Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Herb: 12Ingredient: 1Target: 12Links: 24
Arranging relationship network...
Record Fields
Scalar fields from the final ingredient record.
- Ingredient Id
- 19662
- Core Entity Id
- 25036
- Source Entity Count
- 1
- Preferred Name
- Galuteolin
- Name En
- Pubchem Id
- 5291488
- Smiles Canonical
- C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O
- Molecular Formula
- C21H20O11
- Molecular Weight
- 448.3800
- Inchikey
- KBGKQZVCLWKUDQ-QNDFHXLGSA-N
- Inchi
- InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-9-4-12(25)17-13(26)6-14(31-15(17)5-9)8-1-2-10(23)11(24)3-8/h1-6,16,18-25,27-29H,7H2
- Isomeric Smiles
- C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O
- Cas Id
- Ob Score
- 2.6820
- Mol Logp
- -0.2445
- Num H Donors
- 7
- Num H Acceptors
- 11
- Num Rotatable Bonds
- 4
- Drug Likeness
- 0.2610
- Polar Surface Area
- 186.3600
- Molecular Volume
- 322.4100
- Alogp
- 0.2380
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Galuteolin
Role
preferred
Source
HERB_v2
Preferred
Yes
Name
Galuteolin
Role
preferred
Source
ETCM_v2
Preferred
Yes
Name
Galuteolin
Role
preferred
Source
itcmdb_public
Preferred
Yes
Name
Galuteolin
Role
preferred
Source
TCMBank
Preferred
Yes
Name
Galuteolin
Role
preferred
Source
SymMap_v2
Preferred
Yes
Name
Luteolin-7-O-Beta-D-Galactopyranoside
Role
preferred
Source
SymMap_v2
Preferred
Yes
Name
Luteolin-7-beta-d-glucosid
Role
preferred
Source
itcmdb_public
Preferred
Yes
Name
Luteolin-7-beta-d-glucosid
Role
preferred
Source
HERB_v2
Preferred
Yes
Name
Luteolin-7-o-beta-d-galactopyranoside
Role
preferred
Source
HERB_v2
Preferred
Yes
Name
Luteolin-7-o-beta-d-galactopyranoside
Role
preferred
Source
itcmdb_public
Preferred
Yes
Name
luteolin-7-O-beta-D-galactopyranoside
Role
preferred
Source
TCMBank
Preferred
Yes
Name
luteolin-7-o-beta-d-galactopyranoside
Role
preferred
Source
ETCM_v2
Preferred
Yes
Name
蒲公英
Role
TCM_name
Source
TCMBank
Preferred
No
Name
问荆
Role
TCM_name
Source
TCMBank
Preferred
No
Name
Taraxacum mongolicum
Role
TCM_name2
Source
TCMBank
Preferred
No
Name
WEN JING
Role
TCM_name2
Source
TCMBank
Preferred
No
Name
Bottle-brush
Role
TCM_name_en
Source
TCMBank
Preferred
No
Name
Dandelion
Role
TCM_name_en
Source
TCMBank
Preferred
No
Name
0422AB
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-DIHYDROXYPHENYL)-5-HYDROXY-7-{[3,4,5-TRIHYDROXY-6-(HYDROXYMETHYL)OXAN-2-YL]OXY}CHROMEN-4-ONE
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl hexopyranoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl hexopyranoside
Role
alias
Source
HERB_v2
Preferred
No
Name
2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl hexopyranoside #
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-(4,5,6-trihydroxy-3-(hydroxymethyl)(2-oxanyloxy))-4H-chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-Dihydroxyphenyl)-7-(beta-D-galactopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one
Role
alias
Source
HERB_v2
Preferred
No
Name
2-(3,4-Dihydroxyphenyl)-7-(beta-D-galactopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one
Role
alias
Source
itcmdb_public
Preferred
No
Name
2-(3,4-Dihydroxyphenyl)-7-(beta-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl beta-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-chromone
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)(2H-3,4 ,5,6-tetrahydropyran-2-yloxy)]chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Role
alias
Source
HERB_v2
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Role
alias
Source
itcmdb_public
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-chromone
Role
alias
Source
TCMBank
Preferred
No
Name
2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone
Role
alias
Source
TCMBank
Preferred
No
Name
20344-46-1
Role
alias
Source
TCMBank
Preferred
No
Name
20344-46-1
Role
alias
Source
HERB_v2
Preferred
No
