1-(4-Ethoxy-3-hydroxy-5,7,8-trimethoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)ethanone

Details

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Internal ID 14e01442-e935-4830-b7b2-9cbf177077b9
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 1-(4-ethoxy-3-hydroxy-5,7,8-trimethoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H26O7/c1-8-24-15-11-12(21-5)10(9(2)19)13(22-6)16(23-7)14(11)25-18(3,4)17(15)20/h15,17,20H,8H2,1-7H3
InChI Key AMERCRIYENEJRO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O7
Molecular Weight 354.40 g/mol
Exact Mass 354.16785316 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(4-Ethoxy-3-hydroxy-5,7,8-trimethoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9716 97.16%
Caco-2 + 0.6919 69.19%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7648 76.48%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9005 90.05%
OATP1B3 inhibitior + 0.9706 97.06%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5840 58.40%
P-glycoprotein inhibitior - 0.6139 61.39%
P-glycoprotein substrate - 0.7825 78.25%
CYP3A4 substrate + 0.6008 60.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7344 73.44%
CYP3A4 inhibition - 0.5824 58.24%
CYP2C9 inhibition + 0.7546 75.46%
CYP2C19 inhibition + 0.8583 85.83%
CYP2D6 inhibition - 0.7564 75.64%
CYP1A2 inhibition + 0.8651 86.51%
CYP2C8 inhibition - 0.6948 69.48%
CYP inhibitory promiscuity + 0.6425 64.25%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6527 65.27%
Eye corrosion - 0.9794 97.94%
Eye irritation + 0.5505 55.05%
Skin irritation - 0.7876 78.76%
Skin corrosion - 0.9567 95.67%
Ames mutagenesis - 0.5854 58.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4948 49.48%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.6694 66.94%
skin sensitisation - 0.8418 84.18%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5797 57.97%
Acute Oral Toxicity (c) III 0.5650 56.50%
Estrogen receptor binding + 0.8407 84.07%
Androgen receptor binding - 0.5940 59.40%
Thyroid receptor binding + 0.7242 72.42%
Glucocorticoid receptor binding + 0.7338 73.38%
Aromatase binding - 0.5741 57.41%
PPAR gamma + 0.7844 78.44%
Honey bee toxicity - 0.8464 84.64%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7155 71.55%
Fish aquatic toxicity + 0.8403 84.03%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.73% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.97% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.82% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.45% 97.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.59% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.42% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 84.20% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.91% 97.25%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.54% 94.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.67% 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.
Melicope pteleifolia

Cross-Links

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PubChem 15383043
LOTUS LTS0233648
wikiData Q104914577