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Antipyretic and antinociceptive activity of Diospyros lotus L. in animals.(Z)-2-Phenyl-3-pivaloyl-1,1-dipropyl-guanidine.2-Methyl-6-(4,4,10,13,14-penta-methyl-3-oxo-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetra-deca-hydro-1H-cyclo-penta-[a]phenanthren-17-yl)hept-2-enoic acidCrystal structure of catena-poly[silver(I)-μ-l-tyrosinato-κ(2) O:N].Crystal structure of 3-{(E)-[(3,4-di-chloro-phen-yl)imino]-meth-yl}benzene-1,2-diol.Antipyretic and antinociceptive potential of extract/fractions of Potentilla evestita and its isolated compound, acacetin.Quantitative ethnobotanical survey of medicinal flora thriving in Malakand Pass Hills, Khyber Pakhtunkhwa, Pakistan.Evaluation of Antioxidant, Free Radical Scavenging, and Antimicrobial Activity of Quercus incana Roxb.Bioassay-Guided Isolation of Sesquiterpene Coumarins from Ferula narthex Bioss: A New Anticancer Agent.Biological Evaluation and Docking Analysis of Daturaolone as Potential Cyclooxygenase InhibitorAntidepressent Effect of Two New Benzyl Derivatives from Wild Strawberry Fragaria vesca var. nubicola Lindl. ex Hook.f.A Comprehensive Review on Ebola (EBOV) Virus: Future Prospects.In silico analysis of ChtBD3 domain to find its role in bacterial pathogenesis and beyond.Isolation of Chlorogenic Acid from Soil Borne Fungi Screlotium rolfsii, their Reversal of Multidrug Resistance and anti-proliferative in Mouse Lymphoma cells.A new synthetic methodology for the preparation of biocompatible and organo-soluble barbituric- and thiobarbituric acid based chitosan derivatives for biomedical applications.Adaptogenic herb ginseng (Panax) as medical food: Status quo and future prospects.Triethyl orthoformate mediated a novel crosslinking method for the preparation of hydrogels for tissue engineering applications: characterization and in vitro cytocompatibility analysis.Synthesis of piroxicam loaded novel electrospun biodegradable nanocomposite scaffolds for periodontal regeneration.Anti-tumour-promoting and thermal-induced protein denaturation inhibitory activities of β-sitosterol and lupeol isolated from Diospyros lotus L.Cytotoxic, antitumour-promoting and inhibition of protein denaturation effects of flavonoids, isolated from Potentilla evestita Th. Wolf.Resveratrol as an anti-cancer agent: A review.Phytochemical, ethnomedicinal uses and pharmacological profile of genus Pistacia.Phytofabricated gold nanoparticles and their biomedical applications.Designing, synthesis, and antimicrobial action of oxazoline and thiazoline derivatives of fatty acid esters.In Silico Study of Alkaloids as α-Glucosidase Inhibitors: Hope for the Discovery of Effective Lead CompoundsEdible seeds from Cucurbitaceae family as potential functional foods: Immense promises, few concerns.Diospyros, an under-utilized, multi-purpose plant genus: A review.A holistic review on the autoimmune disease vitiligo with emphasis on the causal factors.Mechanisms Underlying Anti-hyperalgesic Properties of Kaempferol-3,7- di-O-α-L-rhamnopyranoside Isolated from Dryopteris cycadina.Pistagremic acid a new leishmanicidal triterpene isolated from Pistacia integerrima Stewart.Phosphodiesterase-1 Inhibitory Activity of Two Flavonoids Isolated from Pistacia integerrima J. L. Stewart Galls.Novel meloxicam releasing electrospun polymer/ceramic reinforced biodegradable membranes for periodontal regeneration applications.Synthesis and In Vitro Biological Evaluation of 1,3,4-Oxadiazol-2(3H)-one and Tetrahydropyridazine-3,6-dione Derivatives of Fatty Acids.Gastrointestinal Motility and Acute Toxicity of Pistagremic Acid Isolated from the Galls of Pistacia integerrima.In-vivo antinociceptive, anti-inflammatory and antipyretic activity of pistagremic acid isolated from Pistacia integerrima.Assessment of WHO/INRUD core drug use indicators in two tertiary care hospitals of Bahawalpur, Punjab, Pakistan.5-(3,4,5-Trimeth-oxy-phen-yl)-1,3,4-oxadiazole-2(3H)-thione.Phytochemical, spectroscopic and density functional theory study of Diospyrin, and non-bonding interactions of Diospyrin with atmospheric gases.Bioassay-guided isolation of antibacterial constituents from Diospyros lotus roots.Corrigendum: Bioassay-Guided Isolation of Sesquiterpene Coumarins from Ferula narthex Bioss: A New Anticancer Agent.
