Degradable conjugates from oxanorbornadiene reagents - Wikidata - awgldk - TriplyDB

Degradable conjugates from oxanorbornadiene reagents

Degradable conjugates from oxanorbornadiene reagents

http://www.wikidata.org/entity/Q34264123

about

Click chemistry in complex mixtures: bioorthogonal bioconjugation Design of Thiol- and Light-sensitive Degradable Hydrogels using Michael-type Addition Reactions.Acid-labile mPEG-vinyl ether-1,2-dioleylglycerol lipids with tunable pH sensitivity: synthesis and structural effects on hydrolysis rates, DOPE liposome release performance, and pharmacokinetics.Solvent-Free Synthesis and Fluorescence of a Thiol-Reactive Sensor for Undergraduate Organic Laboratories.1,3-Dipolar Cycloaddition with Diazo Groups: Noncovalent Interactions Overwhelm Strain.Albumin-Oxanorbornadiene Conjugates Formed ex Vivo for the Extended Circulation of Hydrophilic Cargo Chemical Protein Modification through Cysteine.Modular degradable hydrogels based on thiol-reactive oxanorbornadiene linkers.Relative performance of alkynes in copper-catalyzed azide-alkyne cycloaddition.Simultaneous introduction of trifluoromethyl and λ(6)-pentafluorosulfanyl substituents using F5S-C≡C-CF3 as a dienophile.

P2860

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P2860

Degradable conjugates from oxanorbornadiene reagents

http://www.wikidata.org/entity/Q34264123

description

2012 nî lūn-bûn

@nan

2012 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի մարտին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Degradable conjugates from oxanorbornadiene reagents

@ast

Degradable conjugates from oxanorbornadiene reagents

@en

Degradable conjugates from oxanorbornadiene reagents

@nl

type

label

Degradable conjugates from oxanorbornadiene reagents

@ast

Degradable conjugates from oxanorbornadiene reagents

@en

Degradable conjugates from oxanorbornadiene reagents

@nl

prefLabel

Degradable conjugates from oxanorbornadiene reagents

@ast

Degradable conjugates from oxanorbornadiene reagents

@en

Degradable conjugates from oxanorbornadiene reagents

@nl

P1433

Q34264123-964E1581-759F-459A-83FC-4B880A4F7420

P1476

Q34264123-3E4A2A67-C1B6-4ED6-9345-6BE73C51E634

P2093

Q34264123-A90943E6-CF39-4E0C-8D67-89049E403EA1

Q34264123-DED7E4B9-7AFD-474B-89D3-159F6D42DF8D

Q34264123-FBD8482C-0348-4F52-A7A9-DA623E119113

P2860

Q34264123-0A8057BF-02DA-48C8-A835-62F0CB1C96E2

Q34264123-0AEFEE86-CFB9-4A0E-810A-3E2C26FDD112

Q34264123-0B03054B-3CD5-4D69-B183-FC1E4824FE33

Q34264123-248CFECF-ED4C-4A31-BF19-FD2061570A0F

Q34264123-26B4EECF-EE06-46F6-894F-8C60CB0FF239

Q34264123-29E41D67-8A77-40EF-82AB-90CC173890D8

Q34264123-3C83981E-492E-4FE6-BEC8-BA0EF666E96E

Q34264123-3C85EB91-09DF-4999-8962-9A8AA2AA2027

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P304

Q34264123-FA33F402-ECA5-42B2-8BCF-CD2C25019970

P31

Q34264123-B8A99BC3-4FA5-4C81-B479-4B04464B59D6

P356

Q34264123-2F15AB1B-D022-4E75-A251-1FBDCD10EAA0

P407

Q34264123-6187081F-5209-4A32-8D5E-03578EFAACC7

P433

Q34264123-B5F3E53C-DA88-4BF8-8804-0B7E6005DFA8

P478

Q34264123-222DE184-4422-438C-A8D0-6F661A887F49

P50

Q34264123-D78E13BB-B759-47CC-984B-535B735C8F87

P577

Q34264123-BA2AE062-7532-42CF-AEFC-6293ADEC4D8F

P5875

Q34264123-27AA38DB-F904-468A-8041-193B19A120DF

P698

Q34264123-387E8813-42CC-4AEA-A149-E397F8C0D106

P932

Q34264123-795925E2-C7E4-468A-AE71-A4054E9FD9DA

P356

P1433

Journal of the American Chemical Society

P1476

Degradable conjugates from oxanorbornadiene reagents

@en

P2093

Alexander A Kislukhin

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

Cody J Higginson

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

Vu P Hong

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

P2860

Thiol-selective fluorogenic probes for labeling and release.

Hexahistidine-tag-specific optical probes for analyses of proteins and their interactions

Reaction of Tris(2-carboxyethyl)phosphine (TCEP) with maleimide and alpha-haloacyl groups: anomalous elution of TCEP by gel filtration

Formation, Reactivity, and Detection of Protein Sulfenic Acids

Aqueous-phase deactivation and intramolecular [2 + 2 + 2] cycloaddition of oxanorbornadiene esters

Experimental pK(a) values of buried residues: analysis with continuum methods and role of water penetration

Metal-free triazole formation as a tool for bioconjugation.

Tapasin and ERp57 form a stable disulfide-linked dimer within the MHC class I peptide-loading complex

Reversible and covalent binding of drugs to human serum albumin: methodological approaches and physiological relevance.

Application of metal-free triazole formation in the synthesis of cyclic RGD-DTPA conjugates.

P304

6491-6497

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

P31

scholarly article

P356

10.1021/JA301491H

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

P407

P433

14

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

P478

134

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

P50

P577

2012-03-28T00:00:00Z

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

P5875

223135235

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P698

22455380

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

P932

3432588

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