3,5-Dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one

Details

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Internal ID 74a87f82-2b3e-4642-a822-b64628d5b752
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O7/c1-22-8-6-11(19)13-12(7-8)24-17(15(21)14(13)20)9-4-3-5-10(18)16(9)23-2/h3-7,15,17-19,21H,1-2H3
InChI Key VSQOAFBYLZTIIC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O7
Molecular Weight 332.30 g/mol
Exact Mass 332.08960285 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,5-Dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-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 + 0.9730 97.30%
Caco-2 + 0.5710 57.10%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8156 81.56%
OATP2B1 inhibitior - 0.7145 71.45%
OATP1B1 inhibitior + 0.9240 92.40%
OATP1B3 inhibitior + 0.9738 97.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7108 71.08%
P-glycoprotein inhibitior - 0.6356 63.56%
P-glycoprotein substrate - 0.9406 94.06%
CYP3A4 substrate + 0.5963 59.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7873 78.73%
CYP3A4 inhibition - 0.5571 55.71%
CYP2C9 inhibition + 0.7766 77.66%
CYP2C19 inhibition + 0.8962 89.62%
CYP2D6 inhibition - 0.7334 73.34%
CYP1A2 inhibition + 0.8679 86.79%
CYP2C8 inhibition + 0.5779 57.79%
CYP inhibitory promiscuity + 0.7750 77.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6135 61.35%
Eye corrosion - 0.9782 97.82%
Eye irritation + 0.5993 59.93%
Skin irritation - 0.6511 65.11%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6890 68.90%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9410 94.10%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5250 52.50%
Acute Oral Toxicity (c) III 0.5602 56.02%
Estrogen receptor binding + 0.6979 69.79%
Androgen receptor binding - 0.5690 56.90%
Thyroid receptor binding + 0.6003 60.03%
Glucocorticoid receptor binding + 0.7718 77.18%
Aromatase binding - 0.6220 62.20%
PPAR gamma + 0.6199 61.99%
Honey bee toxicity - 0.8909 89.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5247 52.47%
Fish aquatic toxicity + 0.8898 88.98%

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 97.69% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.05% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.04% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.58% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 91.62% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.24% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.22% 93.99%
CHEMBL2535 P11166 Glucose transporter 89.15% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.82% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.26% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.15% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.88% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.62% 89.00%
CHEMBL2581 P07339 Cathepsin D 84.82% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.58% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 82.50% 91.19%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.35% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.77% 85.14%

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.
Iris tenuifolia

Cross-Links

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PubChem 162951470
LOTUS LTS0161644
wikiData Q105292446