3aalpha,4,5,6,7,8-Hexahydro-7beta-isopropenyl-1,4beta-dimethylazulene-2(3H)-one

Details

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Internal ID fb37cb3e-c650-4145-9e7d-29463eec3aa8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (5R,8S,8aS)-3,8-dimethyl-5-prop-1-en-2-yl-4,5,6,7,8,8a-hexahydro-1H-azulen-2-one
SMILES (Canonical) CC1CCC(CC2=C(C(=O)CC12)C)C(=C)C
SMILES (Isomeric) C[C@H]1CC[C@H](CC2=C(C(=O)C[C@@H]12)C)C(=C)C
InChI InChI=1S/C15H22O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)14(13)7-12/h10,12-13H,1,5-8H2,2-4H3/t10-,12+,13-/m0/s1
InChI Key CESATEXQMONATC-UHTWSYAYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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AKOS040736159
1??,7??,10??H-Guaia-4,11-dien-3-one
3aalpha,4,5,6,7,8-Hexahydro-7beta-isopropenyl-1,4beta-dimethylazulene-2(3H)-one

2D Structure

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2D Structure of 3aalpha,4,5,6,7,8-Hexahydro-7beta-isopropenyl-1,4beta-dimethylazulene-2(3H)-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8669 86.69%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4682 46.82%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9389 93.89%
OATP1B3 inhibitior + 0.9057 90.57%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8042 80.42%
P-glycoprotein inhibitior - 0.8561 85.61%
P-glycoprotein substrate - 0.8245 82.45%
CYP3A4 substrate - 0.5301 53.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.9196 91.96%
CYP2C9 inhibition - 0.8534 85.34%
CYP2C19 inhibition - 0.7641 76.41%
CYP2D6 inhibition - 0.9356 93.56%
CYP1A2 inhibition - 0.5423 54.23%
CYP2C8 inhibition - 0.9012 90.12%
CYP inhibitory promiscuity - 0.8940 89.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5362 53.62%
Eye corrosion - 0.9375 93.75%
Eye irritation + 0.7961 79.61%
Skin irritation + 0.5941 59.41%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5157 51.57%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.7897 78.97%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.4769 47.69%
Acute Oral Toxicity (c) III 0.7174 71.74%
Estrogen receptor binding - 0.8301 83.01%
Androgen receptor binding - 0.5596 55.96%
Thyroid receptor binding - 0.6532 65.32%
Glucocorticoid receptor binding - 0.7396 73.96%
Aromatase binding - 0.7942 79.42%
PPAR gamma - 0.6247 62.47%
Honey bee toxicity - 0.9211 92.11%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9855 98.55%

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 89.88% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.54% 85.14%
CHEMBL2581 P07339 Cathepsin D 89.24% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.27% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.66% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.13% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.52% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.67% 97.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.25% 94.80%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.24% 93.04%

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.
Agathis lanceolata
Baccharis boliviensis
Daphne aurantiaca
Dracaena concinna
Isodon amethystoides
Neolitsea pulchella
Vigna angularis

Cross-Links

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PubChem 10082128
NPASS NPC20603
LOTUS LTS0187176
wikiData Q104956012