(2S)-5,7-dihydroxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydrochromen-4-one

Details

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Internal ID 2b634f78-fea8-41d4-b62a-c119fd2df0f6
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 4-O-methylated flavonoids
IUPAC Name (2S)-5,7-dihydroxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H18O7/c1-22-15-4-9(5-16(23-2)18(15)24-3)13-8-12(21)17-11(20)6-10(19)7-14(17)25-13/h4-7,13,19-20H,8H2,1-3H3/t13-/m0/s1
InChI Key CTALFFOVOLJORS-ZDUSSCGKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O7
Molecular Weight 346.30 g/mol
Exact Mass 346.10525291 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-5,7-dihydroxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8874 88.74%
Caco-2 + 0.8276 82.76%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.6378 63.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9577 95.77%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6539 65.39%
P-glycoprotein inhibitior - 0.5149 51.49%
P-glycoprotein substrate - 0.9350 93.50%
CYP3A4 substrate + 0.5470 54.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7429 74.29%
CYP3A4 inhibition + 0.6809 68.09%
CYP2C9 inhibition - 0.5296 52.96%
CYP2C19 inhibition + 0.6916 69.16%
CYP2D6 inhibition + 0.5891 58.91%
CYP1A2 inhibition + 0.8447 84.47%
CYP2C8 inhibition - 0.5655 56.55%
CYP inhibitory promiscuity + 0.7549 75.49%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6015 60.15%
Eye corrosion - 0.9871 98.71%
Eye irritation + 0.7181 71.81%
Skin irritation - 0.7515 75.15%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4580 45.80%
Micronuclear + 0.8059 80.59%
Hepatotoxicity - 0.5343 53.43%
skin sensitisation - 0.9327 93.27%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5182 51.82%
Acute Oral Toxicity (c) III 0.5053 50.53%
Estrogen receptor binding + 0.8091 80.91%
Androgen receptor binding - 0.5864 58.64%
Thyroid receptor binding + 0.7290 72.90%
Glucocorticoid receptor binding + 0.8118 81.18%
Aromatase binding - 0.7021 70.21%
PPAR gamma + 0.7546 75.46%
Honey bee toxicity - 0.7382 73.82%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.7807 78.07%

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 98.14% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.30% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.05% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.75% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.06% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.04% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.45% 99.23%
CHEMBL4208 P20618 Proteasome component C5 88.83% 90.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 87.96% 92.68%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.26% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.02% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.43% 86.33%
CHEMBL2535 P11166 Glucose transporter 85.81% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.78% 97.09%
CHEMBL1929 P47989 Xanthine dehydrogenase 83.22% 96.12%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.96% 97.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.38% 99.15%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.09% 82.38%
CHEMBL2581 P07339 Cathepsin D 81.32% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.87% 92.62%

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.
Paulownia tomentosa

Cross-Links

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PubChem 40484424
NPASS NPC338131
LOTUS LTS0084967
wikiData Q104969668