Herqueinone o Isoherqueinone

Details

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Internal ID f2c8a703-6081-4d5a-9b5e-0eaa2f4ab9d0
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name 4,6,7a-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-9H-phenaleno[1,2-b]furan-3,7-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O7/c1-7-6-9(21)11-12-10(7)18-20(25,19(3,4)8(2)27-18)17(24)13(12)15(23)16(26-5)14(11)22/h6,8,22-23,25H,1-5H3
InChI Key PKJJEYCUTMFGJW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H20O7
Molecular Weight 372.40 g/mol
Exact Mass 372.12090297 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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SCHEMBL8274485
BS-1262

2D Structure

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2D Structure of Herqueinone o Isoherqueinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.5261 52.61%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7324 73.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7796 77.96%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4882 48.82%
P-glycoprotein inhibitior - 0.7455 74.55%
P-glycoprotein substrate - 0.7821 78.21%
CYP3A4 substrate + 0.6201 62.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8623 86.23%
CYP3A4 inhibition - 0.6218 62.18%
CYP2C9 inhibition + 0.8113 81.13%
CYP2C19 inhibition - 0.5204 52.04%
CYP2D6 inhibition - 0.7888 78.88%
CYP1A2 inhibition + 0.7544 75.44%
CYP2C8 inhibition - 0.6516 65.16%
CYP inhibitory promiscuity + 0.9020 90.20%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9843 98.43%
Carcinogenicity (trinary) Danger 0.5152 51.52%
Eye corrosion - 0.9835 98.35%
Eye irritation + 0.6422 64.22%
Skin irritation - 0.7063 70.63%
Skin corrosion - 0.9297 92.97%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6190 61.90%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.5178 51.78%
skin sensitisation - 0.7280 72.80%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6502 65.02%
Acute Oral Toxicity (c) III 0.5304 53.04%
Estrogen receptor binding + 0.8874 88.74%
Androgen receptor binding + 0.5999 59.99%
Thyroid receptor binding + 0.6064 60.64%
Glucocorticoid receptor binding + 0.6448 64.48%
Aromatase binding + 0.7108 71.08%
PPAR gamma + 0.8053 80.53%
Honey bee toxicity - 0.8663 86.63%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9836 98.36%

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 98.03% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.17% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.06% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.53% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.42% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.41% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.41% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.74% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.74% 94.75%
CHEMBL2581 P07339 Cathepsin D 83.61% 98.95%

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 9799600
LOTUS LTS0020843
wikiData Q77517512