Dihydroaltersolanol B

Details

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Internal ID a66c15a2-be52-4e40-8706-5707008e26a2
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name (2R,3S,4aS,9aS)-2,3,8-trihydroxy-6-methoxy-3-methyl-2,4,4a,9a-tetrahydro-1H-anthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O6/c1-16(21)6-10-8(5-12(16)18)15(20)13-9(14(10)19)3-7(22-2)4-11(13)17/h3-4,8,10,12,17-18,21H,5-6H2,1-2H3/t8-,10-,12+,16-/m0/s1
InChI Key LTGSEZGUXURGDR-SLLFNTCVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O6
Molecular Weight 306.31 g/mol
Exact Mass 306.11033829 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.92
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dihydroaltersolanol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.4920 49.20%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7542 75.42%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8995 89.95%
OATP1B3 inhibitior + 0.9525 95.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8062 80.62%
P-glycoprotein inhibitior - 0.9312 93.12%
P-glycoprotein substrate - 0.8043 80.43%
CYP3A4 substrate + 0.6351 63.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8070 80.70%
CYP3A4 inhibition - 0.6895 68.95%
CYP2C9 inhibition - 0.9289 92.89%
CYP2C19 inhibition - 0.8884 88.84%
CYP2D6 inhibition - 0.8792 87.92%
CYP1A2 inhibition + 0.6809 68.09%
CYP2C8 inhibition - 0.6866 68.66%
CYP inhibitory promiscuity - 0.9802 98.02%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8832 88.32%
Carcinogenicity (trinary) Non-required 0.5446 54.46%
Eye corrosion - 0.9865 98.65%
Eye irritation - 0.8443 84.43%
Skin irritation - 0.6425 64.25%
Skin corrosion - 0.8986 89.86%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7706 77.06%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.6027 60.27%
skin sensitisation - 0.8142 81.42%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5719 57.19%
Acute Oral Toxicity (c) III 0.6075 60.75%
Estrogen receptor binding + 0.8317 83.17%
Androgen receptor binding + 0.8014 80.14%
Thyroid receptor binding - 0.5287 52.87%
Glucocorticoid receptor binding + 0.8344 83.44%
Aromatase binding - 0.6300 63.00%
PPAR gamma + 0.5989 59.89%
Honey bee toxicity - 0.8644 86.44%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9859 98.59%

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 98.80% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.49% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.30% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.85% 97.09%
CHEMBL4208 P20618 Proteasome component C5 91.01% 90.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.40% 82.69%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.82% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.33% 92.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.61% 96.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.52% 91.07%
CHEMBL2581 P07339 Cathepsin D 87.84% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.52% 86.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.94% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.73% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.47% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 84.92% 95.93%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.56% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.15% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 84.12% 91.19%
CHEMBL2535 P11166 Glucose transporter 83.81% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.85% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.59% 99.23%

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 132562010
LOTUS LTS0026967
wikiData Q75059160