butyl 5-(2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethylamino)-5-oxopentanoate

Details

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Internal ID 1e8d6543-8a7d-4790-b77e-ccc89bbb29b9
Taxonomy Organoheterocyclic compounds > Quinolizines
IUPAC Name butyl 5-(2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethylamino)-5-oxopentanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H34N2O3/c1-2-3-14-24-19(23)11-6-10-18(22)20-15-16-8-7-13-21-12-5-4-9-17(16)21/h16-17H,2-15H2,1H3,(H,20,22)
InChI Key CWJHHOQFXOOROL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H34N2O3
Molecular Weight 338.50 g/mol
Exact Mass 338.25694295 g/mol
Topological Polar Surface Area (TPSA) 58.60 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of butyl 5-(2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethylamino)-5-oxopentanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 - 0.6198 61.98%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.4692 46.92%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9153 91.53%
OATP1B3 inhibitior + 0.9425 94.25%
MATE1 inhibitior - 0.7817 78.17%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7120 71.20%
P-glycoprotein inhibitior - 0.8162 81.62%
P-glycoprotein substrate + 0.5541 55.41%
CYP3A4 substrate + 0.5832 58.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6578 65.78%
CYP3A4 inhibition - 0.6495 64.95%
CYP2C9 inhibition - 0.7358 73.58%
CYP2C19 inhibition - 0.6649 66.49%
CYP2D6 inhibition - 0.8273 82.73%
CYP1A2 inhibition - 0.7598 75.98%
CYP2C8 inhibition - 0.7493 74.93%
CYP inhibitory promiscuity - 0.7487 74.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6695 66.95%
Eye corrosion - 0.9821 98.21%
Eye irritation - 0.8596 85.96%
Skin irritation - 0.8034 80.34%
Skin corrosion - 0.9418 94.18%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4415 44.15%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.6431 64.31%
skin sensitisation - 0.9046 90.46%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding - 0.7905 79.05%
Androgen receptor binding - 0.7230 72.30%
Thyroid receptor binding - 0.5383 53.83%
Glucocorticoid receptor binding - 0.7085 70.85%
Aromatase binding - 0.6222 62.22%
PPAR gamma - 0.7142 71.42%
Honey bee toxicity - 0.9550 95.50%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.7290 72.90%

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
CHEMBL2581 P07339 Cathepsin D 98.32% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.31% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 91.93% 89.63%
CHEMBL5255 O00206 Toll-like receptor 4 91.88% 92.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 90.74% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.64% 99.17%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 90.20% 96.25%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.67% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.00% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.40% 97.09%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.73% 94.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.15% 91.81%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 85.80% 96.00%
CHEMBL1968 P07099 Epoxide hydrolase 1 85.50% 98.57%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.09% 100.00%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 84.57% 97.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.29% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.80% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 83.60% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.24% 93.56%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 82.98% 98.24%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 82.95% 95.27%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.90% 94.00%
CHEMBL4608 P33032 Melanocortin receptor 5 82.16% 97.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.90% 100.00%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 81.85% 97.64%
CHEMBL4040 P28482 MAP kinase ERK2 81.69% 83.82%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.65% 98.33%

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.
Sophora alopecuroides

Cross-Links

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PubChem 12125578
LOTUS LTS0205071
wikiData Q104971316