CID 21635658

Details

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Internal ID ab0de057-93a9-4dae-af1e-402531b4d634
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name
SMILES (Canonical) CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)OC(=O)C
SMILES (Isomeric) C[C@@H]1C[C@@H]([C@@]2([C@@H]([C@@]13C[C@@H](OC3=O)C4=COC=C4)CC[C@@H]([C@]25CO5)O)COC(=O)C)OC(=O)C
InChI InChI=1S/C24H30O9/c1-13-8-20(32-15(3)26)23(11-30-14(2)25)18(4-5-19(27)24(23)12-31-24)22(13)9-17(33-21(22)28)16-6-7-29-10-16/h6-7,10,13,17-20,27H,4-5,8-9,11-12H2,1-3H3/t13-,17-,18-,19+,20+,22-,23+,24-/m1/s1
InChI Key XWQPBOZEAVXNBB-QAGMUIFJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H30O9
Molecular Weight 462.50 g/mol
Exact Mass 462.18898253 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 21635658

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9733 97.33%
Caco-2 - 0.7187 71.87%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8171 81.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7700 77.00%
OATP1B3 inhibitior + 0.8294 82.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7287 72.87%
BSEP inhibitior + 0.5724 57.24%
P-glycoprotein inhibitior - 0.4769 47.69%
P-glycoprotein substrate + 0.5422 54.22%
CYP3A4 substrate + 0.6817 68.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8241 82.41%
CYP3A4 inhibition + 0.6359 63.59%
CYP2C9 inhibition - 0.6254 62.54%
CYP2C19 inhibition - 0.6922 69.22%
CYP2D6 inhibition - 0.9522 95.22%
CYP1A2 inhibition - 0.9008 90.08%
CYP2C8 inhibition + 0.5911 59.11%
CYP inhibitory promiscuity - 0.9021 90.21%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5127 51.27%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9333 93.33%
Skin irritation - 0.6863 68.63%
Skin corrosion - 0.9448 94.48%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8364 83.64%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9209 92.09%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6170 61.70%
Acute Oral Toxicity (c) I 0.5336 53.36%
Estrogen receptor binding + 0.8981 89.81%
Androgen receptor binding + 0.6544 65.44%
Thyroid receptor binding + 0.6019 60.19%
Glucocorticoid receptor binding + 0.8115 81.15%
Aromatase binding + 0.6654 66.54%
PPAR gamma + 0.6449 64.49%
Honey bee toxicity - 0.8359 83.59%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9862 98.62%

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 97.31% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.59% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.08% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.66% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.46% 94.80%
CHEMBL2581 P07339 Cathepsin D 90.21% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.94% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.43% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 85.79% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.60% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.07% 89.00%
CHEMBL2996 Q05655 Protein kinase C delta 83.65% 97.79%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.15% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.94% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.67% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.44% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.83% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.50% 100.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.06% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 80.42% 91.19%
CHEMBL5255 O00206 Toll-like receptor 4 80.30% 92.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.10% 93.00%

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.
Teucrium montanum
Teucrium montbretii

Cross-Links

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PubChem 21635658
LOTUS LTS0239364
wikiData Q105343728