UB Paderborn / Katalog / Suche / in CDI

Activation of Peripheral KCNQ Channels Attenuates Inflammatory Pain

Molecular pain, 2014-02, Vol.10 (1), p.15-15

2014

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Establishment and validation of a new semi-chronic dextran sulfate sodium-induced model of colitis in mice

International immunopharmacology, 2013-01, Vol.15 (1), p.23-29

2013

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Malt1 inactivation attenuates experimental colitis through the regulation of Th17 and Th1/17 cells

Inflammation research, 2019-03, Vol.68 (3), p.223-230

2019

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Formation of Azole-Resistant Candida albicans by Mutation of Sterol 14-Demethylase P450

Antimicrobial Agents and Chemotherapy, 1999-05, Vol.43 (5), p.1163-1169

1999

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Role of Malt1 protease activity in pathogenesis of inflammatory disorders mediated by FcγR signaling

International immunopharmacology, 2018-03, Vol.56, p.193-196

2018

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Reduced Virulence of HWP1-Deficient Mutants of Candida albicans and Their Interactions with Host Cells

Infection and Immunity, 2000-04, Vol.68 (4), p.1997-2002

2000

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Pharmacological evaluation of TAK-828F, a novel orally available RORγt inverse agonist, on murine chronic experimental autoimmune encephalomyelitis model

Journal of neuroimmunology, 2019-10, Vol.335, p.577016-577016, Article 577016

2019

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Pharmacological inhibitory profile of TAK-828F, a potent and selective orally available RORγt inverse agonist

Biochemical pharmacology, 2018-04, Vol.150, p.35-45

2018

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Discovery of [cis-3-({(5R)‑5-[(7-Fluoro-1,1-dimethyl-2,3-dihydro‑1H‑inden-5-yl)carbamoyl]-2-methoxy-7,8-dihydro-1,6-naphthyridin-6(5H)‑yl}carbonyl)cyclobutyl]acetic Acid (TAK-828F) as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor γt Inverse Agonist

Journal of medicinal chemistry, 2018-04, Vol.61 (7), p.2973-2988

2018

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Role of Malt1 protease activity in pathogenesis of inflammatory disorders mediated by Fc?R signaling

International immunopharmacology, 2018-03, Vol.56, p.193

2018

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MLN3126, an antagonist of the chemokine receptor CCR9, ameliorates inflammation in a T cell mediated mouse colitis model

International immunopharmacology, 2018-07, Vol.60, p.160-169

2018

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Pharmacological Evaluation of TAK-828F, a Novel Orally Available RORγt Inverse Agonist, on Murine Colitis Model

Inflammation, 2019-02, Vol.42 (1), p.91-102

2019

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Pharmacological effects of TAK-828F: an orally available RORγt inverse agonist, in mouse colitis model and human blood cells of inflammatory bowel disease

Inflammation research, 2019-06, Vol.68 (6), p.493-509

2019

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In Vitro and In Vivo Antifungal Activities of TAK-456, a Novel Oral Triazole with a Broad Antifungal Spectrum

Antimicrobial Agents and Chemotherapy, 2002-05, Vol.46 (5), p.1388-1393

2002

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Optically Active Antifungal Azoles. VII. Synthesis and Antifungal Activity of Stereoisomers of 2-((1R,2R)-2-(2,4-Difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl)-4-(4-(2,2,3,3-tetrafluoropropoxy)phenyl)-3(2H,4H)-1,2,4-triazolone (TAK-187)

Chemical & pharmaceutical bulletin, 1997, Vol.45 (2), p.321-326

1997

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Optically Active Antifungal Azoles. V. Synthesis and Antifungal Activity of Stereoisomers of 3-Azolyl-2-(substituted phenyl)-1-(1H-1, 2, 4-triazol-1-yl)-2-butanols

Chemical and Pharmaceutical Bulletin, 1995/03/15, Vol.43(3), pp.441-449

1995

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Structure of pyrrolosine: a novel inhibitor of RNA synthesis, from the actinomycete Streptomyces albus

Journal of the American Chemical Society, 1990-12, Vol.112 (26), p.9668-9669

1990

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Isolation and identification of a specific and reversible inhibitor of starfish development

FEBS letters, 1987-06, Vol.218 (2), p.205-208

1987

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Crystal Structure of an Inhibitor of Starfish Embryonic Development, 4-Oxo-7-(β-D-ribofuranosyl)-3H-furo[3, 2-d]pyrimidine: Revision of Pyrrolosine Structure

Analytical Sciences, 1992/12/10, Vol.8(6), pp.897-898

1992

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Significance of an Increase of Intracellular Adenosine Concentration for Dormancy in Starfish Blastulae