Name
20344-46-1
Role
alias
Source
itcmdb_public
Preferred
No
Name
26811-41-6
Role
alias
Source
TCMBank
Preferred
No
Name
373L115
Role
alias
Source
TCMBank
Preferred
No
Name
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-, mono-beta-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-7-hydroxy-
Role
alias
Source
HERB_v2
Preferred
No
Name
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-7-hydroxy-
Role
alias
Source
itcmdb_public
Preferred
No
Name
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-7-hydroxy-
Role
alias
Source
TCMBank
Preferred
No
Name
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(.beta.-D-glucopyranosyloxy)-5-hydroxy-
Role
alias
Source
TCMBank
Preferred
No
Name
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(beta-D-galactopyranosyloxy)-5-hydroxy-
Role
alias
Source
HERB_v2
Preferred
No
Name
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(beta-D-galactopyranosyloxy)-5-hydroxy-
Role
alias
Source
itcmdb_public
Preferred
No
Name
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-7-(
Role
alias
Source
TCMBank
Preferred
No
Name
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-7-(b-D-glucopyranosyloxy)-5-hydroxy-
Role
alias
Source
TCMBank
Preferred
No
Name
5373/11/5
Role
alias
Source
TCMBank
Preferred
No
Name
54985-16-9
Role
alias
Source
HERB_v2
Preferred
No
Name
54985-16-9
Role
alias
Source
itcmdb_public
Preferred
No
Name
569-89-1
Role
alias
Source
TCMBank
Preferred
No
Name
68321-11-9
Role
alias
Source
TCMBank
Preferred
No
Name
68321-11-9
Role
alias
Source
HERB_v2
Preferred
No
Name
68321-11-9
Role
alias
Source
itcmdb_public
Preferred
No
Name
7-(beta-D-glucopyranosyloxy)-5-hydroxy-2-(3,4-dihydroxyphenyl)-4H-chromen-4-one
Role
alias
Source
TCMBank
Preferred
No
Name
7-Glucoluteolin
Role
alias
Source
TCMBank
Preferred
No
Name
7-Glucosylluteolin
Role
alias
Source
TCMBank
Preferred
No
Name
7-O-beta-D-Glucosyl-5,7,3',4'-tetrahydroxyflavone
Role
alias
Source
TCMBank
Preferred
No
Name
98J6XDS46I
Role
alias
Source
TCMBank
Preferred
No
Name
A-D-glucopyranosyloxy)-5-hydroxy-
Role
alias
Source
TCMBank
Preferred
No
Name
A-D-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
A2306/0097227
Role
alias
Source
TCMBank
Preferred
No
Name
AC-6054
Role
alias
Source
TCMBank
Preferred
No
Name
AC1NQXCE
Role
alias
Source
TCMBank
Preferred
No
Name
AC1NRHCY
Role
alias
Source
TCMBank
Preferred
No
Name
AC1NSVN1
Role
alias
Source
TCMBank
Preferred
No
Name
AIDS-219925
Role
alias
Source
TCMBank
Preferred
No
Name
AIDS070478
Role
alias
Source
TCMBank
Preferred
No
Name
AJ-47986
Role
alias
Source
TCMBank
Preferred
No
Name
AJ-86337
Role
alias
Source
TCMBank
Preferred
No
Name
AK-25217
Role
alias
Source
TCMBank
Preferred
No
Name
AK120358
Role
alias
Source
TCMBank
Preferred
No
Name
AKOS001483348
Role
alias
Source
TCMBank
Preferred
No
Name
AKOS015903261
Role
alias
Source
TCMBank
Preferred
No
Name
AKOS016010674
Role
alias
Source
TCMBank
Preferred
No
Name
AKOS021983229
Role
alias
Source
TCMBank
Preferred
No
Name
API0003232
Role
alias
Source
TCMBank
Preferred
No
Name
AX8061581
Role
alias
Source
TCMBank
Preferred
No
Name
AX8245774
Role
alias
Source
TCMBank
Preferred
No
Name
BDBM50241242
Role
alias
Source
TCMBank
Preferred
No
Name
BG01154730
Role
alias
Source
TCMBank
Preferred
No
Name
BG01739205
Role
alias
Source
TCMBank
Preferred
No
Name
BG01739210
Role
alias
Source
TCMBank
Preferred
No
Name
BIDF1013
Role
alias
Source
TCMBank
Preferred
No
Name
Bio-0221
Role
alias
Source
TCMBank
Preferred
No
Name
C-22456
Role
alias
Source
TCMBank
Preferred
No
Name
C03951
Role
alias
Source
TCMBank
Preferred
No
Name
CC-30093
Role
alias
Source
TCMBank
Preferred
No
Name
CHEBI:27994
Role
alias
Source
TCMBank
Preferred
No
Name
CHEMBL233929
Role
alias
Source
TCMBank
Preferred
No
Name
CNI9E8ORF6
Role
alias
Source
itcmdb_public
Preferred
No
Name
CNI9E8ORF6
Role
alias
Source
HERB_v2
Preferred
No
Name
