(1S,9S)-2,2,9-trimethyl-8,12-dioxatricyclo[7.2.1.01,6]dodec-5-ene

Details

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Internal ID 36d96672-5775-4dc1-b756-e5f178919eab
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (1S,9S)-2,2,9-trimethyl-8,12-dioxatricyclo[7.2.1.01,6]dodec-5-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H20O2/c1-11(2)6-4-5-10-9-14-12(3)7-8-13(10,11)15-12/h5H,4,6-9H2,1-3H3/t12-,13+/m0/s1
InChI Key AKKNWGRLXKHQDH-QWHCGFSZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O2
Molecular Weight 208.30 g/mol
Exact Mass 208.146329876 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 2
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 (1S,9S)-2,2,9-trimethyl-8,12-dioxatricyclo[7.2.1.01,6]dodec-5-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.9329 93.29%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5523 55.23%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9262 92.62%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9265 92.65%
P-glycoprotein inhibitior - 0.9687 96.87%
P-glycoprotein substrate - 0.8803 88.03%
CYP3A4 substrate - 0.5136 51.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7728 77.28%
CYP3A4 inhibition - 0.9273 92.73%
CYP2C9 inhibition - 0.6948 69.48%
CYP2C19 inhibition - 0.6145 61.45%
CYP2D6 inhibition - 0.8735 87.35%
CYP1A2 inhibition - 0.6456 64.56%
CYP2C8 inhibition - 0.8532 85.32%
CYP inhibitory promiscuity - 0.7681 76.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5632 56.32%
Eye corrosion - 0.9757 97.57%
Eye irritation + 0.5863 58.63%
Skin irritation - 0.7883 78.83%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.6676 66.76%
skin sensitisation - 0.5514 55.14%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.6787 67.87%
Acute Oral Toxicity (c) III 0.6637 66.37%
Estrogen receptor binding - 0.8923 89.23%
Androgen receptor binding - 0.5552 55.52%
Thyroid receptor binding - 0.7456 74.56%
Glucocorticoid receptor binding - 0.8274 82.74%
Aromatase binding - 0.7227 72.27%
PPAR gamma - 0.8585 85.85%
Honey bee toxicity - 0.8793 87.93%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9620 96.20%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.38% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.13% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.00% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.30% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.22% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.07% 86.33%

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.
Cydonia oblonga

Cross-Links

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PubChem 162889958
LOTUS LTS0060493
wikiData Q104913699