CID 163192599

Details

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Internal ID 627276ed-bc62-4f78-a09f-df6485ba1dc4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H30O8/c1-12(23)28-20(4)16(25)14-15-18(2,17(26)27-14)7-5-8-19(15,3)22(20)11-10-21(30-22)9-6-13(24)29-21/h13-15,24H,5-11H2,1-4H3
InChI Key VOCQGZSCIFRADC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O8
Molecular Weight 422.50 g/mol
Exact Mass 422.19406791 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163192599

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9724 97.24%
Caco-2 - 0.5621 56.21%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7753 77.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8830 88.30%
OATP1B3 inhibitior - 0.2470 24.70%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6821 68.21%
BSEP inhibitior + 0.5857 58.57%
P-glycoprotein inhibitior - 0.4586 45.86%
P-glycoprotein substrate - 0.7477 74.77%
CYP3A4 substrate + 0.6660 66.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8703 87.03%
CYP3A4 inhibition - 0.7014 70.14%
CYP2C9 inhibition - 0.8781 87.81%
CYP2C19 inhibition - 0.7884 78.84%
CYP2D6 inhibition - 0.9717 97.17%
CYP1A2 inhibition - 0.7326 73.26%
CYP2C8 inhibition - 0.6789 67.89%
CYP inhibitory promiscuity - 0.9783 97.83%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5271 52.71%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9116 91.16%
Skin irritation + 0.5561 55.61%
Skin corrosion - 0.8316 83.16%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4707 47.07%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9123 91.23%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.6659 66.59%
Acute Oral Toxicity (c) I 0.3163 31.63%
Estrogen receptor binding + 0.8887 88.87%
Androgen receptor binding + 0.7107 71.07%
Thyroid receptor binding + 0.5908 59.08%
Glucocorticoid receptor binding + 0.8178 81.78%
Aromatase binding + 0.8361 83.61%
PPAR gamma + 0.6565 65.65%
Honey bee toxicity - 0.8536 85.36%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6550 65.50%
Fish aquatic toxicity + 0.9669 96.69%

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 95.67% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.71% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.22% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.50% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.26% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.33% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.96% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.88% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.03% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.77% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.21% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.13% 92.62%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.86% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.75% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 82.26% 91.19%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.82% 93.04%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.41% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.85% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.70% 85.14%

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.
Leonurus cardiaca

Cross-Links

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PubChem 163192599
LOTUS LTS0118859
wikiData Q105290102