CS-5712
Role
alias
Source
TCMBank
Preferred
No
Name
Cinaroside
Role
alias
Source
TCMBank
Preferred
No
Name
Cynaroside
Role
alias
Source
TCMBank
Preferred
No
Name
DTXSID001318842
Role
alias
Source
itcmdb_public
Preferred
No
Name
DTXSID001318842
Role
alias
Source
HERB_v2
Preferred
No
Name
Daphneflavonoloside
Role
alias
Source
TCMBank
Preferred
No
Name
EINECS 226-365-8
Role
alias
Source
TCMBank
Preferred
No
Name
FT-0697969
Role
alias
Source
TCMBank
Preferred
No
Name
Flavon, 3',4',5,7-tetrahydroxy-, glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Flavone, 3',4',5,7-tetrahydroxy-, mono-beta-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Flavopurposide
Role
alias
Source
TCMBank
Preferred
No
Name
Galuteolin
Role
alias
Source
TCMBank
Preferred
No
Name
Glucoluteolin
Role
alias
Source
TCMBank
Preferred
No
Name
HMS2224O21
Role
alias
Source
TCMBank
Preferred
No
Name
HY-N0540
Role
alias
Source
TCMBank
Preferred
No
Name
I14-19110
Role
alias
Source
TCMBank
Preferred
No
Name
KB-290714
Role
alias
Source
TCMBank
Preferred
No
Name
KS-00001FIQ
Role
alias
Source
TCMBank
Preferred
No
Name
LS-39606
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 5-O-glucoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteolin 5-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 5-glucoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin 5-glucoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteolin 7-.beta.-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-.beta.-D-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-O-
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-O-D-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-O-Glucoside, United States Pharmacopeia (USP) Reference Standard
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-O-beta-D-glucoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin 7-O-beta-D-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-O-beta-D-glucoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteolin 7-O-beta-D-glucoside, >=98.0% (HPLC)
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-O-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-b-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-galactoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin 7-galactoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-galactoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteolin 7-glucoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteolin 7-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-glucoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin 7-glucoside, analytical standard
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin 7-glucoside, primary pharmaceutical reference standard
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin monoglucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-5-O-b-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-5-O-beta-D-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-5-O-beta-D-glucoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteolin-5-O-beta-D-glucoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin-5-O-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-5-O-glucoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin-7-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-7-O-.beta.-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-7-O-D-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-7-O-galactoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin-7-O-galactoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteolin-7-O-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-7-glucosid
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteolin-7-glucosid
Role
alias
Source
TCMBank
Preferred
No
Name
Luteolin-7-glucosid
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteollin 5-glucoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
