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(1)H and (13)C NMR data of methyl tetra-O-benzoyl-D-pyranosides in acetone-d(6).(1)H,(13)C and (19)F NMR data of N-substituted 6-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amines in DMSO-d(6).Preparation of pharmaceutical important fluorinated 1-arylethanols using isolated enzymes.Balancing potency, metabolic stability and permeability in pyrrolopyrimidine-based EGFR inhibitors.In vitro baselining of new pyrrolopyrimidine EGFR-TK inhibitors with Erlotinib.Changes in cellular signaling proteins in extracts from A549, H460, and U2OS cells treated with cisplatin or docetaxel.Identification of new 4-N-substituted 6-aryl-7H-pyrrolo[2,3-d]pyrimidine-4-amines as highly potent EGFR-TK inhibitors with Src-family activity.Structure-activity study leading to identification of a highly active thienopyrimidine based EGFR inhibitor.Chiral 6-aryl-furo[2,3-d]pyrimidin-4-amines as EGFR inhibitors.Truncated structures used in search for new lead compounds and in a retrospective analysis of thienopyrimidine-based EGFR inhibitors.Chiral N-benzyl-N-methyl-1-(naphthalen-1-yl)ethanamines and their in vitro antifungal activity against Cryptococcus neoformans, Trichophyton mentagrophytes and Trichophyton rubrum.Synthesis and in vitro EGFR (ErbB1) tyrosine kinase inhibitory activity of 4-N-substituted 6-aryl-7H-pyrrolo[2,3-d]pyrimidine-4-amines.Synthesis of the antistroke drug lubeluzole and its enantiomer. Lipase-catalyzed resolution of chiral building block.Activity of 6-aryl-pyrrolo[2,3-d]pyrimidine-4-amines to Tetrahymena.Single-step microwave-assisted hot water extraction of hemicelluloses from selected lignocellulosic materials - A biorefinery approach.Is literature data useful for identifying enzyme catalysts for new substrates? A case study on reduction of 1-aryl-2-alkanoates.Economical synthesis of 13C-labeled opiates, cocaine derivatives and selected urinary metabolites by derivatization of the natural products.Solvent Effects on Optical Rotation: On the Balance between Hydrogen Bonding and Shifts in Dihedral Angles.On-column trypsinization allows for re-use of matrix in modified multiplexed inhibitor beads assay.Extended structure-activity study of thienopyrimidine-based EGFR inhibitors with evaluation of drug-like properties.Optical Rotation Calculations for Fluorinated Alcohols, Amines, Amides and Esters.Enantiopure derivatives of 1,2-alkanediols: substrate requirements of lipase B from Candida antarcticaChemo-enzymatic synthesis of the antidepressant duloxetine and its enantiomerSynthesis of 1,3-dithianes and 1,3-dithiolanes. Baker's yeast reduction and lipase-catalyzed resolution for synthesis of enantiopure derivativesGas chromatographic enantiomer separation of C-3 and C-4 synthons: prediction of absolute configuration from elution order and enzymatic resolutionResolution of derivatives of 1,2-propanediol with lipase B from Candida antarctica. Effect of substrate structure, medium, water activity and acyl donor on enantiomeric ratioEnantioselectivity, swelling and stability of 4-hydroxyprolinol containing acrylic polymer beads in the asymmetric reduction of ketonesSynthesis of [13C4]-labeled ∆9-tetrahydrocannabinol and 11-nor-9-carboxy-∆9-tetrahydrocannabinol as internal standards for reducing ion suppressing/alteration effects in LC/MS-MS quantification.Benzoylated uronic acid building blocks and synthesis of N-uronate conjugates of lamotrigineSynthesis of [13C6]-labelled phenethylamine derivatives for drug quantification in biological samplesIdentification of fused pyrimidines as interleukin 17 secretion inhibitorsEffect of Auxiliary Donors on 3,8-Phenothiazine Dyes for Dye-Sensitized Solar CellsSynthesis of Novel 3,6-Dithienyl Diketopyrrolopyrrole Dyes by Direct C‒H Arylation
P50
Q33403312-4082EC11-A2F8-4794-AA6B-34B7F5EDE345Q33521330-F2C36C7A-0E5A-4629-A8A8-BEB01FCC97DAQ38151464-A092401F-D519-4F72-A8D4-269F757E4456Q38747045-9ED265C5-7E9B-4600-A57D-205A3A8F3D60Q38841895-6074BAC9-6200-43CF-9E27-B320403311E5Q38861429-7D5E60EA-26A1-4CDE-A23E-5CC2533B8839Q39001062-9D25D750-5CDC-491E-9F6F-F56987A578C9Q39022132-964B1513-AAE4-442D-BF50-BD4E0EDECBDDQ39729027-E142C7DD-4DBD-4F72-A645-D539F89A7B14Q41229031-6C104F15-4375-4581-BD82-12C6E815CD36Q42709345-01B9A158-FBBD-4D63-B5F6-660EFBF2927DQ42725786-A5C215CF-92FD-4E89-9674-07962A277394Q43554669-08F8CCA5-99E4-4E3D-8847-DA51CE2EAEE8Q44946156-131B444A-265B-4437-A27F-5D1B8B96B756Q46307591-18B5C446-536B-44EC-87A7-3790CE484DF0Q47704605-3B36EA1C-7E83-42D5-9099-0AAF405AFFF2Q47729733-AF4BBEB9-BF00-4920-BCBD-07A0DD47887DQ48023080-D790B3FD-6069-4E34-9707-7AF45DF617EEQ51150188-B23F5731-CF49-45D9-AEC9-BD35D2E4EEFAQ51575294-22DA3D10-B747-4FD2-A5CB-F93D1A114DD0Q51800261-CE1DA74D-5A61-40C2-A07D-7A423849BC64Q56953096-FF56E503-42C5-47AF-A574-0E4B98C0469FQ56953465-E1D47432-5394-45B2-9888-58D2A6815A3DQ56953690-C407DD4F-A807-4420-B8FC-B358398830E1Q56953835-2D987C68-E100-4A7C-B8F5-F7D54D4252CAQ56954018-A1929903-046B-4FD1-A7AF-280FB3658364Q57373772-DA373E04-8A67-4867-A3FC-1AABF249C7EEQ64977820-5BF99E1F-A082-419D-9427-F2C4D3CE1AE1Q83307216-C9A0DB30-D727-429A-AC5D-6DC64ED9DF0CQ87452198-3B68CCAB-8D99-4A0D-B579-16889D648E9DQ89126578-2A58340E-09AA-4A86-A949-C23B7FEB929DQ91815813-DF2FC9D3-1FDE-443D-9E84-285E4050113EQ95654861-F2CBC3B8-1EE0-4737-AE71-34945C18BAAB
P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
wetenschapper
@nl
հետազոտող
@hy
name
Bård Helge Hoff
@ast
Bård Helge Hoff
@en
Bård Helge Hoff
@es
Bård Helge Hoff
@nl
Bård Helge Hoff
@sl
type
label
Bård Helge Hoff
@ast
Bård Helge Hoff
@en
Bård Helge Hoff
@es
Bård Helge Hoff
@nl
Bård Helge Hoff
@sl
prefLabel
Bård Helge Hoff
@ast
Bård Helge Hoff
@en
Bård Helge Hoff
@es
Bård Helge Hoff
@nl
Bård Helge Hoff
@sl
P106
P1153
7006223816
P21
P214
376149106007968490490
P31
P496
0000-0001-7859-7810
P569
2000-01-01T00:00:00Z