(4aS,8S,8aR)-8-hydroxy-4a,8-dimethyl-3,4,5,6,7,8a-hexahydro-1H-naphthalen-2-one

Details

Top
Internal ID 2cc37648-2bb3-4956-b421-288f29fb2d40
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (4aS,8S,8aR)-8-hydroxy-4a,8-dimethyl-3,4,5,6,7,8a-hexahydro-1H-naphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20O2/c1-11-5-3-6-12(2,14)10(11)8-9(13)4-7-11/h10,14H,3-8H2,1-2H3/t10-,11+,12+/m1/s1
InChI Key MXEVPBYXRSDNCO-WOPDTQHZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H20O2
Molecular Weight 196.29 g/mol
Exact Mass 196.146329876 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4aS,8S,8aR)-8-hydroxy-4a,8-dimethyl-3,4,5,6,7,8a-hexahydro-1H-naphthalen-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9027 90.27%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6958 69.58%
OATP2B1 inhibitior - 0.8399 83.99%
OATP1B1 inhibitior + 0.9502 95.02%
OATP1B3 inhibitior + 0.9774 97.74%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.7500 75.00%
BSEP inhibitior - 0.8935 89.35%
P-glycoprotein inhibitior - 0.9445 94.45%
P-glycoprotein substrate - 0.9573 95.73%
CYP3A4 substrate - 0.5143 51.43%
CYP2C9 substrate - 0.8272 82.72%
CYP2D6 substrate - 0.8035 80.35%
CYP3A4 inhibition - 0.8337 83.37%
CYP2C9 inhibition - 0.8301 83.01%
CYP2C19 inhibition - 0.8870 88.70%
CYP2D6 inhibition - 0.9616 96.16%
CYP1A2 inhibition - 0.6656 66.56%
CYP2C8 inhibition - 0.9596 95.96%
CYP inhibitory promiscuity - 0.9773 97.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5816 58.16%
Eye corrosion - 0.9639 96.39%
Eye irritation + 0.8771 87.71%
Skin irritation + 0.5712 57.12%
Skin corrosion - 0.8936 89.36%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7431 74.31%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5074 50.74%
skin sensitisation + 0.5332 53.32%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7399 73.99%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6381 63.81%
Acute Oral Toxicity (c) III 0.9024 90.24%
Estrogen receptor binding - 0.8479 84.79%
Androgen receptor binding - 0.7277 72.77%
Thyroid receptor binding - 0.8379 83.79%
Glucocorticoid receptor binding - 0.8129 81.29%
Aromatase binding - 0.7532 75.32%
PPAR gamma - 0.6789 67.89%
Honey bee toxicity - 0.9664 96.64%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8906 89.06%

Targets

Top

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.44% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.36% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.15% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.61% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.57% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.16% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.38% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 84.23% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.49% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.02% 96.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.00% 93.03%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.09% 100.00%

Plants that contains it

Top
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.
Teucrium heterophyllum

Cross-Links

Top
PubChem 101611687
LOTUS LTS0031471
wikiData Q105174028