Luteollin 5-glucoside
Role
alias
Source
HERB_v2
Preferred
No
Name
Luteollin 5-glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
Luteoloside
Role
alias
Source
TCMBank
Preferred
No
Name
MCULE-8064140924
Role
alias
Source
TCMBank
Preferred
No
Name
MCULE-8191036162
Role
alias
Source
TCMBank
Preferred
No
Name
MEGxp0_000562
Role
alias
Source
HERB_v2
Preferred
No
Name
MEGxp0_000562
Role
alias
Source
TCMBank
Preferred
No
Name
MEGxp0_000562
Role
alias
Source
itcmdb_public
Preferred
No
Name
MEGxp0_000619
Role
alias
Source
TCMBank
Preferred
No
Name
MFCD06799436
Role
alias
Source
TCMBank
Preferred
No
Name
MLS002473222
Role
alias
Source
TCMBank
Preferred
No
Name
MolPort-001-740-780
Role
alias
Source
TCMBank
Preferred
No
Name
MolPort-002-708-422
Role
alias
Source
TCMBank
Preferred
No
Name
MolPort-020-005-904
Role
alias
Source
TCMBank
Preferred
No
Name
N1724
Role
alias
Source
TCMBank
Preferred
No
Name
N2724
Role
alias
Source
TCMBank
Preferred
No
Name
NCGC00017208-02
Role
alias
Source
TCMBank
Preferred
No
Name
NCGC00142376-01
Role
alias
Source
TCMBank
Preferred
No
Name
NCGC00163589-01
Role
alias
Source
TCMBank
Preferred
No
Name
NCI60_035927
Role
alias
Source
TCMBank
Preferred
No
Name
NSC-724451
Role
alias
Source
TCMBank
Preferred
No
Name
NSC700145
Role
alias
Source
HERB_v2
Preferred
No
Name
NSC700145
Role
alias
Source
itcmdb_public
Preferred
No
Name
NSC700145
Role
alias
Source
TCMBank
Preferred
No
Name
NSC724451
Role
alias
Source
itcmdb_public
Preferred
No
Name
NSC724451
Role
alias
Source
HERB_v2
Preferred
No
Name
PEFNSGRTCBGNAN-QNDFHXLGSA-N
Role
alias
Source
TCMBank
Preferred
No
Name
Q-100249
Role
alias
Source
TCMBank
Preferred
No
Name
REGID_for_CID_5280637
Role
alias
Source
TCMBank
Preferred
No
Name
REGID_for_CID_657946
Role
alias
Source
TCMBank
Preferred
No
Name
SC-46564
Role
alias
Source
TCMBank
Preferred
No
Name
SCHEMBL149118
Role
alias
Source
TCMBank
Preferred
No
Name
SCHEMBL149119
Role
alias
Source
HERB_v2
Preferred
No
Name
SCHEMBL149119
Role
alias
Source
TCMBank
Preferred
No
Name
SCHEMBL149119
Role
alias
Source
itcmdb_public
Preferred
No
Name
SCHEMBL19523005
Role
alias
Source
HERB_v2
Preferred
No
Name
SCHEMBL19523005
Role
alias
Source
TCMBank
Preferred
No
Name
SCHEMBL19523005
Role
alias
Source
itcmdb_public
Preferred
No
Name
SCHEMBL242602
Role
alias
Source
TCMBank
Preferred
No
Name
SMR000232358
Role
alias
Source
TCMBank
Preferred
No
Name
SR-01000867987
Role
alias
Source
TCMBank
Preferred
No
Name
SR-01000867987-2
Role
alias
Source
TCMBank
Preferred
No
Name
SR-01000867987-3
Role
alias
Source
TCMBank
Preferred
No
Name
ST024704
Role
alias
Source
TCMBank
Preferred
No
Name
ST24047512
Role
alias
Source
TCMBank
Preferred
No
Name
ST2407074
Role
alias
Source
TCMBank
Preferred
No
Name
STK763169
Role
alias
Source
TCMBank
Preferred
No
Name
STK763169
Role
alias
Source
HERB_v2
Preferred
No
Name
STK763169
Role
alias
Source
itcmdb_public
Preferred
No
Name
STOCK1N-08497
Role
alias
Source
TCMBank
Preferred
No
Name
TR-019005
Role
alias
Source
TCMBank
Preferred
No
Name
UNII-98J6XDS46I
Role
alias
Source
TCMBank
Preferred
No
Name
V1543
Role
alias
Source
TCMBank
Preferred
No
Name
ZINC33831307
Role
alias
Source
TCMBank
Preferred
No
Name
ZINC4096258
Role
alias
Source
TCMBank
Preferred
No
Name
ZX-AFC003073
Role
alias
Source
TCMBank
Preferred
No
Name
cid_5280637
Role
alias
Source
TCMBank
Preferred
No
Name
lCynaroside
Role
alias
Source
TCMBank
Preferred
No
Name
luteolin glucoside
Role
alias
Source
TCMBank
Preferred
No
Name
luteolin-5-o-beta-d-glucopyranoside
Role
alias
Source
itcmdb_public
Preferred
No
Name
luteolin-5-o-beta-d-glucopyranoside
Role
alias
Source
TCMBank
Preferred
No
Name
luteolin-5-o-beta-d-glucopyranoside
Role
alias
Source
HERB_v2
Preferred
No
Name
luteolin-7-O-beta-glucoside
Role
alias
Source
TCMBank
Preferred
No
Aliases
Additional names normalized into the restored final schema.
