Methyl 3-(5-methoxy-2,2-dimethylchromen-6-yl)propanoate

Details

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Internal ID 9ae48f8d-1e93-43f2-a8fd-73e899bece40
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name methyl 3-(5-methoxy-2,2-dimethylchromen-6-yl)propanoate
SMILES (Canonical) CC1(C=CC2=C(O1)C=CC(=C2OC)CCC(=O)OC)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=CC(=C2OC)CCC(=O)OC)C
InChI InChI=1S/C16H20O4/c1-16(2)10-9-12-13(20-16)7-5-11(15(12)19-4)6-8-14(17)18-3/h5,7,9-10H,6,8H2,1-4H3
InChI Key XRJVRHOPKCXHKJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O4
Molecular Weight 276.33 g/mol
Exact Mass 276.13615911 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 4
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 Methyl 3-(5-methoxy-2,2-dimethylchromen-6-yl)propanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.9494 94.94%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7173 71.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8975 89.75%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.4669 46.69%
P-glycoprotein inhibitior - 0.9074 90.74%
P-glycoprotein substrate - 0.7606 76.06%
CYP3A4 substrate + 0.5526 55.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8032 80.32%
CYP3A4 inhibition - 0.7019 70.19%
CYP2C9 inhibition - 0.8095 80.95%
CYP2C19 inhibition - 0.6095 60.95%
CYP2D6 inhibition - 0.8903 89.03%
CYP1A2 inhibition + 0.5147 51.47%
CYP2C8 inhibition - 0.6503 65.03%
CYP inhibitory promiscuity - 0.5286 52.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6420 64.20%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.5470 54.70%
Skin irritation - 0.7505 75.05%
Skin corrosion - 0.9499 94.99%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6915 69.15%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5914 59.14%
skin sensitisation - 0.7874 78.74%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.4598 45.98%
Acute Oral Toxicity (c) III 0.5357 53.57%
Estrogen receptor binding + 0.7796 77.96%
Androgen receptor binding - 0.6542 65.42%
Thyroid receptor binding + 0.5612 56.12%
Glucocorticoid receptor binding + 0.6436 64.36%
Aromatase binding + 0.6160 61.60%
PPAR gamma + 0.6957 69.57%
Honey bee toxicity - 0.9015 90.15%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9561 95.61%

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 98.64% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.52% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.59% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.76% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.61% 99.17%
CHEMBL4208 P20618 Proteasome component C5 87.35% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.98% 86.33%
CHEMBL2581 P07339 Cathepsin D 86.32% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.89% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.13% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.17% 94.73%

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.
Hortia oreadica

Cross-Links

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PubChem 11219612
LOTUS LTS0224324
wikiData Q104201276