| Weight | 112.128 g/mol |
|---|---|
| Formula | C6H8O2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
5-Hexynoic acid (53293-00-8)
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- Mechanism of inactivation of .gamma.-aminobutyric acid aminotransferase by 4-amino-5-hexynoic acid (.gamma.-ethynyl GABA) (Journal of the American Chemical Society, 1991)
- 4-Amino-5-Hexynoic AcidA Potent Inhibitor of Tetrapyrrole Biosynthesis in Plants (Plant Physiology, 1988)
- ASYMMETRIC-SYNTHESIS OF S-(+)-4-AMINO-5-HEXYNOIC ACID (Tetrahedron-asymmetry, 1995)
- Inhibition of plant ornithine aminotransferase by gabaculine and 4-amino-5-hexynoic acid (Phytochemistry, 1993)
- 4-Pentynoic and 5-Hexynoic Acid from Jones Oxidation of 5-Hexynol (Synthetic Communications, 1979)
- A kinetic model for the action of the enzyme activated irreversible inhibitor 4-amino-5-hexynoic acid in vivo (Biochemical Pharmacology, 1984)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC#CCCCC(=O)O
-
InChIKeyVPFMEXRVUOPYRG-UHFFFAOYSA-N
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