| Weight | 209.01 g/mol |
|---|---|
| Formula | C9H12BNO4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
4-Borono-L-phenylalanine (76410-58-7)
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- Synthesis and radiation dosimetry of 4-borono-2-[18F]fluoro-D,L-phenylalanine: a target compound for PET and boron neutron capture therapy. (International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1991)
- A CONCISE PREPARATION OF 4-BORONO-L-PHENYLALANINE (L-BPA) FROM L-PHENYLALANINE (Journal of Organic Chemistry, 1998)
- A unique in vivo assessment of 4-[10B]borono-L-phenylalanine in tumour tissues for boron neutron capture therapy of malignant melanomas using positron emission tomography and 4-borono-2-[18F]fluoro-L-phenylalanine (Melanoma Research, 1992)
- Evaluation of 4-Borono-2-18F-Fluoro-l-Phenylalanine-Fructose as a Probe for Boron Neutron Capture Therapy in a Glioma-Bearing Rat Model (The Journal of Nuclear Medicine, 2004)
- Evaluation of Pharmacokinetics of 4-Borono-2-18F-Fluoro-l-Phenylalanine for Boron Neutron Capture Therapy in a Glioma-Bearing Rat Model with Hyperosmolar BloodBrain Barrier Disruption (The Journal of Nuclear Medicine, 2005)
- SYNTHESIS OF 4-BORONO-L-PHENYLALANINE (Synlett, 1996)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESB(C1=CC=C(C=C1)CC(C(=O)O)N)(O)O
-
InChIKeyNFIVJOSXJDORSP-UHFFFAOYSA-N
- Pubchem - 4-Borono-L-phenylalanine
- Wikipedia - boronophenylalanine
Phenylalanine (Phe or F) is an -amino acid with the formula C 9H 11NO 2. It can be viewed as a benzyl group substituted for the methyl group of alanine, or a phenyl group in place of a terminal hydrogen of alanine. This essential amino acid is classified as neutral, and nonpolar because of the inert and hydrophobic nature of the benzyl side chain.
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