CID 162883974

Details

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Internal ID f28cf01f-2dc1-4799-82c6-0c08e1cbd61e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O9/c1-11-17(25)18(26)21(9-29-12(2)23)15(3-4-16(24)22(21)10-30-22)20(11)7-14(31-19(20)27)13-5-6-28-8-13/h5-6,8,11,14-15,17,25H,3-4,7,9-10H2,1-2H3/t11-,14+,15-,17-,20-,21+,22-/m1/s1
InChI Key RWDUFUWSPLPCBX-ZNDGPWFTSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O9
Molecular Weight 432.40 g/mol
Exact Mass 432.14203234 g/mol
Topological Polar Surface Area (TPSA) 133.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 1.13
H-Bond Acceptor 9
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 162883974

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 - 0.7002 70.02%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8714 87.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7869 78.69%
OATP1B3 inhibitior + 0.9099 90.99%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5616 56.16%
P-glycoprotein inhibitior - 0.4928 49.28%
P-glycoprotein substrate - 0.6234 62.34%
CYP3A4 substrate + 0.6491 64.91%
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 + 0.5337 53.37%
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 - 0.9434 94.34%
Skin irritation - 0.7490 74.90%
Skin corrosion - 0.9372 93.72%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7426 74.26%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8871 88.71%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.5967 59.67%
Acute Oral Toxicity (c) I 0.3912 39.12%
Estrogen receptor binding + 0.8593 85.93%
Androgen receptor binding + 0.7057 70.57%
Thyroid receptor binding - 0.5570 55.70%
Glucocorticoid receptor binding + 0.8437 84.37%
Aromatase binding + 0.6406 64.06%
PPAR gamma - 0.5255 52.55%
Honey bee toxicity - 0.7367 73.67%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5300 53.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.96% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.48% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.64% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.92% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.87% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.82% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.36% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.30% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.68% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.11% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.69% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 81.49% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.94% 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 racemosum
Teucrium trifidum

Cross-Links

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PubChem 162883974
LOTUS LTS0188738
wikiData Q105246469