| Weight | 287.322 g/mol |
|---|---|
| Formula | C18H13N3O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 0 |
Rutaecarpine (84-26-4)
Score:
#2155 in Biochemistry
,
#5577 in Chemistry
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- Sigma-Aldrich - Rutaecarpine109.50 - 438.50 USD
- Fisher Scientific - Search for Rutaecarpine
- TCI - Rutaecarpine130.00 - 453.00 USD
- A new class of COX-2 inhibitor, rutaecarpine from Evodia rutaecarpa. (Inflammation Research, 1999)
- Novel inhibitors of acetyl- and butyrylcholinesterase derived from the alkaloids dehydroevodiamine and rutaecarpine. (European Journal of Medicinal Chemistry, 2005)
- Studies of rutaecarpine and related quinazolinocarboline alkaloids (Journal of Organic Chemistry, 1985)
- Progress in the Studies on Rutaecarpine (Molecules, 2008)
- The Alkaloid Rutaecarpine Is a Selective Inhibitor of Cytochrome P450 1A in Mouse and Human Liver Microsomes (Drug Metabolism and Disposition, 2002)
- Vasorelaxing Action of Rutaecarpine: Effects of Rutaecarpine on Calcium Channel Activities in Vascular Endothelial and Smooth Muscle Cells (Journal of Pharmacology and Experimental Therapeutics, 1999)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4
-
InChIKeyACVGWSKVRYFWRP-UHFFFAOYSA-N
- Pubchem - Rutaecarpine
- Wikipedia - rutecarpine
Rutecarpine or rutaecarpine is a COX-2 inhibitor isolated from Euodia ruticarpa.
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