Luteolin-7-O-Beta-D-GalactopyranosideLuteolin-7-beta-d-glucosid蒲公英问荆Taraxacum mongolicumWEN JINGBottle-brushDandelion0422AB2-(3,4-DIHYDROXYPHENYL)-5-HYDROXY-7-{[3,4,5-TRIHYDROXY-6-(HYDROXYMETHYL)OXAN-2-YL]OXY}CHROMEN-4-ONE2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl hexopyranoside2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl hexopyranoside #2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-(4,5,6-trihydroxy-3-(hydroxymethyl)(2-oxanyloxy))-4H-chromen-4-one2-(3,4-Dihydroxyphenyl)-7-(beta-D-galactopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one2-(3,4-Dihydroxyphenyl)-7-(beta-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl beta-D-glucopyranoside2-(3,4-dihydroxyphenyl)-5-hydroxy-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-chromone2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)(2H-3,4 ,5,6-tetrahydropyran-2-yloxy)]chromen-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-chromone2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone20344-46-126811-41-6373L1154H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-, mono-beta-D-glucopyranoside4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-7-hydroxy-4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(.beta.-D-glucopyranosyloxy)-5-hydroxy-4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-(beta-D-galactopyranosyloxy)-5-hydroxy-4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-7-(4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-7-(b-D-glucopyranosyloxy)-5-hydroxy-5373/11/554985-16-9569-89-168321-11-97-(beta-D-glucopyranosyloxy)-5-hydroxy-2-(3,4-dihydroxyphenyl)-4H-chromen-4-one7-Glucoluteolin7-Glucosylluteolin7-O-beta-D-Glucosyl-5,7,3',4'-tetrahydroxyflavone98J6XDS46IA-D-glucopyranosyloxy)-5-hydroxy-A-D-glucosideA2306/0097227AC-6054AC1NQXCEAC1NRHCYAC1NSVN1AIDS-219925AIDS070478AJ-47986AJ-86337AK-25217AK120358AKOS001483348AKOS015903261AKOS016010674AKOS021983229API0003232AX8061581AX8245774BDBM50241242BG01154730BG01739205BG01739210BIDF1013Bio-0221C-22456C03951CC-30093CHEBI:27994CHEMBL233929CNI9E8ORF6CS-5712CinarosideCynarosideDTXSID001318842DaphneflavonolosideEINECS 226-365-8FT-0697969Flavon, 3',4',5,7-tetrahydroxy-, glucosideFlavone, 3',4',5,7-tetrahydroxy-, mono-beta-D-glucopyranosideFlavopurposideGlucoluteolinHMS2224O21HY-N0540I14-19110KB-290714KS-00001FIQLS-39606Luteolin 5-O-glucosideLuteolin 5-glucosideLuteolin 7-.beta.-D-glucopyranosideLuteolin 7-.beta.-D-glucosideLuteolin 7-O-Luteolin 7-O-D-glucosideLuteolin 7-O-Glucoside, United States Pharmacopeia (USP) Reference StandardLuteolin 7-O-beta-D-glucosideLuteolin 7-O-beta-D-glucoside, >=98.0% (HPLC)Luteolin 7-O-glucopyranosideLuteolin 7-b-glucosideLuteolin 7-galactosideLuteolin 7-glucosideLuteolin 7-glucoside, analytical standardLuteolin 7-glucoside, primary pharmaceutical reference standardLuteolin monoglucosideLuteolin-5-O-b-D-glucopyranosideLuteolin-5-O-beta-D-glucosideLuteolin-5-O-glucopyranosideLuteolin-5-O-glucosideLuteolin-7-D-glucopyranosideLuteolin-7-O-.beta.-D-glucopyranosideLuteolin-7-O-D-glucopyranosideLuteolin-7-O-galactosideLuteolin-7-O-glucosideLuteolin-7-glucosidLuteollin 5-glucosideLuteolosideMCULE-8064140924MCULE-8191036162MEGxp0_000562MEGxp0_000619MFCD06799436MLS002473222MolPort-001-740-780MolPort-002-708-422MolPort-020-005-904N1724N2724NCGC00017208-02NCGC00142376-01NCGC00163589-01NCI60_035927NSC-724451NSC700145NSC724451PEFNSGRTCBGNAN-QNDFHXLGSA-NQ-100249REGID_for_CID_5280637REGID_for_CID_657946SC-46564SCHEMBL149118SCHEMBL149119SCHEMBL19523005SCHEMBL242602SMR000232358SR-01000867987SR-01000867987-2SR-01000867987-3ST024704ST24047512ST2407074STK763169STOCK1N-08497TR-019005UNII-98J6XDS46IV1543ZINC33831307ZINC4096258ZX-AFC003073cid_5280637lCynarosideluteolin glucosideluteolin-5-o-beta-d-glucopyranosideluteolin-7-O-beta-glucoside
Cross References
Trusted external identifiers retained for this final record.
