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(Q82960212)
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English
dioncophylline A
chemical compound
7-(4,5-Dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol
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Statements
instance of
type of chemical entity
0 references
subclass of
(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol
1 reference
based on heuristic
inferred from SMILES
Dioncophyllin A
1 reference
based on heuristic
inferred from SMILES
mass
377.199093724
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
(1R,3S)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
chemical formula
C₂₄H₂₇NO₃
0 references
canonical SMILES
OC1=C(C=CC2=C1C(NC(C)C2)C)C3=C4C=CC=C(OC)C4=C(OC)C=C3C
0 references
isomeric SMILES
C[C@@H]1CC2=C([C@H](N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O
0 references
found in taxon
Habropetalum dawei
1 reference
stated in
HPLC−CD On-Line Coupling in Combination with HPLC−NMR and HPLC−MS/MS for the Determination of the Full Absolute Stereostructure of New Metabolites in Plant Extracts
Ancistrocladus korupensis
1 reference
stated in
ancistrobrevine B, the first naphthylisoquinoline alkaloid with A 5,8′-coupling site, and related compounds from Ancistrocladus abbreviatus
Ancistrocladus barteri
1 reference
stated in
Activities of extracts and naphthylisoquinoline alkaloids from Triphyophyllum peltatum, Ancistrocladus abbreviatus and Ancistrocladus barteri against Plasmodium berghei (Anka strain) in vitro
Ancistrocladus letestui
1 reference
stated in
Dioncophylline A, the Principal Cytotoxin fromAncistrocladus letestui
Ancistrocladus tectorius
1 reference
stated in
Molluscicidal activity of naphthylisoquinoline alkaloids from Triphyophyllum and Ancistrocladus species
Dioncophyllum thollonii
1 reference
stated in
Dioncophylline E from Dioncophyllum thollonii, the first 7,3'-coupled dioncophyllaceous naphthylisoquinoline alkaloid
Triphyophyllum peltatum
3 references
stated in
Activity of extracts and naphthylisoquinoline alkaloids from Triphyophyllum peltatum, Ancistrocladus abbreviatus and A. Barteri against Plasmodium falciparum in vitro☆
stated in
Naphthylisoquinoline alkaloids against malaria: evaluation of the curative potentials of dioncophylline C and dioncopeltine A against Plasmodium berghei in vivo.
stated in
In vitro inhibition of liver forms of the rodent malaria parasite Plasmodium berghei by naphthylisoquinoline alkaloids--structure-activity relationships of dioncophyllines A and C and ancistrocladine
Identifiers
InChI
InChI=1S/C24H27NO3/c1-13-11-20(28-5)23-17(7-6-8-19(23)27-4)21(13)18-10-9-16-12-14(2)25-15(3)22(16)24(18)26/h6-11,14-15,25-26H,12H2,1-5H3/t14-,15-/m1/s1
0 references
InChIKey
MXIZZLBQRBAZEX-HUUCEWRRSA-N
0 references
CAS Registry Number
60142-17-8
0 references
PubChem CID
443773
1 reference
matched by identifier from
InChIKey
InChIKey
MXIZZLBQRBAZEX-HUUCEWRRSA-N
ChEBI ID
31504
mapping relation type
exact match
2 references
stated in
ChEBI release 2021-03-01
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C24H27NO3/c1-13-11-20(28-5)23-17(7-6-8-19(23)27-4)21(13)18-10-9-16-12-14(2)25-15(3)22(16)24(18)26/h6-11,14-15,25-26H,12H2,1-5H3/t14-,15-/m1/s1
66272
mapping relation type
exact match
1 reference
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C24H27NO3/c1-13-11-20(28-5)23-17(7-6-8-19(23)27-4)21(13)18-10-9-16-12-14(2)25-15(3)22(16)24(18)26/h6-11,14-15,25-26H,12H2,1-5H3/t14-,15-/m1/s1
UniChem compound ID
93069
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID20975569
1 reference
matched by identifier from
InChIKey
InChIKey
MXIZZLBQRBAZEX-HUUCEWRRSA-N
DSSTOX compound identifier
DTXCID401402968
0 references
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