about
A Structurally-Tunable 3-Hydroxyflavone Motif for Visible Light-Induced Carbon Monoxide-Releasing Molecules (CORMs)Toward Carbon Monoxide-Based Therapeutics: Critical Drug Delivery and Developability IssuesPhotoCORMs: CO release moves into the visible.Heme Oxygenase-1 and Carbon Monoxide in the Heart: The Balancing Act Between Danger Signaling and Pro-Survival.Toward carbon monoxide based therapeutics: carbon monoxide in a pill.Norborn-2-en-7-ones as physiologically-triggered carbon monoxide-releasing prodrugsRational Design of a Robust Fluorescent Probe for the Detection of Endogenous Carbon Monoxide in Living Zebrafish Embryos and Mouse Tissue.Nonmetallic carbon monoxide releasing molecules (CORMs).Hexamethylenetetramine carboxyborane: synthesis, structural characterization and CO releasing properties.Sulfur dioxide prodrugs: triggered release of SO2via a click reaction.Click and Fluoresce: A Bioorthogonally Activated Smart Probe for Wash-Free Fluorescent Labeling of Biomolecules.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.Dissociative reactions of benzonorbornadienes with tetrazines: scope of leaving groups and mechanistic insights.Solution or solid - it doesn't matter: visible light-induced CO release reactivity of zinc flavonolato complexes.An oral redox-sensitive self-immolating prodrug strategy.Enabling [18F]-bicyclo[6.1.0]nonyne for oligonucleotide conjugation for positron emission tomography applications: [18F]-anti-microRNA-21 as an examplepH-Sensitive metal-free carbon monoxide prodrugs with tunable and predictable release rates
P2860
Q36170250-BF0F04FA-20DE-412F-9A0C-1234F1BC227DQ36584960-0ED6CE3F-DFA1-4CB5-A22C-66D45AC4D0FDQ38786408-43D3ED90-6553-4919-BC84-CDD3F172B2B0Q38860810-A11BB27E-A322-4423-85B3-6C3E285950EDQ39428134-EF9792D3-C386-4F2A-9C58-DF11A0F4C4B9Q41883399-16232935-8A19-441C-BA9A-2CBE31EA2286Q47742477-775C268B-DD48-4554-A24A-65950DBC7E13Q47929446-13327F21-C291-4AC5-9703-FCD31D04DC7DQ48126560-C7481E1D-2C18-4821-A7A6-5ECA51D547F9Q48369151-437DD2CC-61DD-43FA-87A9-5CA2A267249AQ48373031-4316B907-849E-4F22-9378-4B3ABE0D3639Q48728819-2E72FABE-15BA-4D4B-9C7A-C84E171E040DQ48925029-D689C512-EFA4-4484-AD1A-9393B8F3E950Q50006616-C2B285C1-D34A-4CDF-A76E-3E6C9EED095DQ50227642-A1DDB1F6-A30F-4F9A-8802-17727BDCDD39Q51004337-8F8D9953-FA26-499A-A281-4C5EBD0214FDQ57621551-117797CA-D0B0-4967-9DE2-ACEE323919B9Q57696870-66EB3A85-0BD2-48A4-9D4F-EA488E1A7A81
P2860
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh
2014年學術文章
@zh-hant
name
A click-and-release approach to CO prodrugs.
@en
type
label
A click-and-release approach to CO prodrugs.
@en
prefLabel
A click-and-release approach to CO prodrugs.
@en
P2093
P2860
P356
P1476
A click-and-release approach to CO prodrugs
@en
P2093
Alexander Draganov
Binghe Wang
Chaofeng Dai
Danzhu Wang
Didier Merlin
Krishna Damera
Yueqing Zheng
P2860
P304
15890-15893
P356
10.1039/C4CC07748B
P577
2014-12-01T00:00:00Z