Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant. - Wikidata - wikimedia - TriplyDB

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

http://www.wikidata.org/entity/Q30725024

about

Rapid Macrocycle Threading by a Fluorescent Dye-Polymer Conjugate in Water with Nanomolar Affinity.Supramolecular Controlled Cargo Release via Near Infrared Tunable Cucurbit[7]uril-Gold Nanostars Stimuli responsive systems constructed using cucurbit[n]uril-type molecular containers.Anion binding by biotin[6]uril in water.Acyclic Cucurbit[n]uril-Type Molecular Containers: Influence of Linker Length on Their Function as Solubilizing Agents.Glycoluril-Derived Molecular Clips are Potent and Selective Receptors for Cationic Dyes in Water.Reversible manipulation of the G-quadruplex structures and enzymatic reactions through supramolecular host-guest interactions Acyclic cucurbit[n]uril-type molecular containers: influence of aromatic walls on their function as solubilizing excipients for insoluble drugs.Acyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agents.A simple assay for quality binders to cucurbiturils.Synthesis of a Disulfonated Derivative of Cucurbit[7]uril and Investigations of its Ability to Solubilize Insoluble Drugs.In Vitro selectivity of an acyclic cucurbit[n]uril molecular container towards neuromuscular blocking agents relative to commonly used drugs.Acyclic Cucurbit[n]uril-Type Molecular Container Enables Systemic Delivery of Effective Doses of Albendazole for Treatment of SK-OV-3 Xenograft Tumors Cationic acyclic cucurbit[n]uril-type containers: synthesis and molecular recognition toward nucleotides.Supramolecular PEGylation of biopharmaceuticals Molecular recognition in chemical and biological systems.A naphthalimide derived fluorescent sensor for solid-phase screening of cucurbit[7]uril-guest interactions.Synthetic mimics of biotin/(strept)avidin.Molecular Shape and the Hydrophobic Effect.Molecular recognition and activation by polyaza macrocyclic compounds based on host-guest interactions.The aqueous supramolecular chemistry of cucurbit[n]urils, pillar[n]arenes and deep-cavity cavitands.Predicting Binding Free Energies: Frontiers and Benchmarks.Surveying macrocyclic chemistry: from flexible crown ethers to rigid cyclophanes.Photoresponsive, reversible immobilization of virus particles on supramolecular platforms.Five-Component Self-Assembly of Cucurbituril-Based Hetero-pseudorotaxanes.Water Structure Recovery in Chaotropic Anion Recognition: High-Affinity Binding of Dodecaborate Clusters to γ-Cyclodextrin A Novel Strategy to Reverse General Anesthesia by Scavenging with the Acyclic Cucurbit[n]uril-type Molecular Container Calabadion 2 Acyclic Cucurbit[n]uril Dendrimers.Enrichment of Specifically Labeled Proteins by an Immobilized Host Molecule.Modulating the oxidation of cucurbit[n]urils.Noncovalent chirality sensing ensembles for the detection and reaction monitoring of amino acids, peptides, proteins, and aromatic drugs.A Hierarchical Bipyridine-Constructed Framework for Highly Efficient Carbon Dioxide Capture and Catalytic Conversion.Solid-state study of the structure and host-guest chemistry of cucurbituril-ferrocene inclusion complexes.Flavylium network of chemical reactions in confined media: modulation of 3',4',7-trihydroxyflavilium reactions by host-guest interactions with cucurbit[7]uril.Molecular Containers Bind Drugs of Abuse in Vitro and Reverse the Hyperlocomotive Effect of Methamphetamine in Rats.Supramolecular polymeric biomaterials.Host-Guest Tethered DNA Transducer: ATP Fueled Release of a Protein Inhibitor from Cucurbit[7]uril.Acyclic cucurbit[n]uril conjugated dextran for drug encapsulation and bioimaging.Host-Guest Complexes of Cyclodextrins and Nanodiamonds as a Strong Non-Covalent Binding Motif for Self-Assembled Nanomaterials.Photochemical behavior of biosupramolecular assemblies of photosensitizers, cucurbit[n]urils and albumins.

