3-O-Methylalaternin-7-O-sulphate

Details

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Internal ID c910db77-6c05-448c-89bc-6c6c4a9b4174
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name (1,8-dihydroxy-6-methoxy-3-methyl-9,10-dioxoanthracen-2-yl) hydrogen sulfate
SMILES (Canonical) CC1=CC2=C(C(=C1OS(=O)(=O)O)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC
SMILES (Isomeric) CC1=CC2=C(C(=C1OS(=O)(=O)O)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC
InChI InChI=1S/C16H12O9S/c1-6-3-8-12(15(20)16(6)25-26(21,22)23)14(19)11-9(13(8)18)4-7(24-2)5-10(11)17/h3-5,17,20H,1-2H3,(H,21,22,23)
InChI Key FMLGIVPYYOHBBX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H12O9S
Molecular Weight 380.30 g/mol
Exact Mass 380.02020313 g/mol
Topological Polar Surface Area (TPSA) 156.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.37
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-O-Methylalaternin-7-O-sulphate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9399 93.99%
Caco-2 + 0.5642 56.42%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5979 59.79%
OATP2B1 inhibitior - 0.7085 70.85%
OATP1B1 inhibitior + 0.9155 91.55%
OATP1B3 inhibitior + 0.9350 93.50%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8390 83.90%
P-glycoprotein inhibitior - 0.7835 78.35%
P-glycoprotein substrate - 0.9366 93.66%
CYP3A4 substrate + 0.5335 53.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8287 82.87%
CYP3A4 inhibition - 0.9590 95.90%
CYP2C9 inhibition - 0.8384 83.84%
CYP2C19 inhibition - 0.8522 85.22%
CYP2D6 inhibition - 0.9184 91.84%
CYP1A2 inhibition + 0.5167 51.67%
CYP2C8 inhibition - 0.5823 58.23%
CYP inhibitory promiscuity - 0.8000 80.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.6640 66.40%
Carcinogenicity (trinary) Non-required 0.6036 60.36%
Eye corrosion - 0.8698 86.98%
Eye irritation - 0.5401 54.01%
Skin irritation - 0.7831 78.31%
Skin corrosion - 0.8536 85.36%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8014 80.14%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.5055 50.55%
skin sensitisation - 0.8648 86.48%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5510 55.10%
Acute Oral Toxicity (c) III 0.6524 65.24%
Estrogen receptor binding + 0.6098 60.98%
Androgen receptor binding + 0.5905 59.05%
Thyroid receptor binding - 0.7403 74.03%
Glucocorticoid receptor binding + 0.6708 67.08%
Aromatase binding - 0.5522 55.22%
PPAR gamma - 0.5325 53.25%
Honey bee toxicity - 0.9229 92.29%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9932 99.32%

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 97.28% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.27% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.56% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.84% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.56% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.54% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.14% 99.23%
CHEMBL4208 P20618 Proteasome component C5 89.11% 90.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.06% 96.21%
CHEMBL3401 O75469 Pregnane X receptor 86.99% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.54% 89.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.27% 92.68%
CHEMBL2535 P11166 Glucose transporter 86.18% 98.75%
CHEMBL2056 P21728 Dopamine D1 receptor 84.30% 91.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.80% 91.07%
CHEMBL4581 P52732 Kinesin-like protein 1 81.22% 93.18%

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 24882469
LOTUS LTS0147283
wikiData Q77385415