2-(4,7-dihydroxy-5-oxo-2-phenyl-7,8-dihydro-6H-naphthalen-1-yl)-6-hydroxypyran-4-one

Details

Top
Internal ID 781d2b0a-dab6-4a73-a591-443837a9cc66
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 2-(4,7-dihydroxy-5-oxo-2-phenyl-7,8-dihydro-6H-naphthalen-1-yl)-6-hydroxypyran-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H16O6/c22-12-6-15-20(18-8-13(23)9-19(26)27-18)14(11-4-2-1-3-5-11)10-17(25)21(15)16(24)7-12/h1-5,8-10,12,22,25-26H,6-7H2
InChI Key XHWVUVJDLYZUFU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H16O6
Molecular Weight 364.30 g/mol
Exact Mass 364.09468823 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(4,7-dihydroxy-5-oxo-2-phenyl-7,8-dihydro-6H-naphthalen-1-yl)-6-hydroxypyran-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9359 93.59%
Caco-2 - 0.6779 67.79%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8155 81.55%
OATP2B1 inhibitior - 0.5791 57.91%
OATP1B1 inhibitior + 0.9049 90.49%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5912 59.12%
P-glycoprotein inhibitior - 0.7756 77.56%
P-glycoprotein substrate - 0.8280 82.80%
CYP3A4 substrate + 0.5502 55.02%
CYP2C9 substrate + 0.6048 60.48%
CYP2D6 substrate - 0.8058 80.58%
CYP3A4 inhibition - 0.8957 89.57%
CYP2C9 inhibition + 0.6640 66.40%
CYP2C19 inhibition - 0.8540 85.40%
CYP2D6 inhibition - 0.9073 90.73%
CYP1A2 inhibition - 0.9101 91.01%
CYP2C8 inhibition + 0.5850 58.50%
CYP inhibitory promiscuity - 0.9288 92.88%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6327 63.27%
Eye corrosion - 0.9945 99.45%
Eye irritation - 0.7678 76.78%
Skin irritation - 0.6273 62.73%
Skin corrosion - 0.9652 96.52%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5618 56.18%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.9252 92.52%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.5987 59.87%
Acute Oral Toxicity (c) I 0.7016 70.16%
Estrogen receptor binding + 0.7150 71.50%
Androgen receptor binding + 0.8558 85.58%
Thyroid receptor binding - 0.6767 67.67%
Glucocorticoid receptor binding + 0.6884 68.84%
Aromatase binding + 0.6160 61.60%
PPAR gamma + 0.9261 92.61%
Honey bee toxicity - 0.8162 81.62%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9598 95.98%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.26% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.01% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.33% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.15% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.69% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.05% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.96% 99.23%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 85.39% 89.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.91% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.13% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.11% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.05% 97.09%

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.
There are no matching plants.

Cross-Links

Top
PubChem 16216910
LOTUS LTS0061706
wikiData Q105328331