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...

Design, synthesis, and STING-agonistic activity of benzo[b]thiophene-2-carboxamide derivatives

Molecular diversity, 2023-10

2023

Volltextzugriff (PDF)

Discovery of Potent Irreversible Pan-Fibroblast Growth Factor Receptor (FGFR) Inhibitors

Journal of medicinal chemistry, 2018-10, Vol.61 (20), p.9085-9104

2018

Volltextzugriff (PDF)

Potent, Selective, and Cell Active Protein Arginine Methyltransferase 5 (PRMT5) Inhibitor Developed by Structure-Based Virtual Screening and Hit Optimization

Journal of medicinal chemistry, 2017-07, Vol.60 (14), p.6289-6304

2017

Volltextzugriff (PDF)

A Novel IRAK4 Inhibitor DW18134 Ameliorates Peritonitis and Inflammatory Bowel Disease

Molecules (Basel, Switzerland), 2024-04, Vol.29 (8), p.1803

2024

Volltextzugriff (PDF)

Catalytic Enantioselective Henry Reactions of Isatins: Application in the Concise Synthesis of (S)-(−)-Spirobrassinin

Chemistry : a European journal, 2011-07, Vol.17 (28), p.7791-7795

2011

Volltextzugriff (PDF)

Organocatalytic Enantioselective Conjugate Additions to Enones

Journal of the American Chemical Society, 2006-10, Vol.128 (39), p.12652-12653

2006

Volltextzugriff (PDF)

Synthesis of Chiral 3-Substituted Phthalides by a Sequential Organocatalytic Enantioselective Aldol-Lactonization Reaction. Three-Step Synthesis of (S)-(−)-3-Butylphthalide

Journal of organic chemistry, 2010-01, Vol.75 (2), p.368-374

2010

Volltextzugriff (PDF)

Organocatalytic Asymmetric Michael Addition of 2,4-Pentandione to Nitroolefins

Organic letters, 2005-10, Vol.7 (21), p.4713-4716

2005

Volltextzugriff (PDF)

A Novel Bifunctional Sulfonamide Primary Amine‐Catalyzed Enantioselective Conjugate Addition of Ketones to Nitroolefins

Advanced synthesis & catalysis, 2008-10, Vol.350 (14‐15), p.2194-2198

2008

Volltextzugriff (PDF)

Simple Cyclohexanediamine-Derived Primary Amine Thiourea Catalyzed Highly Enantioselective Conjugate Addition of Nitroalkanes to Enones

Organic letters, 2009-07, Vol.11 (13), p.2864-2867

2009

Volltextzugriff (PDF)

The NF-kappa B inhibitor, celastrol, could enhance the anti-cancer effect of gambogic acid on oral squamous cell carcinoma

BMC cancer, 2009-09, Vol.9 (1), p.343-343, Article 343

2009

Volltextzugriff (PDF)

Synthesis of triazolotriazine derivatives as c-Met inhibitors

Molecular diversity, 2021-05, Vol.25 (2), p.839-846

2021

Volltextzugriff (PDF)

Growth inhibition and induction of apoptosis in human oral squamous cell carcinoma Tca-8113 cell lines by shikonin was partly through the inactivation of NF-κB pathway

Phytotherapy research, 2008-03, Vol.22 (3), p.407-415

2008

Volltextzugriff (PDF)

Structural insights into a shared mechanism of human STING activation by a potent agonist and an autoimmune disease-associated mutation

Cell discovery, 2022-12, Vol.8 (1), p.133-133, Article 133

2022

Volltextzugriff (PDF)

Gambogic acid inhibits the catalytic activity of human topoisomerase IIα by binding to its ATPase domain

Molecular cancer therapeutics, 2007-09, Vol.6 (9), p.2429-2440

2007

Volltextzugriff (PDF)

Synthesis and Bioevaluation of Shikonin Derivatives

Letters in drug design & discovery, 2018-01, Vol.15 (9), p.945-950

2018

Volltextzugriff (PDF)

A novel strategy for treating oncogene‐mutated tumors by targeting tumor microenvironment and synergistically enhancing anti‐PD‐1 immunotherapy

Cancer communications (London, England), 2024-03, Vol.44 (3), p.438-442

2024

Volltextzugriff (PDF)

Preclinical and early clinical studies of a novel compound SYHA1813 that efficiently crosses the blood–brain barrier and exhibits potent activity against glioblastoma

Acta pharmaceutica Sinica. B, 2023-12, Vol.13 (12), p.4748-4764

2023

Volltextzugriff (PDF)

SH‐7, a new synthesized shikonin derivative, exerting its potent antitumor activities as a topoisomerase inhibitor

International journal of cancer, 2006-09, Vol.119 (5), p.1184-1193

2006

Volltextzugriff (PDF)

Synthesis and biological activity of novel shikonin analogues

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (3), p.735-737

2009

Volltextzugriff (PDF)

Synthesis and antitumor activity of 10-arylcamptothecin derivatives

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (7), p.2071-2074

2011

Volltextzugriff (PDF)

