ46701886-D982D06B-669B-4D7F-88E1-751A3C4DB993Q46711727-54FC1A17-7E74-4CD4-9264-6958E9AF2B9BQ46801275-CD12AD0A-11DA-492F-8F1F-CD75F0AF200EQ46969080-E189229E-F97F-413A-BCCC-6A710E11E3F5Q57464694-429E2DB3-5C78-4F52-91DB-61A9930D9E7DQ79455265-A09B3F21-D201-4F37-B771-3457D9688F01Q79706854-4D48B1C4-1F4A-465C-A780-5C76861B513EQ82520367-6FACC4E3-5825-4B80-A4B6-3BC0C011738DQ85798165-67A4B2F7-F55F-4DB6-A0DF-AD5D63C3E614Q86251954-58F09623-E711-4053-A580-54502E529FEC
P50
description
Forscher
@de
chercheur
@fr
hulumtuese
@sq
investigador
@es
researcher
@en
ricercatore
@it
研究者
@zh
name
Shamsun Nahar Khan
@ast
Shamsun Nahar Khan
@en
Shamsun Nahar Khan
@es
Shamsun Nahar Khan
@nl
type
label
Shamsun Nahar Khan
@ast
Shamsun Nahar Khan
@en
Shamsun Nahar Khan
@es
Shamsun Nahar Khan
@nl
prefLabel
Shamsun Nahar Khan
@ast
Shamsun Nahar Khan
@en
Shamsun Nahar Khan
@es
Shamsun Nahar Khan
@nl
P1960
83FGef0AAAAJ
P21
P31
P496
0000-0002-8966-0480