(2S,4S,8aS)-4,8a-dimethyl-6-propan-2-yl-2,3,4,8-tetrahydro-1H-naphthalen-2-ol

Details

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Internal ID cb548873-339c-4996-8907-fda2f2d15f83
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2S,4S,8aS)-4,8a-dimethyl-6-propan-2-yl-2,3,4,8-tetrahydro-1H-naphthalen-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)12-5-6-15(4)9-13(16)7-11(3)14(15)8-12/h5,8,10-11,13,16H,6-7,9H2,1-4H3/t11-,13-,15-/m0/s1
InChI Key KNUCOFYQBDJBHF-WHOFXGATSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.70
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 (2S,4S,8aS)-4,8a-dimethyl-6-propan-2-yl-2,3,4,8-tetrahydro-1H-naphthalen-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 + 0.9964 99.64%
Caco-2 + 0.8513 85.13%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5419 54.19%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9489 94.89%
OATP1B3 inhibitior + 0.9733 97.33%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6697 66.97%
P-glycoprotein inhibitior - 0.9241 92.41%
P-glycoprotein substrate - 0.6059 60.59%
CYP3A4 substrate + 0.5180 51.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7337 73.37%
CYP3A4 inhibition - 0.8588 85.88%
CYP2C9 inhibition - 0.7114 71.14%
CYP2C19 inhibition - 0.5482 54.82%
CYP2D6 inhibition - 0.9092 90.92%
CYP1A2 inhibition - 0.8373 83.73%
CYP2C8 inhibition - 0.8864 88.64%
CYP inhibitory promiscuity - 0.7004 70.04%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8108 81.08%
Carcinogenicity (trinary) Non-required 0.5288 52.88%
Eye corrosion - 0.9755 97.55%
Eye irritation + 0.7392 73.92%
Skin irritation - 0.5313 53.13%
Skin corrosion - 0.9195 91.95%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6073 60.73%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.6811 68.11%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7378 73.78%
Acute Oral Toxicity (c) III 0.8230 82.30%
Estrogen receptor binding - 0.8322 83.22%
Androgen receptor binding - 0.5323 53.23%
Thyroid receptor binding + 0.5528 55.28%
Glucocorticoid receptor binding - 0.7602 76.02%
Aromatase binding - 0.7417 74.17%
PPAR gamma - 0.7083 70.83%
Honey bee toxicity - 0.8785 87.85%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9195 91.95%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.62% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.46% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.36% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.66% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.61% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.57% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.37% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.29% 96.77%
CHEMBL226 P30542 Adenosine A1 receptor 81.82% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.76% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.20% 100.00%

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.
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Cross-Links

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PubChem 90846193
LOTUS LTS0209561
wikiData Q105143571