Altersolanol N

Details

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Internal ID 543a2aba-c344-4925-890d-4ca227179e4d
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name [(1S,2R,3S,4R)-1,3,4,8-tetrahydroxy-6-methoxy-3-methyl-9,10-dioxo-2,4-dihydro-1H-anthracen-2-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H18O9/c1-6(19)27-17-15(23)11-12(16(24)18(17,2)25)13(21)8-4-7(26-3)5-9(20)10(8)14(11)22/h4-5,15-17,20,23-25H,1-3H3/t15-,16+,17+,18-/m0/s1
InChI Key JDGCLPKEFXLDSC-MLHJIOFPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O9
Molecular Weight 378.30 g/mol
Exact Mass 378.09508215 g/mol
Topological Polar Surface Area (TPSA) 151.00 Ų
XlogP -0.80
Atomic LogP (AlogP) -0.51
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Altersolanol N

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9785 97.85%
Caco-2 - 0.5936 59.36%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7186 71.86%
OATP2B1 inhibitior - 0.5739 57.39%
OATP1B1 inhibitior + 0.9044 90.44%
OATP1B3 inhibitior + 0.9087 90.87%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6554 65.54%
P-glycoprotein inhibitior - 0.6962 69.62%
P-glycoprotein substrate - 0.8247 82.47%
CYP3A4 substrate + 0.6047 60.47%
CYP2C9 substrate - 0.8050 80.50%
CYP2D6 substrate - 0.8701 87.01%
CYP3A4 inhibition - 0.8500 85.00%
CYP2C9 inhibition - 0.7448 74.48%
CYP2C19 inhibition - 0.8345 83.45%
CYP2D6 inhibition - 0.9004 90.04%
CYP1A2 inhibition - 0.6322 63.22%
CYP2C8 inhibition - 0.6207 62.07%
CYP inhibitory promiscuity - 0.7001 70.01%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9297 92.97%
Carcinogenicity (trinary) Non-required 0.4903 49.03%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.7602 76.02%
Skin irritation - 0.6301 63.01%
Skin corrosion - 0.9305 93.05%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7254 72.54%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation - 0.7358 73.58%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7950 79.50%
Acute Oral Toxicity (c) III 0.4638 46.38%
Estrogen receptor binding + 0.8561 85.61%
Androgen receptor binding + 0.6820 68.20%
Thyroid receptor binding - 0.6305 63.05%
Glucocorticoid receptor binding + 0.6496 64.96%
Aromatase binding - 0.6293 62.93%
PPAR gamma + 0.6352 63.52%
Honey bee toxicity - 0.7743 77.43%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9927 99.27%

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 98.28% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.88% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.37% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.72% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.10% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.69% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 92.31% 91.19%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.20% 85.14%
CHEMBL4208 P20618 Proteasome component C5 91.63% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.75% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.43% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.95% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.63% 86.33%
CHEMBL2535 P11166 Glucose transporter 82.21% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.41% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.26% 94.42%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.15% 92.94%

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 57380591
LOTUS LTS0052498
wikiData Q77494045