CID 3984885

Details

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Internal ID 52c5818d-3e67-4956-8ba6-489e873103d9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name
SMILES (Canonical) CC1C(C(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O
SMILES (Isomeric) CC1C(C(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O
InChI InChI=1S/C22H26O8/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/h5,7,9,12,15-17,24H,3-4,6,8,10-11H2,1-2H3
InChI Key OTBYKTCXWWCEQU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O8
Molecular Weight 418.40 g/mol
Exact Mass 418.16276778 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 3984885

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9478 94.78%
Caco-2 - 0.6858 68.58%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8714 87.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7591 75.91%
OATP1B3 inhibitior + 0.9099 90.99%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5950 59.50%
P-glycoprotein inhibitior - 0.5760 57.60%
P-glycoprotein substrate - 0.6194 61.94%
CYP3A4 substrate + 0.6626 66.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8268 82.68%
CYP3A4 inhibition - 0.6198 61.98%
CYP2C9 inhibition - 0.6865 68.65%
CYP2C19 inhibition - 0.7145 71.45%
CYP2D6 inhibition - 0.9463 94.63%
CYP1A2 inhibition - 0.9086 90.86%
CYP2C8 inhibition + 0.5313 53.13%
CYP inhibitory promiscuity - 0.7946 79.46%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5227 52.27%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9574 95.74%
Skin irritation - 0.7490 74.90%
Skin corrosion - 0.9372 93.72%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7537 75.37%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5236 52.36%
skin sensitisation - 0.8871 88.71%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.5923 59.23%
Acute Oral Toxicity (c) I 0.3912 39.12%
Estrogen receptor binding + 0.8937 89.37%
Androgen receptor binding + 0.6996 69.96%
Thyroid receptor binding - 0.5505 55.05%
Glucocorticoid receptor binding + 0.8322 83.22%
Aromatase binding + 0.6799 67.99%
PPAR gamma - 0.5371 53.71%
Honey bee toxicity - 0.7956 79.56%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5750 57.50%
Fish aquatic toxicity + 0.9797 97.97%

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 96.75% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 95.82% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.02% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.67% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.07% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.78% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.43% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.57% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.39% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.34% 94.80%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.27% 85.14%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.55% 95.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.32% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.26% 95.56%
CHEMBL2581 P07339 Cathepsin D 82.22% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.39% 99.23%

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 3984885
LOTUS LTS0049859
wikiData Q105199479