Organic CO Prodrugs: Structure–CO‐Release Rate Relationship Studies
Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized therapeutic effects. A significant challenge in this field is the development of pharmaceutically acceptable forms of CO delivery with controllable an...
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Published in | Chemistry : a European journal Vol. 23; no. 41; pp. 9838 - 9845 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
21.07.2017
Wiley Subscription Services, Inc |
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Online Access | Get full text |
ISSN | 0947-6539 1521-3765 1521-3765 |
DOI | 10.1002/chem.201700936 |
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Abstract | Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized therapeutic effects. A significant challenge in this field is the development of pharmaceutically acceptable forms of CO delivery with controllable and tunable release rates. Herein, the structure–release rate studies of the first class of organic CO prodrugs that release CO in aqueous solution at neutral pH is described.
Structure–CO‐release rate relationship studies of organic CO prodrugs reveal that CO releasing rate can be tuned by modifying the nature of the linker, substituents on dienone ring or linker, and the length of the linker. |
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AbstractList | Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized therapeutic effects. A significant challenge in this field is the development of pharmaceutically acceptable forms of CO delivery with controllable and tunable release rates. Herein, the structure–release rate studies of the first class of organic CO prodrugs that release CO in aqueous solution at neutral pH is described. Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized therapeutic effects. A significant challenge in this field is the development of pharmaceutically acceptable forms of CO delivery with controllable and tunable release rates. Herein, the structure-release rate studies of the first class of organic CO prodrugs that release CO in aqueous solution at neutral pH is described.Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized therapeutic effects. A significant challenge in this field is the development of pharmaceutically acceptable forms of CO delivery with controllable and tunable release rates. Herein, the structure-release rate studies of the first class of organic CO prodrugs that release CO in aqueous solution at neutral pH is described. Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized therapeutic effects. A significant challenge in this field is the development of pharmaceutically acceptable forms of CO delivery with controllable and tunable release rates. Herein, the structure–release rate studies of the first class of organic CO prodrugs that release CO in aqueous solution at neutral pH is described. Structure–CO‐release rate relationship studies of organic CO prodrugs reveal that CO releasing rate can be tuned by modifying the nature of the linker, substituents on dienone ring or linker, and the length of the linker. Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized therapeutic effects. A significant challenge in this field is the development of pharmaceutically acceptable forms of CO delivery with controllable and tunable release rates. Herein, we describe the structure-release rate studies of the first class of organic CO-prodrugs that release CO in aqueous solution at neutral pH. Structure CO-release rate relationship studies of organic CO prodrugs reveals that CO releasing rate can be tuned by modifying the nature of the linker, substituents on dienone ring or linker, and the length of the linker. |
Author | Wang, Binghe Pan, Zhixiang Ji, Kaili Zhu, Mengyuan Li, Wei Zhang, Jun Chittavong, Vayou Ji, Xingyue |
Author_xml | – sequence: 1 givenname: Zhixiang surname: Pan fullname: Pan, Zhixiang organization: Georgia State University – sequence: 2 givenname: Vayou surname: Chittavong fullname: Chittavong, Vayou organization: Georgia State University – sequence: 3 givenname: Wei surname: Li fullname: Li, Wei organization: Jining Medical University – sequence: 4 givenname: Jun surname: Zhang fullname: Zhang, Jun organization: Tianjin Medical University – sequence: 5 givenname: Kaili surname: Ji fullname: Ji, Kaili organization: Georgia State University – sequence: 6 givenname: Mengyuan surname: Zhu fullname: Zhu, Mengyuan organization: Georgia State University – sequence: 7 givenname: Xingyue surname: Ji fullname: Ji, Xingyue email: xji@gsu.edu organization: Georgia State University – sequence: 8 givenname: Binghe surname: Wang fullname: Wang, Binghe email: wang@gsu.edu organization: Georgia State University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28544290$$D View this record in MEDLINE/PubMed |
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Keywords | DESIGN DIELS-ALDER REACTIONS PHOTOCORMS COMPLEXES carbon monoxide click and release prodrugs metal free MOLECULES DELIVERY VISIBLE-LIGHT CARBON-MONOXIDE release rate CLICK FLUORESCENT-PROBE |
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Snippet | Carbon monoxide (CO) is an endogenously produced gasotransmitter in mammals, and may have signaling roles in bacteria as well. It has many recognized... |
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SubjectTerms | Animals Aqueous solutions Bacteria Carbon monoxide Carbon Monoxide - chemistry Carbon Monoxide - metabolism Cell Survival - drug effects Chemical compounds Chemistry Chemistry, Multidisciplinary click and release Drug Design Drugs Hydrogen-Ion Concentration Kinetics Mammals metal free Mice Microscopy, Fluorescence Myoglobin - chemistry Myoglobin - metabolism Physical Sciences Prodrugs Prodrugs - chemical synthesis Prodrugs - chemistry Prodrugs - toxicity RAW 264.7 Cells release rate Science & Technology Water - chemistry |
Title | Organic CO Prodrugs: Structure–CO‐Release Rate Relationship Studies |
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