E-Ocimene oxide

Details

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Internal ID 65ac9e21-51c5-4bf2-816c-90235cb96419
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (2R,3S)-2-ethenyl-2-methyl-3-(3-methylbut-2-enyl)oxirane
SMILES (Canonical) CC(=CCC1C(O1)(C)C=C)C
SMILES (Isomeric) CC(=CC[C@H]1[C@@](O1)(C)C=C)C
InChI InChI=1S/C10H16O/c1-5-10(4)9(11-10)7-6-8(2)3/h5-6,9H,1,7H2,2-4H3/t9-,10+/m0/s1
InChI Key DUBZPCHJCIFTKB-VHSXEESVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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transepoxyocimene
Q67880127

2D Structure

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2D Structure of E-Ocimene oxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 - 0.6598 65.98%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4498 44.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9272 92.72%
OATP1B3 inhibitior + 0.9308 93.08%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8971 89.71%
P-glycoprotein inhibitior - 0.9762 97.62%
P-glycoprotein substrate - 0.9275 92.75%
CYP3A4 substrate - 0.5423 54.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7471 74.71%
CYP3A4 inhibition - 0.8511 85.11%
CYP2C9 inhibition - 0.5973 59.73%
CYP2C19 inhibition + 0.6187 61.87%
CYP2D6 inhibition - 0.9346 93.46%
CYP1A2 inhibition - 0.5210 52.10%
CYP2C8 inhibition - 0.9061 90.61%
CYP inhibitory promiscuity - 0.5597 55.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5344 53.44%
Carcinogenicity (trinary) Non-required 0.4930 49.30%
Eye corrosion - 0.7843 78.43%
Eye irritation + 0.8803 88.03%
Skin irritation + 0.6842 68.42%
Skin corrosion - 0.9055 90.55%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6063 60.63%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5429 54.29%
skin sensitisation + 0.9332 93.32%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.7352 73.52%
Acute Oral Toxicity (c) III 0.7644 76.44%
Estrogen receptor binding - 0.9260 92.60%
Androgen receptor binding - 0.7949 79.49%
Thyroid receptor binding - 0.8589 85.89%
Glucocorticoid receptor binding - 0.7971 79.71%
Aromatase binding - 0.8673 86.73%
PPAR gamma - 0.8756 87.56%
Honey bee toxicity - 0.7180 71.80%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.7942 79.42%

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 94.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.66% 96.09%
CHEMBL240 Q12809 HERG 85.51% 89.76%
CHEMBL3401 O75469 Pregnane X receptor 82.45% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.83% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.59% 94.45%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.82% 97.28%

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.
Artemisia absinthium

Cross-Links

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PubChem 6429141
LOTUS LTS0227173
wikiData Q67880127