3-(2-Hydroxypropan-2-yl)-8a-methyl-5-methylidene-1,4,4a,6,7,8-hexahydronaphthalen-1-ol

Details

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Internal ID 3b4133ba-3c11-4f03-a8d6-2c76c44ea748
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-(2-hydroxypropan-2-yl)-8a-methyl-5-methylidene-1,4,4a,6,7,8-hexahydronaphthalen-1-ol
SMILES (Canonical) CC12CCCC(=C)C1CC(=CC2O)C(C)(C)O
SMILES (Isomeric) CC12CCCC(=C)C1CC(=CC2O)C(C)(C)O
InChI InChI=1S/C15H24O2/c1-10-6-5-7-15(4)12(10)8-11(9-13(15)16)14(2,3)17/h9,12-13,16-17H,1,5-8H2,2-4H3
InChI Key YYKNLMBUHZDCCS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(2-Hydroxypropan-2-yl)-8a-methyl-5-methylidene-1,4,4a,6,7,8-hexahydronaphthalen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.7201 72.01%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5681 56.81%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.8350 83.50%
OATP1B3 inhibitior + 0.7925 79.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8859 88.59%
P-glycoprotein inhibitior - 0.9401 94.01%
P-glycoprotein substrate - 0.7985 79.85%
CYP3A4 substrate + 0.5614 56.14%
CYP2C9 substrate - 0.5811 58.11%
CYP2D6 substrate - 0.7340 73.40%
CYP3A4 inhibition - 0.7054 70.54%
CYP2C9 inhibition - 0.7528 75.28%
CYP2C19 inhibition - 0.5633 56.33%
CYP2D6 inhibition - 0.9236 92.36%
CYP1A2 inhibition - 0.7173 71.73%
CYP2C8 inhibition - 0.8384 83.84%
CYP inhibitory promiscuity - 0.5786 57.86%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6186 61.86%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.6423 64.23%
Skin irritation - 0.5279 52.79%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5950 59.50%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.7074 70.74%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7568 75.68%
Acute Oral Toxicity (c) III 0.8102 81.02%
Estrogen receptor binding - 0.6712 67.12%
Androgen receptor binding + 0.5238 52.38%
Thyroid receptor binding - 0.5523 55.23%
Glucocorticoid receptor binding + 0.5537 55.37%
Aromatase binding - 0.7022 70.22%
PPAR gamma - 0.7217 72.17%
Honey bee toxicity - 0.8130 81.30%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
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 98.00% 97.25%
CHEMBL1977 P11473 Vitamin D receptor 94.48% 99.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.71% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.11% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.58% 95.89%
CHEMBL233 P35372 Mu opioid receptor 85.02% 97.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.64% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.86% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.11% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.97% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.88% 86.33%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 162997167
LOTUS LTS0172727
wikiData Q105368704