P50
Q33628768-75E13100-0E82-456C-BD36-075764C85CA3Q34266141-2B3F0FC4-7634-4559-9D8D-1B90C86793E3Q34639063-D8426195-9A93-477B-9BA0-0EAA41E7B3FCQ35150824-47068A1E-4200-4CB2-9A81-32934878924BQ35259806-E1205498-26CF-4114-BAEF-C8E6130918EEQ35434316-3E51F46E-237A-440D-8B2A-ED90D752FBDFQ35624605-1409D063-3737-4B2E-BD30-D2625CA91A01Q36305502-BB81D1D8-98F3-4468-94EA-4D8AA93DBDEAQ36582512-2030786F-0F6A-4615-8631-1A2083A944BCQ36690580-8AE22D96-E16F-4E55-8D0B-91A094F2FF48Q38633073-90FA0E74-6E75-4DC4-A2C8-AA921BD8E391Q38640421-9717D5CA-89AC-412D-B101-164434534CECQ38651102-16266837-25CF-47DB-8908-F196156B15FEQ38700548-0DB82058-7EA7-4DB3-8971-33843AD913E8Q38769580-693A7655-F6E1-44EB-B521-1AE830E6920FQ38785673-8189CBAF-5CB7-4592-A1AC-6E1C7D3F239DQ38845791-162D0EF6-E4F0-4DA4-8EC9-568FB0FE1595Q38845796-5DEAF317-1667-4733-86C4-7D041444A103Q38857722-F2CE83DF-6F7C-464E-96CA-F54BB2872701Q38920017-978E815D-693D-4A4D-896E-0C2EFA3EB6DAQ39045911-7E35D633-D9A9-45FC-A354-00CEF1D97035Q39052446-07E310EC-56CF-4DF6-A0A4-0A3C0A0E325DQ39156474-373110C1-58E5-47C5-939F-96AF94E6171FQ39228385-B500A64E-11FA-4E25-8D5E-218D3D425D23Q39264108-880CFDB3-C038-4B2D-808E-942006BCF261Q39278294-F11C13AE-2A69-4184-8BF8-9FCFF2256B50Q39302819-E634F3EA-68DF-4F44-A571-B7A2FBDD722BQ39346579-BD0C4FA5-B426-408A-B161-C57C0EE78FF6Q39455906-211FD470-8354-46A0-96B7-36B9BE2FF1A8Q39488588-4DB1D497-2FB2-465A-AB66-97D78CE72D6DQ39763098-19057156-C326-4FBD-82AC-8EE27AD6B276Q39811507-41E4C5B9-A1F4-45AC-85D2-A0FA77E26675Q40028905-9CB8A6C1-CE8E-41C2-93FE-5466CC3717ABQ40084507-6695C0DF-D18D-4F72-A986-C6019957358DQ40180610-23929748-CCD2-4EF1-A33F-C29EB80F5E32Q41166842-8E4B7CF8-B346-4892-B803-5AF25AAC0A29Q41373657-76E29844-7828-4F7C-A573-497B368B5B11Q41467674-0BB76ECA-8D02-45F7-BB9A-FA2BAF48A368Q41471401-FB8487E9-E20C-4A21-AE73-7D8593365436Q42364991-8A73CD11-8ECC-4921-AB3A-56620BA21FE5
P50
description
researcher (ORCID 0000-0003-2429-5491)
@en
name
Abdul Rauf
@en
type
label
Abdul Rauf
@en
prefLabel
Abdul Rauf
@en
P31
P496
0000-0003-2429-5491