5,5,9-Trimethyl-3-oxatricyclo[5.5.1.04,13]tridecane-2,8-dione

Details

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Internal ID 95ec5de3-4b72-409c-bc95-d394cc44196b
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 5,5,9-trimethyl-3-oxatricyclo[5.5.1.04,13]tridecane-2,8-dione
SMILES (Canonical) CC1CCCC2C3C(C1=O)CC(C3OC2=O)(C)C
SMILES (Isomeric) CC1CCCC2C3C(C1=O)CC(C3OC2=O)(C)C
InChI InChI=1S/C15H22O3/c1-8-5-4-6-9-11-10(12(8)16)7-15(2,3)13(11)18-14(9)17/h8-11,13H,4-7H2,1-3H3
InChI Key UEOBEAJSRJXKEQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,5,9-Trimethyl-3-oxatricyclo[5.5.1.04,13]tridecane-2,8-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 + 0.8774 87.74%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5921 59.21%
OATP2B1 inhibitior - 0.8438 84.38%
OATP1B1 inhibitior + 0.8564 85.64%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9326 93.26%
P-glycoprotein inhibitior - 0.8168 81.68%
P-glycoprotein substrate - 0.8703 87.03%
CYP3A4 substrate + 0.5589 55.89%
CYP2C9 substrate - 0.7818 78.18%
CYP2D6 substrate - 0.8392 83.92%
CYP3A4 inhibition - 0.9468 94.68%
CYP2C9 inhibition - 0.8848 88.48%
CYP2C19 inhibition - 0.8629 86.29%
CYP2D6 inhibition - 0.9549 95.49%
CYP1A2 inhibition - 0.6608 66.08%
CYP2C8 inhibition - 0.9129 91.29%
CYP inhibitory promiscuity - 0.9770 97.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6357 63.57%
Eye corrosion - 0.9200 92.00%
Eye irritation - 0.6211 62.11%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.5875 58.75%
Ames mutagenesis - 0.7770 77.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6452 64.52%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.4932 49.32%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.8745 87.45%
Acute Oral Toxicity (c) III 0.6233 62.33%
Estrogen receptor binding - 0.5099 50.99%
Androgen receptor binding + 0.5618 56.18%
Thyroid receptor binding - 0.6017 60.17%
Glucocorticoid receptor binding - 0.6960 69.60%
Aromatase binding - 0.7311 73.11%
PPAR gamma - 0.7003 70.03%
Honey bee toxicity - 0.8917 89.17%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9517 95.17%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.95% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.75% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.37% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.62% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.66% 92.94%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.54% 96.77%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 86.26% 83.57%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.09% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.08% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.89% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.76% 96.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.88% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.53% 97.14%
CHEMBL1902 P62942 FK506-binding protein 1A 83.82% 97.05%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.89% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.25% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 80.16% 92.50%

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.
Asteriscus aquaticus

Cross-Links

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PubChem 73115665
LOTUS LTS0126810
wikiData Q105271025