3-(2-hydroxypropan-2-yl)-5,8a-dimethyl-2,3,3a,4,5,6,7,8-octahydro-1H-azulen-4-ol

Details

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Internal ID 54d7decb-ead6-4649-849a-0dff395d053a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 3-(2-hydroxypropan-2-yl)-5,8a-dimethyl-2,3,3a,4,5,6,7,8-octahydro-1H-azulen-4-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H28O2/c1-10-6-5-8-15(4)9-7-11(14(2,3)17)12(15)13(10)16/h10-13,16-17H,5-9H2,1-4H3
InChI Key SUNRMOIMPOGBOY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O2
Molecular Weight 240.38 g/mol
Exact Mass 240.208930132 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.6541 65.41%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4638 46.38%
OATP2B1 inhibitior - 0.8458 84.58%
OATP1B1 inhibitior + 0.9441 94.41%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9307 93.07%
P-glycoprotein inhibitior - 0.9343 93.43%
P-glycoprotein substrate - 0.9106 91.06%
CYP3A4 substrate + 0.5480 54.80%
CYP2C9 substrate + 0.5942 59.42%
CYP2D6 substrate - 0.7034 70.34%
CYP3A4 inhibition - 0.8847 88.47%
CYP2C9 inhibition - 0.7848 78.48%
CYP2C19 inhibition - 0.8553 85.53%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition + 0.5932 59.32%
CYP2C8 inhibition - 0.8159 81.59%
CYP inhibitory promiscuity - 0.9001 90.01%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6469 64.69%
Eye corrosion - 0.9333 93.33%
Eye irritation + 0.6932 69.32%
Skin irritation + 0.5329 53.29%
Skin corrosion - 0.9220 92.20%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5840 58.40%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.5649 56.49%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7575 75.75%
Acute Oral Toxicity (c) III 0.7373 73.73%
Estrogen receptor binding - 0.7024 70.24%
Androgen receptor binding - 0.5202 52.02%
Thyroid receptor binding + 0.5856 58.56%
Glucocorticoid receptor binding - 0.5285 52.85%
Aromatase binding - 0.6292 62.92%
PPAR gamma - 0.7931 79.31%
Honey bee toxicity - 0.8670 86.70%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9516 95.16%

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 97.71% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.27% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.79% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.70% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.66% 97.09%
CHEMBL4040 P28482 MAP kinase ERK2 87.19% 83.82%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.78% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.38% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.56% 95.89%
CHEMBL2581 P07339 Cathepsin D 82.31% 98.95%

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 162962100
LOTUS LTS0217178
wikiData Q104197666