Phomonaphthalenone A

Details

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Internal ID 494112df-3b98-4ad6-95f7-73e613031a65
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name (1S,9S,12R,14S)-3,6-dihydroxy-4-methoxy-12-methyl-11,15-dioxatetracyclo[10.2.1.02,7.09,14]pentadeca-2(7),3,5-trien-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O6/c1-15-4-6-7(5-20-15)12(17)10-8(16)3-9(19-2)13(18)11(10)14(6)21-15/h3,6-7,14,16,18H,4-5H2,1-2H3/t6-,7+,14-,15+/m0/s1
InChI Key JSFXOJVYQRUNET-XOEPVMSWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O6
Molecular Weight 292.28 g/mol
Exact Mass 292.09468823 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phomonaphthalenone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9552 95.52%
Caco-2 + 0.5144 51.44%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7468 74.68%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8994 89.94%
OATP1B3 inhibitior + 0.9145 91.45%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8131 81.31%
P-glycoprotein inhibitior - 0.8932 89.32%
P-glycoprotein substrate - 0.6473 64.73%
CYP3A4 substrate + 0.6289 62.89%
CYP2C9 substrate - 0.6021 60.21%
CYP2D6 substrate - 0.8194 81.94%
CYP3A4 inhibition - 0.6371 63.71%
CYP2C9 inhibition - 0.8102 81.02%
CYP2C19 inhibition - 0.6168 61.68%
CYP2D6 inhibition - 0.7468 74.68%
CYP1A2 inhibition - 0.7387 73.87%
CYP2C8 inhibition - 0.5577 55.77%
CYP inhibitory promiscuity - 0.7799 77.99%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5862 58.62%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.7106 71.06%
Skin irritation - 0.7836 78.36%
Skin corrosion - 0.9516 95.16%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7948 79.48%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.5045 50.45%
skin sensitisation - 0.7932 79.32%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.5829 58.29%
Acute Oral Toxicity (c) III 0.6064 60.64%
Estrogen receptor binding + 0.8493 84.93%
Androgen receptor binding + 0.7581 75.81%
Thyroid receptor binding + 0.5971 59.71%
Glucocorticoid receptor binding + 0.9077 90.77%
Aromatase binding - 0.7518 75.18%
PPAR gamma + 0.7700 77.00%
Honey bee toxicity - 0.7408 74.08%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5949 59.49%
Fish aquatic toxicity + 0.9639 96.39%

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 99.70% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.30% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.80% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.97% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.52% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.85% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.57% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.06% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.30% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.93% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 86.11% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.47% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.66% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.31% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.96% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 83.61% 91.19%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.65% 96.21%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.79% 97.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.41% 95.50%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.18% 96.00%

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.
There are no matching plants.

Cross-Links

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PubChem 139583689
LOTUS LTS0256000
wikiData Q75065481