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(Q104251609)
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English
n-cis-Feruloyltyramine
chemical compound
In more languages
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No label defined
No description defined
edit
Statements
instance of
type of chemical entity
0 references
subclass of
phenethylamine alkaloid
0 references
cinnamoylamide alkaloid
0 references
mass
313.131408088
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₈H₁₉NO₄
0 references
canonical SMILES
COc1cc(C=CC(=O)NCCc2ccc(O)cc2)ccc1O
0 references
isomeric SMILES
COc1cc(/C=C\C(=O)NCCc2ccc(O)cc2)ccc1O
1 reference
based on heuristic
inferred from InChI
found in taxon
Tinospora crispa
6 references
stated in
Chemistry and Biological Activities of the Genera Tinospora
stated in
Studies on the constituents of the stems of Tinospora tuberculata Beumee. I. N-trans- and N-cis-feruloyl tyramine, and a new phenolic glucoside, tinotuberide.
stated in
Antioxidant and lipophilic constituents of Tinospora crispa
stated in
Studies on the constituents of the stems of Tinospora tuberculata Beumee. I. N-trans- and N-cis-feruloyl tyramine, and a new phenolic glucoside, tinotuberide.
stated in
Antioxidant and lipophilic constituents of Tinospora crispa
stated in
Studies on the constituents of the stems of Tinospora tuberculata Beumee. I. N-trans- and N-cis-feruloyl tyramine, and a new phenolic glucoside, tinotuberide.
Zanthoxylum beecheyanum
2 references
stated in
Chemical and Antiplatelet Constituents from the Stem ofZanthoxylum Beecheyanum
stated in
Chemical and Antiplatelet Constituents from the Stem ofZanthoxylum Beecheyanum
Annona cherimola
3 references
stated in
Amides from stems of annona cherimola
stated in
Amides from stems of annona cherimola
stated in
Amides from stems of annona cherimola
Aristolochia heterophylla
2 references
stated in
The constituents of the root and stem of Aristolochia heterophylla Hemsl
stated in
The constituents of the root and stem of Aristolochia heterophylla Hemsl
Aristolochia kaempferi
2 references
stated in
The constituents of the root and stem of Aristolochia heterophylla Hemsl
stated in
The constituents of the root and stem of Aristolochia heterophylla Hemsl
Balanites aegyptiaca
3 references
stated in
Alkaloids from Balanites aegyptiaca
stated in
Alkaloids from Balanites aegyptiaca
stated in
Alkaloids from Balanites aegyptiaca
Balanites aegyptiacus
3 references
stated in
Alkaloids from Balanites aegyptiaca
stated in
Alkaloids from Balanites aegyptiaca
stated in
Alkaloids from Balanites aegyptiaca
Hibiscus taiwanensis
3 references
stated in
Constituents from the stems of Hibiscus taiwanensis.
stated in
Constituents from the Stems of Hibiscus taiwanensis.
stated in
Constituents from the stems of Hibiscus taiwanensis.
Lindera glauca
3 references
stated in
Alkaloids fromLindera Glauca
stated in
Terpenes from Lindera glauca
stated in
Alkaloids fromLindera Glauca
Peperomia heyneana
3 references
stated in
Bioactive lignans from Peperomia duclouxii
stated in
Bioactive lignans from Peperomia duclouxii
stated in
Bioactive lignans from Peperomia duclouxii
Peperomia leptostachya
3 references
stated in
Chemical and cytotoxic constituents from Peperomia sui
stated in
Chemical and cytotoxic constituents from Peperomia sui
stated in
Chemical and cytotoxic constituents from Peperomia sui
Aristolochia elegans
2 references
stated in
The alkaloids and other constituents from the root and stem of Aristolochia elegans
stated in
The alkaloids and other constituents from the root and stem of Aristolochia elegans
Aristolochia gehrtii
1 reference
stated in
Alkamides and phenethyl derivatives from Aristolochia gehrtii
Aristolochia kankauensis
1 reference
stated in
Aristolochic acids, aristolactam alkaloids and amides from Aristolochia kankauensis
Aristolochia zollingeriana
1 reference
stated in
Aristolochic acids, aristolactam alkaloids and amides from Aristolochia kankauensis
Casearia membranacea
1 reference
stated in
A cytotoxic butenolide, two new dolabellane diterpenoids, a chroman and a benzoquinol derivative formosan Casearia membranacea
Deprea subtriflora
2 references
stated in
Isolation and characterization of miscellaneous secondary metabolites of Deprea subtriflora.
stated in
Isolation and characterization of miscellaneous secondary metabolites of Deprea subtriflora.
