
CAS 1033622-38-6
:Formula:C20H17NO4
InChI:InChI=1S/C20H17NO4/c1-2-11-21(12-19(22)23)20(24)25-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h1,3-10,18H,11-13H2,(H,22,23)
InChI key:BTHZEMFPZILBCR-UHFFFAOYSA-N
SMILES:C#CCN(CC(=O)O)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
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Found 5 products.
2-((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)(Prop-2-Yn-1-Yl)Amino)Acetic Acid
CAS:Formula:C20H17NO4Purity:97%Color and Shape:SolidMolecular weight:335.35332-({[(9h-fluoren-9-yl)methoxy]carbonyl}(prop-2-yn-1-yl)amino)acetic acid
CAS:2-({[(9h-fluoren-9-yl)methoxy]carbonyl}(prop-2-yn-1-yl)amino)acetic acidFormula:C20H17NO4Purity:97%Molecular weight:335.35Fmoc-N-(propargyl)-glycine
CAS:2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(prop-2-yn-1-yl)amino)acetic acidFormula:C20H17NO4Purity:98%Molecular weight:335.35Fmoc-N-(propargyl)-glycine
CAS:Fmoc-N-(propargyl)-glycine (Fmoc-PG) is a synthesized and modified amino acid that can be used in the treatment of cancer. Fmoc-PG has been shown to inhibit the growth of tumor cells when conjugated with positron emission radiotracers, such as 18F-Fluorodeoxyglucose, for use in positron emission tomography. Fmoc-PG also inhibits the glucose analogue, which may lead to an improvement of neurological function. Fmoc-PG has been shown to be metabolized by acid conjugates and conjugates, resulting in increased stability and reduced toxicity.Formula:C20H17NO4Purity:Min. 95%Molecular weight:335.36 g/mol




