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(Q72460180)
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Cyclomorusin
chemical compound
Cyclomulberrochromene
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Statements
instance of
type of chemical entity
0 references
subclass of
3,8C-substituted flavone
0 references
mass
418.141638424
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₂₅H₂₂O₆
0 references
canonical SMILES
O=C1C2=C(O)C=C3OC(C=CC3=C2OC=4C=5C=CC(O)=CC5OC(C=C(C)C)C14)(C)C
0 references
found in taxon
Sorocea bonplandii
1 reference
stated in
Three New Flavanone Derivatives from the Root Bark of Sorocea bonplandii Baillon
Artocarpus elasticus
1 reference
stated in
New prenylflavonoids from Artocarpus communis
Morus nigra
1 reference
stated in
Induction of Biologically Active Flavonoids in Cell Cultures of Morus nigra and Testing their Hypoglycemic Efficacy
Morus australis
1 reference
stated in
[Components of Root Bark of Morus australis.].
Morus indica
1 reference
stated in
[Components of Root Bark of Morus australis.].
breadfruit
3 references
stated in
Three New Prenylflavones from Artocarpus altilis
stated in
New prenylflavonoids from Artocarpus communis
stated in
Antiinflammatory flavonoids from Artocarpus heterophyllus and Artocarpus communis
Morus alba
7 references
stated in
Hypoglycemic effect of Egyptian Morus alba root bark extract: effect on diabetes and lipid peroxidation of streptozotocin-induced diabetic rats.
stated in
Studies on the constituents of the cultivated mulberry tree. I. Three new prenylflavones from the root bark of Morus alba L.
stated in
Isolation of cholinesterase-inhibiting flavonoids from Morus lhou
stated in
Inhibitory effects on mushroom tyrosinase by flavones from the stem barks of Morus lhou (S.) Koidz
stated in
Isoprenylated flavonoids from the root bark of Morus alba and their hepatoprotective and neuroprotective activities
stated in
Four analogues of artocarpin and cyclotocarpin from morus alba
stated in
Phenolic constituents of the cultivated mulberry tree (Morus alba L.).
Morus lhou
2 references
stated in
Isolation of cholinesterase-inhibiting flavonoids from Morus lhou
stated in
Inhibitory effects on mushroom tyrosinase by flavones from the stem barks of Morus lhou (S.) Koidz
Identifiers
InChI
InChI=1S/C25H22O6/c1-12(2)9-19-21-22(28)20-16(27)11-18-15(7-8-25(3,4)31-18)23(20)30-24(21)14-6-5-13(26)10-17(14)29-19/h5-11,19,26-27H,1-4H3
0 references
InChIKey
GDQXJMLXEYSICD-UHFFFAOYSA-N
0 references
CAS Registry Number
62596-34-3
1 reference
InChIKey
GDQXJMLXEYSICD-UHFFFAOYSA-N
stated in
CAS Common Chemistry
retrieved
8 April 2021
reference URL
https://commonchemistry.cas.org/detail?cas_rn=62596-34-3
PubChem CID
5481969
2 references
stated in
PubChem
retrieved
26 December 2021
inferred from
InChIKey
matched by identifier from
InChIKey
InChIKey
GDQXJMLXEYSICD-UHFFFAOYSA-N
ChEBI ID
132868
mapping relation type
exact match
2 references
stated in
ChEBI release 2021-03-01
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C25H22O6/c1-12(2)9-19-21-22(28)20-16(27)11-18-15(7-8-25(3,4)31-18)23(20)30-24(21)14-6-5-13(26)10-17(14)29-19/h5-11,19,26-27H,1-4H3
UniChem compound ID
1092661
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID30978167
1 reference
matched by identifier from
InChIKey
InChIKey
GDQXJMLXEYSICD-UHFFFAOYSA-N
DSSTOX compound identifier
DTXCID001405491
0 references
Human Metabolome Database ID
HMDB0030687
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
GDQXJMLXEYSICD-UHFFFAOYSA-N
LIPID MAPS ID
LMPK12110913
1 reference
stated in
LIPID MAPS
reference URL
http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download
retrieved
30 June 2018
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