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...

Synthesis of Rhodamine-Conjugated Lupane Type Triterpenes of Enhanced Cytotoxicity

Molecules (Basel, Switzerland), 2024-05, Vol.29 (10), p.2346

2024

Volltextzugriff (PDF)

Synthesis and In Silico Docking Study towards M-Pro of Novel Heterocyclic Compounds Derived from Pyrazolopyrimidinone as Putative SARS-CoV-2 Inhibitors

Molecules (Basel, Switzerland), 2022-08, Vol.27 (16), p.5303

2022

Volltextzugriff (PDF)

F16 Hybrids Derived from Steviol or Isosteviol Are Accumulated in the Mitochondria of Tumor Cells and Overcome Drug Resistance

Molecules (Basel, Switzerland), 2024-01, Vol.29 (2), p.381

2024

Volltextzugriff (PDF)

The APOE [varepsilon]4 allele modulates brain white matter integrity in healthy adults

Molecular psychiatry, 2011-09, Vol.16 (9), p.908

2011

Volltextzugriff (PDF)

Rhodamine 101 Conjugates of Triterpenoic Amides Are of Comparable Cytotoxicity as Their Rhodamine B Analogs

Molecules (Basel, Switzerland), 2022-03, Vol.27 (7), p.2220

2022

Volltextzugriff (PDF)

Synthesis and Enzymatic Evaluation of a Small Library of Substituted Phenylsulfonamido-Alkyl Sulfamates towards Carbonic Anhydrase II

Molecules (Basel, Switzerland), 2024-06, Vol.29 (13), p.3015

2024

Volltextzugriff (PDF)

The APOE epsilon 4 allele modulates brain white matter integrity in healthy adults

Molecular psychiatry, 2011-09, Vol.16 (9), p.908-916

2011

Volltextzugriff (PDF)

The Finally Rewarding Search for A Cytotoxic Isosteviol Derivative

Molecules (Basel, Switzerland), 2023-06, Vol.28 (13), p.4951

2023

Volltextzugriff (PDF)

Developing an Amide-Spacered Triterpenoid Rhodamine Hybrid of Nano-Molar Cytotoxicity Combined with Excellent Tumor Cell/Non-Tumor Cell Selectivity

Molecules (Basel, Switzerland), 2023-09, Vol.28 (17), p.6404

2023

Volltextzugriff (PDF)

Stereochemistry matters: Inhibition of carbonic anhydrase II by amino acid derived sulfamates depends on their absolute configuration

European journal of medicinal chemistry reports, 2024-08, Vol.11, p.100162, Article 100162

2024

Volltextzugriff (PDF)

Synthesis and In Silico Docking of New Pyrazolo[4,3-e]pyrido[1,2-a]pyrimidine-based Cytotoxic Agents

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10258

2021

Volltextzugriff (PDF)

Combination of Betulinic Acid Fragments and Carbonic Anhydrase Inhibitors-A New Drug Targeting Approach

Pharmaceutics, 2024-03, Vol.16 (3), p.401

2024

Volltextzugriff (PDF)

Revisiting capsaicin and nonivamide: Their analogs exert strong inhibitory activity against cholinesterases

European journal of medicinal chemistry reports, 2024-12, Vol.12, p.100200, Article 100200

2024

Volltextzugriff (PDF)

(Iso)quinoline amides derived from corosolic acid exhibit high cytotoxicity, and the potential for overcoming drug resistance in human cancer cells

European journal of medicinal chemistry reports, 2024-12, Vol.12, p.100198, Article 100198

2024

Volltextzugriff (PDF)

Betulinic acid derived amides are highly cytotoxic, apoptotic and selective

European journal of medicinal chemistry, 2020-12, Vol.207, p.112815, Article 112815

2020

Volltextzugriff (PDF)

Dehydroabietylamine-substituted trifluorobenzene sulfonamide rhodamine B hybrids as anticancer agents overcoming drug resistance

European journal of medicinal chemistry, 2024-10, Vol.276, p.116667, Article 116667

2024

Volltextzugriff (PDF)

Arylsulfonamido-alkyl-sulfamates act as inhibitors of bovine carbonic anhydrase II

European journal of medicinal chemistry reports, 2024-12, Vol.12, p.100177, Article 100177

2024

Volltextzugriff (PDF)

An asiatic acid derived trisulfamate acts as a nanomolar inhibitor of human carbonic anhydrase VA

Steroids, 2024-05, Vol.205, p.109381-109381, Article 109381

2024

Volltextzugriff (PDF)

Lupane acetates in small molecule drug hybrids: Probing their inhibitory activity for carbonic anhydrase II

European journal of medicinal chemistry reports, 2024-04, Vol.10, p.100139, Article 100139

