Compounds > feruloylputrescine
Page last updated: 2024-12-10

feruloylputrescine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

feruloylputrescine: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5281796
CHEBI ID9299
MeSH IDM0179256

Synonyms (31)

Synonym
nsc602818
nsc-602818
cinnamamide, n-(4-aminobutyl)-4-hydroxy-3-methoxy-
2-propenamide, n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)-
subaphylline
n-feruloylputrescine
4-oxy-3-methoxycinnamylputrescine
n-(4-aminobutyl)-4-hydroxy-3-methoxycinnamamide
feruloylputrescine
501-13-3
(e)-n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide
n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide
CHEBI:9299
trans-n-feruloylputrescine
(2e)-n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)-2-propenamide #
SFUVCMKSYKHYLD-FNORWQNLSA-N
(e)-n-(4-aminobutyl)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enamide
2-propenamide, n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)-, (2e)-
J3HM10B75D ,
n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)-2-propenamide
Q27108351
(e)-n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide
unii-j3hm10b75d
91000-11-2
feruloyl putrescine (isomer of 1178)
DTXSID90904144
A871657
AS-75663
CS-0367848
(2e)-n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide
2-propenamide, n-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)-, (e)-
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
hydroxycinnamic acidAny member of the class of cinnamic acids carrying one or more hydroxy substituents.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (28.57)18.2507
2000's1 (14.29)29.6817
2010's2 (28.57)24.3611
2020's2 (28.57)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 37.78

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index37.78 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index5.03 (4.65)
Search Engine Demand Index39.50 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (37.78)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
agmatine
Agmatine: Decarboxylated arginine, isolated from several plant and animal sources, e.g., pollen, ergot, herring sperm, octopus muscle.		2.2510guanidines;
primary amino compound		Escherichia coli metabolite;
mouse metabolite
putrescine
[no description available]		3.4370alkane-alpha,omega-diamineantioxidant;
fundamental metabolite
spermidine
[no description available]		2.2510polyazaalkane;
triamine		autophagy inducer;
fundamental metabolite;
geroprotector
eflornithine
Eflornithine: An inhibitor of ORNITHINE DECARBOXYLASE, the rate limiting enzyme of the polyamine biosynthetic pathway.. eflornithine : A fluoroamino acid that is ornithine substituted by a difluoromethyl group at position 2.		1.9810alpha-amino acid;
fluoroamino acid		trypanocidal drug
tyramine
[no description available]		2.2510monoamine molecular messenger;
primary amino compound;
tyramines		EC 3.1.1.8 (cholinesterase) inhibitor;
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
neurotransmitter
isoleucine
Isoleucine: An essential branched-chain aliphatic amino acid found in many proteins. It is an isomer of LEUCINE. It is important in hemoglobin synthesis and regulation of blood sugar and energy levels.. isoleucine : A 2-amino-3-methylpentanoic acid having either (2R,3R)- or (2S,3S)-configuration.. L-isoleucine : The L-enantiomer of isoleucine.		2.2510aspartate family amino acid;
isoleucine;
L-alpha-amino acid zwitterion;
L-alpha-amino acid;
proteinogenic amino acid		algal metabolite;
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
plant metabolite;
Saccharomyces cerevisiae metabolite
ethylene
Plastipore: high density polyethylene sponge biocompatible material; used as posts in dental bridges		2.2510alkene;
gas molecular entity		plant hormone;
refrigerant
cyclopentane
Cyclopentanes: A group of alicyclic hydrocarbons with the general formula R-C5H9.. cyclopentanes : Cyclopentane and its derivatives formed by substitution.		2.2510cycloalkane;
cyclopentanes;
volatile organic compound		non-polar solvent
ferulic acid
ferulate : A monocarboxylic acid anion obtained by the deprotonation of the carboxy group of ferulic acid.		2.0110ferulic acidsanti-inflammatory agent;
antioxidant;
apoptosis inhibitor;
cardioprotective agent;
MALDI matrix material;
plant metabolite
feruloyltyramine
feruloyltyramine: structure given in first source; isolated from Cannabis sativa seeds, roots, leaves, and resin; induces hypothermia and motor incoordination in mice; moupinamide is (E)-isomer		2.2510tyraminesmetabolite
jasmonic acid
jasmonic acid: a derivative of alpha-linolenic acid that has a role in plant response to herbivory analogous to the role of prostanoids in inflammation in mammals;. jasmonic acid : An oxo monocarboxylic acid that is (3-oxocyclopentyl)acetic acid substituted by a (2Z)-pent-2-en-1-yl group at position 2 of the cyclopentane ring.		2.2510oxo monocarboxylic acidjasmonates;
plant metabolite
ConditionIndicatedRelationship StrengthStudiesTrials