CID 163097017

Details

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Internal ID d8b968c8-9bfb-4280-bfa0-c35a0d9e506e
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC1CC2C3C(C14CCC5(O4)COC=C5)(CCC(=O)C3(C(=O)O2)C)C
SMILES (Isomeric) C[C@@H]1C[C@@H]2[C@@H]3[C@@]([C@@]14CC[C@@]5(O4)COC=C5)(CCC(=O)[C@@]3(C(=O)O2)C)C
InChI InChI=1S/C20H26O5/c1-12-10-13-15-17(2,5-4-14(21)18(15,3)16(22)24-13)20(12)7-6-19(25-20)8-9-23-11-19/h8-9,12-13,15H,4-7,10-11H2,1-3H3/t12-,13-,15-,17+,18+,19+,20-/m1/s1
InChI Key APJLGTWXFWPNFV-VFKMRLCYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O5
Molecular Weight 346.40 g/mol
Exact Mass 346.17802393 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 5
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 163097017

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 + 0.7449 74.49%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7714 77.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8997 89.97%
OATP1B3 inhibitior + 0.9578 95.78%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.5233 52.33%
P-glycoprotein inhibitior - 0.5427 54.27%
P-glycoprotein substrate - 0.6606 66.06%
CYP3A4 substrate + 0.6233 62.33%
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 + 0.5145 51.45%
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 - 0.9546 95.46%
Skin irritation - 0.5441 54.41%
Skin corrosion - 0.8559 85.59%
Ames mutagenesis + 0.5276 52.76%
Human Ether-a-go-go-Related Gene inhibition + 0.6455 64.55%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6108 61.08%
skin sensitisation - 0.8900 89.00%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6554 65.54%
Acute Oral Toxicity (c) III 0.5900 59.00%
Estrogen receptor binding + 0.8860 88.60%
Androgen receptor binding + 0.6740 67.40%
Thyroid receptor binding + 0.7223 72.23%
Glucocorticoid receptor binding + 0.8041 80.41%
Aromatase binding + 0.8342 83.42%
PPAR gamma + 0.6932 69.32%
Honey bee toxicity - 0.8258 82.58%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5700 57.00%
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
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.68% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.11% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 90.10% 94.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.71% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.51% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.65% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.97% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.29% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.39% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.75% 82.69%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.32% 93.40%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.15% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.02% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.94% 93.04%
CHEMBL2996 Q05655 Protein kinase C delta 82.57% 97.79%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.25% 96.00%

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 thessalum

Cross-Links

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PubChem 163097017
LOTUS LTS0202094
wikiData Q104916345