1-Pyrrolidin-1-ylnonadeca-2,9-dien-1-one

Details

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Internal ID d48ed251-3524-4bf9-b667-33d90b45e701
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-ylnonadeca-2,9-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H41NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-23(25)24-21-18-19-22-24/h10-11,17,20H,2-9,12-16,18-19,21-22H2,1H3
InChI Key WETGLEAOFFOIMU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H41NO
Molecular Weight 347.60 g/mol
Exact Mass 347.318814931 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 8.10
Atomic LogP (AlogP) 6.81
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pyrrolidin-1-ylnonadeca-2,9-dien-1-one

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 + 0.5163 51.63%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4463 44.63%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.8900 89.00%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7105 71.05%
P-glycoprotein inhibitior - 0.6067 60.67%
P-glycoprotein substrate - 0.8395 83.95%
CYP3A4 substrate - 0.5710 57.10%
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 - 0.9383 93.83%
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 + 0.5449 54.49%
Skin irritation + 0.4917 49.17%
Skin corrosion - 0.5199 51.99%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4483 44.83%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5360 53.60%
skin sensitisation - 0.9060 90.60%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7472 74.72%
Acute Oral Toxicity (c) III 0.6425 64.25%
Estrogen receptor binding + 0.6381 63.81%
Androgen receptor binding - 0.5385 53.85%
Thyroid receptor binding + 0.5660 56.60%
Glucocorticoid receptor binding - 0.6839 68.39%
Aromatase binding - 0.8167 81.67%
PPAR gamma + 0.6107 61.07%
Honey bee toxicity - 0.9921 99.21%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.8324 83.24%
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 97.09% 89.63%
CHEMBL2581 P07339 Cathepsin D 96.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.56% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.40% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 92.89% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.57% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.23% 100.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.42% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 86.31% 97.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.07% 94.33%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 83.55% 93.90%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.47% 90.24%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.40% 95.50%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.69% 97.50%

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 peepuloides

Cross-Links

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PubChem 162913256
LOTUS LTS0090695
wikiData Q105303549