CID 163105428

Details

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Internal ID 7bf25ab8-8043-4f69-b073-9a9bc1e31685
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H30O8/c1-14-10-20(31-16(3)26)24(13-29-15(2)25)19(7-4-8-22(24)12-30-22)23(14)11-18(32-21(23)27)17-6-5-9-28-17/h5-6,9,14,18-20H,4,7-8,10-13H2,1-3H3/t14-,18+,19-,20-,22+,23-,24+/m1/s1
InChI Key ORXFTJRKLPXNMD-SMQHAVTGSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H30O8
Molecular Weight 446.50 g/mol
Exact Mass 446.19406791 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163105428

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 - 0.6560 65.60%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7948 79.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8557 85.57%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6144 61.44%
P-glycoprotein inhibitior + 0.5892 58.92%
P-glycoprotein substrate - 0.6462 64.62%
CYP3A4 substrate + 0.6853 68.53%
CYP2C9 substrate - 0.6062 60.62%
CYP2D6 substrate - 0.8370 83.70%
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 + 0.5307 53.07%
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 - 0.9067 90.67%
Skin irritation - 0.7668 76.68%
Skin corrosion - 0.9404 94.04%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8879 88.79%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5351 53.51%
skin sensitisation - 0.8918 89.18%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.7192 71.92%
Acute Oral Toxicity (c) III 0.3853 38.53%
Estrogen receptor binding + 0.9195 91.95%
Androgen receptor binding + 0.6593 65.93%
Thyroid receptor binding + 0.5491 54.91%
Glucocorticoid receptor binding + 0.8109 81.09%
Aromatase binding + 0.6839 68.39%
PPAR gamma + 0.6446 64.46%
Honey bee toxicity - 0.8122 81.22%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
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 97.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.03% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.88% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.85% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.82% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.08% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.94% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.91% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.82% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.55% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.23% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.22% 92.62%
CHEMBL221 P23219 Cyclooxygenase-1 82.37% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.99% 95.89%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.96% 97.28%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.77% 97.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.03% 82.69%

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 fruticans
Teucrium scordium

Cross-Links

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PubChem 163105428
LOTUS LTS0190124
wikiData Q105198530