CID 3500934

Details

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Internal ID 03bd4dee-7672-4055-9456-626a06ee7375
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name
SMILES (Canonical) CC1C(=O)C(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C
SMILES (Isomeric) CC1C(=O)C(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C
InChI InChI=1S/C22H24O8/c1-12-17(24)18(25)22(11-28-13(2)23)16(4-3-6-20(22)10-29-20)21(12)8-15(30-19(21)26)14-5-7-27-9-14/h5,7,9,12,15-16H,3-4,6,8,10-11H2,1-2H3
InChI Key CENICYUALNGAFW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O8
Molecular Weight 416.40 g/mol
Exact Mass 416.14711772 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 3500934

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 - 0.6364 63.64%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8422 84.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7497 74.97%
OATP1B3 inhibitior + 0.9561 95.61%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.4546 45.46%
P-glycoprotein inhibitior + 0.5945 59.45%
P-glycoprotein substrate - 0.6574 65.74%
CYP3A4 substrate + 0.6600 66.00%
CYP2C9 substrate - 0.8097 80.97%
CYP2D6 substrate - 0.8516 85.16%
CYP3A4 inhibition - 0.5581 55.81%
CYP2C9 inhibition - 0.7153 71.53%
CYP2C19 inhibition - 0.6343 63.43%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.8858 88.58%
CYP2C8 inhibition + 0.5889 58.89%
CYP inhibitory promiscuity - 0.6806 68.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5483 54.83%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9142 91.42%
Skin irritation - 0.7860 78.60%
Skin corrosion - 0.9302 93.02%
Ames mutagenesis - 0.6870 68.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8189 81.89%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.6167 61.67%
skin sensitisation - 0.8493 84.93%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.4740 47.40%
Acute Oral Toxicity (c) III 0.4536 45.36%
Estrogen receptor binding + 0.8791 87.91%
Androgen receptor binding + 0.6953 69.53%
Thyroid receptor binding - 0.5084 50.84%
Glucocorticoid receptor binding + 0.7605 76.05%
Aromatase binding + 0.6322 63.22%
PPAR gamma + 0.5479 54.79%
Honey bee toxicity - 0.8334 83.34%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6350 63.50%
Fish aquatic toxicity + 0.9853 98.53%

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 96.49% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.33% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.36% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.96% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.94% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.69% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.36% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.11% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.10% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.22% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.04% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.76% 95.56%
CHEMBL2581 P07339 Cathepsin D 83.29% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.17% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.09% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.93% 92.62%

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 polium

Cross-Links

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PubChem 3500934
LOTUS LTS0211570
wikiData Q104955890