(+)-alpha-Thujone

Details

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Internal ID 8bb0ff14-92e9-4000-aecf-090675f9ca69
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,4S,5S)-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexan-3-one
SMILES (Canonical) CC1C2CC2(CC1=O)C(C)C
SMILES (Isomeric) C[C@H]1[C@@H]2C[C@@]2(CC1=O)C(C)C
InChI InChI=1S/C10H16O/c1-6(2)10-4-8(10)7(3)9(11)5-10/h6-8H,4-5H2,1-3H3/t7-,8-,10+/m0/s1
InChI Key USMNOWBWPHYOEA-OYNCUSHFSA-N
Popularity 124 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) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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(1R,4S,5S)-thujan-3-one
(-)-Thujone
cis-Thujone
.alpha.-Thujone
3-Thujone
(1R,4S,5S)-1-isopropyl-4-methylbicyclo[3.1.0]hexan-3-one
(1R,4S,5S)-4-methyl-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-one
THUJONE
(+)-thujan-3-one
Thujone, cis
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (+)-alpha-Thujone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 - 0.6774 67.74%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5631 56.31%
OATP2B1 inhibitior - 0.8490 84.90%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9635 96.35%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9031 90.31%
P-glycoprotein inhibitior - 0.9518 95.18%
P-glycoprotein substrate - 0.9224 92.24%
CYP3A4 substrate - 0.5690 56.90%
CYP2C9 substrate - 0.7813 78.13%
CYP2D6 substrate - 0.7531 75.31%
CYP3A4 inhibition - 0.9045 90.45%
CYP2C9 inhibition - 0.8726 87.26%
CYP2C19 inhibition - 0.8201 82.01%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition - 0.8544 85.44%
CYP2C8 inhibition - 0.9947 99.47%
CYP inhibitory promiscuity - 0.9607 96.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7817 78.17%
Carcinogenicity (trinary) Non-required 0.6220 62.20%
Eye corrosion - 0.8039 80.39%
Eye irritation + 0.9012 90.12%
Skin irritation + 0.7647 76.47%
Skin corrosion - 0.9359 93.59%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7501 75.01%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.8403 84.03%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7839 78.39%
Acute Oral Toxicity (c) II 0.7356 73.56%
Estrogen receptor binding - 0.9129 91.29%
Androgen receptor binding - 0.5830 58.30%
Thyroid receptor binding - 0.8753 87.53%
Glucocorticoid receptor binding - 0.9044 90.44%
Aromatase binding - 0.8562 85.62%
PPAR gamma - 0.6934 69.34%
Honey bee toxicity - 0.7995 79.95%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9150 91.50%

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 94.88% 97.25%
CHEMBL299 P17252 Protein kinase C alpha 88.52% 98.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.20% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.03% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.96% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.13% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.09% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.98% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.15% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.06% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 82.05% 94.75%

Cross-Links

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PubChem 12304612
NPASS NPC57234
LOTUS LTS0165508
wikiData Q27104745