Alterporriol Q

Details

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Internal ID bde35cb3-68a6-466b-b01d-a2be84448ff8
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 2-(2,8-dihydroxy-6-methoxy-3-methyl-9,10-dioxoanthracen-1-yl)-1,7-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione
SMILES (Canonical) CC1=CC2=C(C=C1O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C4=C(C(=CC5=C4C(=O)C6=C(C5=O)C=C(C=C6O)OC)C)O)O
SMILES (Isomeric) CC1=CC2=C(C=C1O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C4=C(C(=CC5=C4C(=O)C6=C(C5=O)C=C(C=C6O)OC)C)O)O
InChI InChI=1S/C32H22O10/c1-11-5-14-15(9-19(11)33)30(38)24-18(28(14)36)10-21(42-4)25(32(24)40)26-23-16(6-12(2)27(26)35)29(37)17-7-13(41-3)8-20(34)22(17)31(23)39/h5-10,33-35,40H,1-4H3
InChI Key IFLKWZMIHYZTTR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H22O10
Molecular Weight 566.50 g/mol
Exact Mass 566.12129689 g/mol
Topological Polar Surface Area (TPSA) 168.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 10
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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CHEMBL2011668
SCHEMBL23522419

2D Structure

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2D Structure of Alterporriol Q

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 - 0.7726 77.26%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.9160 91.60%
OATP2B1 inhibitior - 0.7143 71.43%
OATP1B1 inhibitior + 0.9157 91.57%
OATP1B3 inhibitior + 0.7900 79.00%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9281 92.81%
P-glycoprotein inhibitior + 0.7542 75.42%
P-glycoprotein substrate - 0.8716 87.16%
CYP3A4 substrate + 0.5772 57.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7976 79.76%
CYP3A4 inhibition - 0.8649 86.49%
CYP2C9 inhibition - 0.6454 64.54%
CYP2C19 inhibition - 0.7697 76.97%
CYP2D6 inhibition - 0.8580 85.80%
CYP1A2 inhibition + 0.8692 86.92%
CYP2C8 inhibition + 0.5391 53.91%
CYP inhibitory promiscuity - 0.5529 55.29%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7929 79.29%
Carcinogenicity (trinary) Non-required 0.5429 54.29%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.6625 66.25%
Skin irritation - 0.7455 74.55%
Skin corrosion - 0.9709 97.09%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3642 36.42%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5180 51.80%
skin sensitisation - 0.9685 96.85%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6549 65.49%
Acute Oral Toxicity (c) II 0.5750 57.50%
Estrogen receptor binding + 0.8741 87.41%
Androgen receptor binding + 0.6873 68.73%
Thyroid receptor binding + 0.5270 52.70%
Glucocorticoid receptor binding + 0.7743 77.43%
Aromatase binding + 0.5519 55.19%
PPAR gamma + 0.6486 64.86%
Honey bee toxicity - 0.8673 86.73%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9881 98.81%

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
CHEMBL1860 P10827 Thyroid hormone receptor alpha 97.47% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.94% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.59% 91.11%
CHEMBL4208 P20618 Proteasome component C5 92.74% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.11% 94.00%
CHEMBL2581 P07339 Cathepsin D 91.68% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.28% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.10% 89.00%
CHEMBL2535 P11166 Glucose transporter 87.82% 98.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.34% 96.21%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.43% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.74% 86.33%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 83.29% 92.68%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.93% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.47% 99.17%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.16% 97.36%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.94% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 80.52% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.13% 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 57332381
LOTUS LTS0159294
wikiData Q77500292