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Fórmula empírica (notación de Hill):
C17H19NO3
Número CAS:
Peso molecular:
285.34
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-348-0
Beilstein/REAXYS Number:
90741
MDL number:
Assay:
≥97%
Form:
crystalline, powder, crystals or chunks, solid
Servicio técnico
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Permítanos ayudarleassay
≥97%
form
crystalline, powder, crystals or chunks, solid
mp
131-135 °C (lit.)
SMILES string
O=C(\C=C\C=C\c1ccc2OCOc2c1)N3CCCCC3
InChI
1S/C17H19NO3/c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15/h2-3,6-9,12H,1,4-5,10-11,13H2/b6-2+,7-3+
InChI key
MXXWOMGUGJBKIW-YPCIICBESA-N
Gene Information
human ... CYP3A4(1576)
Application
Reactant for synthesis of:
- Dimeric amide alkaloids
- Piperoyl-amino acid conjugates used for antileishmanial activity
- Piperine derived amides with TRPV1 activity
- Piperine analogues as S. aureus NorA efflux pump inhibitors
- Bioactive conjugates of curcumin with antimicrobial and antiproliferative properties
- Piperine derivatives for use as trypanocidal agents
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2
Clase de almacenamiento
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Piperine is the main active component of Piper longum L., which is also the main component of anti-sciatica Mongolian medicine Naru Sanwei pill. It has many pharmacological activities such as anti-inflammatory and immune regulation. This paper aims to preliminarily explore
V. R. S. Rao, et al.,
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Welisson da Silva Ferreira et al.
Bioorganic & medicinal chemistry, 16(6), 2984-2991 (2008-01-30)
We herein describe the synthesis and characterization of nine new 1,3,4-thiadiazolium-2-phenylamine chlorides derived from natural piperine. We evaluate their toxic effects against the different evolutive forms of Trypanosoma cruzi, and the host cell (murine macrophages). The results obtained show that

