Swerilactone F

Details

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Internal ID 60a655e0-bdc9-4672-a128-575862070bd4
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 1,2,5,6,8,9-hexahydroisochromeno[7,6-f]isochromene-4,11-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O4/c17-15-12-2-1-9-7-10-3-5-19-16(18)14(10)8-13(9)11(12)4-6-20-15/h7-8H,1-6H2
InChI Key CACOEDMTMUFXDB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O4
Molecular Weight 270.28 g/mol
Exact Mass 270.08920892 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1,2,5,6,8,9-hexahydroisochromeno[7,6-f]isochromene-4,11-dione
1,2,5,6,8,9-Hexahydro-4H,11H-isochromeno[7,6-f]isochromene-4,11-dione

2D Structure

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2D Structure of Swerilactone F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 + 0.6203 62.03%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8627 86.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9363 93.63%
OATP1B3 inhibitior + 0.9619 96.19%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6088 60.88%
P-glycoprotein inhibitior - 0.8865 88.65%
P-glycoprotein substrate - 0.9480 94.80%
CYP3A4 substrate - 0.5807 58.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8285 82.85%
CYP3A4 inhibition - 0.7505 75.05%
CYP2C9 inhibition - 0.6168 61.68%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7599 75.99%
CYP1A2 inhibition + 0.5549 55.49%
CYP2C8 inhibition - 0.9347 93.47%
CYP inhibitory promiscuity - 0.7869 78.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6741 67.41%
Eye corrosion - 0.9187 91.87%
Eye irritation + 0.9250 92.50%
Skin irritation - 0.8149 81.49%
Skin corrosion - 0.9632 96.32%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5292 52.92%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.7173 71.73%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6294 62.94%
Acute Oral Toxicity (c) III 0.4763 47.63%
Estrogen receptor binding + 0.6699 66.99%
Androgen receptor binding + 0.6589 65.89%
Thyroid receptor binding - 0.6055 60.55%
Glucocorticoid receptor binding + 0.5863 58.63%
Aromatase binding - 0.5700 57.00%
PPAR gamma + 0.6106 61.06%
Honey bee toxicity - 0.8900 89.00%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9803 98.03%

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 92.35% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.53% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.65% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 89.55% 91.49%
CHEMBL2581 P07339 Cathepsin D 86.80% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 86.50% 89.63%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.95% 93.40%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 80.27% 98.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.21% 100.00%

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 46209730
NPASS NPC78617
LOTUS LTS0081810
wikiData Q104950941