CID 162852394

Details

Top
Internal ID f2bc5107-c1af-4d93-9117-1146fd69b44d
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC1CC2C3C(CCCC3(C14CC(=O)C5(O4)CCOC5)C)(C(=O)O2)C
SMILES (Isomeric) CC1CC2C3C(CCCC3(C14CC(=O)C5(O4)CCOC5)C)(C(=O)O2)C
InChI InChI=1S/C20H28O5/c1-12-9-13-15-17(2,16(22)24-13)5-4-6-18(15,3)20(12)10-14(21)19(25-20)7-8-23-11-19/h12-13,15H,4-11H2,1-3H3
InChI Key BGAUDCJZMKIQAR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H28O5
Molecular Weight 348.40 g/mol
Exact Mass 348.19367399 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 162852394

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9745 97.45%
Caco-2 + 0.7571 75.71%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6693 66.93%
OATP2B1 inhibitior - 0.8639 86.39%
OATP1B1 inhibitior + 0.9079 90.79%
OATP1B3 inhibitior + 0.9704 97.04%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.6663 66.63%
P-glycoprotein inhibitior - 0.6192 61.92%
P-glycoprotein substrate - 0.6920 69.20%
CYP3A4 substrate + 0.6178 61.78%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8455 84.55%
CYP3A4 inhibition - 0.8006 80.06%
CYP2C9 inhibition - 0.9208 92.08%
CYP2C19 inhibition - 0.8663 86.63%
CYP2D6 inhibition - 0.9556 95.56%
CYP1A2 inhibition - 0.8893 88.93%
CYP2C8 inhibition - 0.6389 63.89%
CYP inhibitory promiscuity - 0.9791 97.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4923 49.23%
Eye corrosion - 0.9846 98.46%
Eye irritation - 0.9095 90.95%
Skin irritation - 0.7204 72.04%
Skin corrosion - 0.8768 87.68%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6004 60.04%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8980 89.80%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.9109 91.09%
Acute Oral Toxicity (c) III 0.5700 57.00%
Estrogen receptor binding + 0.8630 86.30%
Androgen receptor binding + 0.6763 67.63%
Thyroid receptor binding + 0.7331 73.31%
Glucocorticoid receptor binding + 0.8196 81.96%
Aromatase binding + 0.8165 81.65%
PPAR gamma + 0.6395 63.95%
Honey bee toxicity - 0.7591 75.91%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9553 95.53%

Targets

Top

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.44% 85.14%
CHEMBL230 P35354 Cyclooxygenase-2 92.75% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.23% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.94% 82.69%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.85% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.11% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.50% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.15% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.15% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.58% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.47% 93.04%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.42% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.33% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.27% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 82.93% 94.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.39% 95.71%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 81.31% 98.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.01% 86.33%
CHEMBL2581 P07339 Cathepsin D 80.52% 98.95%

Plants that contains it

Top
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 anisodon

Cross-Links

Top
PubChem 162852394
LOTUS LTS0261780
wikiData Q104935145