Weight | 271.316 g/mol |
---|---|
Formula | C16H17NO3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 4 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Higenamine (106032-53-5, 5843-65-2)
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- Higenamine reduces apoptotic cell death by induction of heme oxygenase-1 in rat myocardial ischemia-reperfusion injury (Apoptosis, 2006)
- Enantioselective synthesis of (R)-(+)- and (S)-(-)-higenamine and their analogues with effects on platelet aggregation and experimental animal model of disseminated intravascular coagulation. (Bioorganic & Medicinal Chemistry Letters, 2008)
- Different pharmacological characteristics of structurally similar benzylisoquinoline analogs, papaverine, higenamine, and GS 389, on isolated rat aorta and heart (Canadian Journal of Physiology and Pharmacology, 1994)
- Higenamine reduces HMGB1 during hypoxia-induced brain injury by induction of heme oxygenase-1 through PI3K/Akt/Nrf-2 signal pathways (Apoptosis, 2012)
- Inhibition of Activation of Nuclear Factor B Is Responsible for Inhibition of Inducible Nitric Oxide Synthase Expression by Higenamine, an Active Component of Aconite Root (Journal of Pharmacology and Experimental Therapeutics, 1999)
- Identification of higenamine in Radix Aconiti Lateralis Preparata as a beta2-adrenergic receptor agonist (Acta Pharmacologica Sinica, 2008)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNC(C2=CC(=C(C=C21)O)O)CC3=CC=C(C=C3)O
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InChIKeyWZRCQWQRFZITDX-UHFFFAOYSA-N
- Pubchem - Higenamine
- Wikipedia - higenamine
Higenamine (norcoclaurine) is a chemical compound found in a variety of plants including Nandina domestica (fruit), Aconitum carmichaelii (root), Asarum heterotropioides, Galium divaricatum (stem and vine), Annona squamosa, and Nelumbo nucifera (lotus seeds).
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Synthesis
dopamine
+
Reactant
(Alkylation of primary amines)
Phenol
+
Reactant
(Friedel-Crafts alkylation)
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