CID 14314530

Details

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Internal ID 6dd4fb04-0477-49cf-a7b2-8ed8ec7acb89
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name
SMILES (Canonical) CC1=C(C(=O)C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCCC25CO5)COC(=O)C)O
SMILES (Isomeric) CC1=C(C(=O)C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCCC25CO5)COC(=O)C)O
InChI InChI=1S/C24H28O9/c1-13-19(27)20(28)24(12-30-14(2)25)18(5-4-7-22(24)11-31-22)23(13)9-17(16-6-8-29-10-16)33-21(23)32-15(3)26/h6,8,10,17-18,21,27H,4-5,7,9,11-12H2,1-3H3
InChI Key HIPMUUMEVGAKCD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28O9
Molecular Weight 460.50 g/mol
Exact Mass 460.17333247 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 14314530

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9719 97.19%
Caco-2 - 0.6554 65.54%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8635 86.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7521 75.21%
OATP1B3 inhibitior + 0.8853 88.53%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7868 78.68%
P-glycoprotein inhibitior + 0.5876 58.76%
P-glycoprotein substrate - 0.6449 64.49%
CYP3A4 substrate + 0.6774 67.74%
CYP2C9 substrate - 0.8162 81.62%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.6760 67.60%
CYP2C9 inhibition - 0.7526 75.26%
CYP2C19 inhibition - 0.7826 78.26%
CYP2D6 inhibition - 0.9295 92.95%
CYP1A2 inhibition - 0.7957 79.57%
CYP2C8 inhibition + 0.6524 65.24%
CYP inhibitory promiscuity - 0.7042 70.42%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4491 44.91%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.8860 88.60%
Skin irritation - 0.6479 64.79%
Skin corrosion - 0.9419 94.19%
Ames mutagenesis - 0.6654 66.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7580 75.80%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5410 54.10%
skin sensitisation - 0.8570 85.70%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5573 55.73%
Acute Oral Toxicity (c) I 0.6071 60.71%
Estrogen receptor binding + 0.8661 86.61%
Androgen receptor binding + 0.7207 72.07%
Thyroid receptor binding - 0.5318 53.18%
Glucocorticoid receptor binding + 0.8653 86.53%
Aromatase binding + 0.7422 74.22%
PPAR gamma + 0.6630 66.30%
Honey bee toxicity - 0.8312 83.12%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5150 51.50%
Fish aquatic toxicity + 0.9933 99.33%

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 96.86% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.63% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 95.66% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.03% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.37% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.36% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.31% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 87.89% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.86% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.13% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.02% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.89% 99.23%
CHEMBL221 P23219 Cyclooxygenase-1 84.98% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.63% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.05% 85.14%
CHEMBL5255 O00206 Toll-like receptor 4 82.81% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.06% 100.00%

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 lanigerum

Cross-Links

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PubChem 14314530
LOTUS LTS0027720
wikiData Q105028951