3'-O-Methylastilbin

Details

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Internal ID aebe1cd2-376a-454b-bd3b-5a2854496897
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name (2R,3R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O
InChI InChI=1S/C22H24O11/c1-8-16(26)18(28)19(29)22(31-8)33-21-17(27)15-12(25)6-10(23)7-14(15)32-20(21)9-3-4-11(24)13(5-9)30-2/h3-8,16,18-26,28-29H,1-2H3/t8-,16-,18+,19+,20+,21-,22-/m0/s1
InChI Key HIFPGFAGQUHMAU-XYECQVTLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O11
Molecular Weight 464.40 g/mol
Exact Mass 464.13186158 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.34
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3'-O-Methylastilbin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7980 79.80%
Caco-2 - 0.8114 81.14%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.6676 66.76%
OATP2B1 inhibitior - 0.5651 56.51%
OATP1B1 inhibitior + 0.9245 92.45%
OATP1B3 inhibitior + 0.9220 92.20%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5736 57.36%
P-glycoprotein inhibitior - 0.6374 63.74%
P-glycoprotein substrate - 0.7788 77.88%
CYP3A4 substrate + 0.6117 61.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8557 85.57%
CYP3A4 inhibition - 0.6056 60.56%
CYP2C9 inhibition - 0.9236 92.36%
CYP2C19 inhibition - 0.8201 82.01%
CYP2D6 inhibition - 0.8906 89.06%
CYP1A2 inhibition - 0.7268 72.68%
CYP2C8 inhibition + 0.5897 58.97%
CYP inhibitory promiscuity - 0.5508 55.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6071 60.71%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.7856 78.56%
Skin irritation - 0.6906 69.06%
Skin corrosion - 0.9434 94.34%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6091 60.91%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation - 0.9206 92.06%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.5897 58.97%
Acute Oral Toxicity (c) III 0.4825 48.25%
Estrogen receptor binding + 0.7521 75.21%
Androgen receptor binding - 0.5440 54.40%
Thyroid receptor binding + 0.5857 58.57%
Glucocorticoid receptor binding + 0.6750 67.50%
Aromatase binding - 0.5814 58.14%
PPAR gamma + 0.5851 58.51%
Honey bee toxicity - 0.7968 79.68%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9150 91.50%

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 99.43% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.96% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.22% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.85% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.05% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.61% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.35% 94.00%
CHEMBL2535 P11166 Glucose transporter 90.66% 98.75%
CHEMBL2581 P07339 Cathepsin D 90.37% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.15% 99.23%
CHEMBL4208 P20618 Proteasome component C5 88.79% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.64% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 87.07% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 86.72% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.74% 99.17%
CHEMBL3194 P02766 Transthyretin 84.43% 90.71%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.45% 97.36%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.94% 97.14%

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.
Smilax china
Smilax glabra

Cross-Links

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PubChem 101473436
NPASS NPC100400