Artemiseole

Details

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Internal ID 3103eff6-a920-4c24-9b62-16acb0f42d9a
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name 6-ethenyl-1,4,4-trimethyl-3-oxabicyclo[3.1.0]hexane
SMILES (Canonical) CC1(C2C(C2(CO1)C)C=C)C
SMILES (Isomeric) CC1(C2C(C2(CO1)C)C=C)C
InChI InChI=1S/C10H16O/c1-5-7-8-9(2,3)11-6-10(7,8)4/h5,7-8H,1,6H2,2-4H3
InChI Key HHDOWVHECSBICN-UHFFFAOYSA-N
Popularity 3 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) 9.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1,6,6-Trimethyl-4-ethenyl-exo-2-oxabicyclo[3.1.0] hexane
DTXSID80880781
HHDOWVHECSBICN-UHFFFAOYSA-N
60485-46-3
Q67879700
1,4,4-Trimethyl-6-vinyl-3-oxabicyclo[3.1.0]hexane #

2D Structure

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2D Structure of Artemiseole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.8074 80.74%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5798 57.98%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9465 94.65%
OATP1B3 inhibitior + 0.9200 92.00%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9578 95.78%
P-glycoprotein inhibitior - 0.9662 96.62%
P-glycoprotein substrate - 0.9430 94.30%
CYP3A4 substrate - 0.5308 53.08%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7559 75.59%
CYP3A4 inhibition - 0.7255 72.55%
CYP2C9 inhibition - 0.7387 73.87%
CYP2C19 inhibition - 0.5222 52.22%
CYP2D6 inhibition - 0.9127 91.27%
CYP1A2 inhibition + 0.5600 56.00%
CYP2C8 inhibition - 0.8901 89.01%
CYP inhibitory promiscuity - 0.6185 61.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7617 76.17%
Carcinogenicity (trinary) Non-required 0.4989 49.89%
Eye corrosion - 0.8889 88.89%
Eye irritation + 0.9395 93.95%
Skin irritation - 0.5190 51.90%
Skin corrosion - 0.9000 90.00%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7595 75.95%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5290 52.90%
skin sensitisation + 0.6829 68.29%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.7744 77.44%
Acute Oral Toxicity (c) III 0.6533 65.33%
Estrogen receptor binding - 0.7663 76.63%
Androgen receptor binding - 0.7871 78.71%
Thyroid receptor binding - 0.8210 82.10%
Glucocorticoid receptor binding - 0.7756 77.56%
Aromatase binding - 0.8481 84.81%
PPAR gamma - 0.8303 83.03%
Honey bee toxicity - 0.5000 50.00%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9253 92.53%

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 89.01% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.92% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.78% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.05% 94.45%

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 arbuscula
Artemisia cana
Artemisia tridentata

Cross-Links

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PubChem 521927
LOTUS LTS0165934
wikiData Q67879700