(1S,2S,4aR,8aS)-1,4a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-2,8a-diol

Details

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Internal ID 59e7ec88-85f2-4bdf-ba0c-fa0239cef336
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (1S,2S,4aR,8aS)-1,4a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-2,8a-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H22O2/c1-9-10(13)5-8-11(2)6-3-4-7-12(9,11)14/h9-10,13-14H,3-8H2,1-2H3/t9-,10-,11+,12-/m0/s1
InChI Key ISGNFBBRJRWYOB-YFKTTZPYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H22O2
Molecular Weight 198.30 g/mol
Exact Mass 198.161979940 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2S,4aR,8aS)-1,4a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-2,8a-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.8015 80.15%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5455 54.55%
OATP2B1 inhibitior - 0.8452 84.52%
OATP1B1 inhibitior + 0.9316 93.16%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8538 85.38%
P-glycoprotein inhibitior - 0.9689 96.89%
P-glycoprotein substrate - 0.8784 87.84%
CYP3A4 substrate - 0.5150 51.50%
CYP2C9 substrate - 0.5641 56.41%
CYP2D6 substrate - 0.7203 72.03%
CYP3A4 inhibition - 0.8283 82.83%
CYP2C9 inhibition - 0.7746 77.46%
CYP2C19 inhibition - 0.8486 84.86%
CYP2D6 inhibition - 0.9468 94.68%
CYP1A2 inhibition + 0.6313 63.13%
CYP2C8 inhibition - 0.9686 96.86%
CYP inhibitory promiscuity - 0.9238 92.38%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5672 56.72%
Eye corrosion - 0.9734 97.34%
Eye irritation + 0.5581 55.81%
Skin irritation + 0.5170 51.70%
Skin corrosion - 0.8460 84.60%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6971 69.71%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5554 55.54%
skin sensitisation - 0.6316 63.16%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8641 86.41%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8179 81.79%
Acute Oral Toxicity (c) III 0.7676 76.76%
Estrogen receptor binding - 0.8100 81.00%
Androgen receptor binding - 0.5329 53.29%
Thyroid receptor binding - 0.7606 76.06%
Glucocorticoid receptor binding - 0.7957 79.57%
Aromatase binding - 0.7532 75.32%
PPAR gamma - 0.8585 85.85%
Honey bee toxicity - 0.9082 90.82%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8914 89.14%

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 96.06% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 92.02% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.41% 91.11%
CHEMBL206 P03372 Estrogen receptor alpha 89.98% 97.64%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.87% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.78% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.57% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.24% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.98% 100.00%
CHEMBL237 P41145 Kappa opioid receptor 81.93% 98.10%
CHEMBL259 P32245 Melanocortin receptor 4 81.74% 95.38%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.17% 92.94%
CHEMBL2581 P07339 Cathepsin D 80.69% 98.95%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 80.05% 98.99%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 130929216
LOTUS LTS0205157
wikiData Q105119496