4-Isopropyl-1,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene

Details

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Internal ID b146c70b-f0f7-4b55-99eb-17d3ac3a653c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,6-dimethyl-4-propan-2-yl-1,2,4a,5,8,8a-hexahydronaphthalene
SMILES (Canonical) CC1CC=C(C2C1CC=C(C2)C)C(C)C
SMILES (Isomeric) CC1CC=C(C2C1CC=C(C2)C)C(C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5,8,10,12,14-15H,6-7,9H2,1-4H3
InChI Key BODHEYZMWPRRPR-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 4.00
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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4-Isopropyl-1,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene
14087-01-5

2D Structure

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2D Structure of 4-Isopropyl-1,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.9072 90.72%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6507 65.07%
OATP2B1 inhibitior - 0.8490 84.90%
OATP1B1 inhibitior + 0.9543 95.43%
OATP1B3 inhibitior + 0.9349 93.49%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7923 79.23%
P-glycoprotein inhibitior - 0.9535 95.35%
P-glycoprotein substrate - 0.7971 79.71%
CYP3A4 substrate - 0.5928 59.28%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.8454 84.54%
CYP2C9 inhibition - 0.7576 75.76%
CYP2C19 inhibition - 0.6915 69.15%
CYP2D6 inhibition - 0.8908 89.08%
CYP1A2 inhibition - 0.7087 70.87%
CYP2C8 inhibition - 0.9341 93.41%
CYP inhibitory promiscuity - 0.5095 50.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.4445 44.45%
Eye corrosion - 0.8655 86.55%
Eye irritation + 0.6438 64.38%
Skin irritation - 0.5477 54.77%
Skin corrosion - 0.9263 92.63%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7124 71.24%
Micronuclear - 0.9367 93.67%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8565 85.65%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5239 52.39%
Acute Oral Toxicity (c) III 0.6727 67.27%
Estrogen receptor binding - 0.9379 93.79%
Androgen receptor binding - 0.6462 64.62%
Thyroid receptor binding - 0.7339 73.39%
Glucocorticoid receptor binding - 0.8342 83.42%
Aromatase binding - 0.8490 84.90%
PPAR gamma - 0.8656 86.56%
Honey bee toxicity - 0.7614 76.14%
Biodegradation - 0.6750 67.50%
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 92.89% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 91.35% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.37% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.66% 93.56%
CHEMBL2581 P07339 Cathepsin D 87.86% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.46% 94.80%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.81% 97.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.46% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.33% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.46% 89.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.59% 91.11%

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.
Acritopappus confertus
Artemisia vulgaris

Cross-Links

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PubChem 85125935
LOTUS LTS0228664
wikiData Q105224615