Esterase-Sensitive Prodrugs with Tunable Release Rates and Direct Generation of Hydrogen Sulfide.
about
Self-Immolative Thiocarbamates Provide Access to Triggered H2S Donors and Analyte Replacement Fluorescent ProbesA Novel Esterase-sensitive Prodrug Approach for Controllable Delivery of Persulfide Species.Cardioprotection by H2S Donors: Nitric Oxide-Dependent and ‑Independent Mechanisms.Hydrogen Sulfide Donors Activated by Reactive Oxygen Species.Toward Hydrogen Sulfide Based Therapeutics: Critical Drug Delivery and Developability Issues.A Single Fluorescent Probe to Visualize Hydrogen Sulfide and Hydrogen Polysulfides with Different Fluorescence Signals."On demand" redox buffering by H2S contributes to antibiotic resistance revealed by a bacteria-specific H2S donor.Light-responsive paper strips as CO-releasing material with a colourimetric response.Hydrogen Sulfide: A Worthwhile Tool in the Design of New Multitarget Drugs.Recent Development of Hydrogen Sulfide Releasing/Stimulating Reagents and Their Potential Applications in Cancer and Glycometabolic Disorders.Therapeutic Delivery of H2S via COS: Small Molecule and Polymeric Donors with Benign Byproducts.A review of hydrogen sulfide (H2S) donors: Chemistry and potential therapeutic applications.Inhibition of Mitochondrial Bioenergetics by Esterase-Triggered COS/H2S Donors.International Union of Basic and Clinical Pharmacology. CII: Pharmacological Modulation of H2S Levels: H2S Donors and H2S Biosynthesis Inhibitors.Kinetic Insights into Hydrogen Sulfide Delivery from Caged-Carbonyl Sulfide Isomeric Donor Platforms.Triggered and Tunable Hydrogen Sulfide Release from Photogenerated Thiobenzaldehydes.Glyceride-Mimetic Prodrugs Incorporating Self-Immolative Spacers Promote Lymphatic Transport, Avoid First-Pass Metabolism, and Enhance Oral Bioavailability.Sulfur dioxide prodrugs: triggered release of SO2via a click reaction.An esterase-activated click and release approach to metal-free CO-prodrugs.Click and Release: A Chemical Strategy toward Developing Gasotransmitter Prodrugs by Using an Intramolecular Diels-Alder Reaction.Esterase-sensitive sulfur dioxide prodrugs inspired by modified Julia olefination.
P2860
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P2860
Esterase-Sensitive Prodrugs with Tunable Release Rates and Direct Generation of Hydrogen Sulfide.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Esterase-Sensitive Prodrugs wi ...... eneration of Hydrogen Sulfide.
@en
Esterase-Sensitive Prodrugs wi ...... eneration of Hydrogen Sulfide.
@nl
type
label
Esterase-Sensitive Prodrugs wi ...... eneration of Hydrogen Sulfide.
@en
Esterase-Sensitive Prodrugs wi ...... eneration of Hydrogen Sulfide.
@nl
prefLabel
Esterase-Sensitive Prodrugs wi ...... eneration of Hydrogen Sulfide.
@en
Esterase-Sensitive Prodrugs wi ...... eneration of Hydrogen Sulfide.
@nl
P2093
P2860
P356
P1476
Esterase-Sensitive Prodrugs wi ...... Generation of Hydrogen Sulfide
@en
P2093
Bingchen Yu
Vayou Chittavong
Yueqin Zheng
Zhixiang Pan
P2860
P304
P356
10.1002/ANIE.201511244
P407
P50
P577
2016-01-28T00:00:00Z