(2E,4E,8Z,11Z)-1-pyrrolidin-1-yltetradeca-2,4,8,11-tetraen-1-one

Details

Top
Internal ID cd702456-892d-4488-b0cb-1fcd866f69cb
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name (2E,4E,8Z,11Z)-1-pyrrolidin-1-yltetradeca-2,4,8,11-tetraen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H27NO/c1-2-3-4-5-6-7-8-9-10-11-12-15-18(20)19-16-13-14-17-19/h3-4,6-7,10-12,15H,2,5,8-9,13-14,16-17H2,1H3/b4-3-,7-6-,11-10+,15-12+
InChI Key JMJYEEGIQCTDMB-ABWRRPSRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H27NO
Molecular Weight 273.40 g/mol
Exact Mass 273.209264485 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.41
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2E,4E,8Z,11Z)-1-pyrrolidin-1-yltetradeca-2,4,8,11-tetraen-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 + 0.8525 85.25%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.3641 36.41%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.8783 87.83%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.7165 71.65%
P-glycoprotein inhibitior - 0.8300 83.00%
P-glycoprotein substrate - 0.8161 81.61%
CYP3A4 substrate - 0.5807 58.07%
CYP2C9 substrate + 0.5844 58.44%
CYP2D6 substrate - 0.8890 88.90%
CYP3A4 inhibition - 0.9802 98.02%
CYP2C9 inhibition - 0.8186 81.86%
CYP2C19 inhibition - 0.5323 53.23%
CYP2D6 inhibition - 0.8119 81.19%
CYP1A2 inhibition - 0.7005 70.05%
CYP2C8 inhibition - 0.9468 94.68%
CYP inhibitory promiscuity - 0.6779 67.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.4900 49.00%
Eye corrosion - 0.6251 62.51%
Eye irritation - 0.4815 48.15%
Skin irritation - 0.5506 55.06%
Skin corrosion - 0.5977 59.77%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5227 52.27%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.9015 90.15%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.8134 81.34%
Acute Oral Toxicity (c) III 0.5648 56.48%
Estrogen receptor binding + 0.5962 59.62%
Androgen receptor binding - 0.7437 74.37%
Thyroid receptor binding + 0.5202 52.02%
Glucocorticoid receptor binding - 0.5423 54.23%
Aromatase binding - 0.5764 57.64%
PPAR gamma + 0.8278 82.78%
Honey bee toxicity - 0.9802 98.02%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.6776 67.76%

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 96.28% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.18% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 90.88% 83.57%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.39% 86.33%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 83.58% 93.90%
CHEMBL230 P35354 Cyclooxygenase-2 82.21% 89.63%
CHEMBL4208 P20618 Proteasome component C5 81.76% 90.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.24% 94.33%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.72% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.24% 95.56%

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.
Achillea ageratifolia

Cross-Links

Top
PubChem 13846817
LOTUS LTS0057645
wikiData Q105131484