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(Q83000308)
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Gemin D
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
chemical compound
0 references
mass
634.080613864
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₂₇H₂₂O₁₈
0 references
canonical SMILES
O=CC(O)C(OC(=O)C1=CC(O)=C(O)C(O)=C1)C2OC(=O)C3=CC(O)=C(O)C(O)=C3C=4C(O)=C(O)C(O)=CC4C(=O)OCC2O
0 references
found in taxon
Woodfordia fruticosa
1 reference
stated in
Woodfordin C, a macro-ring hydrolyzable tannin dimer with antitumor activity, and accompanying dimers from Woodfordia fruticosa flowers
Schima wallichii
1 reference
stated in
Tannins and Related Polyphenols of Theaceous Plants. IV. Monomeric and Dimeric Hydrolyzable Tannins Having a Dilactonized Valoneoyl Group from Schima wallichii KORTH.
Camellia japonica
3 references
stated in
Tannins of theaceous plants. III. Camelliatannins A and B, two new complex tannins from Camellia japonica L.
stated in
Gemins D, E and F, ellagitannins from Geum japonicum
stated in
Tannins of theaceous plants. II. Camelliins A and B, two new dimeric hydrolyzable tannins from flower buds of Camellia japonica L. and Camellia sasanqua Thunb.
Reaumuria hirtella
1 reference
stated in
Tannins of Tamaricaceous Plants. II. New Monomeric and Dimeric Hydrolyzable Tannins from Reaumuria hirtella and Tamarix pakistanica.
Eucalyptus alba
1 reference
stated in
Eucalbanins A,B and C, Monomeric and Dimeric Hydrolyzable Tannins from Eucalyptus alba REINW.
Alnus japonica
1 reference
stated in
Dimeric ellagitannins from Alnus japonica
Loropetalum chinense
1 reference
stated in
Hydrolysable tannins from Loropetalum chinense
clove
2 references
stated in
Tannins and Related Compounds. CXXIII. Chromone, Acetophenone and Phenylpropanoid Glycosides and Their Galloyl and /or Hexahydroxydiphenoyl Esters from the Leaves of Syzygium aromaticum MERR. et PERRY.
stated in
Syzyginins A and B, two ellagitannins from Syzygium aromaticum
Tamarix aphylla
1 reference
stated in
Ellagitannins, gallotannins, and gallo-ellagitannins from the galls of Tamarix aphylla.
Balanophora japonica
1 reference
stated in
Caffeoyl, coumaroyl, galloyl, and hexahydroxydiphenoyl glucoses from Balanophora japonica.
Camellia sasanqua
1 reference
stated in
Tannins of theaceous plants. II. Camelliins A and B, two new dimeric hydrolyzable tannins from flower buds of Camellia japonica L. and Camellia sasanqua Thunb.
Camptotheca acuminata
1 reference
stated in
Camptothins A and B, new dimeric hydrolyzable tannins from Camptotheca acuminata DECNE.
Castanea mollissima
1 reference
stated in
Hydrolysable tannins and related compounds from Castanea mollissima
Coriaria japonica
1 reference
stated in
Tannins of Coriaria japonica A. Gray. II Coriariins C, D, E and F, new dimeric and monomeric hydrolyzable tannins.
Cornus controversa
1 reference
stated in
Phenolic compounds from the leaves of Cornus controversa
Geum japonicum
1 reference
stated in
Gemins D, E and F, ellagitannins from Geum japonicum
Oenothera erythrosepala
1 reference
stated in
Oenothein B, a dimeric, hydrolysable tannin with macrocyclic structure, and accompanying tannins from Oenothera erythrosepala
Geum macrophyllum
1 reference
stated in
Gemins D, E and F, ellagitannins from Geum japonicum
Camellia oleifera
2 references
stated in
Tannins of theaceous plants. II. Camelliins A and B, two new dimeric hydrolyzable tannins from flower buds of Camellia japonica L. and Camellia sasanqua Thunb.
stated in
A dimeric hydrolysable tannin from Camellia oleifera.
Oenothera glazioviana
1 reference
stated in
Oenothein B, a dimeric, hydrolysable tannin with macrocyclic structure, and accompanying tannins from Oenothera erythrosepala
Identifiers
InChI
InChI=1S/C27H22O18/c28-5-14(33)23(44-25(40)7-1-10(29)18(35)11(30)2-7)24-15(34)6-43-26(41)8-3-12(31)19(36)21(38)16(8)17-9(27(42)45-24)4-13(32)20(37)22(17)39/h1-5,14-15,23-24,29-39H,6H2
0 references
InChIKey
XKVYZLLWKHGKMT-UHFFFAOYSA-N
0 references
CAS Registry Number
84744-46-7
0 references
PubChem CID
471119
1 reference
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
UniChem compound ID
63305501
1 reference
stated in
UniChem
DSSTox substance ID
DTXSID701005046
0 references
DSSTOX compound identifier
DTXCID001431935
0 references
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