(3S)-1-ethoxy-8-methoxy-3,5-dimethyl-3,4-dihydro-1H-isochromen-6-ol

Details

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Internal ID 67659427-709b-4a49-ba06-507233b750da
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3S)-1-ethoxy-8-methoxy-3,5-dimethyl-3,4-dihydro-1H-isochromen-6-ol
SMILES (Canonical) CCOC1C2=C(C=C(C(=C2CC(O1)C)C)O)OC
SMILES (Isomeric) CCOC1C2=C(C=C(C(=C2C[C@@H](O1)C)C)O)OC
InChI InChI=1S/C14H20O4/c1-5-17-14-13-10(6-8(2)18-14)9(3)11(15)7-12(13)16-4/h7-8,14-15H,5-6H2,1-4H3/t8-,14?/m0/s1
InChI Key CLAXJTXPHPPOCK-BVVIDWAXSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H20O4
Molecular Weight 252.31 g/mol
Exact Mass 252.13615911 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.71
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 (3S)-1-ethoxy-8-methoxy-3,5-dimethyl-3,4-dihydro-1H-isochromen-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9647 96.47%
Caco-2 + 0.8644 86.44%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5708 57.08%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.8919 89.19%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7981 79.81%
P-glycoprotein inhibitior - 0.9019 90.19%
P-glycoprotein substrate - 0.7326 73.26%
CYP3A4 substrate + 0.5263 52.63%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate + 0.4060 40.60%
CYP3A4 inhibition - 0.8657 86.57%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5600 56.00%
CYP2D6 inhibition - 0.8671 86.71%
CYP1A2 inhibition + 0.6798 67.98%
CYP2C8 inhibition - 0.6287 62.87%
CYP inhibitory promiscuity + 0.5111 51.11%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9013 90.13%
Carcinogenicity (trinary) Non-required 0.6468 64.68%
Eye corrosion - 0.9860 98.60%
Eye irritation + 0.5866 58.66%
Skin irritation - 0.8214 82.14%
Skin corrosion - 0.9689 96.89%
Ames mutagenesis - 0.5391 53.91%
Human Ether-a-go-go-Related Gene inhibition - 0.4512 45.12%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.5031 50.31%
skin sensitisation - 0.8639 86.39%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7032 70.32%
Acute Oral Toxicity (c) III 0.4806 48.06%
Estrogen receptor binding - 0.6050 60.50%
Androgen receptor binding + 0.5537 55.37%
Thyroid receptor binding + 0.6310 63.10%
Glucocorticoid receptor binding - 0.6562 65.62%
Aromatase binding - 0.8630 86.30%
PPAR gamma - 0.5386 53.86%
Honey bee toxicity - 0.8889 88.89%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9231 92.31%

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 96.64% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.25% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 94.65% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.08% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.77% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.96% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.77% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.92% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.69% 90.00%
CHEMBL2581 P07339 Cathepsin D 84.39% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.76% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.39% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 81.20% 94.73%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.04% 89.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.91% 89.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.78% 91.79%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.12% 97.36%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11345759
LOTUS LTS0015764
wikiData Q104963134