about
Toxicology and drug delivery by cucurbit[n]uril type molecular containersSelf-association of facially amphiphilic methylene bridged glycoluril dimers.Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.Acyclic CB[n]-type molecular containers: effect of solubilizing group on their function as solubilizing excipients.Stimuli responsive systems constructed using cucurbit[n]uril-type molecular containers.Molecular-recognition properties of a water-soluble cucurbit[6]uril analogue.Acyclic Cucurbit[n]uril-Type Molecular Containers: Influence of Linker Length on Their Function as Solubilizing Agents.Uptake of Hydrocarbons in Aqueous Solution by Encapsulation in Acyclic Cucurbit[n]uril-Type Molecular Containers.Glycoluril-Derived Molecular Clips are Potent and Selective Receptors for Cationic Dyes in Water.Blind prediction of host-guest binding affinities: a new SAMPL3 challenge.New small-molecule inhibitors effectively blocking picornavirus replicationThe cucurbit[n]uril family: prime components for self-sorting systems.The ex vivo neurotoxic, myotoxic and cardiotoxic activity of cucurbituril-based macrocyclic drug delivery vehicles.Acyclic cucurbit[n]uril-type molecular containers: influence of aromatic walls on their function as solubilizing excipients for insoluble drugs.Mesoporous Silica Nanoparticles Coated by Layer-by-Layer Self-assembly Using Cucurbit[7]uril for in Vitro and in Vivo Anticancer Drug ReleaseAcyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agents.Synthesis of a Disulfonated Derivative of Cucurbit[7]uril and Investigations of its Ability to Solubilize Insoluble Drugs.A synthetic host-guest system achieves avidin-biotin affinity by overcoming enthalpy-entropy compensationCucurbit[7]uril containers for targeted delivery of oxaliplatin to cancer cellsSynthetic mimics of biotin/(strept)avidin.Acyclic cucurbit[n]uril molecular containers enhance the solubility and bioactivity of poorly soluble pharmaceuticals.Multianalyte sensing of addictive over-the-counter (OTC) drugs.Reasons why aldehydes do not generally participate in cucurbit[n]uril forming reactions.Biological catalysis regulated by cucurbit[7]uril molecular containers.Supramolecular rhombic grids formed from bimolecular building blocks.Diastereoselective formation of glycoluril dimers: isomerization mechanism and implications for cucurbit[n]uril synthesis.Methylene-bridged glycoluril dimers: synthetic methods.Supramolecular ladders from dimeric cucurbit[6]uril.Self-sorting: the exception or the rule?Acyclic congener of cucurbituril: synthesis and recognition properties.Calabadion: A new agent to reverse the effects of benzylisoquinoline and steroidal neuromuscular-blocking agents.Tetrameric molecular bowl assembled from glycoluril building blocks.Molecular Containers Bind Drugs of Abuse in Vitro and Reverse the Hyperlocomotive Effect of Methamphetamine in Rats.Shape-Controllable and Fluorescent Supramolecular Organic Frameworks Through Aqueous Host-Guest Complexation.Host-Guest Tethered DNA Transducer: ATP Fueled Release of a Protein Inhibitor from Cucurbit[7]uril.Supramolecular Sensors for Opiates and Their Metabolites.Cucurbit[7]uril-Tetramethylrhodamine Conjugate for Direct Sensing and Cellular Imaging.From Packed "Sandwich" to "Russian Doll": Assembly by Charge-Transfer Interactions in Cucurbit[10]uril.Self-assembly of cucurbit[7]uril based triangular [4]molecular necklaces and their fluorescence properties.Unraveling the Structure-Affinity Relationship between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids.
P50
Q28473864-0F4EADB2-C74D-4991-B898-88994BD8CE05Q30661322-B17BE9C3-29D4-44FB-94CC-D3F2623B9BA6Q30725024-B747131A-C36B-433A-BAF9-8A507BEDB124Q30770195-3B654615-4459-422E-86EA-FF4A8CC2581EQ30812330-A8DF5FC8-AA4D-451C-895D-EF48BB7E4366Q31030664-6855C27B-23A2-4900-80AF-6ADC7ED5DF56Q31060481-7C004867-FB48-4C40-BAF5-B19E9270B2ACQ31095509-8C231D3D-4A68-49CF-8EA4-8C23571A610BQ31119698-2689E90A-A395-43B4-8DCF-B0015768AC8AQ34257034-A02C554F-8055-4BA6-B54F-C46D94727FAFQ34261753-8B015B5E-403A-41E9-8210-BC2BCB372AEAQ34466152-CD387EA8-2F72-4FFD-9CE4-6B184C7D9424Q34523282-30569288-54EC-4DDA-A2B9-B6B3093145EEQ34631587-8EF933E1-D666-4C43-B112-88AB68B8EB0CQ34986234-B4577D78-3F8C-49CF-B63B-8CBEF354322FQ35196330-72172E03-FE86-4E6E-9B5D-482351337431Q35546753-BF8173A6-007E-4B36-9B81-04EB8CB9D585Q36696316-2377BD5C-D9F1-4318-B114-674D8DA32F77Q37638514-ED10A4AA-E642-42E0-AE1E-1D72D9259EECQ38758309-33F41F67-AF88-45C9-9C31-49333CC674C1Q39344797-FCD202EB-C85B-4675-97B6-96C6AEE63836Q39356571-EF5B4033-B275-43FC-BC37-53D5258D2623Q43117613-9D3BF706-C710-4E5A-87A3-26CD10515E2FQ43139373-533FBF4A-4BAC-4740-AF00-A725C3641770Q43282586-72EEE960-F619-4017-AD36-F93F35C1F265Q44054114-FBF6031E-7388-444E-9D4F-BB8DB0DEB0C1Q44086309-8A8AC2AB-1442-443E-A660-367D89799557Q44384387-051D835E-489B-45C9-9C36-5ED4AC8F9EA2Q44404348-362382FA-55FC-4D6B-A8FB-EF87EBEF7E74Q44534939-FBA1B0F1-7A67-4D70-8193-BD3D949696F4Q45422589-7275DC8A-6CC7-41F1-A93F-4F502B45BCA6Q46506927-56355095-5BC1-47BD-A308-C9B78D3B0811Q47288519-773BACD3-6247-45CC-ACCC-F8A3C75E2AEAQ47295809-06E9B994-5946-4681-A641-55E046539E97Q47840257-2934F9C2-D329-432C-8E2C-2EB82BC57366Q47923279-E38E5E1A-6995-4789-B053-6CCF7EC46882Q48133046-C25E69A3-EBDF-4471-B234-8F2AFAE92E10Q48215619-29C29F43-361D-4E39-8A98-4782DC94C884Q48225355-A45EA313-2E88-413D-8191-0E4AB4442700Q48256778-F50ACE8F-233C-4C7C-AAF6-AEDA7B25066C
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Lyle D Isaacs
@ast
Lyle D Isaacs
@en
Lyle D Isaacs
@es
Lyle D Isaacs
@nl
Lyle D Isaacs
@sl
type
label
Lyle D Isaacs
@ast
Lyle D Isaacs
@en
Lyle D Isaacs
@es
Lyle D Isaacs
@nl
Lyle D Isaacs
@sl
altLabel
Lyle D. Isaacs
@en
Lyle David Isaacs
@en
prefLabel
Lyle D Isaacs
@ast
Lyle D Isaacs
@en
Lyle D Isaacs
@es
Lyle D Isaacs
@nl
Lyle D Isaacs
@sl
P1053
B-4472-2009
P106
P21
P31
P3829
P496
0000-0002-4079-332X