about
Titanium (III) ChlorideReceptor-specific mediation by immunoglobulin E of antigen-induced contraction of tracheal and lung parenchymal strips isolated from the guinea pig.Screening of terpenes and derivatives for antimycobacterial activity; identification of geranylgeraniol and geranylgeranyl acetate as potent inhibitors of Mycobacterium tuberculosis in vitro.Antimicrobial and antineoplastic activities of agelasine analogs modified in the purine 2-position.Screening of agelasine D and analogs for inhibitory activity against pathogenic protozoa; identification of hits for visceral leishmaniasis and Chagas disease.Synthesis, antimicrobial and antineoplastic activities for agelasine and agelasimine analogs with a beta-cyclocitral derived substituent.Antifouling activity of the sponge metabolite agelasine D and synthesised analogs on Balanus improvisus.Antimicrobial and cytotoxic activity of agelasine and agelasimine analogs.(+)-agelasine D: improved synthesis and evaluation of antibacterial and cytotoxic activities.Selective anti-tubercular purines: synthesis and chemotherapeutic properties of 6-aryl- and 6-heteroaryl-9-benzylpurines.Cytotoxic activity of 6-alkynyl- and 6-alkenylpurines.(E)-9-(But-2-en-1-yl)-6-chloro-9H-purine.Synthesis and antimycobacterial activities of non-purine analogs of 6-aryl-9-benzylpurines: Imidazopyridines, pyrrolopyridines, benzimidazoles, and indoles.Synthesis of non-purine analogs of 6-aryl-9-benzylpurines, and their antimycobacterial activities. Compounds modified in the imidazole ring.Synthesis and biological evaluation of pyrimidine analogs of antimycobacterial purines.Synthesis of imidazole derivatives with antimycobacterial activity.Synthesis, structure, and antimycobacterial activity of 6-[1(3H)-isobenzofuranylidenemethyl]purines and analogs.Cytotoxic and antibacterial activity of 2-oxopurine derivatives.Synthesis and antimycobacterial activity of 6-arylpurines: the requirements for the N-9 substituent in active antimycobacterial purines.Antimycobacterial activity of 1-substituted indolizines.Indolizines as novel potent inhibitors of 15-lipoxygenase.Synthesis and antimycobacterial activity of agelasine E and analogs.Synthesis and antimycobacterial activity of 5-formylaminopyrimidines; analogs of antibacterial purines.Synthesis, biological activity, and SAR of antimycobacterial 9-aryl-, 9-arylsulfonyl-, and 9-benzyl-6-(2-furyl)purines.Indolizine 1-sulfonates as potent inhibitors of 15-lipoxygenase from soybeans.6-substituted purines as inhibitors of 15-lipoxygenase; a structure-activity study.Synthesis of indolizine derivatives with selective antibacterial activity against Mycobacterium tuberculosis.Synthesis, biological activity, and SAR of antimycobacterial 2- and 8-substituted 6-(2-furyl)-9-(p-methoxybenzyl)purines.Mechanistic Insights on the Stereoselective Nucleophilic 1,2-Addition to Sulfinyl IminesRegiochemistry and Stereochemistry in Pd(0)-Catalyzed Allylic Alkylation of Nucleoside BasesWhen Inhibitors Do Not Inhibit: Critical Evaluation of Rational Drug Design Targeting Chorismate Mutase fromMycobacterium tuberculosis
P50
Q29026400-56C772A7-084F-4302-BE05-4183C4A77A28Q34608541-BB4B4F70-5582-4FDA-AB34-264CEEFBC80CQ34699704-705B74C7-2768-4AE1-92AB-5A3FACA949DFQ39405935-FCF23505-E835-4075-A998-E429355C0AB2Q39560746-C9780743-4F77-4CC0-B6FC-43A0284713FBQ40053846-BD3C11A2-C32B-430E-95C2-9F2484BAA4BAQ40103274-983C5C98-1790-4C00-996C-F1BAFA87E82DQ40144068-9B139847-2E2E-4737-9CAD-99C8C65F7336Q40300304-FDE17718-0D5D-44DB-AF7A-909ED73BDE8AQ40388730-19A22CCD-7F1D-4C11-8C41-4EB4DCCE3221Q40666560-FA09AA22-27DC-42B8-853F-E2EB2F92C58AQ42160525-5F227941-0551-45F3-8420-7A1FCC7AFDC3Q42740931-9225FEE0-992F-4251-92CE-B5DF19EB82F1Q42910311-44CA53D6-C7F9-473E-944C-BF86E2C77403Q43058040-9BF850B4-1A13-458E-8777-50D8BA0A4C25Q43231193-5300FAB1-D5AD-4454-B362-971B03DD48F5Q43285384-EBE22923-DC34-428E-87AA-A5504FB9B08DQ43886180-E5743AA9-833E-4569-AB8E-2E97789E890DQ43907816-8224D872-ABF6-43D2-8A30-D81379642813Q44488306-9BC044D6-2EF3-4A4B-A1A6-6303A7653EE8Q44671747-6800D464-D2A1-4A00-8910-F570FA04B841Q45306173-D0AC3D9B-8C03-41B2-9540-225C183F7C62Q46019500-8EF5905B-BA3D-40D0-9B79-BB1C0D294025Q46414137-F2589738-0CB4-4D6C-9740-4B858BE34D75Q46421152-B36D3B5E-538C-4A91-88F3-7FFAC60199A4Q46466973-EFEFAF51-3369-4CF5-A2B8-32C1C6510C25Q53779132-70178FCA-1BF1-4F65-A66F-358F5AEC1357Q54434937-BFBADB97-D9E5-403D-8AE1-0C132A9B1C98Q57400158-E1E4392F-8909-47BB-BB9C-406D6A7EEF6CQ58039789-CD21CA26-4A56-4610-A38F-32B2CC7CA088Q58378507-7F3D745C-D8FB-4D85-B3D6-493FD44AF265
P50
description
Noors professor
@nl
Norwegian chemist and professor at University of Oslo
@en
norsk kjemiker og professor ved Universitetet i Oslo
@nb
norsk kjemiker og professor ved Universitetet i Oslo
@nn
name
Lise-Lotte Gundersen
@ast
Lise-Lotte Gundersen
@ca
Lise-Lotte Gundersen
@da
Lise-Lotte Gundersen
@de
Lise-Lotte Gundersen
@en
Lise-Lotte Gundersen
@es
Lise-Lotte Gundersen
@fr
Lise-Lotte Gundersen
@ga
Lise-Lotte Gundersen
@nb
Lise-Lotte Gundersen
@nl
type
label
Lise-Lotte Gundersen
@ast
Lise-Lotte Gundersen
@ca
Lise-Lotte Gundersen
@da
Lise-Lotte Gundersen
@de
Lise-Lotte Gundersen
@en
Lise-Lotte Gundersen
@es
Lise-Lotte Gundersen
@fr
Lise-Lotte Gundersen
@ga
Lise-Lotte Gundersen
@nb
Lise-Lotte Gundersen
@nl
prefLabel
Lise-Lotte Gundersen
@ast
Lise-Lotte Gundersen
@ca
Lise-Lotte Gundersen
@da
Lise-Lotte Gundersen
@de
Lise-Lotte Gundersen
@en
Lise-Lotte Gundersen
@es
Lise-Lotte Gundersen
@fr
Lise-Lotte Gundersen
@ga
Lise-Lotte Gundersen
@nb
Lise-Lotte Gundersen
@nl
P106
P1015
P1015
P19
P21
P214
323149196273774790780
P2287
P27
P31
P569
1963-01-01T00:00:00Z
P734
P7859
viaf-323149196273774790780