CID 162986920

Details

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Internal ID 7f3836a4-6932-4794-9ff8-d95a9aef40cf
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tetracarboxylic acids and derivatives
IUPAC Name
SMILES (Canonical) CC1CC(C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)OC(=O)C
SMILES (Isomeric) CC1CC(C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)OC(=O)C
InChI InChI=1S/C28H36O11/c1-15-10-24(37-18(4)31)27(13-34-16(2)29)22(6-7-23(36-17(3)30)28(27)14-35-28)26(15)11-21(20-8-9-33-12-20)39-25(26)38-19(5)32/h8-9,12,15,21-25H,6-7,10-11,13-14H2,1-5H3
InChI Key RWRDJADIWOOIQG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H36O11
Molecular Weight 548.60 g/mol
Exact Mass 548.22576196 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 11
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162986920

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9812 98.12%
Caco-2 - 0.7515 75.15%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7948 79.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7955 79.55%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9781 97.81%
P-glycoprotein inhibitior + 0.7890 78.90%
P-glycoprotein substrate + 0.5121 51.21%
CYP3A4 substrate + 0.6705 67.05%
CYP2C9 substrate - 0.6020 60.20%
CYP2D6 substrate - 0.8412 84.12%
CYP3A4 inhibition + 0.5084 50.84%
CYP2C9 inhibition - 0.7242 72.42%
CYP2C19 inhibition - 0.6712 67.12%
CYP2D6 inhibition - 0.9445 94.45%
CYP1A2 inhibition - 0.8933 89.33%
CYP2C8 inhibition + 0.6256 62.56%
CYP inhibitory promiscuity - 0.7598 75.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5173 51.73%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.8691 86.91%
Skin irritation - 0.7668 76.68%
Skin corrosion - 0.9404 94.04%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8729 87.29%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8918 89.18%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5829 58.29%
Acute Oral Toxicity (c) III 0.3853 38.53%
Estrogen receptor binding + 0.9032 90.32%
Androgen receptor binding + 0.6914 69.14%
Thyroid receptor binding + 0.6106 61.06%
Glucocorticoid receptor binding + 0.8156 81.56%
Aromatase binding + 0.6829 68.29%
PPAR gamma + 0.7407 74.07%
Honey bee toxicity - 0.8351 83.51%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9922 99.22%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.89% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.44% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.45% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.57% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.65% 94.80%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.03% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.35% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.15% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.18% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.82% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.99% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.95% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.74% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.44% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.25% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.14% 99.17%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.77% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.91% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.18% 95.50%

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.
Teucrium pyrenaicum

Cross-Links

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PubChem 162986920
LOTUS LTS0149528
wikiData Q105246688