Halawanone D

Details

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Internal ID 5ecd09dd-4a41-4657-bc52-a04dc21c7c91
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 3-[(2S,4R,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-1-ethyl-8-hydroxyanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H22O7/c1-3-11-7-12(29-17-9-16(24)20(25)10(2)28-17)8-14-18(11)22(27)19-13(21(14)26)5-4-6-15(19)23/h4-8,10,16-17,20,23-25H,3,9H2,1-2H3/t10-,16-,17+,20-/m1/s1
InChI Key XAPCBICNZSELEW-OKZQZZHASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O7
Molecular Weight 398.40 g/mol
Exact Mass 398.13655304 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 7
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 Halawanone D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8939 89.39%
Caco-2 - 0.6832 68.32%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6892 68.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9132 91.32%
OATP1B3 inhibitior + 0.9065 90.65%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9476 94.76%
P-glycoprotein inhibitior - 0.6062 60.62%
P-glycoprotein substrate - 0.5385 53.85%
CYP3A4 substrate + 0.6200 62.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.9448 94.48%
CYP2C9 inhibition - 0.8615 86.15%
CYP2C19 inhibition - 0.8753 87.53%
CYP2D6 inhibition - 0.9616 96.16%
CYP1A2 inhibition - 0.6623 66.23%
CYP2C8 inhibition - 0.7517 75.17%
CYP inhibitory promiscuity - 0.9357 93.57%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6643 66.43%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9367 93.67%
Skin irritation - 0.8002 80.02%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis + 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6538 65.38%
Micronuclear + 0.6859 68.59%
Hepatotoxicity + 0.5427 54.27%
skin sensitisation - 0.8745 87.45%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5352 53.52%
Acute Oral Toxicity (c) III 0.5609 56.09%
Estrogen receptor binding + 0.8070 80.70%
Androgen receptor binding + 0.5531 55.31%
Thyroid receptor binding - 0.6017 60.17%
Glucocorticoid receptor binding + 0.7401 74.01%
Aromatase binding + 0.6249 62.49%
PPAR gamma + 0.7831 78.31%
Honey bee toxicity - 0.8237 82.37%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9573 95.73%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.67% 91.49%
CHEMBL2581 P07339 Cathepsin D 98.96% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.78% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 96.99% 95.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.05% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.71% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.55% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.78% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.64% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.82% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 91.09% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.28% 94.00%
CHEMBL4208 P20618 Proteasome component C5 88.27% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.76% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.72% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.28% 90.71%
CHEMBL2535 P11166 Glucose transporter 84.75% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.55% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.44% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.00% 100.00%

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 10501038
LOTUS LTS0126990
wikiData Q77310287