Phenatic acid B

Details

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Internal ID be1080d5-45bc-4688-8645-fcdb2a1e8896
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 2-[2-(2-hydroxy-3,5-dimethylbenzoyl)-5-oxooxolan-3-yl]acetic acid
SMILES (Canonical) CC1=CC(=C(C(=C1)C(=O)C2C(CC(=O)O2)CC(=O)O)O)C
SMILES (Isomeric) CC1=CC(=C(C(=C1)C(=O)C2C(CC(=O)O2)CC(=O)O)O)C
InChI InChI=1S/C15H16O6/c1-7-3-8(2)13(19)10(4-7)14(20)15-9(5-11(16)17)6-12(18)21-15/h3-4,9,15,19H,5-6H2,1-2H3,(H,16,17)
InChI Key XMMWCOYSUBFDCF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O6
Molecular Weight 292.28 g/mol
Exact Mass 292.09468823 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.60
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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2-[2-(2-hydroxy-3,5-dimethylbenzoyl)-5-oxooxolan-3-yl]acetic acid

2D Structure

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2D Structure of Phenatic acid B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8722 87.22%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8070 80.70%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.8302 83.02%
OATP1B3 inhibitior + 0.9108 91.08%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9080 90.80%
P-glycoprotein inhibitior - 0.9398 93.98%
P-glycoprotein substrate - 0.8478 84.78%
CYP3A4 substrate - 0.5763 57.63%
CYP2C9 substrate + 0.6230 62.30%
CYP2D6 substrate - 0.8836 88.36%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.7872 78.72%
CYP2C19 inhibition - 0.7840 78.40%
CYP2D6 inhibition - 0.9193 91.93%
CYP1A2 inhibition - 0.8030 80.30%
CYP2C8 inhibition - 0.7502 75.02%
CYP inhibitory promiscuity - 0.8360 83.60%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8811 88.11%
Carcinogenicity (trinary) Non-required 0.6309 63.09%
Eye corrosion - 0.9560 95.60%
Eye irritation - 0.5612 56.12%
Skin irritation - 0.6401 64.01%
Skin corrosion - 0.8641 86.41%
Ames mutagenesis - 0.6428 64.28%
Human Ether-a-go-go-Related Gene inhibition - 0.6050 60.50%
Micronuclear + 0.6394 63.94%
Hepatotoxicity + 0.7806 78.06%
skin sensitisation - 0.7498 74.98%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7639 76.39%
Acute Oral Toxicity (c) III 0.4361 43.61%
Estrogen receptor binding - 0.5637 56.37%
Androgen receptor binding + 0.6662 66.62%
Thyroid receptor binding - 0.6417 64.17%
Glucocorticoid receptor binding + 0.5885 58.85%
Aromatase binding - 0.8224 82.24%
PPAR gamma - 0.4846 48.46%
Honey bee toxicity - 0.9497 94.97%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8444 84.44%

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
CHEMBL2581 P07339 Cathepsin D 96.05% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.74% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.08% 93.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.73% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.54% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.44% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.15% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.68% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.15% 89.00%
CHEMBL4530 P00488 Coagulation factor XIII 80.82% 96.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11471869
LOTUS LTS0090401
wikiData Q75064117