| Weight | 285.343 g/mol |
|---|---|
| Formula | C17H19NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
piperine (7780-20-3, 94-62-2)
piperine, (Z,Z)-isomer · 1-piperoylpiperidine · piperine, (E,Z)-isomer
Score:
#3188 in Biology
,
#3988 in Chemistry
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- Influence of Piperine on the Pharmacokinetics of Curcumin in Animals and Human Volunteers (Planta Medica, 1998)
- Nanoparticle encapsulation improves oral bioavailability of curcumin by at least 9-fold when compared to curcumin administered with piperine as absorption enhancer. (European Journal of Pharmaceutical Sciences, 2009)
- Black Pepper and its Pungent Principle-Piperine: A Review of Diverse Physiological Effects (Critical Reviews in Food Science and Nutrition, 2007)
- Piperine, a Major Constituent of Black Pepper, Inhibits Human P-glycoprotein and CYP3A4 (Journal of Pharmacology and Experimental Therapeutics, 2002)
- Targeting breast stem cells with the cancer preventive compounds curcumin and piperine (Breast Cancer Research and Treatment, 2010)
- Immunomodulatory and antitumor activity of Piper longum Linn. and piperine (Journal of Ethnopharmacology, 2004)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - piperine, (Z,Z)-isomer
- 1-piperoylpiperidine
- piperine, (E,Z)-isomer
- (1-(5-(1,3)-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl)piperidine
- piperine, (E,E)-isomer
- piperine, (Z,E)-isomer
- ((1-5-(1,3)-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl)piperidine
-
SMILESC1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3
-
InChIKeyMXXWOMGUGJBKIW-UHFFFAOYSA-N
- Pubchem - piperine
- Wikipedia - piperine
Piperine, along with its isomer chavicine, is the alkaloid responsible for the pungency of black pepper and long pepper. It has been used in some forms of traditional medicine.
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Reactant
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piperine
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