(3S,3aR,4S)-3-acetyl-7-methyl-4-propan-2-yl-2,3,3a,4,5,6-hexahydroinden-1-one

Details

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Internal ID 2785e2e7-71d9-41e1-988f-138f94af4b21
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3S,3aR,4S)-3-acetyl-7-methyl-4-propan-2-yl-2,3,3a,4,5,6-hexahydroinden-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-8(2)11-6-5-9(3)14-13(17)7-12(10(4)16)15(11)14/h8,11-12,15H,5-7H2,1-4H3/t11-,12+,15+/m0/s1
InChI Key XTEXPKPDBRKBPS-YWPYICTPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,3aR,4S)-3-acetyl-7-methyl-4-propan-2-yl-2,3,3a,4,5,6-hexahydroinden-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 + 1.0000 100.00%
Caco-2 + 0.8077 80.77%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6056 60.56%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8178 81.78%
P-glycoprotein inhibitior - 0.8515 85.15%
P-glycoprotein substrate - 0.7845 78.45%
CYP3A4 substrate - 0.5156 51.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.9391 93.91%
CYP2C9 inhibition - 0.8116 81.16%
CYP2C19 inhibition - 0.7494 74.94%
CYP2D6 inhibition - 0.9209 92.09%
CYP1A2 inhibition - 0.7153 71.53%
CYP2C8 inhibition - 0.9827 98.27%
CYP inhibitory promiscuity - 0.8756 87.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5414 54.14%
Eye corrosion - 0.9399 93.99%
Eye irritation + 0.7954 79.54%
Skin irritation + 0.6306 63.06%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5629 56.29%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.8413 84.13%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6239 62.39%
Acute Oral Toxicity (c) III 0.7132 71.32%
Estrogen receptor binding - 0.7541 75.41%
Androgen receptor binding + 0.6110 61.10%
Thyroid receptor binding - 0.7102 71.02%
Glucocorticoid receptor binding - 0.6290 62.90%
Aromatase binding - 0.8895 88.95%
PPAR gamma - 0.7624 76.24%
Honey bee toxicity - 0.9113 91.13%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9422 94.22%

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 95.49% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.74% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 86.84% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.72% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.30% 91.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.40% 93.03%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.33% 96.47%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.08% 95.56%
CHEMBL1871 P10275 Androgen Receptor 81.87% 96.43%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.73% 93.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.42% 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.
Ambrosia artemisioides

Cross-Links

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PubChem 14164886
LOTUS LTS0066555
wikiData Q105341520