Page last updated: 2024-12-07

sinapine

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

Description

sinapine: black mustard seeds, seeds of Brassica nigra; RN given refers to parent; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

sinapine : An acylcholine in which the acyl group specified is sinapoyl. [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]

FloraRankFlora DefinitionFamilyFamily Definition
BrassicagenusA plant genus of the family Cruciferae. It contains many species and cultivars used as food including cabbage, cauliflower, broccoli, Brussel sprouts, kale, collard greens, MUSTARD PLANT; (B. alba, B. junica, and B. nigra), turnips (BRASSICA NAPUS) and rapeseed (BRASSICA RAPA).[MeSH]BrassicaceaeA plant family of the order Capparales, subclass Dilleniidae, class Magnoliopsida. They are mostly herbaceous plants with peppery-flavored leaves, due to gluconapin (GLUCOSINOLATES) and its hydrolysis product butenylisotrhiocyanate. The family includes many plants of economic importance that have been extensively altered and domesticated by humans. Flowers have 4 petals. Podlike fruits contain a number of seeds. Cress is a general term used for many in the Brassicacea family. Rockcress is usually ARABIS; Bittercress is usually CARDAMINE; Yellowcress is usually RORIPPA; Pennycress is usually THLASPI; Watercress refers to NASTURTIUM; or RORIPPA or TROPAEOLUM; Gardencress refers to LEPIDIUM; Indiancress refers to TROPAEOLUM.[MeSH]

Cross-References

ID SourceID
PubMed CID5280385
CHEBI ID16353
MeSH IDM0047385

Synonyms (42)

Synonym
CHEBI:16353
o-sinapoylcholine ,
2-[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]-n,n,n-trimethylethanaminium
2-(4-hydroxy-3,5-dimethoxycinnamoyloxy)-n,n,n-trimethylethanaminium
MEGXP0_001763
C00933
18696-26-9
sinapoylcholine
sinapine
ACON1_000255
BRD-K21295184-064-01-0
2-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]ethyl-trimethylazanium
2-[(e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxyethyl-trimethylazanium
S3235
2-((3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propenyl)oxy)-n,n,n-trimethylethanaminium
4-hydroxy-3,5-dimethoxycinnamate choline
ethanaminium, 2-((3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propenyl)oxy)-n,n,n-trimethyl-
sinapine thiocyanate
sinapine cation
sinapine [mi]
sinapin
ethanaminium, 2-(((2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propen-1-yl)oxy)-n,n,n-trimethyl-
2-((3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propen-1-yl)oxy)-n,n,n-trimethylethanaminium
trans-sinapoylcholine
trans-sinapine
ethanaminium, 2-((3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propen-1-yl)oxy)-n,n,n-trimethyl-
sinapine ion
choline, 4-hydroxy-3,5-dimethoxycinnamate (ester)
cinnamic acid, 4-hydroxy-3,5-dimethoxy-, choline ester
84123-22-8
09211A0HHL ,
AC-34366
Q-100224
unii-09211a0hhl
DTXSID10171957
choline 4-hydroxy-3,5-dimethoxycinnamate, 8ci
2-[[3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propenyl]oxy]-n,n,n- trimethylethanaminium, 9ci
2-((3-(4-hydroxy-3,5-dimethoxyphenyl)acryloyl)oxy)-n,n,n-trimethylethan-1-aminium
AKOS030626997
Q891772
CS-0032305
HY-N5077
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
photosynthetic electron-transport chain inhibitornull
antioxidantA substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role 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]

Drug Classes (1)

ClassDescription
acylcholineA choline ester formed from choline and a carboxylic acid.
[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]

Pathways (1)

PathwayProteinsCompounds
sinapate ester biosynthesis221

Research

Studies (59)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (10.17)18.7374
1990's3 (5.08)18.2507
2000's14 (23.73)29.6817
2010's24 (40.68)24.3611
2020's12 (20.34)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.67%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other59 (98.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]