Apigenin-4'-glucoside

Details

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Internal ID bcdd5b5e-a080-4fd1-8a04-442a5044e38f
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name 5,7-dihydroxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
SMILES (Canonical) C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C21H20O10/c22-8-16-18(26)19(27)20(28)21(31-16)29-11-3-1-9(2-4-11)14-7-13(25)17-12(24)5-10(23)6-15(17)30-14/h1-7,16,18-24,26-28H,8H2/t16-,18-,19+,20-,21-/m1/s1
InChI Key ICLVCWSZHUZEFT-QNDFHXLGSA-N
Popularity 3 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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20486-34-4
Apigenin 4'-O-glucoside
Apigenin-4'-O-glucoside
Apigenin 4'-glucoside
Flavone, 4',5,7-trihydroxy-, 4'-beta-D-glucopyranoside
Apigenin 4 inverted exclamation marka-O-|A-D-glucopyranoside
5,7-dihydroxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
4'-O-beta-D-Glucosylapigenin
Apigenin 4'-beta-D-glucoside
Apigenin 4'-O-beta-glucoside
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-4'-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 - 0.9005 90.05%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6433 64.33%
OATP2B1 inhibitior - 0.5530 55.30%
OATP1B1 inhibitior + 0.9430 94.30%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5618 56.18%
P-glycoprotein inhibitior - 0.6071 60.71%
P-glycoprotein substrate - 0.8591 85.91%
CYP3A4 substrate + 0.5804 58.04%
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 + 0.7238 72.38%
CYP inhibitory promiscuity - 0.7833 78.33%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6688 66.88%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.9224 92.24%
Skin irritation - 0.8111 81.11%
Skin corrosion - 0.9715 97.15%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5425 54.25%
Micronuclear + 0.6133 61.33%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.9256 92.56%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8260 82.60%
Acute Oral Toxicity (c) III 0.4522 45.22%
Estrogen receptor binding + 0.6991 69.91%
Androgen receptor binding + 0.7190 71.90%
Thyroid receptor binding + 0.5351 53.51%
Glucocorticoid receptor binding + 0.5742 57.42%
Aromatase binding + 0.6560 65.60%
PPAR gamma + 0.8382 83.82%
Honey bee toxicity - 0.7002 70.02%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6550 65.50%
Fish aquatic toxicity + 0.7773 77.73%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.50% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.34% 94.00%
CHEMBL2581 P07339 Cathepsin D 95.34% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.28% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.70% 99.15%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.38% 83.57%
CHEMBL3194 P02766 Transthyretin 92.94% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.93% 86.92%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.88% 97.09%
CHEMBL220 P22303 Acetylcholinesterase 89.31% 94.45%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.17% 95.78%
CHEMBL3401 O75469 Pregnane X receptor 87.89% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.67% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.46% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.98% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 85.40% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.12% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.87% 90.71%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.76% 96.21%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 81.69% 80.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.37% 94.45%
CHEMBL4208 P20618 Proteasome component C5 80.13% 90.00%

Cross-Links

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PubChem 5491384
NPASS NPC143851
LOTUS LTS0246588
wikiData Q76309703