Weight | 285.475 g/mol |
---|---|
Formula | C20H31N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
1446-61-3 (1446-61-3)
dehydroabietylamine
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- Sigma-Aldrich - 1446-61-396.10 USD
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- Adsorption of the anionic dye Congo red from aqueous solution onto natural zeolites modified with N,N-dimethyl dehydroabietylamine oxide (Chemical Engineering Journal, 2014)
- Synthesis and antitumor activity of novel aminophosphonates from diterpenic dehydroabietylamine (Heteroatom Chemistry, 2008)
- Corrosion inhibition and adsorption behavior of 2-((dehydroabietylamine) methyl)-6-methoxyphenol on mild steel surface in seawater (Thin Solid Films, 2011)
- Topical antiinflammatory dehydroabietylamine derivatives. IV (Bioorganic & Medicinal Chemistry Letters, 1993)
- Cytotoxic effects and pro-apoptotic mechanism of TBIDOM, a novel dehydroabietylamine derivative, on human hepatocellular carcinoma SMMC-7721 cells (Journal of Pharmacy and Pharmacology, 2008)
- N-Benzoyl-12-nitrodehydroabietylamine-7-one, a novel dehydroabietylamine derivative, induces apoptosis and inhibits proliferation in HepG2 cells (Chemico-Biological Interactions, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dehydroabietylamine
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SMILESCC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CN)C
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InChIKeyJVVXZOOGOGPDRZ-UHFFFAOYSA-N
- Pubchem - 1446-61-3
- Wikipedia - dehydroabietylamine
Leelamine (dehydroabietylamine) is a diterpene amine that has weak affinity for the cannabinoid receptors CB1 and CB2, as well as being an inhibitor of pyruvate dehydrogenase kinase. Optically active leelamine is also used as a chiral resolving agent for carboxylic acids. Leelamine has been shown to be effective against certain cancer cells, independent from its activity on Cannabinoids or PDK1.
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