5-hydroxy-6,8-dimethoxy-2,3-dimethyl-4H-naphtho(2,3-b)pyran-4-one

Details

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Internal ID a3ab2f23-e281-4005-bc30-6dc0d54d8eeb
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 5-hydroxy-6,8-dimethoxy-2,3-dimethylbenzo[g]chromen-4-one
SMILES (Canonical) CC1=C(OC2=CC3=CC(=CC(=C3C(=C2C1=O)O)OC)OC)C
SMILES (Isomeric) CC1=C(OC2=CC3=CC(=CC(=C3C(=C2C1=O)O)OC)OC)C
InChI InChI=1S/C17H16O5/c1-8-9(2)22-13-6-10-5-11(20-3)7-12(21-4)14(10)17(19)15(13)16(8)18/h5-7,19H,1-4H3
InChI Key FZYRENRMDAPHEM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O5
Molecular Weight 300.30 g/mol
Exact Mass 300.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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5-hydroxy-6,8-dimethoxy-2,3-dimethyl-4H-naphtho[2,3-b]pyran-4-one

2D Structure

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2D Structure of 5-hydroxy-6,8-dimethoxy-2,3-dimethyl-4H-naphtho(2,3-b)pyran-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 + 0.8010 80.10%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7237 72.37%
OATP2B1 inhibitior - 0.7187 71.87%
OATP1B1 inhibitior + 0.9014 90.14%
OATP1B3 inhibitior + 0.9931 99.31%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6535 65.35%
P-glycoprotein inhibitior - 0.4728 47.28%
P-glycoprotein substrate - 0.8622 86.22%
CYP3A4 substrate + 0.5097 50.97%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate - 0.8410 84.10%
CYP3A4 inhibition - 0.6586 65.86%
CYP2C9 inhibition - 0.9427 94.27%
CYP2C19 inhibition - 0.5570 55.70%
CYP2D6 inhibition - 0.8684 86.84%
CYP1A2 inhibition + 0.9717 97.17%
CYP2C8 inhibition - 0.6090 60.90%
CYP inhibitory promiscuity + 0.5065 50.65%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.6188 61.88%
Eye corrosion - 0.9710 97.10%
Eye irritation + 0.6341 63.41%
Skin irritation - 0.7051 70.51%
Skin corrosion - 0.9897 98.97%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4716 47.16%
Micronuclear + 0.8259 82.59%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.9571 95.71%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6656 66.56%
Acute Oral Toxicity (c) II 0.5409 54.09%
Estrogen receptor binding + 0.8837 88.37%
Androgen receptor binding + 0.6177 61.77%
Thyroid receptor binding + 0.5908 59.08%
Glucocorticoid receptor binding + 0.7900 79.00%
Aromatase binding + 0.8594 85.94%
PPAR gamma + 0.8093 80.93%
Honey bee toxicity - 0.9052 90.52%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8938 89.38%

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 96.35% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.32% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.92% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.15% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.10% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.05% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.44% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.37% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.28% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.70% 94.42%
CHEMBL2581 P07339 Cathepsin D 85.39% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.98% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.66% 94.73%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.42% 92.94%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.14% 93.65%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.73% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.19% 96.00%
CHEMBL4208 P20618 Proteasome component C5 81.01% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10685604
LOTUS LTS0037598
wikiData Q77380015