Weight | 337.372 g/mol |
---|---|
Formula | C17H23NO6 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 7 |
Boc-Glu-OBzl (30924-93-7)
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- Crystal structure of the -helical undecapeptide Boc-L-Ala-Aib-Ala-Aib-Ala-Glu(OBzl)-Ala-Aib-Ala-Aib-Ala-OMe (Biopolymers, 1985)
- Crystal structure of Boc-Leu-Aib-Pro-Val-Aib-Aib-Glu(OBzl)-Gln-PhlH2O, the C-terminal nonapeptide of the voltage-dependent ionophore alamethicin (Biopolymers, 1985)
- Circular dichroism and conformational analysis of the membrane-modifying peptide -N-t-Boc-(Aib-L-Ala)5-Gly-Ala-Aib-Pro-Ala-Aib-Aib-Glu-(OBzl)-Gln-OMe with respect to alamethicin (Biopolymers, 1980)
- The -helical conformation of the undecapeptide boc-l-Ala-[Aib-Ala]2-Glu(OBzl)-Ala-[Aib-Ala]2-OMe: Synthesis, X-Ray crystal structure, and conformation in solution (European Journal of Organic Chemistry, 1982)
- Parallel zippers formed by alpha-helical peptide columns in crystals of Boc-Aib-Glu(OBzl)-Leu-Aib-Ala-Leu-Aib-Ala-Lys(Z)-Aib-OMe (Proceedings of the National Academy of Sciences of the United States of America, 1990)
- High Yield Preparation of Boc-Glu(OBzl) Avoiding a Serious Side Reaction of Intramolecular Cyclization (ChemInform, 1992)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)OC(=O)NC(CCC(=O)O)C(=O)OCC1=CC=CC=C1
-
InChIKeyCVZUKWBYQQYBTF-UHFFFAOYSA-N
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Synthesis
Reactant
+
Benzyl Alcohol
(O-acylation)
tert-Butyl carbamate
+
Reactant
(Alkylation of primary amines)
Reactant
+
2-Chloro-2-methylpropane
(Ester from carboxilic acid(SN2))
Reactant
+
4-amino-5-oxo-5-phenylmethoxypentanoic acid
(Schotten-Baumann amide from acyl chloride)
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