(2R)-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromene-5,8-dione

Details

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Internal ID fccb1791-85e4-4429-a1f6-001696339f0b
Taxonomy Organoheterocyclic compounds > Benzopyrans
IUPAC Name (2R)-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromene-5,8-dione
SMILES (Canonical) COC1=C(C=C(C=C1)C2CCC3=C(O2)C(=O)C(=CC3=O)OC)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)[C@H]2CCC3=C(O2)C(=O)C(=CC3=O)OC)OC
InChI InChI=1S/C18H18O6/c1-21-14-6-4-10(8-15(14)22-2)13-7-5-11-12(19)9-16(23-3)17(20)18(11)24-13/h4,6,8-9,13H,5,7H2,1-3H3/t13-/m1/s1
InChI Key NGGBXUMUYRBLPC-CYBMUJFWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O6
Molecular Weight 330.30 g/mol
Exact Mass 330.11033829 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromene-5,8-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8570 85.70%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8167 81.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7522 75.22%
P-glycoprotein inhibitior + 0.6164 61.64%
P-glycoprotein substrate - 0.8531 85.31%
CYP3A4 substrate + 0.5673 56.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7726 77.26%
CYP3A4 inhibition + 0.6209 62.09%
CYP2C9 inhibition - 0.6300 63.00%
CYP2C19 inhibition + 0.6094 60.94%
CYP2D6 inhibition - 0.9059 90.59%
CYP1A2 inhibition + 0.7734 77.34%
CYP2C8 inhibition - 0.6903 69.03%
CYP inhibitory promiscuity + 0.7666 76.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9618 96.18%
Carcinogenicity (trinary) Non-required 0.5966 59.66%
Eye corrosion - 0.9785 97.85%
Eye irritation - 0.7412 74.12%
Skin irritation - 0.7567 75.67%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3848 38.48%
Micronuclear - 0.5341 53.41%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.7978 79.78%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6289 62.89%
Acute Oral Toxicity (c) III 0.4540 45.40%
Estrogen receptor binding + 0.8662 86.62%
Androgen receptor binding + 0.5643 56.43%
Thyroid receptor binding + 0.5151 51.51%
Glucocorticoid receptor binding + 0.7929 79.29%
Aromatase binding - 0.7481 74.81%
PPAR gamma - 0.5390 53.90%
Honey bee toxicity - 0.8557 85.57%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9021 90.21%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.53% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.26% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.98% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.44% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.37% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.10% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.79% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.65% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.32% 93.99%
CHEMBL2581 P07339 Cathepsin D 86.10% 98.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.70% 95.89%
CHEMBL2535 P11166 Glucose transporter 85.44% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.34% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.53% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.43% 97.14%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.01% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.23% 91.11%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.70% 94.03%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.46% 96.38%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.29% 96.00%

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.
Ilex centrochinensis

Cross-Links

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PubChem 53349838
LOTUS LTS0014925
wikiData Q105178892