CID 162968353

Details

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Internal ID c085b48a-e33b-46b6-a928-455841d7b77d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha-acyloxy carbonyl compounds > Alpha-acyloxy ketones
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H30O8/c1-12(23)29-20(4)16(25)14-15-18(2,17(26)28-14)6-5-7-19(15,3)22(20)9-8-21(30-22)10-13(24)27-11-21/h13-15,24H,5-11H2,1-4H3/t13-,14+,15+,18+,19+,20+,21-,22+/m1/s1
InChI Key YPFSOWQXNOLVDV-UFLPTDMQSA-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 1.50
Atomic LogP (AlogP) 1.66
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 162968353

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9729 97.29%
Caco-2 - 0.5499 54.99%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8220 82.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8582 85.82%
OATP1B3 inhibitior + 0.9031 90.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5864 58.64%
BSEP inhibitior - 0.5573 55.73%
P-glycoprotein inhibitior - 0.4662 46.62%
P-glycoprotein substrate - 0.6592 65.92%
CYP3A4 substrate + 0.6690 66.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8741 87.41%
CYP3A4 inhibition - 0.7633 76.33%
CYP2C9 inhibition - 0.8408 84.08%
CYP2C19 inhibition - 0.8656 86.56%
CYP2D6 inhibition - 0.9722 97.22%
CYP1A2 inhibition - 0.8657 86.57%
CYP2C8 inhibition - 0.6587 65.87%
CYP inhibitory promiscuity - 0.9740 97.40%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5367 53.67%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.8874 88.74%
Skin irritation - 0.5361 53.61%
Skin corrosion - 0.9143 91.43%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4256 42.56%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9382 93.82%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.6414 64.14%
Acute Oral Toxicity (c) I 0.3272 32.72%
Estrogen receptor binding + 0.9090 90.90%
Androgen receptor binding + 0.7212 72.12%
Thyroid receptor binding + 0.6402 64.02%
Glucocorticoid receptor binding + 0.7981 79.81%
Aromatase binding + 0.8420 84.20%
PPAR gamma + 0.6116 61.16%
Honey bee toxicity - 0.8156 81.56%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6550 65.50%
Fish aquatic toxicity + 0.9622 96.22%

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 96.10% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.84% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.95% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.71% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.42% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.18% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.97% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.38% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.12% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.84% 97.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.29% 82.69%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 85.08% 95.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.81% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.72% 93.03%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.16% 97.28%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.61% 96.77%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.33% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.29% 94.00%
CHEMBL5028 O14672 ADAM10 80.21% 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.
Leonurus cardiaca

Cross-Links

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PubChem 162968353
LOTUS LTS0008801
wikiData Q105351660