CID 163040799

Details

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Internal ID 5ee9418b-ed0b-46bd-8cd3-5eb1180ad907
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name
SMILES (Canonical) CC1C(C(=O)C2(C(C13CC(OC3O)C4=COC=C4)CCCC25CO5)COC(=O)C)O
SMILES (Isomeric) CC1C(C(=O)C2(C(C13CC(OC3O)C4=COC=C4)CCCC25CO5)COC(=O)C)O
InChI InChI=1S/C22H28O8/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/h5,7,9,12,15-17,19,24,26H,3-4,6,8,10-11H2,1-2H3
InChI Key GZLKMBIXFMGIDE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O8
Molecular Weight 420.50 g/mol
Exact Mass 420.17841785 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163040799

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9405 94.05%
Caco-2 - 0.7309 73.09%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8892 88.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7462 74.62%
OATP1B3 inhibitior + 0.9226 92.26%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8037 80.37%
BSEP inhibitior - 0.4618 46.18%
P-glycoprotein inhibitior - 0.6528 65.28%
P-glycoprotein substrate - 0.5725 57.25%
CYP3A4 substrate + 0.6656 66.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8417 84.17%
CYP3A4 inhibition - 0.6898 68.98%
CYP2C9 inhibition - 0.7103 71.03%
CYP2C19 inhibition - 0.7370 73.70%
CYP2D6 inhibition - 0.9482 94.82%
CYP1A2 inhibition - 0.8927 89.27%
CYP2C8 inhibition + 0.4816 48.16%
CYP inhibitory promiscuity - 0.8191 81.91%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5334 53.34%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9691 96.91%
Skin irritation - 0.7645 76.45%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.6070 60.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7383 73.83%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.5398 53.98%
skin sensitisation - 0.9083 90.83%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4603 46.03%
Acute Oral Toxicity (c) I 0.4524 45.24%
Estrogen receptor binding + 0.8916 89.16%
Androgen receptor binding + 0.7382 73.82%
Thyroid receptor binding - 0.5619 56.19%
Glucocorticoid receptor binding + 0.7817 78.17%
Aromatase binding + 0.7053 70.53%
PPAR gamma - 0.5899 58.99%
Honey bee toxicity - 0.8309 83.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5450 54.50%
Fish aquatic toxicity + 0.9828 98.28%

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 97.83% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.83% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.76% 97.09%
CHEMBL2581 P07339 Cathepsin D 93.62% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.88% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.14% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 91.25% 83.82%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.49% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.47% 94.80%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.26% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.43% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.14% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.09% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.68% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.17% 99.23%
CHEMBL221 P23219 Cyclooxygenase-1 83.70% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 81.56% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.84% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.56% 96.00%
CHEMBL5028 O14672 ADAM10 80.48% 97.50%

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 163040799
LOTUS LTS0018216
wikiData Q105024438