3,8-Dimethyl-5-propan-2-ylidene-4,4a,6,7,8,8a-hexahydronaphthalen-1-one

Details

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Internal ID f0cc2a60-c4d2-4de5-965b-3168e3d03f97
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,8-dimethyl-5-propan-2-ylidene-4,4a,6,7,8,8a-hexahydronaphthalen-1-one
SMILES (Canonical) CC1CCC(=C(C)C)C2C1C(=O)C=C(C2)C
SMILES (Isomeric) CC1CCC(=C(C)C)C2C1C(=O)C=C(C2)C
InChI InChI=1S/C15H22O/c1-9(2)12-6-5-11(4)15-13(12)7-10(3)8-14(15)16/h8,11,13,15H,5-7H2,1-4H3
InChI Key OYGMKZAGBMAOKO-UHFFFAOYSA-N
Popularity 0 references 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 3.20
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,8-Dimethyl-5-propan-2-ylidene-4,4a,6,7,8,8a-hexahydronaphthalen-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 + 0.9314 93.14%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4429 44.29%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.9189 91.89%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8413 84.13%
P-glycoprotein inhibitior - 0.9404 94.04%
P-glycoprotein substrate - 0.8670 86.70%
CYP3A4 substrate - 0.5154 51.54%
CYP2C9 substrate - 0.8170 81.70%
CYP2D6 substrate - 0.8598 85.98%
CYP3A4 inhibition - 0.9292 92.92%
CYP2C9 inhibition - 0.6605 66.05%
CYP2C19 inhibition - 0.5566 55.66%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.5741 57.41%
CYP2C8 inhibition - 0.9119 91.19%
CYP inhibitory promiscuity - 0.6660 66.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5309 53.09%
Eye corrosion - 0.9316 93.16%
Eye irritation + 0.6087 60.87%
Skin irritation + 0.5198 51.98%
Skin corrosion - 0.9462 94.62%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6493 64.93%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.8586 85.86%
skin sensitisation + 0.9024 90.24%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6327 63.27%
Acute Oral Toxicity (c) III 0.6219 62.19%
Estrogen receptor binding - 0.8862 88.62%
Androgen receptor binding + 0.7251 72.51%
Thyroid receptor binding - 0.6812 68.12%
Glucocorticoid receptor binding - 0.6830 68.30%
Aromatase binding - 0.8766 87.66%
PPAR gamma - 0.8279 82.79%
Honey bee toxicity - 0.9337 93.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9931 99.31%

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 93.53% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.81% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.47% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.77% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.88% 85.14%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.26% 86.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.42% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.17% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.83% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.00% 92.94%

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.
Cyperus articulatus

Cross-Links

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PubChem 72796189
LOTUS LTS0235013
wikiData Q105203187