10-Hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),9-triene-6,11-dione

Details

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Internal ID 6c20ebf5-d5ba-4ed4-9b8a-5627a5212677
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 10-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),9-triene-6,11-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O4/c1-6-4-9(16)10-7(2)5-19-15-8(3)13(17)14(18)11(6)12(10)15/h6-7,18H,4-5H2,1-3H3
InChI Key AKDXIPQJXIUTOK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.80
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),9-triene-6,11-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9698 96.98%
Caco-2 + 0.6482 64.82%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7697 76.97%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9173 91.73%
OATP1B3 inhibitior + 0.9715 97.15%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5787 57.87%
P-glycoprotein inhibitior - 0.8564 85.64%
P-glycoprotein substrate - 0.8059 80.59%
CYP3A4 substrate - 0.5449 54.49%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8642 86.42%
CYP3A4 inhibition - 0.7847 78.47%
CYP2C9 inhibition - 0.8060 80.60%
CYP2C19 inhibition - 0.8020 80.20%
CYP2D6 inhibition - 0.9163 91.63%
CYP1A2 inhibition - 0.6222 62.22%
CYP2C8 inhibition - 0.9630 96.30%
CYP inhibitory promiscuity - 0.8885 88.85%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5946 59.46%
Eye corrosion - 0.9842 98.42%
Eye irritation + 0.8572 85.72%
Skin irritation - 0.6036 60.36%
Skin corrosion - 0.9505 95.05%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7336 73.36%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5803 58.03%
skin sensitisation - 0.8134 81.34%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5057 50.57%
Acute Oral Toxicity (c) III 0.4494 44.94%
Estrogen receptor binding - 0.5344 53.44%
Androgen receptor binding - 0.5672 56.72%
Thyroid receptor binding + 0.5480 54.80%
Glucocorticoid receptor binding + 0.6112 61.12%
Aromatase binding - 0.8400 84.00%
PPAR gamma - 0.7411 74.11%
Honey bee toxicity - 0.8802 88.02%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9043 90.43%

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
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.93% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.54% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.14% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.47% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.73% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 81.05% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Thespesia populnea

Cross-Links

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PubChem 21589523
LOTUS LTS0175593
wikiData Q104913570