ITCMDBv1
IngredientID 8216

7alpha-l-rhamnosyl-6-methoxyluteolin

C22H22O11

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Relationship Network

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Herb: 1Ingredient: 1Links: 1
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Record Fields

Scalar fields from the final ingredient record.

Ingredient Id
8216
Core Entity Id
12305
Source Entity Count
1
Preferred Name
7alpha-l-rhamnosyl-6-methoxyluteolin
Name En
Pubchem Id
442617
Smiles Canonical
CC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)OC)O)O)O
Molecular Formula
C22H22O11
Molecular Weight
462.4070
Inchikey
UXCXDWDJBSJZOU-CKPDRDNLSA-N
Inchi
InChI=1S/C22H22O11/c1-8-17(26)19(28)20(29)22(31-8)33-15-7-14-16(18(27)21(15)30-2)12(25)6-13(32-14)9-3-4-10(23)11(24)5-9/h3-8,17,19-20,22-24,26-29H,1-2H3/t8-,17-,19+,20+,22-/m0/s1
Isomeric Smiles
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)OC)O)O)O
Cas Id
Ob Score
Mol Logp
0.7917
Num H Donors
6
Num H Acceptors
11
Num Rotatable Bonds
4
Drug Likeness
0.3020
Polar Surface Area
Molecular Volume
Alogp

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
7alpha-l-rhamnosyl-6-methoxyluteolin
Role
preferred
Source
HERB_v2
Preferred
Yes
Name
7alpha-l-rhamnosyl-6-methoxyluteolin
Role
preferred
Source
itcmdb_public
Preferred
Yes
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-chromen-7-yl 6-deoxy-alpha-L-mannopyranoside
Role
alias
Source
HERB_v2
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-chromen-7-yl 6-deoxy-alpha-L-mannopyranoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
Role
alias
Source
itcmdb_public
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
Role
alias
Source
HERB_v2
Preferred
No
Name
35682-55-4
Role
alias
Source
HERB_v2
Preferred
No
Name
35682-55-4
Role
alias
Source
itcmdb_public
Preferred
No
Name
6-Methoxyluteolin 7-rhamnoside
Role
alias
Source
HERB_v2
Preferred
No
Name
6-Methoxyluteolin 7-rhamnoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
6-methoxyluteolin 7-alpha-L-rhamnoside
Role
alias
Source
HERB_v2
Preferred
No
Name
6-methoxyluteolin 7-alpha-L-rhamnoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
CHEBI:28314
Role
alias
Source
HERB_v2
Preferred
No
Name
CHEBI:28314
Role
alias
Source
itcmdb_public
Preferred
No
Name
DTXSID60331882
Role
alias
Source
HERB_v2
Preferred
No
Name
DTXSID60331882
Role
alias
Source
itcmdb_public
Preferred
No
Name
Q27103631
Role
alias
Source
HERB_v2
Preferred
No
Name
Q27103631
Role
alias
Source
itcmdb_public
Preferred
No

Aliases

Additional names normalized into the restored final schema.

2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-chromen-7-yl 6-deoxy-alpha-L-mannopyranoside2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one35682-55-46-Methoxyluteolin 7-rhamnoside6-methoxyluteolin 7-alpha-L-rhamnosideCHEBI:28314DTXSID60331882Q27103631

Cross References

Trusted external identifiers retained for this final record.

Herb
HBIN013047
Tcmid
18728
Pub Chem
442617

Attributes

Merged source attributes and domain-specific metadata.

In Ch I
InChI=1S/C22H22O11/c1-8-17(26)19(28)20(29)22(31-8)33-15-7-14-16(18(27)21(15)30-2)12(25)6-13(32-14)9-3-4-10(23)11(24)5-9/h3-8,17,19-20,22-24,26-29H,1-2H3/t8-,17-,19+,20+,22-/m0/s1
Mol Wt
462.4070000000001
Mol Log P
0.7916999999999994
In Ch Ikey
UXCXDWDJBSJZOU-CKPDRDNLSA-N
Num Hdonors
6
Drug Likeness
0.302
Num Hacceptors
11
Isomeric Smiles
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)OC)O)O)O
Canonical Smiles
CC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)OC)O)O)O
Herb Alias Names
6-Methoxyluteolin 7-rhamnoside35682-55-46-methoxyluteolin 7-alpha-L-rhamnoside2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-chromen-7-yl 6-deoxy-alpha-L-mannopyranosideCHEBI:28314DTXSID60331882Q27103631
Molecular Formula
C22H22O11
Num Rotatable Bonds
4