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serinol

Known as: 2-amino-1,3-propanediol, 2-aminopropane-1,3-diol 
National Institutes of Health

Related topics

Related topics

3 relations
1-aminopropanediol

Broader (2)

PropanolaminesPropylene Glycols

Papers overview

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2015
2015
Ultrasensitive Molecular Beacon Designed with Totally Serinol Nucleic Acid (SNA) for Monitoring mRNA in Cells
An artificial nucleic acid based on acyclic serinol building blocks and termed “serinol nucleic acid” (SNA) was used to construct… 
2013
2013
Siladenoserinols A-L: new sulfonated serinol derivatives from a tunicate as inhibitors of p53-Hdm2 interaction.
Siladenoserinols A-L were isolated from a tunicate as inhibitors of p53-Hdm2 interaction, a promising target for cancer… 
2008
2008
Phospholipase D-catalyzed synthesis of new phospholipids with polar head groups.
2006
2006
Induction of promotive rather than suppressive immune responses from a novel NKT cell repertoire Valpha19 NKT cell with alpha-mannosyl ceramide analogues consisting of the immunosuppressant ISP-I as…
Review
2003
Review
2003
Structures of polysaccharides and oligosaccharides of some Gram-negative marine Proteobacteria.
2002
2002
Stereoselective synthesis of a C-glycoside analogue of N-Fmoc-serine beta-N-acetylglucosaminide by Ramberg-Bäcklund rearrangement.
2001
2001
Enhancing sequence-specific cleavage of RNA within a duplex region: incorporation of 1,3-propanediol linkers into oligonucleotide conjugates of serinol-terpyridine.
The syntheses and RNA cleavage efficiencies of a new series of oligonucleotide conjugates of Cu(II)-serinol-terpyridine and 1,3… 
1998
1998
Structure of the acidic polysaccharide chain of the lipopolysaccharide of Shewanella alga 48055.
Highly Cited
1990
Highly Cited
1990
(1-Pyrenylmethyl)amino alcohols, a new class of antitumor DNA intercalators. Discovery and initial amine side chain structure-activity studies.
In the series of 1-pyrenylmethylamines studied in this work the relationships among structure, interaction with DNA, and murine… 
Highly Cited
1975
Highly Cited
1975
Competitive inhibitors of renin. Inhibitors effective at physiological pH.
Previously we reported the development of competitive inhibitors of renin effective at pH 5.5 (Poulsen, K., Burton, J., and Haber… 
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