Peptides & Peptide Synthesis Products

Fmoc-Ser-OH

Fmoc-Ser-OH
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Fmoc-Ser-OH, Catalog No: 41097
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoic acid, CAS: 73724-45-5, MW: 327.33, Formula: C18H17NO5
Catalog No: 41097
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoic acid, CAS: 73724-45-5, MW: 327.33, Formula: C18H17NO5
Description

Details

(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoic acid
Additional Information

Additional Information

Catalog Number 41097
CAS 73724-45-5
M.W. 327.33
Formula C18H17NO5
IUPAC Name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoic acid
Synonym No
Also Known As
  • (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoic acid
  • (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-propanoic acid
  • (2S)-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]-3-hydroxypropanoic acid
  • (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-propionic acid
  • 47601_FLUKA
  • Fmoc-L-serine
  • Fmoc-Ser-OH
InChIKey JZTKZVJMSCONAK-INIZCTEOSA-N
InChI InChI=1S/C18H17NO5/c20-9-16(17(21)22)19-18(23)24-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16,20H,9-10H2,(H,19,23)(H,21,22)/t16-/m0/s1
SMILES C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@@H](CO)C(=O)O
Cited Uses

Details

1. Avitabile C et al, "? sulphate PNA (PNA S): Highly Selective DNA Binding Molecule Showing Promising Antigene Activity", PLoS ONE, 7(5) pp.e35774 ().
2. Carrillo AK et al, "Synthesis of the AviMeCys-Containing D-Ring of Mersacidin", Organic letters, 14(4) pp.1034-1037 (2012 Feb 17).
3. Lefever MR et al, "Glycosylation of ?-amino acids by sugar acetate donors with InBr3. Minimally competent Lewis acids", Carbohydrate Research, 351() pp.121-125 (2012 Apr 1).
4. Schroll AL et al, "The use of 2,2?-Dithiobis(5-nitropyridine) (DTNP) for Deprotection and Diselenide Formation in Protected Selenocysteine-Containing Peptides", Journal of peptide science : an official publication of the European Peptide Society, 18(3) pp.155-162 (2012 Mar).
5. Ravi S et al, "Maleimide-thiol coupling of a bioactive peptide to an elastin-like protein polymer", Acta biomaterialia, 8(2) pp.10.1016/j.actbio.2011.10.027 (2012 Feb).
6. Yao N et al, "Facile synthesis of glycosylated Fmoc amino acid building blocks assisted by microwave irradiation", Carbohydrate research, 345(15) pp.2277-2281 (2010 Oct 13).
7. Harris KS et al, "Rapid Optimization of a Peptide Inhibitor of Malaria Parasite Invasion by Comprehensive N-Methyl Scanning", The Journal of Biological Chemistry, 284(14) pp.9361-9371 (2009 Apr 3).
8. Clark KM et al, "Expressed Protein Ligation for Metalloprotein Design and Engineering", Methods in enzymology, 462() pp.97-115 (2009).
9. Sun D et al, "Solid-Phase Synthesis and Biological Evaluation of a Uridinyl Branched Peptide Urea Library", Bioorganic & medicinal chemistry letters, 17(24) pp.6899-6904 (2007 Dec 15).
10. Borgia J et al, "Difficulties encountered during glycopeptide syntheses", Journal of Biomolecular Techniques : JBT, 12(3) pp.44-68 (2001 Sep).
11. Yan X et al, "The specificity of the protein kinase C alpha, betaII and gamma isoforms as assessed by an unnatural alcohol-appended peptide library.", Biochemical Journal, 349(Pt 3) pp.709-715 (2000 Aug 1).
12. Pawlak M et al, "Template-assembled melittin: structural and functional characterization of a designed, synthetic channel-forming protein.", Protein Science : A Publication of the Protein Society, 3(10) pp.1788-1805 (1994 Oct).
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