UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Novel molecular hybrids of cinnamic acids and guanylhydrazones as potential antitubercular agents

Bioorganic & medicinal chemistry letters, 2010-03, Vol.20 (5), p.1623-1625

2010

Volltextzugriff (PDF)

Design, synthesis, and biological evaluation of 4-(5-nitrofuran-2-yl)prop-2-en-1-one derivatives as potent antitubercular agents

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (21), p.6175-6178

2010

Volltextzugriff (PDF)

Aromatic amide derivatives of 5,6-dimethoxy-2,3-dihydro-1H -inden ( -1 -yl )acetic acid as anti-inflammatory agents free of ulcerogenic liability

Bioorganic & medicinal chemistry letters, 2007-12, Vol.17 (24), p.6790-6796

2007

Volltextzugriff (PDF)

Versatile synthesis of new cytotoxic agents structurally related to hemiasterlins

Bioorganic & medicinal chemistry letters, 2010-06, Vol.20 (11), p.3431-3435

2010

Volltextzugriff (PDF)

The identification of potent, selective and CNS penetrant furan-based inhibitors of B-Raf kinase

Bioorganic & medicinal chemistry, 2008-08, Vol.18 (15), p.4373-4376

2008

Volltextzugriff (PDF)

HSP60/10 chaperonin systems are inhibited by a variety of approved drugs, natural products, and known bioactive molecules

Bioorganic & medicinal chemistry letters, 2019-05, Vol.29 (9), p.1106-1112

2019

Volltextzugriff (PDF)

Structure–activity relationship study of beta-carboline derivatives as haspin kinase inhibitors

Bioorganic & medicinal chemistry letters, 2012-03, Vol.22 (5), p.2015-2019

2012

Volltextzugriff (PDF)

Dual-targeting GroEL/ES chaperonin and protein tyrosine phosphatase B (PtpB) inhibitors: A polypharmacology strategy for treating Mycobacterium tuberculosis infections

Bioorganic & medicinal chemistry letters, 2019-07, Vol.29 (13), p.1665-1672

2019

Volltextzugriff (PDF)

Identification of a novel class of quinoline–oxadiazole hybrids as anti-tuberculosis agents

Bioorganic & medicinal chemistry letters, 2016-01, Vol.26 (2), p.645-649

2016

Volltextzugriff (PDF)

Activation loop targeting strategy for design of receptor-interacting protein kinase 2 (RIPK2) inhibitors

Bioorganic & medicinal chemistry letters, 2018-02, Vol.28 (4), p.577-583

2018

Volltextzugriff (PDF)

Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (22), p.6483-6488

2010

Volltextzugriff (PDF)

Design, synthesis and antimycobacterial activity of cinnamide derivatives: A molecular hybridization approach

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (7), p.1997-1999

2011

Volltextzugriff (PDF)

Quinazolinethiones and quinazolinediones, novel inhibitors of inosine monophosphate dehydrogenase: synthesis and initial structure–activity relationships

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (3), p.751-754

2005

Volltextzugriff (PDF)

Adenosine analogue inhibitors of S-adenosylhomocysteine hydrolase

Bioorganic & medicinal chemistry letters, 2014-06, Vol.24 (12), p.2737-2740

2014

Volltextzugriff (PDF)

Novel 7-methoxy-6-oxazol-5-yl-2,3-dihydro-1H-quinazolin-4-ones as IMPDH inhibitors

Bioorganic & medicinal chemistry letters, 2005-12, Vol.15 (23), p.5335-5339

2005

Volltextzugriff (PDF)

Rational drug design based synthesis of novel arylquinolines as anti-tuberculosis agents

Bioorganic & medicinal chemistry letters, 2013-11, Vol.23 (22), p.6097-6105

2013

Volltextzugriff (PDF)

Synthesis and preliminary biological evaluation of novel N-(3-aryl-1,2,4-triazol-5-yl) cinnamamide derivatives as potential antimycobacterial agents: An operational Topliss Tree approach

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6523-6526

2011

Volltextzugriff (PDF)

Approaches towards the development of chimeric DPP4/ACE inhibitors for treating metabolic syndrome

Bioorganic & medicinal chemistry letters, 2017-06, Vol.27 (11), p.2313-2318

2017

Volltextzugriff (PDF)

Structure-guided design of α-amino acid-derived Pin1 inhibitors

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.586-590

2010

Volltextzugriff (PDF)

Preparation of novel aza-1,7-annulated indoles and their conversion to potent indolocarbazole kinase inhibitors

Bioorganic & medicinal chemistry letters, 2004-08, Vol.14 (15), p.3925-3928

2004

Volltextzugriff (PDF)

A novel class of 3-(phenoxy-phenyl-methyl)-pyrrolidines as potent and balanced norepinephrine and serotonin reuptake inhibitors: Synthesis and structure–activity relationships

Bioorganic & medicinal chemistry letters, 2013-03, Vol.23 (5), p.1456-1461

2013

Volltextzugriff (PDF)

