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(Q104403243)
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Chalcomoracin
group of stereoisomers with the chemical formula C₃₉H₃₆O₉
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Statements
instance of
group of stereoisomers
0 references
subclass of
biogenic benzofuran
1 reference
inferred from
biogenic benzofuran
mass
648.235932732
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₃₉H₃₆O₉
0 references
canonical SMILES
O=C(C1=CC=C(O)C(=C1O)CC=C(C)C)C2C(C=C(C)CC2C3=CC=C(O)C=C3O)C4=C(O)C=C(C=C4O)C=5OC=6C=C(O)C=CC6C5
0 references
found in taxon
Sorocea guilleminiana
2 references
stated in
Prenylated flavanones from Sorocea ilicifolia
stated in
A new phenolic glycoside from Sorocea ilicifolia stem bark
Morus bombycis
1 reference
stated in
Absolute Configuration of Natural Diels-Alder Type Adducts from the Morus Root Bark
Morus australis
1 reference
stated in
Absolute Configuration of Natural Diels-Alder Type Adducts from the Morus Root Bark
Morus alba
10 references
stated in
UV-B induced changes in the secondary metabolites of Morus alba L. leaves
stated in
Dynamic participation of primary metabolites in the biosynthesis of chalcomoracin and?-sitosterol inMorus alba cell cultures
stated in
Biosynthesis of optically active Diels–Alder type adducts revealed by an aberrant metabolism of O-methylated precursors in Morus alba cell cultures
stated in
Biosynthesis of chalcomoracin and kuwanon J, the Diels-Alder type adducts, in Morus alba L. cell cultures.
stated in
Dual p-Coumaroyl CoA Biosynthesis in Morus alba Cell Cultures
stated in
Late Stage of Biosynthesis of Intermolecular Diels-Alder Type Adducts in Morus alba L. Cell Cultures
stated in
Parallel Contribution of L-Phenylalanine and L-Tyrosine to the Biosynthesis of Prenylchalcones in Morus alba Cell Cultures
stated in
A Chimeric Hemiterpene Biosynthesis in Morus alba Cell Cultures
stated in
Mulberry moracins: scavengers of UV stress-generated free radicals
stated in
A chimeric hemiterpene biosynthesis inMorus alba cell cultures
Sorocea hilarii
2 references
stated in
A new phenolic glycoside from Sorocea ilicifolia stem bark
stated in
Prenylated flavanones from Sorocea ilicifolia
Morus indica
1 reference
stated in
Absolute Configuration of Natural Diels-Alder Type Adducts from the Morus Root Bark
Sorocea bonplandii
2 references
stated in
Prenylated flavanones from Sorocea ilicifolia
stated in
A new phenolic glycoside from Sorocea ilicifolia stem bark
Identifiers
InChI
InChI=1S/C39H36O9/c1-19(2)4-8-26-30(42)11-10-27(38(26)46)39(47)36-28(25-9-7-23(40)17-31(25)43)12-20(3)13-29(36)37-32(44)14-22(15-33(37)45)34-16-21-5-6-24(41)18-35(21)48-34/h4-7,9-11,13-18,28-29,36,40-46H,8,12H2,1-3H3
0 references
InChIKey
SEHVRKPXIDOTRX-UHFFFAOYSA-N
0 references
PubChem CID
434768
2 references
stated in
PubChem
retrieved
26 December 2021
inferred from
InChIKey
matched by identifier from
InChIKey
InChIKey
SEHVRKPXIDOTRX-UHFFFAOYSA-N
ChEBI ID
178143
mapping relation type
exact match
2 references
stated in
ChEBI release 2022-06-13
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C39H36O9/c1-19(2)4-8-26-30(42)11-10-27(38(26)46)39(47)36-28(25-9-7-23(40)17-31(25)43)12-20(3)13-29(36)37-32(44)14-22(15-33(37)45)34-16-21-5-6-24(41)18-35(21)48-34/h4-7,9-11,13-18,28-29,36,40-46H,8,12H2,1-3H3
UniChem compound ID
32016982
1 reference
stated in
UniChem
MassBank accession ID
MSBNK-Fac_Eng_Univ_Tokyo-JP000159
0 references
MSBNK-Fac_Eng_Univ_Tokyo-JP000160
0 references
MSBNK-Fac_Eng_Univ_Tokyo-JP000161
0 references
Human Metabolome Database ID
HMDB0030069
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
SEHVRKPXIDOTRX-UHFFFAOYSA-N
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