Cas
20344-46-1
Herb
HBIN020619HBIN022474HBIN027069HBIN027070HBIN028029HBIN033824HBIN033829HBIN033832HBIN033839HBIN033842HBIN033843HBIN033852HBIN033854HBIN033863HBIN033867
Npass
NPC115334NPC228834NPC85550
Tcmid
33832359368119
Tcmsp
MOL008377MOL011763
Sym Map
SMIT01427SMIT09681SMIT12618
Tcm Id
1083410835108361083713285132861328713288132891685116852168531685416855203332033420335203362033720338232632326623267232684210
Pub Chem
529148853174715488493
Tcmbank
TCMBANKIN032236TCMBANKIN052839TCMBANKIN058145
Etcm Ingredient
Galuteolinluteolin-7-o-beta-d-galactopyranoside
Itcmdb Generated
ITX-INGREDIENT-1583B3A6EA18ITX-INGREDIENT-3E61705CC81EITX-INGREDIENT-7AAFC53242F9ITX-INGREDIENT-92CE2EE11DCFITX-INGREDIENT-FF051EA21247
Attributes
Merged source attributes and domain-specific metadata.
Ic
4.132044.15563
Jx
1.541581.58252
Jy
1.642571.68627
Bic
0.761490.76583
Cic
0.844360.86795
Phi
6.20161
Sic
0.82640.83112
Log D
-0.3940.219
Sc 0
32
Sc 1
35
Sc 2
52
Type
Other ingredients
Alog P
0.238
Chi 0
23.154
Chi 1
15.1888
Chi 2
14.365814.3877
In Ch I
InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-9-4-12(25)17-13(26)6-14(31-15(17)5-9)8-1-2-10(23)11(24)3-8/h1-6,16,18-25,27-29H,7H2InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-9-4-12(25)17-13(26)6-14(31-15(17)5-9)8-1-2-10(23)11(24)3-8/h1-6,16,18-25,27-29H,7H2/t16-,18+,19+,20-,21-/m1/s1InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)31-15-5-9(23)4-14-17(15)12(26)6-13(30-14)8-1-2-10(24)11(25)3-8/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1
Mol Wt
448.3800000000001
Pmi X
254.069397.069
Energy
35.6347.02
Sc 3 C
14
Sc 3 P
71
Smiles
C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)Oc1(O[H])c([H])c(OC(c2c([H])c(O[H])c(O[H])c([H])c2[H])=C([H])C3=O)c3c(O[C@@]4([H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@]([H])(O[H])[C@@]([H])(C([H])([H])O[H])O4)c1[H]c1([H])c(OC(c2c([H])c(O[H])c(O[H])c([H])c2[H])=C([H])C3=O)c3c(O[H])c([H])c1O[C@]4([H])O[C@]([H])(C([H])([H])O[H])[C@]([H])(O[H])[C@]([H])(O[H])[C@@]4([H])O[H]
Zagreb
174
37 Flag
37
Chi 3 C
2.668722.68424
Chi 3 P
12.622612.6969
Chi V 0
16.3214
Chi V 1
9.49691
Chi V 2
7.309057.31056
C Count
21
Kappa 1
25.1037
Kappa 2
10.318
Kappa 3
5.17754
Mol Log P
-0.2444999999999991
N Count
0
O Count
11
P Count
0
Sc 3 Ch
0
S Count
0
Version
v1,v2
Alog P Mr
106.253
Chi 3 Ch
0
Dipole X
-0.25258-3.09894
Dipole Y
-0.506471.93673
Dipole Z
-0.28299-2.19139
Iac Mean
1.53253
In Ch Ikey
KBGKQZVCLWKUDQ-QNDFHXLGSA-NPEFNSGRTCBGNAN-OBJCFNGXSA-NPEFNSGRTCBGNAN-UHFFFAOYSA-N
Is Chiral
0
Ob Score
2.6822.6822299032.70051752524.08574;7.292677;2.68223
Suppress
01
Tcm Name
蒲公英问荆
Chi V 3 C
0.994280.99515
Chi V 3 P
5.130755.14399
Es Sum D O
12.53312.85
Es Sum T N
0
E Adj Equ
513.528
E Adj Mag
696.846
