PAPRAZINE
Compound with spectra: 8 NMR, and 3 MS (GC)
| SpectraBase Compound ID | 3QnMBIqAwJY |
|---|---|
| InChI | InChI=1S/C17H17NO3/c19-15-6-1-13(2-7-15)5-10-17(21)18-12-11-14-3-8-16(20)9-4-14/h1-10,19-20H,11-12H2,(H,18,21)/b10-5+ |
| InChIKey | RXGUTQNKCXHALN-BJMVGYQFSA-N |
| Mol Weight | 283.33 g/mol |
| Molecular Formula | C17H17NO3 |
| Exact Mass | 283.120843 g/mol |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | PYRIDINE-D5 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
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| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C5D5N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | T-68-3780-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | CD-589-0-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | QA-48-813-5 |
- N-TRANS-COUMAROYL-TYRAMINE
- N-(TRANS)-PARA-COUMAROYL-TYRAMINE
- TRANS-N-COUMAROYLTYRAMINE
- N-PARA-COUMAROYLTYRAMINE
- 2-Propenamide, 3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-
- N-p-coumaroyltyramine
PARA-COUMAROYL-BETA-PHENETHYLAMINE
Cinnamamide, N-(p-hydroxyphenethyl)-
(2E)-3-(4-bromophenyl)-N-(2-phenylethyl)-2-propenamide
(Z)-N-[2-(4-Hydroxyphenyl)ethyl]-3-methyldodec-2-enamide
PARA-COUMAROYL-D-ALANINE
P-COUMAROY-D-ALANINE
(2E)-3-(4-isopropylphenyl)-N-(3-{[(2E)-3-(4-isopropylphenyl)-2-propenoyl]amino}propyl)-2-propenamide
N-(3-hydroxy-2-oxopropyl)-(E)-3-(4-methoxyphenyl)acrylamide
N-(2,3-dihydroxypropyl)-(E)-3-(4-methoxyphenyl)acrylamide
| Title | Journal or Book | Year |
|---|---|---|
| Constituintes químicos de Solanum buddleifolium Sendtn | Química Nova | 2013 |
| Phenolic Compounds and Antioxidant Activities of Liriope muscari | Molecules | 2012 |
| Occurrence, biological activities and 13C NMR data of amides from Piper (Piperaceae) | Química Nova | 2012 |
| Bioactive Phenolic Amides from Celtis africana | Molecules | 2012 |
| Alkaloids of Fumaria indica | Phytochemistry | 1992 |
| Additional Bioactive Compounds and Trilobacin, a Novel Highly Cytotoxic Acetogenin, from the Bark of Asimina triloba | Journal of Natural Products | 1992 |
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