P2860

Q27336853-8910BC57-B085-498F-BBC6-63CF5EB03621 Q30389377-8D3E430D-09A8-4325-9A79-22D2C3A61B7B Q30812330-060D520B-FBB2-40CF-9D05-411ECD0A564B Q30870498-B621EFBF-E4A7-4A7F-BD6B-0FACA411132A Q31060481-C3C1EDB8-5E72-4DB4-B471-643F8F6FD518 Q31119698-31E0ED81-BD32-4A55-8BFF-C288B9BF780B Q33557676-F19161F7-31B2-41B1-92E4-0248BBEAF7CF Q34631587-7653B250-E51E-462E-B5A3-8A4A0B27C12D Q35196330-F9D0F9EA-496B-43DF-AEDA-BF3BCC59337C Q35209831-E8540990-DC99-4CEC-AEA2-94F65C2AB1F1 Q35546753-D50B0E5E-461A-4D23-901D-EC51500384F5 Q36483980-496F2C8E-8881-4897-9A37-9673CAABE1A0 Q36665183-07542337-A926-4384-A2DF-17D756ECAED1 Q37337547-D0B9BC53-30A3-4829-800F-BDB986D4FE92 Q37515001-4B4C98B1-46CA-4D3B-B496-D9DBC73A0D13 Q38335784-A47E2EDE-8B90-46EF-BBD8-F7354C900569 Q38543431-BA542618-0CA0-4E5A-B579-E5A1B5A0EB86 Q38758309-1448E793-B39A-406B-B534-F9B2986CB951 Q38842249-E4F9625F-48A0-4C87-AC5A-D951E8885184 Q38887341-B610034E-ED8A-41B4-BC07-D9E7D238A4C1 Q39198168-884016B6-B29F-4A77-A007-BDDDBA299D7C Q39235195-BE66C6BE-08BE-4A59-A33C-F97C3964FB4F Q39277880-1EF19237-A96D-4DEA-82C6-FFE586B58253 Q40367297-51B76691-591F-4646-BF45-3AE016F886D8 Q41989806-0F9BFB14-79BA-46A9-B71F-5C9E229DAD86 Q42110410-7B6C1CE7-8CC9-4AB3-AAE7-5C526915E8B8 Q42409442-CB4879AF-886F-4071-AFFF-1A90DE71DB63 Q43142603-3C2ADFC7-957E-4DF4-BFAE-928F6F3C80B5 Q46424833-3D80CFA6-EA4E-46C8-B91E-D9999E0BA457 Q46434118-C2480BD9-A9B5-4879-AEF3-A60C28794917 Q46442397-8442807A-00CB-420C-9CC2-2A194C155064 Q46458126-CD2BEA36-32B2-40CB-A0E0-9F55EB091BA7 Q46471975-7E57021F-210E-4197-AC88-FE2240BA0108 Q46889877-BF68DC9D-2913-4876-BFE2-D2AEF73127E4 Q47288519-E19C05D7-1947-417A-A06E-E615AAC66ECC Q47325065-E146163C-E0A5-40AC-A83D-1D7BDF6EA1B9 Q47840257-4B7E33D3-5363-482C-9210-D0E97D2DC012 Q47964320-0AAFF59A-171A-466F-8CC0-F118712593CF Q48054478-A3D0EC61-DC84-40C6-AA31-B40C2363B930 Q48088568-1BFD3A8E-79BA-4B2A-AC30-88F7573A89FC

P2860

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

http://www.wikidata.org/entity/Q30725024

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

@ast

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

@en

type

label

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

@ast

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

@en

prefLabel

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

@ast

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant.

@en

P1433

Q30725024-90E1B686-4BB1-47FB-975F-3368F7ED819D

P1476

Q30725024-59185885-A09D-4345-9AD7-75197989511C

P2093

Q30725024-5B63BB32-46CE-4932-AFEB-AE509BE83CD1

Q30725024-69CB90D3-7D88-415E-878C-C2D59F5346E5

P2860

Q30725024-25DCE38E-B97E-4E0D-93A5-656FBCD53672

Q30725024-2616E97F-BADC-406C-B84D-898148D568EF

Q30725024-2B8EEB0E-2163-4D84-B0A9-9948BA5F8FCC

Q30725024-2E7F89D5-3093-4203-9987-F47882227319

Q30725024-347952DE-B006-42BC-B7E2-B8723451214E

Q30725024-5387F34F-21A7-4B6C-BA3E-AD61549B44CE

Q30725024-7156175C-5C74-42E7-A5EC-384F76B8512A

Q30725024-75C6525B-5D32-4110-815A-31DF6C33BC97

Q30725024-804CF9C9-A6B2-483C-9181-84D8891A737C

Q30725024-9E1AF06F-517C-4D94-A81B-3C07680C2A8A

P304

Q30725024-D4197E2F-BBE4-4955-A66E-A280083CD0B1

P31

Q30725024-C867F44C-4707-403C-85BD-A64636631399

P356

Q30725024-9A472A20-0AC5-47CD-9DEE-813732622239

P407

Q30725024-7A55348D-1F4D-465F-9913-ED4767BA10F0

P433

Q30725024-FB4BED3D-C40D-483A-A216-B91CCA972EB3

P478

Q30725024-3FA4CEB6-E26D-46AC-AAF5-47C441FE7F1D

P50

Q30725024-6AF251FE-E53E-4C43-A537-760D2DEA1D68

Q30725024-884FE4DA-23EB-40BB-A5C0-EAFB9067F8F3

Q30725024-B747131A-C36B-433A-BAF9-8A507BEDB124

Q30725024-B755D0B8-5CCB-40CF-875B-BD465AD2AA50

P577

Q30725024-AD24AA92-9E18-4238-979B-2A2561963E54

P698

Q30725024-CDA4D600-0776-4842-B370-6E9B0CFE0CE5

P356

P1433

Angewandte Chemie International Edition

P1476

Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant

@en

P2093

Liping Cao

http://www.w3.org/2001/XMLSchema#string

Robert Glaser

http://www.w3.org/2001/XMLSchema#string

P2860

A streptavidin variant with slower biotin dissociation and increased mechanostability

The origins of femtomolar protein-ligand binding: hydrogen-bond cooperativity and desolvation energetics in the biotin-(strept)avidin binding site

Grid inhomogeneous solvation theory: hydration structure and thermodynamics of the miniature receptor cucurbit[7]uril

Complexation of ferrocene derivatives by the cucurbit[7]uril host: a comparative study of the cucurbituril and cyclodextrin host families.

Cucurbit[10]uril.

Biomolecule-directed assembly of self-supported, nanoporous, conductive, and luminescent single-walled carbon nanotube scaffolds.

The cucurbit[n]uril family: prime components for self-sorting systems.

New ultrahigh affinity host-guest complexes of cucurbit[7]uril with bicyclo[2.2.2]octane and adamantane guests: thermodynamic analysis and evaluation of M2 affinity calculations

The cucurbit[n]uril family.

A synthetic host-guest system achieves avidin-biotin affinity by overcoming enthalpy-entropy compensation

P304

988-993

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/ANIE.201309635

http://www.w3.org/2001/XMLSchema#string

P407

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

53

http://www.w3.org/2001/XMLSchema#string

P50

Kata Mlinarić-Majerski

Marina Šekutor

P577

2014-01-02T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

24382654

http://www.w3.org/2001/XMLSchema#string