Hba Count
4
Hbd Count
7
Iac Total
79.6919
Jurs Rasa
0.434320.43488
Jurs Rncg
0.09888
Jurs Rncs
3.220935.0643
Jurs Rpcg
0.120530.12054
Jurs Rpcs
0.902490.96077
Jurs Rpsa
0.565110.56567
Jurs Sasa
612.03633.395
Jurs Tasa
266.162275.098
Jurs Tpsa
345.868358.297
Num Atoms
32
Num Bonds
35
Num Rings
4
Shadow Xy
115.534119.068
Shadow Xz
59.439861.7791
Shadow Yz
35.741438.3555
Shadow Nu
3.311944.61534
Tcm Name2
Taraxacum mongolicumWEN JING
V Adj Equ
368.406
V Adj Mag
429.05
Mol2 Path
/TCM_database/2.清热药(64-64)/3.清热解毒药(30-30)/蒲公英/Taraxacum mongolicum/Structure/luteolin-7-O-beta-D-galactopyranoside.mol2/TCM_database/2003_3d_all/3220.mol2
Reference
6
Chi V 3 Ch
0
Dipole Mag
0.632754.26104
Es Sum Aa N
0
Es Sum Aa O
0
Es Sum D Nh
0
Es Sum Dd C
0
Es Sum Ds N
0
Es Sum S Oh
68.56668.646
Es Sum Ss O
16.42416.484
Es Sum T Ch
0
Es Sum Ts C
0
Kappa 1 Am
22.6371
Kappa 2 Am
8.76666
Kappa 3 Am
4.25366
Num Hdonors
7
Num Chains
10
Num Rings3
0
Num Rings4
0
Num Rings5
0
Num Rings6
4
Num Rings7
0
Num Rings8
0
Es Count D O
1
Es Count T N
0
Es Sum Aa Ch
6.046.125
Es Sum Aa Nh
0
Es Sum Aaa C
0
Es Sum Aas C
-1.313-1.349
Es Sum Aas N
0
Es Sum D Ch2
0
Es Sum Dds N
0
Es Sum Ds Ch
1.1021.103
Es Sum Dss C
-0.562-0.574
Es Sum S Ch3
0
Es Sum S Nh2
0
Es Sum S Nh3
0
Es Sum Ss Nh
0
Es Sum Sss N
0
Jurs Dpsa 1
-273.41-309.75
Jurs Dpsa 3
141.858147.115
Jurs Fnsa 1
0.723360.74451
Jurs Fnsa 2
-2.87888-2.96317
Jurs Fnsa 3
-0.20781-0.20887
Jurs Fpsa 1
0.255480.27663
Jurs Fpsa 2
0.40970.44357
Jurs Fpsa 3
0.02340.02397
Jurs Pnsa 1
442.72471.573
Jurs Pnsa 2
-1761.95-1876.85
Jurs Pnsa 3
-127.185-132.291
Jurs Ppsa 1
161.823169.31
Jurs Ppsa 3
14.673414.8238
Jurs Wnsa 1
270.958298.692
Jurs Wnsa 2
-1078.37-1188.79
Jurs Wnsa 3
-77.841-83.7928
Jurs Wpsa 1
102.498103.623
Jurs Wpsa 3
8.980539.38933
Num Pi Bonds
0
Tcm Name En
Bottle-brushDandelion
Level1 Name
2.清热药(64-64)
Level2 Name
3.清热解毒药(30-30)
Admet Psa 2 D
189.799
Es Count Aa N
0
Es Count Aa O
0
Es Count D Nh
0
Es Count Dd C
0
Es Count Ds N
0
Es Count S Oh
7
Es Count Ss O
3
Es Count T Ch
0
Es Count Ts C
0
Es Sum Ss Ch2
-0.648-0.671
Es Sum Ss Nh2
0
Es Sum Sss Ch
-7.609-7.823
Es Sum Sss Nh
0
Es Sum Ssss C
0
Es Sum Ssss N
0
Nplus O Count
11
Num H Donors
7
Admet Alog P98
0.238
Admet Ext Ppb
-15.3714-17.4466
Drug Likeness
0.261
Es Count Aa Ch
5
Es Count Aa Nh
0
Es Count Aaa C
0
Es Count Aas C
7
Es Count Aas N
0
Es Count D Ch2
0
Es Count Dds N
0
Es Count Ds Ch
1
Es Count Dss C
2
Es Count S Ch3
0
Es Count S Nh2
0
Es Count S Nh3
0
Es Count Ss Nh
0
Es Count Sss N
0
Es Sum Sssss P
0
Num Hacceptors
11
Num Fragments
1
Num Hydrogens
20
Num Ring Bonds
23
Organic Count
32
Rad Of Gyration
3.863744.09642
Shadow Xyfrac
0.535880.57855
Shadow Xzfrac
0.633370.74196
Shadow Yzfrac
0.636120.74242
