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Volumn 14, Issue 4, 2016, Pages 1277-1287

In Vitro selectivity of an acyclic cucurbit[n]uril molecular container towards neuromuscular blocking agents relative to commonly used drugs

(4) Ganapati, Shweta a Zavalij, Peter Y a Eikermann, Matthias b Isaacs, Lyle a

a UNIVERSITY OF MARYLAND (United States)

b MASSACHUSETTS GENERAL HOSPITAL (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING ENERGY; BINS; CONTAINERS; DRUG INTERACTIONS;

BINDING AFFINITIES; CUCURBIT[N]URIL; EQUILIBRIUM CONCENTRATION; GAMMA-CYCLODEXTRIN; MOLECULAR CONTAINERS; NEUROMUSCULAR BLOCKING AGENTS; NUMBER OF FACTORS; RECOVERY TIME;

DRUG DOSAGE;

CHOLINERGIC RECEPTOR; CUCURBITURIL; MACROCYCLIC COMPOUND; NEUROMUSCULAR BLOCKING AGENT;

CHEMISTRY; CONFORMATION; DOSE RESPONSE; HUMAN; IN VITRO STUDY; METABOLISM; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION;

DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; IN VITRO TECHNIQUES; MACROCYCLIC COMPOUNDS; MOLECULAR CONFORMATION; NEUROMUSCULAR BLOCKING AGENTS; RECEPTORS, CHOLINERGIC; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84955459147 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c5ob02356d Document Type: Article

Times cited : (24)

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