2024

Volltextzugriff (PDF)

Isosteviol – A new scaffold for the synthesis of carbonic anhydrase II inhibitors

Results in Chemistry, 2024-01, Vol.7, p.101426, Article 101426

2024

Volltextzugriff (PDF)

Dehydroabietylamine derived bistetrazoles from ultrasound-assisted pseudo-seven-component Ugi reactions act as efficient and selective inhibitors of cholinesterases

European journal of medicinal chemistry reports, 2024-04, Vol.10, p.100124, Article 100124

2024

Volltextzugriff (PDF)

An improved partial synthesis of corosolic acid and its conversion to highly cytotoxic mitocans

European journal of medicinal chemistry reports, 2022-12, Vol.6, p.100073, Article 100073

2022

Volltextzugriff (PDF)

Asiatic acid as a leading structure for derivatives combining sub-nanomolar cytotoxicity, high selectivity, and the ability to overcome drug resistance in human preclinical tumor models

European journal of medicinal chemistry, 2023-03, Vol.250, p.115189-115189, Article 115189

2023

Volltextzugriff (PDF)

Inhibitory properties of quinopimaric acid derivatives towards cholinesterases

Natural product research, 2024-11, Vol.38 (22), p.3893-3901

2024

Volltextzugriff (PDF)

Diethoxyphosphoryloxy‐oleanolic acid is a nanomolar‐inhibitor of butyrylcholinesterase

Chemical biology & drug design, 2024-03, Vol.103 (3), p.e14506-n/a

2024

Volltextzugriff (PDF)

1 – 25 von 345

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(299)
Mit Volltextzugriff
(279)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Synthesis of Rhodamine-Conjugated Lupane Type Triterpenes of Enhanced Cytotoxicity

Synthesis and In Silico Docking Study towards M-Pro of Novel Heterocyclic Compounds Derived from Pyrazolopyrimidinone as Putative SARS-CoV-2 Inhibitors

F16 Hybrids Derived from Steviol or Isosteviol Are Accumulated in the Mitochondria of Tumor Cells and Overcome Drug Resistance

The APOE [varepsilon]4 allele modulates brain white matter integrity in healthy adults

Rhodamine 101 Conjugates of Triterpenoic Amides Are of Comparable Cytotoxicity as Their Rhodamine B Analogs

Synthesis and Enzymatic Evaluation of a Small Library of Substituted Phenylsulfonamido-Alkyl Sulfamates towards Carbonic Anhydrase II

The APOE epsilon 4 allele modulates brain white matter integrity in healthy adults

The Finally Rewarding Search for A Cytotoxic Isosteviol Derivative

Developing an Amide-Spacered Triterpenoid Rhodamine Hybrid of Nano-Molar Cytotoxicity Combined with Excellent Tumor Cell/Non-Tumor Cell Selectivity

Stereochemistry matters: Inhibition of carbonic anhydrase II by amino acid derived sulfamates depends on their absolute configuration

Synthesis and In Silico Docking of New Pyrazolo[4,3-e]pyrido[1,2-a]pyrimidine-based Cytotoxic Agents

Combination of Betulinic Acid Fragments and Carbonic Anhydrase Inhibitors-A New Drug Targeting Approach

Revisiting capsaicin and nonivamide: Their analogs exert strong inhibitory activity against cholinesterases

(Iso)quinoline amides derived from corosolic acid exhibit high cytotoxicity, and the potential for overcoming drug resistance in human cancer cells

Betulinic acid derived amides are highly cytotoxic, apoptotic and selective

Dehydroabietylamine-substituted trifluorobenzene sulfonamide rhodamine B hybrids as anticancer agents overcoming drug resistance

Arylsulfonamido-alkyl-sulfamates act as inhibitors of bovine carbonic anhydrase II

An asiatic acid derived trisulfamate acts as a nanomolar inhibitor of human carbonic anhydrase VA

Lupane acetates in small molecule drug hybrids: Probing their inhibitory activity for carbonic anhydrase II

Isosteviol – A new scaffold for the synthesis of carbonic anhydrase II inhibitors

Dehydroabietylamine derived bistetrazoles from ultrasound-assisted pseudo-seven-component Ugi reactions act as efficient and selective inhibitors of cholinesterases

An improved partial synthesis of corosolic acid and its conversion to highly cytotoxic mitocans

Asiatic acid as a leading structure for derivatives combining sub-nanomolar cytotoxicity, high selectivity, and the ability to overcome drug resistance in human preclinical tumor models

Inhibitory properties of quinopimaric acid derivatives towards cholinesterases

Diethoxyphosphoryloxy‐oleanolic acid is a nanomolar‐inhibitor of butyrylcholinesterase

Suchergebnisse filtern