Strain Energy
37.5645.62
Es Count Ss Ch2
1
Es Count Ss Nh2
0
Es Count Sss Ch
5
Es Count Sss Nh
0
Es Count Ssss C
0
Es Count Ssss N
0
Molecular Mass
448.101
Molecular Sasa
607.295
Num Metal Atoms
0
Num Rings9 Plus
0
Shadow Xlength
17.629919.6034
Shadow Ylength
11.327111.3342
Shadow Zlength
4.247435.32312
Level1 Name En
heat-clearing medicinal
Level2 Name En
heat-clearing and detoxicating medicinal
Admet Bbb Level
4
Isomeric Smiles
C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)OC1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)O)O)O)O)O)OC1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O)O
Molecular Savol
538.901
Molecule Weight
448.41
Num Atom Classes
32
Num Bridge Bonds
0
Num H Acceptors
11
Num Repeat Units
0
Admet Ext Cyp2 D6
-1.70772-2.56
Admet Solubility
-3.328-3.364
Canonical Smiles
C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)OC1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O
Herb Alias Names
20344-46-1Luteolin-5-O-glucosideLuteolin 5-glucosideLuteollin 5-glucosideLuteolin 5-O-glucoside4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-7-hydroxy-CNI9E8ORF62-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-oneluteolin-5-o-beta-d-glucopyranosideLuteolin-5-O-beta-D-glucoside
Minimized Energy
-1.931.4
Molecular Weight
448.100
Molecular Volume
322.41323.1
Molecular Weight
448.377448.4 g/mol
Molecule Formula
C21H20O11
Num Macro Chains
0
Molecular Formula
C21H20O11
Molecular Formula
C21H20O11
Molecular Formula
C21H20O11
Num Rotatable Bonds
4
Num Aromatic Bonds
12
Num Aromatic Rings
2
Num Explicit Atoms
32
Num Explicit Bonds
35
Num Negative Atoms
0
Num Positive Atoms
0
Link Ingredient Id
1427.0
Num Macro Residues
0
Num Ring Assemblies
3
Num Rotatable Bonds
4
Molecular Polar Sasa
310.094
Num Bridge Head Atoms
0
Num Chain Assemblies
10
Num Meso Stereo Atoms
0
Molecular Solubility
-1.757-1.779
Admet Ext Hepatotoxic
-2.80748-4.34172
Admet Unknown Alog P98
0
Molecular Surface Area
401.95
Num Explicit Hydrogens
0
Num H Donors Lipinski
7
Num Pseudo Stereo Atoms
0
Admet Absorption Level
3
Admet Solubility Level
3
Admet Ext Ppb#Prediction
0
Num H Acceptors Lipinski
11
Molecular Polar Surface Area
186.36
Admet Ext Cyp2 D6#Prediction
0
Molecular Fractional Polar Sasa
0.51
Admet Ext Ppb Applicability#Md
12.8047
Fda Maximum Daily Dose (Fdamdd)
0.0190.033
Admet Ext Hepatotoxic#Prediction
01
Admet Ext Cyp2 D6 Applicability#Md
13.868414.7657
Admet Ext Ppb Applicability#Mdpvalue
0.010696
Molecular Fractional Polar Surface Area
0.463
Admet Ext Hepatotoxic Applicability#Md
10.600811.3842
Admet Ext Cyp2 D6 Applicability#Mdpvalue
0.0000374e-06
Admet Ext Hepatotoxic Applicability#Mdpvalue
0.0017020.020392
Quantitative Estimate Of Drug Likeness（Qed）
0.261