Weight | 143.186 g/mol |
---|---|
Formula | C7H13NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
4-Aminocyclohexanecarboxylic acid
3685-23-2, 1776-53-0, 3685-25-4
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- Stereoselective Routes to 3-Hydroxy and 3,4-Dihydroxy Derivatives of 2-Aminocyclohexanecarboxylic Acid. (Tetrahedron Letters, 2004)
- Synthesis and opioid activity of dynorphin A-(1-13)NH2 analogues containing cis- and trans-4-aminocyclohexanecarboxylic acid. (Journal of Medicinal Chemistry, 1993)
- The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid (Beilstein Journal of Organic Chemistry, 2006)
- Probiotics: Antistaphylococcal Activity of 4-Aminocyclohexanecarboxylic Acid, Aminobenzoic Acid, and Their Derivatives and StructureActivity Relationships (Journal of Pharmaceutical Sciences, 1977)
- Syntheses of di- and tripeptides containing 4-aminocyclohexanecarboxylic acid. (Journal of Organic Chemistry, 1975)
- Cytotoxic T lymphocyte epitope analogues containing cis- or trans-4-aminocyclohexanecarboxylic acid residues (Bioorganic & Medicinal Chemistry, 2002)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC(CCC1C(=O)O)N
-
InChIKeyDRNGLYHKYPNTEA-UHFFFAOYSA-N
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