Oxolobaric acid

Details

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Internal ID a5808dec-e800-4d6a-89fa-2265f6d65a6f
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 3-hydroxy-9-methoxy-6-oxo-7-(4-oxopentanoyl)-1-pentylbenzo[b][1,4]benzodioxepine-2-carboxylic acid
SMILES (Canonical) CCCCCC1=C(C(=CC2=C1OC3=CC(=CC(=C3C(=O)O2)C(=O)CCC(=O)C)OC)O)C(=O)O
SMILES (Isomeric) CCCCCC1=C(C(=CC2=C1OC3=CC(=CC(=C3C(=O)O2)C(=O)CCC(=O)C)OC)O)C(=O)O
InChI InChI=1S/C25H26O9/c1-4-5-6-7-15-21(24(29)30)18(28)12-20-23(15)33-19-11-14(32-3)10-16(22(19)25(31)34-20)17(27)9-8-13(2)26/h10-12,28H,4-9H2,1-3H3,(H,29,30)
InChI Key MWCXCMJYRLNDGU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O9
Molecular Weight 470.50 g/mol
Exact Mass 470.15768240 g/mol
Topological Polar Surface Area (TPSA) 136.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.71
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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3-hydroxy-9-methoxy-6-oxo-7-(4-oxopentanoyl)-1-pentylbenzo[b][1,4]benzodioxepine-2-carboxylic acid
3-hydroxy-9-methoxy-6-oxo-7-(4-oxopentanoyl)-1-pentylbenzo(b)(1,4)benzodioxepine-2-carboxylic acid
RefChem:168983
CHEBI:201679

2D Structure

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2D Structure of Oxolobaric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8309 83.09%
Caco-2 - 0.6804 68.04%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6125 61.25%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior - 0.6349 63.49%
OATP1B3 inhibitior - 0.5698 56.98%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8467 84.67%
P-glycoprotein inhibitior + 0.6995 69.95%
P-glycoprotein substrate - 0.6385 63.85%
CYP3A4 substrate + 0.6131 61.31%
CYP2C9 substrate + 0.8036 80.36%
CYP2D6 substrate - 0.8592 85.92%
CYP3A4 inhibition - 0.7594 75.94%
CYP2C9 inhibition - 0.8060 80.60%
CYP2C19 inhibition - 0.7398 73.98%
CYP2D6 inhibition - 0.8885 88.85%
CYP1A2 inhibition - 0.6677 66.77%
CYP2C8 inhibition + 0.7929 79.29%
CYP inhibitory promiscuity - 0.7751 77.51%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6757 67.57%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.7325 73.25%
Skin irritation - 0.7763 77.63%
Skin corrosion - 0.9244 92.44%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3757 37.57%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5109 51.09%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7936 79.36%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4885 48.85%
Acute Oral Toxicity (c) III 0.4277 42.77%
Estrogen receptor binding + 0.7023 70.23%
Androgen receptor binding + 0.6188 61.88%
Thyroid receptor binding - 0.6395 63.95%
Glucocorticoid receptor binding + 0.8004 80.04%
Aromatase binding + 0.5677 56.77%
PPAR gamma + 0.6478 64.78%
Honey bee toxicity - 0.8495 84.95%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9917 99.17%

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%
CHEMBL2581 P07339 Cathepsin D 98.02% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 95.83% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.18% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.13% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.40% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 92.38% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.19% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.22% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.36% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.59% 95.50%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.46% 92.08%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.50% 97.21%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.87% 91.71%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.43% 94.80%
CHEMBL230 P35354 Cyclooxygenase-2 84.33% 89.63%
CHEMBL1907 P15144 Aminopeptidase N 82.50% 93.31%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.88% 93.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.83% 92.62%

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 139584339
LOTUS LTS0031419
wikiData Q77310506