5,8-dihydroxy-4a,8-dimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one

Details

Top
Internal ID 44799249-23fe-44ca-9dc9-966e82836637
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 5,8-dihydroxy-4a,8-dimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O3/c1-11-5-3-8(13)7-9(11)12(2,15)6-4-10(11)14/h3,5,9-10,14-15H,4,6-7H2,1-2H3
InChI Key MUCHMZHLNORELV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H18O3
Molecular Weight 210.27 g/mol
Exact Mass 210.125594432 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.04
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5,8-dihydroxy-4a,8-dimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.6615 66.15%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8041 80.41%
OATP2B1 inhibitior - 0.8489 84.89%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.9829 98.29%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5901 59.01%
BSEP inhibitior - 0.9388 93.88%
P-glycoprotein inhibitior - 0.9698 96.98%
P-glycoprotein substrate - 0.9017 90.17%
CYP3A4 substrate + 0.5845 58.45%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate - 0.8802 88.02%
CYP3A4 inhibition - 0.6985 69.85%
CYP2C9 inhibition - 0.9273 92.73%
CYP2C19 inhibition - 0.9325 93.25%
CYP2D6 inhibition - 0.9590 95.90%
CYP1A2 inhibition - 0.8007 80.07%
CYP2C8 inhibition - 0.9690 96.90%
CYP inhibitory promiscuity - 0.9355 93.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5537 55.37%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.8865 88.65%
Skin irritation + 0.6069 60.69%
Skin corrosion - 0.9415 94.15%
Ames mutagenesis - 0.8440 84.40%
Human Ether-a-go-go-Related Gene inhibition - 0.7970 79.70%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5174 51.74%
skin sensitisation - 0.5536 55.36%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8641 86.41%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.6115 61.15%
Acute Oral Toxicity (c) III 0.7471 74.71%
Estrogen receptor binding - 0.7378 73.78%
Androgen receptor binding - 0.6526 65.26%
Thyroid receptor binding - 0.7476 74.76%
Glucocorticoid receptor binding - 0.7512 75.12%
Aromatase binding - 0.8023 80.23%
PPAR gamma - 0.6903 69.03%
Honey bee toxicity - 0.9592 95.92%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9837 98.37%

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
CHEMBL1994 P08235 Mineralocorticoid receptor 91.51% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.67% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.19% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.05% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.25% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.67% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.40% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.35% 89.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.64% 82.69%

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 ramosissimum

Cross-Links

Top
PubChem 75038227
LOTUS LTS0212097
wikiData Q105172135