(3R,7R)-4,8,8-trimethyl-2-oxatricyclo[5.1.0.01,3]oct-4-ene

Details

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Internal ID 99d08eee-c2d6-4005-b202-d6be0d3c767f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (3R,7R)-4,8,8-trimethyl-2-oxatricyclo[5.1.0.01,3]oct-4-ene
SMILES (Canonical) CC1=CCC2C(C23C1O3)(C)C
SMILES (Isomeric) CC1=CC[C@@H]2C(C23[C@@H]1O3)(C)C
InChI InChI=1S/C10H14O/c1-6-4-5-7-9(2,3)10(7)8(6)11-10/h4,7-8H,5H2,1-3H3/t7-,8-,10?/m1/s1
InChI Key OOMNRJSJIJYWGT-SZBHIRRCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.13
H-Bond Acceptor 1
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 (3R,7R)-4,8,8-trimethyl-2-oxatricyclo[5.1.0.01,3]oct-4-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.5779 57.79%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6822 68.22%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9541 95.41%
P-glycoprotein inhibitior - 0.9521 95.21%
P-glycoprotein substrate - 0.9529 95.29%
CYP3A4 substrate - 0.5470 54.70%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.7447 74.47%
CYP3A4 inhibition - 0.9372 93.72%
CYP2C9 inhibition - 0.6510 65.10%
CYP2C19 inhibition + 0.5689 56.89%
CYP2D6 inhibition - 0.9071 90.71%
CYP1A2 inhibition + 0.5378 53.78%
CYP2C8 inhibition - 0.9143 91.43%
CYP inhibitory promiscuity - 0.6041 60.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6936 69.36%
Carcinogenicity (trinary) Non-required 0.5368 53.68%
Eye corrosion - 0.9045 90.45%
Eye irritation + 0.9018 90.18%
Skin irritation + 0.6667 66.67%
Skin corrosion - 0.9200 92.00%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4900 49.00%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.7461 74.61%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5835 58.35%
Acute Oral Toxicity (c) III 0.7028 70.28%
Estrogen receptor binding - 0.7186 71.86%
Androgen receptor binding - 0.5381 53.81%
Thyroid receptor binding - 0.8716 87.16%
Glucocorticoid receptor binding - 0.8901 89.01%
Aromatase binding - 0.8886 88.86%
PPAR gamma - 0.7070 70.70%
Honey bee toxicity - 0.8945 89.45%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.8463 84.63%

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 86.97% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.12% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.01% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.38% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.72% 86.00%

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.
Zieria smithii

Cross-Links

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PubChem 163189893
LOTUS LTS0175607
wikiData Q105195478