| Weight | 394.471 g/mol |
|---|---|
| Formula | C23H26N2O4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
BRUCINE (357-57-3)
dimethoxystrychnine · 10,11-dimethoxystrychnine · bruzin
Score:
#525 in Biochemistry
,
#1916 in Chemistry
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- Analgesic and anti-inflammatory properties of brucine and brucine N-oxide extracted from seeds of Strychnos nux-vomica. (Journal of Ethnopharmacology, 2003)
- Subtype-Selective Positive Cooperative Interactions between Brucine Analogues and Acetylcholine at Muscarinic Receptors: Radioligand Binding Studies (Molecular Pharmacology, 1998)
- Brucine Method for the Determination of Nitrate in Ocean, Estuarine, and Fresh Waters. (Analytical Chemistry, 1964)
- Subtype-Selective Positive Cooperative Interactions Between Brucine Analogs and Acetylcholine at Muscarinic Receptors: Functional Studies (Molecular Pharmacology, 1999)
- Brucine-derived amino alcohol catalyzed asymmetric Henry reaction: an orthogonal enantioselectivity approach. (Organic Letters, 2009)
- Reversal of Enantioselectivity between the Copper(I) and Silver(I)Catalyzed 1,3Dipolar Cycloaddition Reactions Using a BrucineDerived Amino Alcohol Ligand (Angewandte Chemie, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H300: Fatal if swallowed
Danger Acute toxicity, oral - Category 1, 2 - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 - H412: Harmful to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 3 - dimethoxystrychnine
- 10,11-dimethoxystrychnine
- bruzin
-
SMILESCOC1=C(C=C2C(=C1)C34CCN5C3CC6C7C4N2C(=O)CC7OCC=C6C5)OC
-
InChIKeyRRKTZKIUPZVBMF-UHFFFAOYSA-N
- Pubchem - BRUCINE
- Wikipedia - brucine
Brucine, an alkaloid closely related to strychnine, is most commonly found in the Strychnos nux-vomica tree. Brucine poisoning is rare, since it is usually ingested with strychnine, and strychnine is more toxic than brucine. In synthetic chemistry, it can be used as a tool for stereospecific chemical syntheses.
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