Asperthecin

Details

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Internal ID c2711e04-9d73-4bb8-b8e9-f1a3158f84a8
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 1,2,5,6,8-pentahydroxy-3-(hydroxymethyl)anthracene-9,10-dione
SMILES (Canonical) C1=C(C(=C(C2=C1C(=O)C3=C(C2=O)C(=CC(=C3O)O)O)O)O)CO
SMILES (Isomeric) C1=C(C(=C(C2=C1C(=O)C3=C(C2=O)C(=CC(=C3O)O)O)O)O)CO
InChI InChI=1S/C15H10O8/c16-3-4-1-5-8(15(23)11(4)19)14(22)9-6(17)2-7(18)13(21)10(9)12(5)20/h1-2,16-19,21,23H,3H2
InChI Key DLOLMYKOOZLTPY-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O8
Molecular Weight 318.23 g/mol
Exact Mass 318.03756727 g/mol
Topological Polar Surface Area (TPSA) 156.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 0.48
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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10089-00-6
1,2,5,6,8-pentahydroxy-3-(hydroxymethyl)anthracene-9,10-dione
CHEBI:64161
1,2,5,6,8-Pentahydroxy-3-(hydroxymethyl)-9,10-anthracenedione
DTXSID80143560
9,10-Anthracenedione, 1,2,5,6,8-pentahydroxy-3-(hydroxymethyl)-
RefChem:906655
DTXCID3066051
Anthraquinone, 1,2,5,6,8-pentahydroxy-3-(hydroxymethyl)-
SCHEMBL31273981
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Asperthecin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8617 86.17%
Caco-2 - 0.8946 89.46%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5269 52.69%
OATP2B1 inhibitior - 0.5485 54.85%
OATP1B1 inhibitior + 0.8961 89.61%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9387 93.87%
P-glycoprotein inhibitior - 0.9646 96.46%
P-glycoprotein substrate - 0.9276 92.76%
CYP3A4 substrate - 0.5723 57.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8256 82.56%
CYP3A4 inhibition - 0.8441 84.41%
CYP2C9 inhibition - 0.8314 83.14%
CYP2C19 inhibition - 0.9110 91.10%
CYP2D6 inhibition - 0.9138 91.38%
CYP1A2 inhibition + 0.6558 65.58%
CYP2C8 inhibition - 0.9022 90.22%
CYP inhibitory promiscuity - 0.8390 83.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8975 89.75%
Carcinogenicity (trinary) Non-required 0.6561 65.61%
Eye corrosion - 0.9947 99.47%
Eye irritation + 0.9183 91.83%
Skin irritation - 0.6200 62.00%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis + 0.7609 76.09%
Human Ether-a-go-go-Related Gene inhibition - 0.7072 70.72%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.6659 66.59%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.5697 56.97%
Acute Oral Toxicity (c) III 0.5039 50.39%
Estrogen receptor binding + 0.6949 69.49%
Androgen receptor binding + 0.6804 68.04%
Thyroid receptor binding - 0.6911 69.11%
Glucocorticoid receptor binding + 0.8558 85.58%
Aromatase binding + 0.5523 55.23%
PPAR gamma + 0.7174 71.74%
Honey bee toxicity - 0.9239 92.39%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9651 96.51%

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 99.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.32% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.18% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.63% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.48% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.44% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.27% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 85.25% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.56% 91.71%
CHEMBL226 P30542 Adenosine A1 receptor 83.79% 95.93%
CHEMBL4208 P20618 Proteasome component C5 82.52% 90.00%
CHEMBL3194 P02766 Transthyretin 81.79% 90.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 3084060
LOTUS LTS0232067
wikiData Q27133084