Aurasperone H

Details

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Internal ID 54a63778-5bc5-4f4e-954b-7fddec1d599c
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 5-hydroxy-7-[5-hydroxy-2-(2-hydroxypropyl)-6,8-dimethoxy-4-oxobenzo[g]chromen-10-yl]-6,8-dimethoxy-2-methylbenzo[g]chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H30O11/c1-14(35)7-18-12-21(37)29-32(39)26-19(11-17(40-3)13-23(26)42-5)27(34(29)45-18)30-22(41-4)9-16-10-24-28(20(36)8-15(2)44-24)31(38)25(16)33(30)43-6/h8-14,35,38-39H,7H2,1-6H3
InChI Key FEUIXQJXKYASCV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H30O11
Molecular Weight 614.60 g/mol
Exact Mass 614.17881177 g/mol
Topological Polar Surface Area (TPSA) 150.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.55
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Aurasperone H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9694 96.94%
Caco-2 - 0.7827 78.27%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8178 81.78%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8504 85.04%
OATP1B3 inhibitior + 0.8741 87.41%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9406 94.06%
P-glycoprotein inhibitior + 0.8304 83.04%
P-glycoprotein substrate + 0.5741 57.41%
CYP3A4 substrate + 0.6471 64.71%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.7891 78.91%
CYP3A4 inhibition - 0.8818 88.18%
CYP2C9 inhibition - 0.8152 81.52%
CYP2C19 inhibition - 0.8372 83.72%
CYP2D6 inhibition - 0.8159 81.59%
CYP1A2 inhibition - 0.6883 68.83%
CYP2C8 inhibition + 0.6246 62.46%
CYP inhibitory promiscuity - 0.7473 74.73%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.5820 58.20%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.8839 88.39%
Skin irritation - 0.8467 84.67%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7857 78.57%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.9341 93.41%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.9443 94.43%
Acute Oral Toxicity (c) III 0.5693 56.93%
Estrogen receptor binding + 0.8612 86.12%
Androgen receptor binding + 0.7231 72.31%
Thyroid receptor binding + 0.5826 58.26%
Glucocorticoid receptor binding + 0.8055 80.55%
Aromatase binding + 0.6309 63.09%
PPAR gamma + 0.6962 69.62%
Honey bee toxicity - 0.8279 82.79%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9025 90.25%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.16% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.04% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.66% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.00% 99.15%
CHEMBL2581 P07339 Cathepsin D 94.79% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.44% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 93.83% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.85% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.64% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.53% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.90% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.23% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.19% 86.33%
CHEMBL2535 P11166 Glucose transporter 88.06% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.79% 99.23%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.41% 86.92%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.72% 92.62%
CHEMBL4581 P52732 Kinesin-like protein 1 84.67% 93.18%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.50% 90.71%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.24% 96.21%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 80.99% 95.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.36% 96.00%

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 139587018
LOTUS LTS0225656
wikiData Q77519615