4,4,7,8,8a-Pentamethyl-1,2,3,4a,5,6-hexahydronaphthalene

Details

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Internal ID 1690420f-e009-454b-b265-c1c3918f3e17
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 4,4,7,8,8a-pentamethyl-1,2,3,4a,5,6-hexahydronaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26/c1-11-7-8-13-14(3,4)9-6-10-15(13,5)12(11)2/h13H,6-10H2,1-5H3
InChI Key VSURQKXDWDMWKL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26
Molecular Weight 206.37 g/mol
Exact Mass 206.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.95
H-Bond Acceptor 0
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 4,4,7,8,8a-Pentamethyl-1,2,3,4a,5,6-hexahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.9361 93.61%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.6698 66.98%
OATP2B1 inhibitior - 0.8435 84.35%
OATP1B1 inhibitior + 0.9509 95.09%
OATP1B3 inhibitior + 0.8227 82.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8271 82.71%
P-glycoprotein inhibitior - 0.9329 93.29%
P-glycoprotein substrate - 0.9633 96.33%
CYP3A4 substrate - 0.5052 50.52%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8356 83.56%
CYP2C9 inhibition - 0.7959 79.59%
CYP2C19 inhibition - 0.6340 63.40%
CYP2D6 inhibition - 0.9415 94.15%
CYP1A2 inhibition - 0.8515 85.15%
CYP2C8 inhibition - 0.7770 77.70%
CYP inhibitory promiscuity - 0.5069 50.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4897 48.97%
Eye corrosion - 0.9624 96.24%
Eye irritation + 0.9368 93.68%
Skin irritation - 0.6409 64.09%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4124 41.24%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5145 51.45%
skin sensitisation + 0.8697 86.97%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6400 64.00%
Acute Oral Toxicity (c) III 0.6452 64.52%
Estrogen receptor binding - 0.8018 80.18%
Androgen receptor binding - 0.5825 58.25%
Thyroid receptor binding - 0.7173 71.73%
Glucocorticoid receptor binding - 0.8792 87.92%
Aromatase binding - 0.6724 67.24%
PPAR gamma - 0.8052 80.52%
Honey bee toxicity - 0.9500 95.00%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.43% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.96% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.34% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.21% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.17% 93.99%
CHEMBL259 P32245 Melanocortin receptor 4 81.91% 95.38%
CHEMBL1871 P10275 Androgen Receptor 81.66% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.11% 95.56%
CHEMBL1914 P06276 Butyrylcholinesterase 80.53% 95.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.34% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.29% 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.
Senegalia pennata

Cross-Links

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PubChem 75227550
LOTUS LTS0203565
wikiData Q105292553