Isoaurasperone

Details

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Internal ID ffbb785a-8ec9-4287-8820-69f33d81a112
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 6-hydroxy-7-(6-hydroxy-5,8-dimethoxy-2-methyl-4-oxobenzo[g]chromen-10-yl)-5,8-dimethoxy-2-methylbenzo[g]chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H26O10/c1-13-7-18(33)26-22(41-13)10-15-9-21(38-4)28(29(36)23(15)30(26)39-5)25-17-11-16(37-3)12-20(35)24(17)31(40-6)27-19(34)8-14(2)42-32(25)27/h7-12,35-36H,1-6H3
InChI Key LQQLPCZPXCJFRH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H26O10
Molecular Weight 570.50 g/mol
Exact Mass 570.15259702 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 5.94
H-Bond Acceptor 10
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isoaurasperone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9657 96.57%
Caco-2 - 0.6591 65.91%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8810 88.10%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8777 87.77%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7468 74.68%
P-glycoprotein inhibitior + 0.8578 85.78%
P-glycoprotein substrate - 0.5979 59.79%
CYP3A4 substrate + 0.6306 63.06%
CYP2C9 substrate - 0.8348 83.48%
CYP2D6 substrate - 0.8294 82.94%
CYP3A4 inhibition - 0.8272 82.72%
CYP2C9 inhibition - 0.6322 63.22%
CYP2C19 inhibition - 0.6817 68.17%
CYP2D6 inhibition - 0.8618 86.18%
CYP1A2 inhibition + 0.6337 63.37%
CYP2C8 inhibition + 0.7212 72.12%
CYP inhibitory promiscuity + 0.5096 50.96%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.5571 55.71%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.8240 82.40%
Skin irritation - 0.7763 77.63%
Skin corrosion - 0.9710 97.10%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8038 80.38%
Micronuclear + 0.8500 85.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9631 96.31%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7939 79.39%
Acute Oral Toxicity (c) III 0.5395 53.95%
Estrogen receptor binding + 0.8646 86.46%
Androgen receptor binding + 0.7408 74.08%
Thyroid receptor binding + 0.5905 59.05%
Glucocorticoid receptor binding + 0.8061 80.61%
Aromatase binding + 0.6252 62.52%
PPAR gamma + 0.6944 69.44%
Honey bee toxicity - 0.8440 84.40%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9309 93.09%

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 98.92% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.73% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.47% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.29% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.93% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 90.66% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.36% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 89.79% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.76% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.71% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.05% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.75% 96.21%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.33% 94.42%
CHEMBL4208 P20618 Proteasome component C5 85.28% 90.00%
CHEMBL2535 P11166 Glucose transporter 83.25% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.12% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.79% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.59% 93.99%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.90% 80.78%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.51% 86.92%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.39% 93.65%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.19% 95.50%
CHEMBL3194 P02766 Transthyretin 80.72% 90.71%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.59% 100.00%

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 101419810
LOTUS LTS0121773
wikiData Q105155681