2,2-Dimethyl-6-carboxyethenyl-2h-1-benzopyran

Details

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Internal ID bc455e65-f248-4a97-bbfb-2f5030d4a788
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 3-(2,2-dimethylchromen-6-yl)prop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O3/c1-14(2)8-7-11-9-10(4-6-13(15)16)3-5-12(11)17-14/h3-9H,1-2H3,(H,15,16)
InChI Key IHRUERBZEZCICE-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O3
Molecular Weight 230.26 g/mol
Exact Mass 230.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2,2-dimethyl-6-carboxyethenyl-2h-1-benzopyran

2D Structure

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2D Structure of 2,2-Dimethyl-6-carboxyethenyl-2h-1-benzopyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.8411 84.11%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7635 76.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9277 92.77%
OATP1B3 inhibitior + 0.9723 97.23%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6425 64.25%
P-glycoprotein inhibitior - 0.9490 94.90%
P-glycoprotein substrate - 0.8976 89.76%
CYP3A4 substrate - 0.5348 53.48%
CYP2C9 substrate - 0.6079 60.79%
CYP2D6 substrate - 0.8686 86.86%
CYP3A4 inhibition - 0.7656 76.56%
CYP2C9 inhibition + 0.6182 61.82%
CYP2C19 inhibition - 0.7467 74.67%
CYP2D6 inhibition - 0.8729 87.29%
CYP1A2 inhibition - 0.6922 69.22%
CYP2C8 inhibition + 0.4689 46.89%
CYP inhibitory promiscuity - 0.6581 65.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8313 83.13%
Carcinogenicity (trinary) Non-required 0.6349 63.49%
Eye corrosion - 0.9555 95.55%
Eye irritation + 0.8894 88.94%
Skin irritation + 0.5313 53.13%
Skin corrosion - 0.9260 92.60%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5285 52.85%
Micronuclear - 0.5041 50.41%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.5536 55.36%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6219 62.19%
Acute Oral Toxicity (c) III 0.7071 70.71%
Estrogen receptor binding + 0.8100 81.00%
Androgen receptor binding + 0.6464 64.64%
Thyroid receptor binding - 0.5568 55.68%
Glucocorticoid receptor binding - 0.6319 63.19%
Aromatase binding + 0.5201 52.01%
PPAR gamma + 0.7324 73.24%
Honey bee toxicity - 0.9524 95.24%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6952 69.52%
Fish aquatic toxicity + 0.9579 95.79%

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 95.11% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.64% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.30% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 90.01% 91.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.69% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.35% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.83% 95.56%
CHEMBL4208 P20618 Proteasome component C5 87.06% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.63% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.47% 85.14%
CHEMBL2581 P07339 Cathepsin D 82.76% 98.95%

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.
Baccharis linearis

Cross-Links

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PubChem 53916933
LOTUS LTS0028986
wikiData Q105113222