N-2,4-Eicosadienoylpyrrolidin

Details

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Internal ID 336d3f5f-2d82-4310-b9ff-8c079e47fcbe
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-ylicosa-2,4-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H43NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-24(26)25-22-19-20-23-25/h16-18,21H,2-15,19-20,22-23H2,1H3
InChI Key RIDFJCCEYZWOSP-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C24H43NO
Molecular Weight 361.60 g/mol
Exact Mass 361.334464995 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 9.20
Atomic LogP (AlogP) 7.20
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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DTXSID80954794
1-(Pyrrolidin-1-yl)icosa-2,4-dien-1-one

2D Structure

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2D Structure of N-2,4-Eicosadienoylpyrrolidin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 - 0.6412 64.12%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.4463 44.63%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.9070 90.70%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7384 73.84%
P-glycoprotein inhibitior - 0.6098 60.98%
P-glycoprotein substrate - 0.7986 79.86%
CYP3A4 substrate - 0.5629 56.29%
CYP2C9 substrate + 0.5844 58.44%
CYP2D6 substrate - 0.8890 88.90%
CYP3A4 inhibition - 0.9797 97.97%
CYP2C9 inhibition - 0.8174 81.74%
CYP2C19 inhibition + 0.5075 50.75%
CYP2D6 inhibition - 0.8237 82.37%
CYP1A2 inhibition - 0.6111 61.11%
CYP2C8 inhibition - 0.9241 92.41%
CYP inhibitory promiscuity - 0.8349 83.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5335 53.35%
Eye corrosion - 0.6626 66.26%
Eye irritation + 0.6401 64.01%
Skin irritation + 0.4917 49.17%
Skin corrosion - 0.5199 51.99%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6928 69.28%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6735 67.35%
skin sensitisation - 0.9060 90.60%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6597 65.97%
Acute Oral Toxicity (c) III 0.6425 64.25%
Estrogen receptor binding + 0.5790 57.90%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.6183 61.83%
Glucocorticoid receptor binding - 0.5109 51.09%
Aromatase binding - 0.6623 66.23%
PPAR gamma + 0.6213 62.13%
Honey bee toxicity - 0.9902 99.02%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.8240 82.40%
Fish aquatic toxicity + 0.6933 69.33%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.26% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.14% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.49% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.83% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 93.10% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.31% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.04% 92.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.97% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.29% 95.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.70% 94.33%
CHEMBL1781 P11387 DNA topoisomerase I 82.62% 97.00%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 82.31% 93.90%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 81.36% 95.27%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.01% 90.24%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 80.60% 96.25%

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.
Piper guineense
Piper trichostachyon

Cross-Links

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PubChem 85296773
LOTUS LTS0189677
wikiData Q82934201