(4aS,8S,8aS)-3,8-dimethyl-5-prop-1-en-2-yl-4a,7,8,8a-tetrahydro-1H-naphthalen-2-one

Details

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Internal ID d325e887-176d-45a9-90b3-56d88b0af396
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aS,8S,8aS)-3,8-dimethyl-5-prop-1-en-2-yl-4a,7,8,8a-tetrahydro-1H-naphthalen-2-one
SMILES (Canonical) CC1CC=C(C2C1CC(=O)C(=C2)C)C(=C)C
SMILES (Isomeric) C[C@H]1CC=C([C@H]2[C@H]1CC(=O)C(=C2)C)C(=C)C
InChI InChI=1S/C15H20O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h6-7,10,13-14H,1,5,8H2,2-4H3/t10-,13-,14-/m0/s1
InChI Key QVTBIFDNDSHCEB-BPNCWPANSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O
Molecular Weight 216.32 g/mol
Exact Mass 216.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4aS,8S,8aS)-3,8-dimethyl-5-prop-1-en-2-yl-4a,7,8,8a-tetrahydro-1H-naphthalen-2-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 + 0.8676 86.76%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4200 42.00%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.9324 93.24%
OATP1B3 inhibitior + 0.9150 91.50%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8636 86.36%
P-glycoprotein inhibitior - 0.9410 94.10%
P-glycoprotein substrate - 0.8382 83.82%
CYP3A4 substrate - 0.5060 50.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.6055 60.55%
CYP2C9 inhibition - 0.8602 86.02%
CYP2C19 inhibition - 0.5703 57.03%
CYP2D6 inhibition - 0.9170 91.70%
CYP1A2 inhibition - 0.5631 56.31%
CYP2C8 inhibition - 0.8983 89.83%
CYP inhibitory promiscuity - 0.6663 66.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.4837 48.37%
Eye corrosion - 0.9589 95.89%
Eye irritation + 0.6748 67.48%
Skin irritation + 0.5483 54.83%
Skin corrosion - 0.9566 95.66%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5241 52.41%
Micronuclear - 0.8541 85.41%
Hepatotoxicity + 0.7533 75.33%
skin sensitisation + 0.8607 86.07%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5651 56.51%
Acute Oral Toxicity (c) III 0.5653 56.53%
Estrogen receptor binding - 0.9099 90.99%
Androgen receptor binding - 0.5391 53.91%
Thyroid receptor binding - 0.7180 71.80%
Glucocorticoid receptor binding - 0.8002 80.02%
Aromatase binding - 0.8259 82.59%
PPAR gamma - 0.6945 69.45%
Honey bee toxicity - 0.6390 63.90%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9936 99.36%

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 90.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.44% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.93% 86.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.14% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.33% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.21% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 80.08% 94.75%

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.
Smallanthus uvedalia

Cross-Links

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PubChem 162959030
LOTUS LTS0068424
wikiData Q105228895