| Weight | 326.396 g/mol |
|---|---|
| Formula | C19H22N2O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 7 |
Phe-phe-ome (13082-29-6)
Score:
#2386 in Physics
,
#2973 in Biochemistry
,
#7279 in Chemistry
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- Crystal and molecular structure of Boc-D-Ala-Phe-Gly-Phe-D-Ala-OMe : a 310-helical dehydropeptide (Biopolymers, 1990)
- Structure of the protected dipeptide Ac-Val-Phe-OMe in the gas phase: Towards a -sheet model system (Journal of Chemical Physics, 2003)
- Structures of the protected amino acid AcPheOMe and its dimer: A -sheet model system in the gas phase (Physical Chemistry Chemical Physics, 2002)
- The Mo(-allyl)(CO)2 Moiety as a Robust Marker Group in Bioorganometallic Chemistry. Unusual Crystal Structure of the Phenylalanine Derivative Mo(C5H4-CO-Phe-OMe)(-allyl)(CO)2 (Organometallics, 2000)
- Synthesis, conformation, and activity of HCO-Met-Z Leu-Phe-Ome, an active analogue of chemotactic N-formyltripeptides (Biopolymers, 1993)
- Two For-MetLeuPhe-OMe analogues trigger selective neutrophil responses: A differential effect on cytosolic free Ca2+ (Biochimica et Biophysica Acta, 1997)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)C(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)N
-
InChIKeyFBKRSZZALAQRNH-UHFFFAOYSA-N
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Synthesis
H-Phe-NH2
+
Reactant
(Alkylation of primary amines)
benzene
+
Reactant
(Friedel-Crafts alkylation)
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