| Weight | 164.208 g/mol |
|---|---|
| Formula | C9H12N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
H-Phe-NH2 (5241-58-7)
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- [3H]-[H-D-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr-NH2] ([3H]CTOP), a potent and highly selective peptide for mu opioid receptors in rat brain. (Journal of Pharmacology and Experimental Therapeutics, 1989)
- Antinociceptive and Respiratory Effects of Intrathecal H-Tyr-d-Arg-Phe-Lys-NH2 (DALDA) and [Dmt1]DALDA (Journal of Pharmacology and Experimental Therapeutics, 2001)
- Dicarba Analogues of the Cyclic Enkephalin Peptides H-Tyr-c[D-Cys-Gly-Phe-D(or L)-Cys]NH2 Retain High Opioid Activity (Journal of Medicinal Chemistry, 2007)
- Synthesis of Stereoisomeric Analogues of Endomorphin-2, H-Tyr-Pro-Phe-Phe-NH2, and Examination of Their Opioid Receptor Binding Activities and Solution Conformation (Biochemical and Biophysical Research Communications, 2000)
- Potent analgesic activity of the enkephalin-like tetrapeptide H-Tyr-D-Ala-Gly-Phe-NH2. (Life Sciences, 1978)
- Synthesis and biological evaluation of constrained analogues of the opioid peptide H-Tyr-D-Ala-Phe-Gly-NH2 using the 4-amino-2-benzazepin-3-one scaffold. (Journal of Peptide Research, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)CC(C(=O)N)N
-
InChIKeyOBSIQMZKFXFYLV-UHFFFAOYSA-N
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