1,6-dimethyl-4-propan-2-yl-4,4a,7,8-tetrahydro-3H-naphthalen-2-one

Details

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Internal ID 5f41f9c0-9176-4a5d-867a-bb853bd5e911
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,6-dimethyl-4-propan-2-yl-4,4a,7,8-tetrahydro-3H-naphthalen-2-one
SMILES (Canonical) CC1=CC2C(CC(=O)C(=C2CC1)C)C(C)C
SMILES (Isomeric) CC1=CC2C(CC(=O)C(=C2CC1)C)C(C)C
InChI InChI=1S/C15H22O/c1-9(2)13-8-15(16)11(4)12-6-5-10(3)7-14(12)13/h7,9,13-14H,5-6,8H2,1-4H3
InChI Key VFACPFXGWGDKEY-UHFFFAOYSA-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 2.90
Atomic LogP (AlogP) 3.90
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 1,6-dimethyl-4-propan-2-yl-4,4a,7,8-tetrahydro-3H-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 + 0.9265 92.65%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5297 52.97%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.9443 94.43%
OATP1B3 inhibitior + 0.9655 96.55%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7551 75.51%
P-glycoprotein inhibitior - 0.8875 88.75%
P-glycoprotein substrate - 0.8883 88.83%
CYP3A4 substrate - 0.5979 59.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.9246 92.46%
CYP2C9 inhibition - 0.8208 82.08%
CYP2C19 inhibition - 0.6768 67.68%
CYP2D6 inhibition - 0.9275 92.75%
CYP1A2 inhibition - 0.6616 66.16%
CYP2C8 inhibition - 0.9730 97.30%
CYP inhibitory promiscuity - 0.7259 72.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9210 92.10%
Carcinogenicity (trinary) Non-required 0.5152 51.52%
Eye corrosion - 0.9691 96.91%
Eye irritation - 0.6155 61.55%
Skin irritation + 0.6266 62.66%
Skin corrosion - 0.9505 95.05%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4451 44.51%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.8935 89.35%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.5633 56.33%
Acute Oral Toxicity (c) III 0.6729 67.29%
Estrogen receptor binding - 0.9431 94.31%
Androgen receptor binding - 0.5372 53.72%
Thyroid receptor binding - 0.6586 65.86%
Glucocorticoid receptor binding - 0.7392 73.92%
Aromatase binding - 0.8810 88.10%
PPAR gamma - 0.5668 56.68%
Honey bee toxicity - 0.7924 79.24%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9792 97.92%

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 93.28% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.91% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.35% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 83.52% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.41% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.32% 90.71%
CHEMBL2996 Q05655 Protein kinase C delta 82.40% 97.79%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.15% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.68% 99.23%

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.
Heterotheca grandiflora

Cross-Links

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PubChem 162931185
LOTUS LTS0017061
wikiData Q105284953