Conphysodalic acid

Details

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Internal ID 03f5053e-0f31-410d-8f3a-7568dfd57fdc
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-(acetyloxymethyl)-3,9-dihydroxy-10-(hydroxymethyl)-1,7-dimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O10/c1-7-4-12(23)10(5-21)17-13(7)20(27)30-18-11(6-28-9(3)22)15(24)14(19(25)26)8(2)16(18)29-17/h4,21,23-24H,5-6H2,1-3H3,(H,25,26)
InChI Key ADGOFPAXWRMONQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O10
Molecular Weight 418.30 g/mol
Exact Mass 418.08999677 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Conphysodalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8857 88.57%
Caco-2 - 0.5703 57.03%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.4522 45.22%
OATP2B1 inhibitior - 0.7149 71.49%
OATP1B1 inhibitior - 0.3298 32.98%
OATP1B3 inhibitior - 0.2212 22.12%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7549 75.49%
P-glycoprotein inhibitior - 0.7096 70.96%
P-glycoprotein substrate - 0.8301 83.01%
CYP3A4 substrate + 0.5510 55.10%
CYP2C9 substrate + 0.7843 78.43%
CYP2D6 substrate - 0.8881 88.81%
CYP3A4 inhibition - 0.8972 89.72%
CYP2C9 inhibition - 0.8145 81.45%
CYP2C19 inhibition - 0.8372 83.72%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition - 0.8346 83.46%
CYP2C8 inhibition + 0.6435 64.35%
CYP inhibitory promiscuity - 0.8307 83.07%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7214 72.14%
Eye corrosion - 0.9898 98.98%
Eye irritation + 0.6497 64.97%
Skin irritation - 0.8182 81.82%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis + 0.7340 73.40%
Human Ether-a-go-go-Related Gene inhibition + 0.6810 68.10%
Micronuclear - 0.5226 52.26%
Hepatotoxicity - 0.6465 64.65%
skin sensitisation - 0.8498 84.98%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5918 59.18%
Acute Oral Toxicity (c) III 0.5379 53.79%
Estrogen receptor binding + 0.8799 87.99%
Androgen receptor binding + 0.6210 62.10%
Thyroid receptor binding - 0.6724 67.24%
Glucocorticoid receptor binding + 0.6059 60.59%
Aromatase binding - 0.5393 53.93%
PPAR gamma + 0.5593 55.93%
Honey bee toxicity - 0.9183 91.83%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9745 97.45%

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 98.12% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.79% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.81% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.67% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.03% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.77% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.64% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.33% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.98% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.91% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.54% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 84.63% 91.49%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.51% 91.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.71% 94.42%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.12% 96.95%

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 122209035
LOTUS LTS0233999
wikiData Q77370025