Efficient, Enantioselective Organocatalytic Synthesis of Trichostatin A

Advanced synthesis & catalysis, 2006-07, Vol.348 (10-11), p.1228-1234

2006

Volltextzugriff (PDF)

An enantioselective synthesis of (+)-( S)-[ n]-gingerols via the l-proline-catalyzed aldol reaction

Bioorganic & medicinal chemistry letters, 2009-07, Vol.19 (14), p.3909-3911

2009

Volltextzugriff (PDF)

Discovery of a New Series of Naphthamides as Potent VEGFR‑2 Kinase Inhibitors

ACS medicinal chemistry letters, 2014-05, Vol.5 (5), p.592-597

2014

Volltextzugriff (PDF)

Evaluation of Deuterium-Labeled JNJ38877605: Pharmacokinetic, Metabolic, and in Vivo Antitumor Profiles

Chemical research in toxicology, 2018-11, Vol.31 (11), p.1213-1218

2018

Volltextzugriff (PDF)

1 – 25 von 130

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieTetrahedron Letters

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(105)
Mit Volltextzugriff
(124)

Publikationsform

Sprache

Englisch
(129)
Japanisch
(18)

Erscheinungsjahr

n.n

Thema

Science & Technology
(89)
Life Sciences & Biomedicine
(64)
Pharmacology & Pharmacy
(43)
Physical Sciences
(41)
Chemistry, Medicinal
(40)
Chemistry
(38)
Humans
(36)
Chemistry, Organic
(20)
Animals
(19)
Cell Line, Tumor
(17)
Molecular Structure
(15)
Antineoplastic Agents - Pharmacology
(14)
Cell Proliferation - Drug Effects
(14)
Mice
(14)
Structure-Activity Relationship
(14)
Chemistry, Multidisciplinary
(13)
Stereoisomerism
(13)
Catalysis
(12)
Biochemistry & Molecular Biology
(11)
Biological And Medical Sciences
(11)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Design, synthesis, and STING-agonistic activity of benzo[b]thiophene-2-carboxamide derivatives

Discovery of Potent Irreversible Pan-Fibroblast Growth Factor Receptor (FGFR) Inhibitors

Potent, Selective, and Cell Active Protein Arginine Methyltransferase 5 (PRMT5) Inhibitor Developed by Structure-Based Virtual Screening and Hit Optimization

A Novel IRAK4 Inhibitor DW18134 Ameliorates Peritonitis and Inflammatory Bowel Disease

Catalytic Enantioselective Henry Reactions of Isatins: Application in the Concise Synthesis of (S)-(−)-Spirobrassinin

Organocatalytic Enantioselective Conjugate Additions to Enones

Synthesis of Chiral 3-Substituted Phthalides by a Sequential Organocatalytic Enantioselective Aldol-Lactonization Reaction. Three-Step Synthesis of (S)-(−)-3-Butylphthalide

Organocatalytic Asymmetric Michael Addition of 2,4-Pentandione to Nitroolefins

A Novel Bifunctional Sulfonamide Primary Amine‐Catalyzed Enantioselective Conjugate Addition of Ketones to Nitroolefins

Simple Cyclohexanediamine-Derived Primary Amine Thiourea Catalyzed Highly Enantioselective Conjugate Addition of Nitroalkanes to Enones

The NF-kappa B inhibitor, celastrol, could enhance the anti-cancer effect of gambogic acid on oral squamous cell carcinoma

Synthesis of triazolotriazine derivatives as c-Met inhibitors

Growth inhibition and induction of apoptosis in human oral squamous cell carcinoma Tca-8113 cell lines by shikonin was partly through the inactivation of NF-κB pathway

Structural insights into a shared mechanism of human STING activation by a potent agonist and an autoimmune disease-associated mutation

Gambogic acid inhibits the catalytic activity of human topoisomerase IIα by binding to its ATPase domain

Synthesis and Bioevaluation of Shikonin Derivatives

A novel strategy for treating oncogene‐mutated tumors by targeting tumor microenvironment and synergistically enhancing anti‐PD‐1 immunotherapy

Preclinical and early clinical studies of a novel compound SYHA1813 that efficiently crosses the blood–brain barrier and exhibits potent activity against glioblastoma

SH‐7, a new synthesized shikonin derivative, exerting its potent antitumor activities as a topoisomerase inhibitor

Synthesis and biological activity of novel shikonin analogues

Synthesis and antitumor activity of 10-arylcamptothecin derivatives

Efficient, Enantioselective Organocatalytic Synthesis of Trichostatin A

An enantioselective synthesis of (+)-( S)-[ n]-gingerols via the l-proline-catalyzed aldol reaction

Discovery of a New Series of Naphthamides as Potent VEGFR‑2 Kinase Inhibitors

Evaluation of Deuterium-Labeled JNJ38877605: Pharmacokinetic, Metabolic, and in Vivo Antitumor Profiles

Aktive Filter

Suchergebnisse filtern