5-methoxy-2-(4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol

Details

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Internal ID 6da5d716-5a69-40c3-86d5-e8746e86ba27
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 5-O-methylated flavonoids
IUPAC Name 5-methoxy-2-(4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol
SMILES (Canonical) COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3OC)O
SMILES (Isomeric) COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3OC)O
InChI InChI=1S/C17H18O4/c1-19-13-5-3-11(4-6-13)15-8-7-14-16(20-2)9-12(18)10-17(14)21-15/h3-6,9-10,15,18H,7-8H2,1-2H3
InChI Key PVKZZNPKFFWKRA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O4
Molecular Weight 286.32 g/mol
Exact Mass 286.12050905 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-methoxy-2-(4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9807 98.07%
Caco-2 + 0.7501 75.01%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7695 76.95%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9846 98.46%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6933 69.33%
P-glycoprotein inhibitior - 0.7617 76.17%
P-glycoprotein substrate - 0.8997 89.97%
CYP3A4 substrate + 0.5568 55.68%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate + 0.6029 60.29%
CYP3A4 inhibition - 0.5177 51.77%
CYP2C9 inhibition - 0.5334 53.34%
CYP2C19 inhibition + 0.6747 67.47%
CYP2D6 inhibition - 0.8405 84.05%
CYP1A2 inhibition + 0.8144 81.44%
CYP2C8 inhibition + 0.5640 56.40%
CYP inhibitory promiscuity + 0.6266 62.66%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6320 63.20%
Eye corrosion - 0.9791 97.91%
Eye irritation - 0.4899 48.99%
Skin irritation - 0.7724 77.24%
Skin corrosion - 0.9635 96.35%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4711 47.11%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.9102 91.02%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.4812 48.12%
Acute Oral Toxicity (c) III 0.7134 71.34%
Estrogen receptor binding + 0.6072 60.72%
Androgen receptor binding + 0.6845 68.45%
Thyroid receptor binding + 0.6784 67.84%
Glucocorticoid receptor binding + 0.5968 59.68%
Aromatase binding - 0.5178 51.78%
PPAR gamma + 0.6345 63.45%
Honey bee toxicity - 0.9473 94.73%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7051 70.51%
Fish aquatic toxicity - 0.4588 45.88%

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 97.85% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.56% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.31% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.51% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.42% 92.94%
CHEMBL4208 P20618 Proteasome component C5 90.18% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.94% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.38% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.32% 95.89%
CHEMBL3438 Q05513 Protein kinase C zeta 87.86% 88.48%
CHEMBL2535 P11166 Glucose transporter 87.20% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.19% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.81% 94.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.33% 93.40%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.13% 82.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.94% 86.33%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 82.72% 91.79%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.51% 99.15%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.35% 95.78%

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.
Imperata cylindrica

Cross-Links

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PubChem 74977228
LOTUS LTS0272888
wikiData Q105215492