CID 162877710

Details

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Internal ID 12e119bd-600f-49d0-824a-7d08c9ee960c
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O6/c1-11-8-12-15-17(2,5-4-13(21)18(15,3)16(23)25-12)20(11)9-14(22)19(26-20)6-7-24-10-19/h6-7,11-12,15H,4-5,8-10H2,1-3H3/t11-,12-,15-,17+,18+,19+,20-/m1/s1
InChI Key WYWQNESKFYQJBN-KCEYAEAJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O6
Molecular Weight 360.40 g/mol
Exact Mass 360.15728848 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162877710

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.6486 64.86%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7714 77.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9079 90.79%
OATP1B3 inhibitior + 0.9578 95.78%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.7405 74.05%
P-glycoprotein inhibitior - 0.5521 55.21%
P-glycoprotein substrate - 0.6386 63.86%
CYP3A4 substrate + 0.6267 62.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8523 85.23%
CYP3A4 inhibition - 0.8157 81.57%
CYP2C9 inhibition - 0.9378 93.78%
CYP2C19 inhibition - 0.9247 92.47%
CYP2D6 inhibition - 0.9626 96.26%
CYP1A2 inhibition - 0.8397 83.97%
CYP2C8 inhibition + 0.4853 48.53%
CYP inhibitory promiscuity - 0.9470 94.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4839 48.39%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9532 95.32%
Skin irritation - 0.5441 54.41%
Skin corrosion - 0.8559 85.59%
Ames mutagenesis + 0.6130 61.30%
Human Ether-a-go-go-Related Gene inhibition - 0.4123 41.23%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6558 65.58%
skin sensitisation - 0.8900 89.00%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.8475 84.75%
Acute Oral Toxicity (c) III 0.5900 59.00%
Estrogen receptor binding + 0.8336 83.36%
Androgen receptor binding + 0.7029 70.29%
Thyroid receptor binding + 0.7124 71.24%
Glucocorticoid receptor binding + 0.7321 73.21%
Aromatase binding + 0.7929 79.29%
PPAR gamma + 0.7003 70.03%
Honey bee toxicity - 0.7982 79.82%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9891 98.91%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.90% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.81% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 92.79% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.72% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.16% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.25% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.22% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.37% 97.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.23% 93.40%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.94% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.02% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.30% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.71% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.28% 86.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.30% 93.04%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.96% 95.71%
CHEMBL2996 Q05655 Protein kinase C delta 82.40% 97.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.75% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.76% 89.00%

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.
Marrubium velutinum

Cross-Links

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PubChem 162877710
LOTUS LTS0260953
wikiData Q105322779