3,8-Dimethyl-5-propan-2-yl-4,4a,5,6-tetrahydronaphthalen-2-ol

Details

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Internal ID f40572c0-bb96-4a2f-a82b-b6f6a05faf91
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,8-dimethyl-5-propan-2-yl-4,4a,5,6-tetrahydronaphthalen-2-ol
SMILES (Canonical) CC1=C(C=C2C(C1)C(CC=C2C)C(C)C)O
SMILES (Isomeric) CC1=C(C=C2C(C1)C(CC=C2C)C(C)C)O
InChI InChI=1S/C15H22O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h5,8-9,12,14,16H,6-7H2,1-4H3
InChI Key QXELPXQYJPSRCP-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) 20.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,8-Dimethyl-5-propan-2-yl-4,4a,5,6-tetrahydronaphthalen-2-ol

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 + 0.8712 87.12%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4974 49.74%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.8968 89.68%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9443 94.43%
P-glycoprotein inhibitior - 0.9728 97.28%
P-glycoprotein substrate - 0.7133 71.33%
CYP3A4 substrate - 0.5506 55.06%
CYP2C9 substrate + 0.5852 58.52%
CYP2D6 substrate - 0.7893 78.93%
CYP3A4 inhibition - 0.7464 74.64%
CYP2C9 inhibition - 0.7106 71.06%
CYP2C19 inhibition - 0.6910 69.10%
CYP2D6 inhibition - 0.8745 87.45%
CYP1A2 inhibition - 0.5787 57.87%
CYP2C8 inhibition - 0.9111 91.11%
CYP inhibitory promiscuity - 0.5511 55.11%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5337 53.37%
Eye corrosion - 0.9664 96.64%
Eye irritation - 0.5747 57.47%
Skin irritation - 0.5736 57.36%
Skin corrosion - 0.8988 89.88%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3758 37.58%
Micronuclear - 0.8782 87.82%
Hepatotoxicity + 0.5565 55.65%
skin sensitisation + 0.7063 70.63%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6571 65.71%
Acute Oral Toxicity (c) III 0.6695 66.95%
Estrogen receptor binding - 0.9145 91.45%
Androgen receptor binding - 0.5215 52.15%
Thyroid receptor binding - 0.4871 48.71%
Glucocorticoid receptor binding - 0.6959 69.59%
Aromatase binding - 0.8266 82.66%
PPAR gamma - 0.5659 56.59%
Honey bee toxicity - 0.9241 92.41%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9956 99.56%

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 91.44% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.61% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.78% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.53% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.81% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.11% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.34% 97.25%

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 inuloides

Cross-Links

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PubChem 163186211
LOTUS LTS0240495
wikiData Q103813421