Parallel synthesis of N-biaryl quinolone carboxylic acids as selective M 1 positive allosteric modulators

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.531-536

2010

Volltextzugriff (PDF)

Quinolizidinone carboxylic acid selective M1 allosteric modulators: SAR in the piperidine series

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (6), p.1710-1715

2011

Volltextzugriff (PDF)

1,7-Annulated indolocarbazoles as cyclin-dependent kinase inhibitors

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3217-3220

2004

Volltextzugriff (PDF)

Triazine and pyrimidine based ROCK inhibitors with efficacy in spontaneous hypertensive rat model

Bioorganic & medicinal chemistry letters, 2009-11, Vol.19 (21), p.6027-6031

2009

Volltextzugriff (PDF)

1 – 25 von 53

Suche als RSS-Feed

Aktive Filter

KollektionWiley Online Library

Zeitschrift / SerieInorganic Chemistry

Zeitschrift / SerieJournal Of The American Chemical Society

Zeitschrift / SerieTetrahedron Letters

Zeitschrift / SerieBioorganic & Medicinal Chemistry Letters

ThemaChemistry

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(53)

Publikationsform

Artikel
(53)

Sprache

Englisch
(53)

Erscheinungsjahr

n.n

Thema

Chemistry, Medicinal
(53)
Chemistry, Organic
(53)
Life Sciences & Biomedicine
(53)
Pharmacology & Pharmacy
(53)
Physical Sciences
(53)
Science & Technology
(53)
Biological And Medical Sciences
(35)
Medical Sciences
(35)
Pharmacology. Drug Treatments
(35)
Structure-Activity Relationship
(29)
Animals
(28)
Humans
(22)
Molecular Structure
(14)
Rats
(14)
Miscellaneous
(11)
Drug Design
(10)
Antibiotics. Antiinfectious Agents. Antiparasitic Agents
(9)
Models, Molecular
(9)
Enzyme Inhibitors - Pharmacology
(8)

14 weitere anzeigen...

Weniger anzeigen...

Kollektion

1 weiteren anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Bioorganic & Medicinal Chemistry
(1)

Menü

Weitere Dienste

Einstellungen

Novel molecular hybrids of cinnamic acids and guanylhydrazones as potential antitubercular agents

Design, synthesis, and biological evaluation of 4-(5-nitrofuran-2-yl)prop-2-en-1-one derivatives as potent antitubercular agents

Aromatic amide derivatives of 5,6-dimethoxy-2,3-dihydro-1H -inden ( -1 -yl )acetic acid as anti-inflammatory agents free of ulcerogenic liability

Versatile synthesis of new cytotoxic agents structurally related to hemiasterlins

The identification of potent, selective and CNS penetrant furan-based inhibitors of B-Raf kinase

HSP60/10 chaperonin systems are inhibited by a variety of approved drugs, natural products, and known bioactive molecules

Structure–activity relationship study of beta-carboline derivatives as haspin kinase inhibitors

Dual-targeting GroEL/ES chaperonin and protein tyrosine phosphatase B (PtpB) inhibitors: A polypharmacology strategy for treating Mycobacterium tuberculosis infections

Identification of a novel class of quinoline–oxadiazole hybrids as anti-tuberculosis agents

Activation loop targeting strategy for design of receptor-interacting protein kinase 2 (RIPK2) inhibitors

Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution

Design, synthesis and antimycobacterial activity of cinnamide derivatives: A molecular hybridization approach

Quinazolinethiones and quinazolinediones, novel inhibitors of inosine monophosphate dehydrogenase: synthesis and initial structure–activity relationships

Adenosine analogue inhibitors of S-adenosylhomocysteine hydrolase

Novel 7-methoxy-6-oxazol-5-yl-2,3-dihydro-1H-quinazolin-4-ones as IMPDH inhibitors

Rational drug design based synthesis of novel arylquinolines as anti-tuberculosis agents

Synthesis and preliminary biological evaluation of novel N-(3-aryl-1,2,4-triazol-5-yl) cinnamamide derivatives as potential antimycobacterial agents: An operational Topliss Tree approach

Approaches towards the development of chimeric DPP4/ACE inhibitors for treating metabolic syndrome

Structure-guided design of α-amino acid-derived Pin1 inhibitors

Preparation of novel aza-1,7-annulated indoles and their conversion to potent indolocarbazole kinase inhibitors

A novel class of 3-(phenoxy-phenyl-methyl)-pyrrolidines as potent and balanced norepinephrine and serotonin reuptake inhibitors: Synthesis and structure–activity relationships

Parallel synthesis of N-biaryl quinolone carboxylic acids as selective M 1 positive allosteric modulators

Quinolizidinone carboxylic acid selective M1 allosteric modulators: SAR in the piperidine series

1,7-Annulated indolocarbazoles as cyclin-dependent kinase inhibitors

Triazine and pyrimidine based ROCK inhibitors with efficacy in spontaneous hypertensive rat model

Aktive Filter

Suchergebnisse filtern