Development, growth & differentiation, 1988-10, Vol.30 (5), p.553-562

1988

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Penicillin-binding protein 5 as an inhibitory target of cefozopran in Enterococcus faecalis

Journal of antimicrobial chemotherapy, 1996-03, Vol.37 (3), p.605-609

1996

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Therapeutic effects of cefozopran against experimental mixed urinary tract infection with Enterococcus faecalis and Pseudomonas aeruginosa in mice

Journal of antimicrobial chemotherapy, 1997-03, Vol.39 (3), p.423-425

1997

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Optically Active Antifungal Azoles. VII. Synthesis and Antifungal Activity of Stereoisomers of 2-[(1R, 2R)-2-(2, 4-Difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1, 2, 4-triazol-1-yl)propyl]-4-[4-(2, 2, 3, 3-tetrafluoropropoxy)phenyl]-3(2H, 4H)-1, 2, 4-triazolone (TAK-187)

Chemical and Pharmaceutical Bulletin, 1997/02/15, Vol.45(2), pp.321-326

1997

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サルモネラ菌は宿主の細胞内シグナル伝達分子を操る

ファルマシア, 2000/05/01, Vol.36(5), pp.414-415

土森, 登

2000

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Adenosine induces dormancy in starfish blastulae

Development (Cambridge), 1988-06, Vol.103 (2), p.345-351

1988

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Activation of Peripheral KCNQ Channels Attenuates Inflammatory Pain

Establishment and validation of a new semi-chronic dextran sulfate sodium-induced model of colitis in mice

Malt1 inactivation attenuates experimental colitis through the regulation of Th17 and Th1/17 cells

Formation of Azole-Resistant Candida albicans by Mutation of Sterol 14-Demethylase P450

Role of Malt1 protease activity in pathogenesis of inflammatory disorders mediated by FcγR signaling

Reduced Virulence of HWP1-Deficient Mutants of Candida albicans and Their Interactions with Host Cells

Pharmacological evaluation of TAK-828F, a novel orally available RORγt inverse agonist, on murine chronic experimental autoimmune encephalomyelitis model

Pharmacological inhibitory profile of TAK-828F, a potent and selective orally available RORγt inverse agonist

Role of Malt1 protease activity in pathogenesis of inflammatory disorders mediated by Fc?R signaling

MLN3126, an antagonist of the chemokine receptor CCR9, ameliorates inflammation in a T cell mediated mouse colitis model

Pharmacological Evaluation of TAK-828F, a Novel Orally Available RORγt Inverse Agonist, on Murine Colitis Model

Pharmacological effects of TAK-828F: an orally available RORγt inverse agonist, in mouse colitis model and human blood cells of inflammatory bowel disease

In Vitro and In Vivo Antifungal Activities of TAK-456, a Novel Oral Triazole with a Broad Antifungal Spectrum

Optically Active Antifungal Azoles. VII. Synthesis and Antifungal Activity of Stereoisomers of 2-((1R,2R)-2-(2,4-Difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl)-4-(4-(2,2,3,3-tetrafluoropropoxy)phenyl)-3(2H,4H)-1,2,4-triazolone (TAK-187)

Optically Active Antifungal Azoles. V. Synthesis and Antifungal Activity of Stereoisomers of 3-Azolyl-2-(substituted phenyl)-1-(1H-1, 2, 4-triazol-1-yl)-2-butanols

Structure of pyrrolosine: a novel inhibitor of RNA synthesis, from the actinomycete Streptomyces albus

Isolation and identification of a specific and reversible inhibitor of starfish development

Crystal Structure of an Inhibitor of Starfish Embryonic Development, 4-Oxo-7-(β-D-ribofuranosyl)-3H-furo[3, 2-d]pyrimidine: Revision of Pyrrolosine Structure

Significance of an Increase of Intracellular Adenosine Concentration for Dormancy in Starfish Blastulae

Penicillin-binding protein 5 as an inhibitory target of cefozopran in Enterococcus faecalis

Therapeutic effects of cefozopran against experimental mixed urinary tract infection with Enterococcus faecalis and Pseudomonas aeruginosa in mice

Optically Active Antifungal Azoles. VII. Synthesis and Antifungal Activity of Stereoisomers of 2-[(1R, 2R)-2-(2, 4-Difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1, 2, 4-triazol-1-yl)propyl]-4-[4-(2, 2, 3, 3-tetrafluoropropoxy)phenyl]-3(2H, 4H)-1, 2, 4-triazolone (TAK-187)

サルモネラ菌は宿主の細胞内シグナル伝達分子を操る

Adenosine induces dormancy in starfish blastulae

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