Hibiscus syriacus
2 references
stated in
An antioxidant lignan and other constituents from the root bark of Hibiscus syriacus
stated in
An antioxidant lignan and other constituents from the root bark of Hibiscus syriacus
Piper argyrophyllum
1 reference
stated in
Neolignans and alkaloids from Piper argyrophylum
Solanum aculeatissimum
1 reference
stated in
Formation of hydroxycinnamoylamides and α-hydroxyacetovanillone in cell cultures of Solanum khasianum
Tetradium glabrifolium
2 references
stated in
The heartwood constituents of Tetradium glabrifolium
stated in
The heartwood constituents of Tetradium glabrifolium
Nelumbo nucifera
1 reference
stated in
Chemical constituents from Nelumbo nucifera leaves and their anti-obesity effects
Hornstedtia reticulata
1 reference
stated in
Chemical constituents from the roots of Cinnamomum reticulatum
Antidesma montanum var. montanum
1 reference
stated in
Chemical Constituents from the Root ofAntidesma Pentandrumvar.Barbatum
Antidesma pentandrum var. barbatum
1 reference
stated in
Chemical Constituents from the Root ofAntidesma Pentandrumvar.Barbatum
Capsicum annuum var. annuum
1 reference
stated in
A New Lignan Amide, Grossamide, from Bell Pepper (Capsicum annuumvar.grossurri)
Cinnamomum reticulatum
1 reference
stated in
Chemical constituents from the roots of Cinnamomum reticulatum
Fibraurea tinctoria
1 reference
stated in
Anti-inflammatory activities of furanoditerpenoids and other constituents from Fibraurea tinctoria
Talipariti tiliaceum
1 reference
stated in
A new cytotoxic amide from the stem wood of Hibiscus tiliaceus
Illigera luzonensis
1 reference
stated in
Aporphine alkaloids and cytotoxic lignans from the roots of Illigera luzonensis
Magnolia compressa
1 reference
stated in
Chemical constituents from the leaves of Michelia compressa var. formosana
Piper caninum
1 reference
stated in
Phenolic acid amides: a new type of DNA strand scission agent from Piper caninum
Polyalthia longifolia
1 reference
stated in
Anti-inflammatory and cytotoxic diterpenes from formosan Polyalthia longifolia var. pendula.
Schizanthus litoralis
1 reference
stated in
Tropane alkaloids from Schizanthus litoralis
Synsepalum dulcificum
1 reference
stated in
Chemical constituents from the roots of Synsepalum dulcificum
Triclisia sacleuxii
1 reference
stated in
Alkaloids and amides from Triclisia sacleuxii
Capsicum annuum
2 references
stated in
A New Lignan Amide, Grossamide, from Bell Pepper (Capsicum annuumvar.grossurri)
stated in
New sesquiterpenes from Capsicum annuum
Acorus gramineus
1 reference
stated in
Phenolic constituents from the rhizomes of Acorus gramineus and their biological evaluation on antitumor and anti-inflammatory activities
potato
1 reference
stated in
Characterization of cross-linked hydroxycinnamic acid amides isolated from potato common scab lesions
Aristolochia littoralis
1 reference
stated in
The alkaloids and other constituents from the root and stem of Aristolochia elegans
Portulaca oleracea
1 reference
stated in
Homoisoflavonoids from the medicinal plant Portulaca oleracea
Peperomia humilis
1 reference
stated in
Chemical and cytotoxic constituents from Peperomia sui
Piper lanatum
1 reference
stated in
Phenolic acid amides: a new type of DNA strand scission agent from Piper caninum
Identifiers
InChI
InChI=1S/C18H19NO4/c1-23-17-12-14(4-8-16(17)21)5-9-18(22)19-11-10-13-2-6-15(20)7-3-13/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)/b9-5-
0 references
InChIKey
NPNNKDMSXVRADT-UITAMQMPSA-N
0 references
CAS Registry Number
80510-09-4
1 reference
stated in
CAS (formerly Chemical Abstracts Service)
retrieved
25 January 2022
PubChem CID
6440659
2 references
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
NPNNKDMSXVRADT-UITAMQMPSA-N
ChEBI ID
185384
mapping relation type
exact match
2 references
stated in
ChEBI release 2022-06-13
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C18H19NO4/c1-23-17-12-14(4-8-16(17)21)5-9-18(22)19-11-10-13-2-6-15(20)7-3-13/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)/b9-5-
SureChEMBL ID
SCHEMBL17693085
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
NPNNKDMSXVRADT-UITAMQMPSA-N
UniChem compound ID
98148
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID101313914
1 reference
matched by identifier from
InChIKey
InChIKey
NPNNKDMSXVRADT-UITAMQMPSA-N
Human Metabolome Database ID
HMDB0036381
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
NPNNKDMSXVRADT-UITAMQMPSA-N
KNApSAcK ID
C00025324
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
NPNNKDMSXVRADT-UITAMQMPSA-N
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