Apigenin 7-O-glucoside

Details

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Internal ID e37226ba-919d-4850-a095-28dfde288667
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 5-hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical) C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O
InChI InChI=1S/C21H20O10/c22-8-16-18(26)19(27)20(28)21(31-16)29-11-5-12(24)17-13(25)7-14(30-15(17)6-11)9-1-3-10(23)4-2-9/h1-7,16,18-24,26-28H,8H2
InChI Key KMOUJOKENFFTPU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O10
Molecular Weight 432.40 g/mol
Exact Mass 432.10564683 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.05
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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Apigenin 7-O-glucoside
Apigenin-7-O-glucoside
Apigenin 7-beta-D-glucoside
Anthemoside
Apigenin 7-O-.beta.-D-glucoside
7-O-(.beta.-D-Glucosyl)apigenin
Apigenin 7-O-.beta.-D-glucopyranoside
APIGENIN, 7-B-D-GLYCOPYRANOSIDE
apigenin7-glucoside
Oprea1_225308
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Apigenin 7-O-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5548 55.48%
Caco-2 - 0.9236 92.36%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6433 64.33%
OATP2B1 inhibitior - 0.5298 52.98%
OATP1B1 inhibitior + 0.9514 95.14%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4704 47.04%
P-glycoprotein inhibitior - 0.8532 85.32%
P-glycoprotein substrate - 0.8587 85.87%
CYP3A4 substrate + 0.5537 55.37%
CYP2C9 substrate - 0.6762 67.62%
CYP2D6 substrate - 0.8575 85.75%
CYP3A4 inhibition - 0.9192 91.92%
CYP2C9 inhibition - 0.9435 94.35%
CYP2C19 inhibition - 0.9426 94.26%
CYP2D6 inhibition - 0.9501 95.01%
CYP1A2 inhibition - 0.9203 92.03%
CYP2C8 inhibition + 0.6928 69.28%
CYP inhibitory promiscuity - 0.7833 78.33%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6688 66.88%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.8716 87.16%
Skin irritation - 0.8111 81.11%
Skin corrosion - 0.9715 97.15%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5745 57.45%
Micronuclear + 0.6133 61.33%
Hepatotoxicity - 0.8696 86.96%
skin sensitisation - 0.9256 92.56%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7945 79.45%
Acute Oral Toxicity (c) III 0.4522 45.22%
Estrogen receptor binding + 0.6847 68.47%
Androgen receptor binding + 0.7434 74.34%
Thyroid receptor binding + 0.5224 52.24%
Glucocorticoid receptor binding + 0.5840 58.40%
Aromatase binding + 0.6524 65.24%
PPAR gamma + 0.8225 82.25%
Honey bee toxicity - 0.6936 69.36%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6450 64.50%
Fish aquatic toxicity + 0.7773 77.73%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1825 P01375 TNF-alpha 200 nM
Kd
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.32% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.74% 94.00%
CHEMBL2581 P07339 Cathepsin D 95.39% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.51% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.74% 99.15%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.90% 86.92%
CHEMBL3194 P02766 Transthyretin 91.80% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 89.31% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.73% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 88.56% 94.73%
CHEMBL242 Q92731 Estrogen receptor beta 87.75% 98.35%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 87.54% 95.78%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.44% 94.45%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.10% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.28% 86.33%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.61% 83.57%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.41% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.50% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.44% 91.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.74% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.42% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.32% 85.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.77% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Achillea collina
Achillea roseo-alba
Allium rotundum
Aloe castellorum
Ammoides pusilla
Apium graveolens
Arnica longifolia
Artemisia austriaca
Asphodeline damascena
Aster koraiensis
Astragalus kadshorensis
Baptisia australis
Bellis perennis
Biebersteinia orphanidis
Blasia pusilla
Bombax ceiba
Broussonetia papyrifera
Buddleja officinalis
Callistephus chinensis
Capsicum annuum
Centaurea cyanus
Centaurea sphaerocephala
Centaurea urvillei
Chrysanthemum indicum
Cichorium intybus
Cichorium pumilum
Cirsium arvense
Cirsium oleraceum
Colchicum speciosum
Cosmos bipinnatus
Crocus chrysanthus
Cryptomeria japonica
Daphne gnidium
Daphne sericea
Dracocephalum multicaule
Dracocephalum nutans
Dracocephalum tanguticum
Echinops echinatus
Elsholtzia ciliata
Elsholtzia rugulosa
Erica cinerea
Euphorbia granulata
Farsetia aegyptia
Galinsoga parviflora
Galium album subsp. prusense
Galium verum subsp. verum
Ginkgo biloba
Glebionis coronaria
Glechoma grandis
Glechoma longituba
Gratiola officinalis
Hedlundia thuringiaca
Helichrysum arenarium
Hieracium gymnocephalum
Humulopsis scandens
Humulus scandens
Hypericum perforatum
Hyssopus officinalis
Itoa orientalis
Lagotis brevituba
Launaea nudicaulis
Lavandula angustifolia subsp. angustifolia
Leucas cephalotes
Leucophyllum ambiguum
Ligustrum vulgare
Linum salsoloides
Lobelia chinensis
Lonicera japonica
Lycianthes synanthera
Lygodium japonicum
Marrubium vulgare
Mentha arvensis
Mentha canadensis
Monarda punctata
Morinda morindoides
Mosla chinensis
Nepeta tenuifolia
Nepeta velutina
Ocimum tenuiflorum
Onosma hispida
Origanum vulgare
Passiflora bryonioides
Perilla frutescens
Phagnalon rupestre
Phlomis bovei
Phlomis herba-venti
Phlomis nissolii
Phlomoides rotata
Platycodon grandiflorus
Pogostemon stellatus
Prosopis farcta
Reynoutria japonica
Rosa rugosa
Rubus amabilis
Salix acutifolia
Salix babylonica
Salix gilgiana
Salvia bucharica
Salvia fruticosa
Salvia officinalis
Saussurea medusa
Scutellaria barbata
Scutellaria immaculata
Scutellaria phyllostachya
Scutellaria schachristanica
Sedum sarmentosum
Senna italica subsp. italica
Senna occidentalis
Shorea roxburghii
Sideritis raeseri
Spartium junceum
Spiraea canescens
Spirodela polyrhiza
Stachys byzantina
Stevia rebaudiana
Tanacetum parthenium
Tanacetum vulgare
Thymus collinus
Thymus quinquecostatus
Thymus vulgaris
Trichosanthes kirilowii
Trichosanthes rosthornii
Turnera diffusa
Valeriana cardamines
Veratrum grandiflorum
Verbascum phlomoides
Vicia sativa
Vitex altissima
Vitex glabrata
Vitex negundo

Cross-Links

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PubChem 5385553
NPASS NPC85473
LOTUS LTS0157591
wikiData Q104170422