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(Q105172754)
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English
methyl 2-(6'-ethenyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl)-3-methoxyprop-2-enoate
group of stereoisomers with the chemical formula C₂₂H₂₆N₂O₄
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Statements
instance of
group of stereoisomers
0 references
subclass of
mitraphylline-type alkaloid
1 reference
inferred from
mitraphylline-type alkaloid
mass
382.18925731199994
dalton
1 reference
based on heuristic
inferred from InChI
chemical formula
C₂₂H₂₆N₂O₄
0 references
canonical SMILES
C=CC1CN2CCC3(C(=O)Nc4ccccc43)C2CC1C(=COC)C(=O)OC
0 references
found in taxon
Uncaria attenuata
1 reference
stated in
Alkaloids from the leaves of Uncaria rhynchophylla and their inhibitory activity on NO production in lipopolysaccharide-activated microglia
Uncaria lanosa
1 reference
stated in
Alkaloids from the leaves of Uncaria rhynchophylla and their inhibitory activity on NO production in lipopolysaccharide-activated microglia
Uncaria longiflora
1 reference
stated in
Alkaloids from the leaves of Uncaria rhynchophylla and their inhibitory activity on NO production in lipopolysaccharide-activated microglia
Uncaria macrophylla
1 reference
stated in
Alkaloids from the leaves of Uncaria rhynchophylla and their inhibitory activity on NO production in lipopolysaccharide-activated microglia
Uncaria borneensis
1 reference
stated in
Alkaloids from the leaves of Uncaria rhynchophylla and their inhibitory activity on NO production in lipopolysaccharide-activated microglia
Mitragyna speciosa
2 references
stated in
A new 9-methoxyyohimbine-type indole alkaloid from Mitragyna africanus
stated in
Chemistry and pharmacology of analgesic indole alkaloids from the rubiaceous plant, Mitragyna speciosa
Mitragyna inermis
1 reference
stated in
The Mitragyna Species of Asia
Uncaria rhynchophylla
1 reference
stated in
Geissoschizine methyl ether, a corynanthean-type indole alkaloid from Uncaria rhynchophylla as a potential acetylcholinesterase inhibitor
Uncaria sinensis
1 reference
stated in
Alkaloids from the leaves of Uncaria rhynchophylla and their inhibitory activity on NO production in lipopolysaccharide-activated microglia
Mitragyna parvifolia
1 reference
stated in
The conversion of pseudo heteroyohimbine alkaloids to oxindoles. II. In vivo studies in Mitragyna parvifolia (Roxb.) Korth
Identifiers
InChI
InChI=1S/C22H26N2O4/c1-4-14-12-24-10-9-22(17-7-5-6-8-18(17)23-21(22)26)19(24)11-15(14)16(13-27-2)20(25)28-3/h4-8,13-15,19H,1,9-12H2,2-3H3,(H,23,26)
0 references
InChIKey
MUVGVMUWMAGNSY-UHFFFAOYSA-N
0 references
PubChem CID
73081505
2 references
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
MUVGVMUWMAGNSY-UHFFFAOYSA-N
UniChem compound ID
69514952
1 reference
stated in
UniChem
Human Metabolome Database ID
HMDB0250480
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
MUVGVMUWMAGNSY-UHFFFAOYSA-N
Probes And Drugs ID
PD086904
0 references
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