CID 100988747

Details

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Internal ID 5cc1fd80-2ac7-44ae-9bfc-90a5d91bb526
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name
SMILES (Canonical) CC1=C(C(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O
SMILES (Isomeric) CC1=C(C(=O)[C@@]2([C@@H]([C@@]13C[C@H](OC3=O)C4=COC=C4)CCC[C@]25CO5)COC(=O)C)O
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/h5,7,9,15-16,24H,3-4,6,8,10-11H2,1-2H3/t15-,16+,20-,21+,22-/m0/s1
InChI Key YDZIRCARTNHGTH-ZEIJQVPMSA-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) 116.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 2.79
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 100988747

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9722 97.22%
Caco-2 - 0.6718 67.18%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8847 88.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7479 74.79%
OATP1B3 inhibitior + 0.9101 91.01%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6297 62.97%
P-glycoprotein inhibitior - 0.5815 58.15%
P-glycoprotein substrate - 0.6709 67.09%
CYP3A4 substrate + 0.6575 65.75%
CYP2C9 substrate - 0.8231 82.31%
CYP2D6 substrate - 0.8771 87.71%
CYP3A4 inhibition - 0.7011 70.11%
CYP2C9 inhibition - 0.7617 76.17%
CYP2C19 inhibition - 0.8006 80.06%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.8008 80.08%
CYP2C8 inhibition + 0.6182 61.82%
CYP inhibitory promiscuity - 0.6788 67.88%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4672 46.72%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9281 92.81%
Skin irritation - 0.6643 66.43%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis - 0.5870 58.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7783 77.83%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5939 59.39%
skin sensitisation - 0.8429 84.29%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.4903 49.03%
Acute Oral Toxicity (c) I 0.5503 55.03%
Estrogen receptor binding + 0.8766 87.66%
Androgen receptor binding + 0.6870 68.70%
Thyroid receptor binding - 0.5653 56.53%
Glucocorticoid receptor binding + 0.8609 86.09%
Aromatase binding + 0.7279 72.79%
PPAR gamma + 0.5616 56.16%
Honey bee toxicity - 0.8283 82.83%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5850 58.50%
Fish aquatic toxicity + 0.9936 99.36%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 96.40% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.59% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.83% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.68% 94.45%
CHEMBL230 P35354 Cyclooxygenase-2 89.87% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.78% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.17% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.08% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.47% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.27% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.24% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.02% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 82.44% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.97% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 81.50% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.95% 97.25%

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 100988747
LOTUS LTS0272230
wikiData Q104401897