7-Methoxy-2,2-dimethylchromene-6-carboxylic acid

Details

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Internal ID fec5d156-e4d4-4be4-9e44-74ee5e40ef0d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 7-methoxy-2,2-dimethylchromene-6-carboxylic acid
SMILES (Canonical) CC1(C=CC2=CC(=C(C=C2O1)OC)C(=O)O)C
SMILES (Isomeric) CC1(C=CC2=CC(=C(C=C2O1)OC)C(=O)O)C
InChI InChI=1S/C13H14O4/c1-13(2)5-4-8-6-9(12(14)15)11(16-3)7-10(8)17-13/h4-7H,1-3H3,(H,14,15)
InChI Key WVJWSWIKHOYGHH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O4
Molecular Weight 234.25 g/mol
Exact Mass 234.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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179457-70-6
7-methoxy-2,2-dimethylchromene-6-carboxylic acid
HY-N9733
AKOS040761007
CS-0203718

2D Structure

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2D Structure of 7-Methoxy-2,2-dimethylchromene-6-carboxylic 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 + 0.8813 88.13%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7278 72.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9778 97.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7582 75.82%
P-glycoprotein inhibitior - 0.9105 91.05%
P-glycoprotein substrate - 0.9051 90.51%
CYP3A4 substrate - 0.5793 57.93%
CYP2C9 substrate + 0.5872 58.72%
CYP2D6 substrate - 0.8678 86.78%
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 - 0.6306 63.06%
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 + 0.9446 94.46%
Skin irritation - 0.7038 70.38%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6417 64.17%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.5324 53.24%
skin sensitisation - 0.8625 86.25%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6288 62.88%
Acute Oral Toxicity (c) II 0.4681 46.81%
Estrogen receptor binding + 0.7885 78.85%
Androgen receptor binding - 0.8474 84.74%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5755 57.55%
Aromatase binding + 0.5583 55.83%
PPAR gamma + 0.6992 69.92%
Honey bee toxicity - 0.9412 94.12%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7700 77.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.70% 96.09%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.31% 87.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.97% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.42% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.04% 81.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.80% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.50% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.87% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 84.54% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.52% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.70% 90.00%
CHEMBL2535 P11166 Glucose transporter 83.42% 98.75%
CHEMBL1811 P34995 Prostanoid EP1 receptor 83.20% 95.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.98% 94.42%
CHEMBL2581 P07339 Cathepsin D 82.93% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.87% 95.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.11% 93.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.70% 96.77%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.39% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.97% 94.00%

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.
Gentiana lutea
Gentiana macrophylla

Cross-Links

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PubChem 5319400
LOTUS LTS0066073
wikiData Q104399844