1,6-Dimethyl-4-propan-2-yl-1,2,3,4,4a,8a-hexahydronaphthalene

Details

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Internal ID 04e34e2b-679a-4f8b-b0c1-8449d663e971
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,8a-hexahydronaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5,7,9-10,12-15H,6,8H2,1-4H3
InChI Key PAYPBTPGBHRBLY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.44
H-Bond Acceptor 0
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-1,2,3,4,4a,8a-hexahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.9332 93.32%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5099 50.99%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.8763 87.63%
OATP1B3 inhibitior + 0.9060 90.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9242 92.42%
P-glycoprotein inhibitior - 0.9652 96.52%
P-glycoprotein substrate - 0.7086 70.86%
CYP3A4 substrate - 0.5578 55.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7535 75.35%
CYP3A4 inhibition - 0.9220 92.20%
CYP2C9 inhibition - 0.8599 85.99%
CYP2C19 inhibition - 0.7267 72.67%
CYP2D6 inhibition - 0.8753 87.53%
CYP1A2 inhibition - 0.6870 68.70%
CYP2C8 inhibition - 0.9320 93.20%
CYP inhibitory promiscuity - 0.5289 52.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4216 42.16%
Eye corrosion - 0.8868 88.68%
Eye irritation - 0.7408 74.08%
Skin irritation + 0.5761 57.61%
Skin corrosion - 0.8379 83.79%
Ames mutagenesis - 0.7654 76.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6456 64.56%
Micronuclear - 0.9741 97.41%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.9096 90.96%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7206 72.06%
Acute Oral Toxicity (c) III 0.7432 74.32%
Estrogen receptor binding - 0.9006 90.06%
Androgen receptor binding - 0.7160 71.60%
Thyroid receptor binding - 0.6473 64.73%
Glucocorticoid receptor binding - 0.8062 80.62%
Aromatase binding - 0.9269 92.69%
PPAR gamma - 0.8524 85.24%
Honey bee toxicity - 0.8960 89.60%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9912 99.12%

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
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.21% 94.80%
CHEMBL2581 P07339 Cathepsin D 90.74% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 90.38% 97.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.33% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 90.22% 86.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.88% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.68% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.48% 97.09%

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.
Pinus pinaster

Cross-Links

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PubChem 12144808
LOTUS LTS0015464
wikiData Q105204962