1,8-dihydroxy-3a,6-dimethyl-1-propan-2-yl-3,7,8,8a-tetrahydro-2H-azulen-4-one

Details

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Internal ID 024144c5-8de5-4166-8430-45ac85bbec5c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,8-dihydroxy-3a,6-dimethyl-1-propan-2-yl-3,7,8,8a-tetrahydro-2H-azulen-4-one
SMILES (Canonical) CC1=CC(=O)C2(CCC(C2C(C1)O)(C(C)C)O)C
SMILES (Isomeric) CC1=CC(=O)C2(CCC(C2C(C1)O)(C(C)C)O)C
InChI InChI=1S/C15H24O3/c1-9(2)15(18)6-5-14(4)12(17)8-10(3)7-11(16)13(14)15/h8-9,11,13,16,18H,5-7H2,1-4H3
InChI Key IDUCKAORVITGQK-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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AKOS024278473

2D Structure

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2D Structure of 1,8-dihydroxy-3a,6-dimethyl-1-propan-2-yl-3,7,8,8a-tetrahydro-2H-azulen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.7565 75.65%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5062 50.62%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9275 92.75%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8433 84.33%
P-glycoprotein inhibitior - 0.9515 95.15%
P-glycoprotein substrate - 0.7770 77.70%
CYP3A4 substrate + 0.5454 54.54%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8871 88.71%
CYP3A4 inhibition - 0.8564 85.64%
CYP2C9 inhibition - 0.6218 62.18%
CYP2C19 inhibition - 0.7596 75.96%
CYP2D6 inhibition - 0.9337 93.37%
CYP1A2 inhibition - 0.6441 64.41%
CYP2C8 inhibition - 0.9635 96.35%
CYP inhibitory promiscuity - 0.8459 84.59%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5206 52.06%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8726 87.26%
Skin irritation + 0.6034 60.34%
Skin corrosion - 0.9122 91.22%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4763 47.63%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5860 58.60%
skin sensitisation - 0.5881 58.81%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.4949 49.49%
Acute Oral Toxicity (c) I 0.3478 34.78%
Estrogen receptor binding - 0.6096 60.96%
Androgen receptor binding + 0.5725 57.25%
Thyroid receptor binding - 0.5228 52.28%
Glucocorticoid receptor binding - 0.6377 63.77%
Aromatase binding - 0.7309 73.09%
PPAR gamma - 0.7673 76.73%
Honey bee toxicity - 0.8934 89.34%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9225 92.25%

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
CHEMBL2581 P07339 Cathepsin D 94.49% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.53% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.14% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.65% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.03% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.97% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.83% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.27% 94.75%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.11% 86.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.79% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.79% 95.89%

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.
Ferula communis subsp. linkii

Cross-Links

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PubChem 14239510
LOTUS LTS0189311
wikiData Q104402363