(3R)-3,8-dihydroxy-3,4-dihydro-2H-naphthalen-1-one

Details

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Internal ID ae6d7d9c-0b52-4d06-a62d-4272ee4d115a
Taxonomy Benzenoids > Tetralins
IUPAC Name (3R)-3,8-dihydroxy-3,4-dihydro-2H-naphthalen-1-one
SMILES (Canonical) C1C(CC(=O)C2=C1C=CC=C2O)O
SMILES (Isomeric) C1[C@H](CC(=O)C2=C1C=CC=C2O)O
InChI InChI=1S/C10H10O3/c11-7-4-6-2-1-3-8(12)10(6)9(13)5-7/h1-3,7,11-12H,4-5H2/t7-/m1/s1
InChI Key AQTKGZASUQVMEJ-SSDOTTSWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H10O3
Molecular Weight 178.18 g/mol
Exact Mass 178.062994177 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.88
H-Bond Acceptor 3
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 (3R)-3,8-dihydroxy-3,4-dihydro-2H-naphthalen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8845 88.45%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8167 81.67%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9555 95.55%
OATP1B3 inhibitior + 0.9763 97.63%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9579 95.79%
P-glycoprotein inhibitior - 0.9884 98.84%
P-glycoprotein substrate - 0.9278 92.78%
CYP3A4 substrate - 0.5928 59.28%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.8240 82.40%
CYP2C9 inhibition - 0.6467 64.67%
CYP2C19 inhibition + 0.5460 54.60%
CYP2D6 inhibition - 0.8157 81.57%
CYP1A2 inhibition + 0.7732 77.32%
CYP2C8 inhibition - 0.9712 97.12%
CYP inhibitory promiscuity - 0.7445 74.45%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8124 81.24%
Carcinogenicity (trinary) Warning 0.4953 49.53%
Eye corrosion - 0.9730 97.30%
Eye irritation + 0.9727 97.27%
Skin irritation + 0.7384 73.84%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8328 83.28%
Micronuclear - 0.5341 53.41%
Hepatotoxicity + 0.6928 69.28%
skin sensitisation + 0.4773 47.73%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.5614 56.14%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5367 53.67%
Acute Oral Toxicity (c) III 0.7069 70.69%
Estrogen receptor binding - 0.9154 91.54%
Androgen receptor binding - 0.5877 58.77%
Thyroid receptor binding - 0.7162 71.62%
Glucocorticoid receptor binding - 0.7141 71.41%
Aromatase binding - 0.9296 92.96%
PPAR gamma + 0.6808 68.08%
Honey bee toxicity - 0.9044 90.44%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8585 85.85%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.28% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.47% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.23% 95.56%
CHEMBL217 P14416 Dopamine D2 receptor 89.11% 95.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.70% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.49% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.42% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.47% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 81.97% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.89% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.75% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.76% 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.
Artemisia gilvescens
Datura stramonium
Oenanthe fistulosa

Cross-Links

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PubChem 11789771
NPASS NPC91824
LOTUS LTS0125922
wikiData Q104917056