feruloyl putrescine
2-propenamide, N-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)- (9CI)
Identification
| Name | feruloyl putrescine |
| IUPAC | (E)-N-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide |
| CAS Number | 501-13-3 |
| FDA UNII | Search |
| Molecular Formula | C14 H20 N2 O3 |
| Molecular Weight | 264.32500000 |
| MDL Number | MFCD01736565 |
| Nikkaji Number | J11.793E |
| XlogP3 | 1.00 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 511.50 °C. @ 760.00 mm Hg (est) |
| Flash Point | 506.00 °F. TCC ( 263.20 °C. ) (est) |
| logP (o/w) | 0.620 (est) |
| Soluble in | water, 5647 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | intraperitoneal-mouse LD50 225 mg/kg |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements', 'VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION\nBEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for feruloyl putrescine usage levels up to | not for fragrance use. |
| Recommendation for feruloyl putrescine flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
(E)-N-(4-
aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide
N-(4-
aminobutyl)-4-hydroxy-3-methoxycinnamamide
cinnamamide, N-(4-aminobutyl)-4-hydroxy-3-methoxy-
cinnamamide, N-(4-aminobutyl)-4-hydroxy-3-methoxy-
feruloylputrescine
N-
feruloylputrescine
4-oxy-3-
methoxycinnamyl putrescine
4-oxy-3-
methoxycinnamylputrescine
2-
propenamide, N-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)- (9CI)
subaphyllin
PubMed:
Studies on the alkaloids of the bark of Magnolia officinalis: isolation and on-line analysis by HPLC-ESI-MS(n).
PubMed:
Accumulation of hydroxycinnamic acid amides induced by pathogen infection and identification of agmatine coumaroyltransferase in Arabidopsis thaliana.
PubMed:
Antioxidant and antimelanogenic activities of polyamine conjugates from corn bran and related hydroxycinnamic acids.
PubMed:
Metabolic flux analysis of the phenylpropanoid pathway in elicitor-treated potato tuber tissue.
PubMed:
Inhibition of aflatoxin biosynthesis in Aspergillus flavus by diferuloylputrescine and p-coumaroylferuloylputrescine.
PubMed:
Inhibitory activity of corn-derived bisamide compounds against alpha-glucosidase.
PubMed:
Diferuloylputrescine and p-coumaroyl-feruloylputrescine, abundant polyamine conjugates in lipid extracts of maize kernels.
PubMed:
Changing root system architecture through inhibition of putrescine and feruloyl putrescine accumulation.
PubMed:
Effects of pollen-extract components, diamines and derivatives of feruloylputrescine on isolated bladder and urethral smooth muscles of mice.
PubMed:
Feruloylputrescine and Caffeoylputrescine Are Not Involved in Growth and Floral Bud Formation of Stem Explants from Nicotiana tabacum L. var Xanthi nc.
PubMed:
Feruloylputrescine: isolation and identification from citrus leaves and fruit.
PubMed:
[Structure of subaphyllin alkaloid].