3,4,5-Trihydroxy-6-[[13-(2-methoxy-2-oxoethyl)-11-methyl-2,9-dioxo-12,15-dioxatetracyclo[8.4.1.01,10.03,8]pentadeca-3(8),4,6-trien-7-yl]oxy]oxane-2-carboxylic acid

Details

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Internal ID d81ef43f-b7c9-40b0-b6a3-207e726b8501
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones > Naphthopyranone glycosides
IUPAC Name 3,4,5-trihydroxy-6-[[13-(2-methoxy-2-oxoethyl)-11-methyl-2,9-dioxo-12,15-dioxatetracyclo[8.4.1.01,10.03,8]pentadeca-3(8),4,6-trien-7-yl]oxy]oxane-2-carboxylic acid
SMILES (Canonical) CC1C23C(=O)C4=C(C=CC=C4OC5C(C(C(C(O5)C(=O)O)O)O)O)C(=O)C2(O3)CC(O1)CC(=O)OC
SMILES (Isomeric) CC1C23C(=O)C4=C(C=CC=C4OC5C(C(C(C(O5)C(=O)O)O)O)O)C(=O)C2(O3)CC(O1)CC(=O)OC
InChI InChI=1S/C23H24O13/c1-8-23-19(29)13-10(18(28)22(23,36-23)7-9(33-8)6-12(24)32-2)4-3-5-11(13)34-21-16(27)14(25)15(26)17(35-21)20(30)31/h3-5,8-9,14-17,21,25-27H,6-7H2,1-2H3,(H,30,31)
InChI Key MXKQICKYJJNJEK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O13
Molecular Weight 508.40 g/mol
Exact Mass 508.12169082 g/mol
Topological Polar Surface Area (TPSA) 199.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -1.42
H-Bond Acceptor 12
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4,5-Trihydroxy-6-[[13-(2-methoxy-2-oxoethyl)-11-methyl-2,9-dioxo-12,15-dioxatetracyclo[8.4.1.01,10.03,8]pentadeca-3(8),4,6-trien-7-yl]oxy]oxane-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7578 75.78%
Caco-2 - 0.8564 85.64%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.4850 48.50%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.8643 86.43%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6717 67.17%
P-glycoprotein inhibitior - 0.4628 46.28%
P-glycoprotein substrate + 0.5595 55.95%
CYP3A4 substrate + 0.6816 68.16%
CYP2C9 substrate - 0.5992 59.92%
CYP2D6 substrate - 0.8722 87.22%
CYP3A4 inhibition - 0.8023 80.23%
CYP2C9 inhibition - 0.9429 94.29%
CYP2C19 inhibition - 0.8690 86.90%
CYP2D6 inhibition - 0.9134 91.34%
CYP1A2 inhibition - 0.8964 89.64%
CYP2C8 inhibition + 0.6504 65.04%
CYP inhibitory promiscuity - 0.9333 93.33%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6640 66.40%
Eye corrosion - 0.9841 98.41%
Eye irritation - 0.9097 90.97%
Skin irritation - 0.7311 73.11%
Skin corrosion - 0.9109 91.09%
Ames mutagenesis - 0.5054 50.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5286 52.86%
Micronuclear + 0.5459 54.59%
Hepatotoxicity - 0.6895 68.95%
skin sensitisation - 0.8185 81.85%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.5581 55.81%
Acute Oral Toxicity (c) III 0.5348 53.48%
Estrogen receptor binding + 0.7522 75.22%
Androgen receptor binding + 0.6867 68.67%
Thyroid receptor binding - 0.5718 57.18%
Glucocorticoid receptor binding + 0.6951 69.51%
Aromatase binding + 0.5920 59.20%
PPAR gamma + 0.6632 66.32%
Honey bee toxicity - 0.8465 84.65%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8707 87.07%

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
CHEMBL2581 P07339 Cathepsin D 98.21% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.45% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.48% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.37% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.33% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 94.79% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.93% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.60% 95.89%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 90.53% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.40% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.91% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.62% 99.23%
CHEMBL5028 O14672 ADAM10 86.29% 97.50%
CHEMBL1951 P21397 Monoamine oxidase A 85.17% 91.49%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.72% 91.07%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.49% 96.00%
CHEMBL2535 P11166 Glucose transporter 82.54% 98.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.60% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.15% 99.17%

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 162814222
LOTUS LTS0028060
wikiData Q104172146