CID 85209523

Details

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Internal ID 5fa1a587-401c-49d1-a7a2-0b664f4778fe
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)CC(CC25CO5)O)COC(=O)C)OC(=O)C
SMILES (Isomeric) CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CC(CC25CO5)O)COC(=O)C)OC(=O)C
InChI InChI=1S/C24H30O9/c1-13-6-20(32-15(3)26)24(12-30-14(2)25)19(7-17(27)8-22(24)11-31-22)23(13)9-18(33-21(23)28)16-4-5-29-10-16/h4-5,10,13,17-20,27H,6-9,11-12H2,1-3H3
InChI Key HUPBOJIWABTVPP-UHFFFAOYSA-N
Popularity 1 reference 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 85209523

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9741 97.41%
Caco-2 - 0.7320 73.20%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7405 74.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7816 78.16%
OATP1B3 inhibitior + 0.8599 85.99%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5511 55.11%
P-glycoprotein inhibitior - 0.4631 46.31%
P-glycoprotein substrate - 0.5416 54.16%
CYP3A4 substrate + 0.6719 67.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8241 82.41%
CYP3A4 inhibition + 0.5113 51.13%
CYP2C9 inhibition - 0.6711 67.11%
CYP2C19 inhibition - 0.7043 70.43%
CYP2D6 inhibition - 0.9452 94.52%
CYP1A2 inhibition - 0.8988 89.88%
CYP2C8 inhibition + 0.5378 53.78%
CYP inhibitory promiscuity - 0.8381 83.81%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5182 51.82%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.8958 89.58%
Skin irritation - 0.7311 73.11%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8651 86.51%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8664 86.64%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.7197 71.97%
Acute Oral Toxicity (c) I 0.5320 53.20%
Estrogen receptor binding + 0.9014 90.14%
Androgen receptor binding + 0.6790 67.90%
Thyroid receptor binding + 0.5515 55.15%
Glucocorticoid receptor binding + 0.8097 80.97%
Aromatase binding + 0.6696 66.96%
PPAR gamma + 0.6240 62.40%
Honey bee toxicity - 0.7770 77.70%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9919 99.19%

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 97.96% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 96.80% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.38% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.12% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.10% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.98% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.26% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.30% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.19% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.15% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.70% 94.80%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.20% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 81.94% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.86% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.36% 94.00%
CHEMBL2581 P07339 Cathepsin D 81.35% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 80.63% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.27% 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.
Teucrium massiliense

Cross-Links

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PubChem 85209523
LOTUS LTS0114670
wikiData Q105033956