5-(2-hydroxypropan-2-yl)-3,8-dimethyl-3,4,5,6,7,8-hexahydro-2H-azulen-1-one

Details

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Internal ID 5d0a4e55-739d-41ba-aeea-1943788da707
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 5-(2-hydroxypropan-2-yl)-3,8-dimethyl-3,4,5,6,7,8-hexahydro-2H-azulen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-9-5-6-11(15(3,4)17)8-12-10(2)7-13(16)14(9)12/h9-11,17H,5-8H2,1-4H3
InChI Key CKROUOLVUCKMJT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.10
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(2-hydroxypropan-2-yl)-3,8-dimethyl-3,4,5,6,7,8-hexahydro-2H-azulen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.8017 80.17%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6596 65.96%
OATP2B1 inhibitior - 0.8493 84.93%
OATP1B1 inhibitior + 0.9424 94.24%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.8806 88.06%
P-glycoprotein inhibitior - 0.8922 89.22%
P-glycoprotein substrate - 0.8741 87.41%
CYP3A4 substrate - 0.5190 51.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8829 88.29%
CYP3A4 inhibition - 0.8959 89.59%
CYP2C9 inhibition - 0.6729 67.29%
CYP2C19 inhibition - 0.6152 61.52%
CYP2D6 inhibition - 0.9359 93.59%
CYP1A2 inhibition - 0.5902 59.02%
CYP2C8 inhibition - 0.9309 93.09%
CYP inhibitory promiscuity - 0.9065 90.65%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5235 52.35%
Eye corrosion - 0.9706 97.06%
Eye irritation + 0.7768 77.68%
Skin irritation + 0.6322 63.22%
Skin corrosion - 0.9601 96.01%
Ames mutagenesis - 0.8624 86.24%
Human Ether-a-go-go-Related Gene inhibition - 0.6514 65.14%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6855 68.55%
skin sensitisation + 0.5649 56.49%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.5517 55.17%
Acute Oral Toxicity (c) III 0.7522 75.22%
Estrogen receptor binding - 0.7104 71.04%
Androgen receptor binding - 0.7332 73.32%
Thyroid receptor binding + 0.5733 57.33%
Glucocorticoid receptor binding - 0.5253 52.53%
Aromatase binding - 0.8346 83.46%
PPAR gamma - 0.6997 69.97%
Honey bee toxicity - 0.9223 92.23%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9597 95.97%

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 96.01% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.99% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.58% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.79% 91.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.80% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.54% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.06% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.06% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 82.10% 97.05%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163018486
LOTUS LTS0016226
wikiData Q104962712