Peptides & Peptide Synthesis Products

Fmoc-Tyr(tBu)-OH

Fmoc-Tyr(tBu)-OH
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Fmoc-Tyr(tBu)-OH, Catalog No: 41014
Nα-Fmoc-O-tert-butyl-L-tyrosine, CAS: 71989-38-3, MW: 459.53, Formula: C28H29NO5
Catalog No: 41014
Nα-Fmoc-O-tert-butyl-L-tyrosine, CAS: 71989-38-3, MW: 459.53, Formula: C28H29NO5

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Description

Details

Nα-Fmoc-O-tert-butyl-L-tyrosine
Additional Information

Additional Information

Catalog Number 41014
CAS 71989-38-3
M.W. 459.53
Formula C28H29NO5
IUPAC Name 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoic acid
Synonym Nα-Fmoc-O-tert-butyl-L-tyrosine
Also Known As
  • 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoic acid
  • 3-(4-tert-butoxyphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid
  • 3-(4-tert-butoxyphenyl)-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]propanoic acid
  • 3-(4-tert-butoxyphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propionic acid
  • 71989-38-3
  • EINECS 276-262-7
  • O-(tert-Butyl)-N-((9H-fluoren-9-ylmethoxy)carbonyl)-L-tyrosine
  • ST5411679
  • L-Tyrosine, O-(1,1-dimethyethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
  • NSC334301
InChIKey JAUKCFULLJFBFN-UHFFFAOYSA-N
InChI InChI=1S/C28H29NO5/c1-28(2,3)34-19-14-12-18(13-15-19)16-25(26(30)31)29-27(32)33-17-24-22-10-6-4-8-20(22)21-9-5-7-11-23(21)24/h4-15,24-25H,16-17H2,1-3H3,(H,29,32)(H,30,31)
SMILES CC(C)(C)OC1=CC=C(C=C1)CC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
Cited Uses

Details

1. Varamini P et al, "Lipo-Endomorphin-1 Derivatives with Systemic Activity against Neuropathic Pain without Producing Constipation", PLoS ONE, 7(8) pp.e41909 ().
2. Nagorny P et al, "On the Emerging Role of Chemistry in the Fashioning of Biologics: Synthesis of a Bidomainal Fucosyl GM1-Based Vaccine, for the Treatment of Small Cell Lung Cancer", The Journal of organic chemistry, 74(15) pp.5157-5162 (2009 Aug 7).
3. Statz AR et al, "Experimental and Theoretical Investigation of Chain Length and Surface Coverage on Fouling of Surface Grafted Polypeptoids", Biointerphases, 4(2) pp.FA22-FA32 (2009 Jun 1).
4. Kumar A et al, "Synthesis and Structure-Activity Relationships of Linear and Conformationally Constrained Peptide Analogs of CIYKYY as Src Tyrosine Kinase Inhibitors", Journal of medicinal chemistry, 49(11) pp.3395-3401 (2006 Jun 1).
5. Agnes RS et al, "Structure-Activity Relationships of Bifunctional Peptides Based on Overlapping Pharmacophores at Opioid and Cholecystokinin Receptors", Journal of medicinal chemistry, 49(10) pp.2868-2875 (2006 May 18).
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