N-(2-methyl-3-oxodec-8-enoyl)-2-pyrroline

Details

Top
Internal ID 5a7802da-04d1-4c4d-86d5-fba9dd4d64b7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > 1,3-dicarbonyl compounds
IUPAC Name 1-(2,3-dihydropyrrol-1-yl)-2-methyldec-8-ene-1,3-dione
SMILES (Canonical) CC=CCCCCC(=O)C(C)C(=O)N1CCC=C1
SMILES (Isomeric) CC=CCCCCC(=O)C(C)C(=O)N1CCC=C1
InChI InChI=1S/C15H23NO2/c1-3-4-5-6-7-10-14(17)13(2)15(18)16-11-8-9-12-16/h3-4,8,11,13H,5-7,9-10,12H2,1-2H3
InChI Key JGNMZTXDOHXIJQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H23NO2
Molecular Weight 249.35 g/mol
Exact Mass 249.172878976 g/mol
Topological Polar Surface Area (TPSA) 37.40 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.07
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of N-(2-methyl-3-oxodec-8-enoyl)-2-pyrroline

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9703 97.03%
Caco-2 + 0.8133 81.33%
Blood Brain Barrier + 0.9330 93.30%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6605 66.05%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.8691 86.91%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6067 60.67%
BSEP inhibitior - 0.5414 54.14%
P-glycoprotein inhibitior - 0.9160 91.60%
P-glycoprotein substrate - 0.6694 66.94%
CYP3A4 substrate - 0.5596 55.96%
CYP2C9 substrate + 0.5587 55.87%
CYP2D6 substrate - 0.8556 85.56%
CYP3A4 inhibition - 0.9619 96.19%
CYP2C9 inhibition - 0.7722 77.22%
CYP2C19 inhibition - 0.5541 55.41%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.7189 71.89%
CYP2C8 inhibition - 0.9323 93.23%
CYP inhibitory promiscuity - 0.8135 81.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5274 52.74%
Eye corrosion - 0.9182 91.82%
Eye irritation - 0.8358 83.58%
Skin irritation - 0.7611 76.11%
Skin corrosion - 0.8321 83.21%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4041 40.41%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.9022 90.22%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5538 55.38%
Nephrotoxicity - 0.8730 87.30%
Acute Oral Toxicity (c) III 0.7106 71.06%
Estrogen receptor binding - 0.6408 64.08%
Androgen receptor binding - 0.7591 75.91%
Thyroid receptor binding - 0.7002 70.02%
Glucocorticoid receptor binding - 0.4656 46.56%
Aromatase binding - 0.7159 71.59%
PPAR gamma + 0.5728 57.28%
Honey bee toxicity - 0.9498 94.98%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.8211 82.11%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.07% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.14% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.16% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.36% 94.45%
CHEMBL4208 P20618 Proteasome component C5 87.78% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.14% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.13% 97.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.24% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.59% 95.56%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 82.45% 98.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.80% 94.33%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.36% 96.47%
CHEMBL4588 P22894 Matrix metalloproteinase 8 80.04% 94.66%

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.
There are no matching plants.

Cross-Links

Top
PubChem 53954211
LOTUS LTS0257332
wikiData Q104169506