Corynesidone A

Details

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Internal ID 63205b83-7f7e-4cd1-b166-0c80b2e06729
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 3,9-dihydroxy-1,7-dimethylbenzo[b][1,4]benzodioxepin-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O5/c1-7-3-9(16)5-11-13(7)15(18)20-12-6-10(17)4-8(2)14(12)19-11/h3-6,16-17H,1-2H3
InChI Key KCAVPBLHZJMMLN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O5
Molecular Weight 272.25 g/mol
Exact Mass 272.06847348 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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CHEMBL3221175

2D Structure

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2D Structure of Corynesidone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9721 97.21%
Caco-2 + 0.7920 79.20%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7193 71.93%
OATP2B1 inhibitior - 0.7181 71.81%
OATP1B1 inhibitior + 0.8416 84.16%
OATP1B3 inhibitior - 0.2933 29.33%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6394 63.94%
P-glycoprotein inhibitior - 0.8930 89.30%
P-glycoprotein substrate - 0.9759 97.59%
CYP3A4 substrate - 0.6033 60.33%
CYP2C9 substrate - 0.5906 59.06%
CYP2D6 substrate - 0.8638 86.38%
CYP3A4 inhibition - 0.8190 81.90%
CYP2C9 inhibition - 0.7578 75.78%
CYP2C19 inhibition - 0.8142 81.42%
CYP2D6 inhibition - 0.8832 88.32%
CYP1A2 inhibition - 0.6677 66.77%
CYP2C8 inhibition - 0.7432 74.32%
CYP inhibitory promiscuity - 0.7771 77.71%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6086 60.86%
Eye corrosion - 0.9830 98.30%
Eye irritation + 0.9776 97.76%
Skin irritation - 0.5455 54.55%
Skin corrosion - 0.9617 96.17%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4833 48.33%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.8063 80.63%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5780 57.80%
Acute Oral Toxicity (c) II 0.5481 54.81%
Estrogen receptor binding + 0.8677 86.77%
Androgen receptor binding - 0.5534 55.34%
Thyroid receptor binding + 0.5552 55.52%
Glucocorticoid receptor binding + 0.7687 76.87%
Aromatase binding + 0.8300 83.00%
PPAR gamma + 0.5464 54.64%
Honey bee toxicity - 0.9344 93.44%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9553 95.53%

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 96.05% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.65% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 93.65% 94.73%
CHEMBL2581 P07339 Cathepsin D 91.27% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.13% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.94% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.19% 99.23%
CHEMBL4208 P20618 Proteasome component C5 83.85% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.83% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.52% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.43% 94.80%

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 42611455
LOTUS LTS0118835
wikiData Q104170139