3-[[(2R,3S,4S,5R,6S)-6-(1,8-dihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid

Details

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Internal ID ab76c09a-fe0e-4902-baf8-e8f29df6bf63
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 3-[[(2R,3S,4S,5R,6S)-6-(1,8-dihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid
SMILES (Canonical) CC1=CC2=C(C(=C1OC3C(C(C(C(O3)COC(=O)CC(=O)O)O)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O
SMILES (Isomeric) CC1=CC2=C(C(=C1O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)COC(=O)CC(=O)O)O)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O
InChI InChI=1S/C24H22O13/c1-8-5-10-16(19(31)15-9(17(10)29)3-2-4-11(15)25)20(32)23(8)37-24-22(34)21(33)18(30)12(36-24)7-35-14(28)6-13(26)27/h2-5,12,18,21-22,24-25,30,32-34H,6-7H2,1H3,(H,26,27)/t12-,18-,21+,22-,24+/m1/s1
InChI Key BWQJNUIZXDNIAY-XDMDMBRJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H22O13
Molecular Weight 518.40 g/mol
Exact Mass 518.10604075 g/mol
Topological Polar Surface Area (TPSA) 217.00 Ų
XlogP 0.60
Atomic LogP (AlogP) -0.61
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-[[(2R,3S,4S,5R,6S)-6-(1,8-dihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4768 47.68%
Caco-2 - 0.8732 87.32%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6090 60.90%
OATP2B1 inhibitior - 0.5694 56.94%
OATP1B1 inhibitior + 0.8486 84.86%
OATP1B3 inhibitior + 0.9299 92.99%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7916 79.16%
P-glycoprotein inhibitior - 0.4720 47.20%
P-glycoprotein substrate - 0.7067 70.67%
CYP3A4 substrate + 0.6396 63.96%
CYP2C9 substrate - 0.6262 62.62%
CYP2D6 substrate - 0.8788 87.88%
CYP3A4 inhibition - 0.8598 85.98%
CYP2C9 inhibition - 0.9273 92.73%
CYP2C19 inhibition - 0.8891 88.91%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition - 0.7835 78.35%
CYP2C8 inhibition + 0.6139 61.39%
CYP inhibitory promiscuity - 0.9200 92.00%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6853 68.53%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.9007 90.07%
Skin irritation - 0.8266 82.66%
Skin corrosion - 0.9529 95.29%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5309 53.09%
Micronuclear + 0.6518 65.18%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.9058 90.58%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7488 74.88%
Acute Oral Toxicity (c) III 0.6612 66.12%
Estrogen receptor binding + 0.7957 79.57%
Androgen receptor binding - 0.5217 52.17%
Thyroid receptor binding - 0.5793 57.93%
Glucocorticoid receptor binding + 0.6763 67.63%
Aromatase binding + 0.5768 57.68%
PPAR gamma + 0.5829 58.29%
Honey bee toxicity - 0.9083 90.83%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9517 95.17%

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 98.80% 91.49%
CHEMBL2581 P07339 Cathepsin D 98.75% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.41% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.69% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.64% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.54% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 95.36% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.72% 85.14%
CHEMBL220 P22303 Acetylcholinesterase 93.37% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.63% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.24% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.09% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.97% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.83% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.57% 99.17%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.67% 96.38%
CHEMBL2535 P11166 Glucose transporter 81.75% 98.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.09% 96.67%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.03% 93.56%
CHEMBL5028 O14672 ADAM10 80.51% 97.50%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 80.09% 83.00%

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.
Hemerocallis fulva

Cross-Links

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PubChem 10918342
LOTUS LTS0138109
wikiData Q104947521