|
Volumn 12, Issue 24, 2002, Pages 3525-3528
|
Vacuolar-type H+-ATPase inhibitory activity of synthetic analogues of the concanamycins: Is the hydrogen bond network involving the lactone carbonyl, the hemiacetal hydroxy group, and the C-19 hydroxy group essential for the biological activity of the concanamycins?
a
KEIO UNIVERSITY
(Japan)
|
Author keywords
[No Author keywords available]
|
Indexed keywords
ACETAL DERIVATIVE;
ADENOSINE TRIPHOSPHATASE;
EPIDERMAL GROWTH FACTOR RECEPTOR;
HYDROXYL GROUP;
KANAMYCIN DERIVATIVE;
LACTONE DERIVATIVE;
ANTIINFECTIVE AGENT;
CONCANAMYCIN F;
ENZYME INHIBITOR;
EPIDERMAL GROWTH FACTOR;
MACROLIDE;
PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;
TUMOR PROTEIN;
ACIDIFICATION;
APOPTOSIS;
ARTICLE;
CANCER CELL CULTURE;
CONTROLLED STUDY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
HYDROGEN BOND;
STRUCTURE ACTIVITY RELATION;
X RAY CRYSTALLOGRAPHY;
CELL SURVIVAL;
CHEMISTRY;
DOSE RESPONSE;
DRUG ANTAGONISM;
DRUG EFFECT;
PH;
PHYSIOLOGY;
ANTI-BACTERIAL AGENTS;
APOPTOSIS;
CELL SURVIVAL;
DOSE-RESPONSE RELATIONSHIP, DRUG;
ENZYME INHIBITORS;
EPIDERMAL GROWTH FACTOR;
HUMANS;
HYDROGEN BONDING;
HYDROGEN-ION CONCENTRATION;
MACROLIDES;
NEOPLASM PROTEINS;
RECEPTOR, EPIDERMAL GROWTH FACTOR;
STRUCTURE-ACTIVITY RELATIONSHIP;
VACUOLAR PROTON-TRANSLOCATING ATPASES;
|
EID: 0036889972
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0960-894X(02)00806-5 Document Type: Article |
Times cited : (10)
|
References (18)
|