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

Details

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Internal ID 45136d17-d4d3-4293-ae6d-ebb8ad418969
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4,7-dimethyl-1-propan-2-ylidene-3,4,4a,5,6,8a-hexahydronaphthalen-2-one
SMILES (Canonical) CC1CC(=O)C(=C(C)C)C2C1CCC(=C2)C
SMILES (Isomeric) CC1CC(=O)C(=C(C)C)C2C1CCC(=C2)C
InChI InChI=1S/C15H22O/c1-9(2)15-13-7-10(3)5-6-12(13)11(4)8-14(15)16/h7,11-13H,5-6,8H2,1-4H3
InChI Key QUSMBBMIOONIAC-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 3.60
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 4,7-Dimethyl-1-propan-2-ylidene-3,4,4a,5,6,8a-hexahydronaphthalen-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 + 0.9603 96.03%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5311 53.11%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.9418 94.18%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8755 87.55%
P-glycoprotein inhibitior - 0.9123 91.23%
P-glycoprotein substrate - 0.8715 87.15%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8170 81.70%
CYP2D6 substrate - 0.8598 85.98%
CYP3A4 inhibition - 0.8776 87.76%
CYP2C9 inhibition - 0.8218 82.18%
CYP2C19 inhibition - 0.6410 64.10%
CYP2D6 inhibition - 0.9562 95.62%
CYP1A2 inhibition - 0.6424 64.24%
CYP2C8 inhibition - 0.8989 89.89%
CYP inhibitory promiscuity - 0.7364 73.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5390 53.90%
Eye corrosion - 0.9631 96.31%
Eye irritation + 0.5893 58.93%
Skin irritation + 0.6062 60.62%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4883 48.83%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation + 0.9212 92.12%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6180 61.80%
Acute Oral Toxicity (c) III 0.4568 45.68%
Estrogen receptor binding - 0.9441 94.41%
Androgen receptor binding - 0.5803 58.03%
Thyroid receptor binding - 0.7142 71.42%
Glucocorticoid receptor binding - 0.7274 72.74%
Aromatase binding - 0.9217 92.17%
PPAR gamma - 0.8590 85.90%
Honey bee toxicity - 0.8891 88.91%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9913 99.13%

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 93.69% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.78% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.60% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.50% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.90% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.16% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.70% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.73% 93.03%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.56% 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.
Baccharis boliviensis
Neomirandea guevarii

Cross-Links

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PubChem 14219449
LOTUS LTS0015592
wikiData Q105228402