3-(7-Methoxy-2,2-dimethylchromen-6-yl)prop-2-enoic acid

Details

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Internal ID 6363a8b9-4d0b-4ec4-958c-23b80ab5978f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 3-(7-methoxy-2,2-dimethylchromen-6-yl)prop-2-enoic acid
SMILES (Canonical) CC1(C=CC2=CC(=C(C=C2O1)OC)C=CC(=O)O)C
SMILES (Isomeric) CC1(C=CC2=CC(=C(C=C2O1)OC)C=CC(=O)O)C
InChI InChI=1S/C15H16O4/c1-15(2)7-6-11-8-10(4-5-14(16)17)12(18-3)9-13(11)19-15/h4-9H,1-3H3,(H,16,17)
InChI Key KFKMQYCHFDVMKG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 3
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 3-(7-Methoxy-2,2-dimethylchromen-6-yl)prop-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.8698 86.98%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7278 72.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8623 86.23%
OATP1B3 inhibitior + 0.9778 97.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6893 68.93%
P-glycoprotein inhibitior - 0.9159 91.59%
P-glycoprotein substrate - 0.8247 82.47%
CYP3A4 substrate + 0.5359 53.59%
CYP2C9 substrate - 0.6079 60.79%
CYP2D6 substrate - 0.8686 86.86%
CYP3A4 inhibition - 0.5446 54.46%
CYP2C9 inhibition - 0.7950 79.50%
CYP2C19 inhibition - 0.5380 53.80%
CYP2D6 inhibition - 0.8696 86.96%
CYP1A2 inhibition + 0.5516 55.16%
CYP2C8 inhibition + 0.5694 56.94%
CYP inhibitory promiscuity - 0.5840 58.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Danger 0.4706 47.06%
Eye corrosion - 0.9724 97.24%
Eye irritation + 0.8539 85.39%
Skin irritation - 0.7038 70.38%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.5926 59.26%
skin sensitisation - 0.8625 86.25%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.5863 58.63%
Acute Oral Toxicity (c) II 0.4681 46.81%
Estrogen receptor binding + 0.8779 87.79%
Androgen receptor binding - 0.5741 57.41%
Thyroid receptor binding + 0.5874 58.74%
Glucocorticoid receptor binding + 0.5549 55.49%
Aromatase binding + 0.7265 72.65%
PPAR gamma + 0.8658 86.58%
Honey bee toxicity - 0.9009 90.09%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6955 69.55%
Fish aquatic toxicity + 0.9660 96.60%

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 96.27% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.51% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.45% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.34% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.22% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.24% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.14% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.77% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.67% 85.14%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.41% 89.50%
CHEMBL4208 P20618 Proteasome component C5 81.68% 90.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.34% 85.30%

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.
Ficus subcuneata

Cross-Links

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PubChem 162986156
LOTUS LTS0265087
wikiData Q105140433