1-Pyrrolidin-1-yltetradeca-2,4-dien-8-yn-1-one

Details

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Internal ID 932dd0db-d46f-48a4-9cff-8f1dfd07bd40
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-yltetradeca-2,4-dien-8-yn-1-one
SMILES (Canonical) CCCCCC#CCCC=CC=CC(=O)N1CCCC1
SMILES (Isomeric) CCCCCC#CCCC=CC=CC(=O)N1CCCC1
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/h10-12,15H,2-5,8-9,13-14,16-17H2,1H3
InChI Key NJYJQJLVTPRPFK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H27NO
Molecular Weight 273.40 g/mol
Exact Mass 273.209264485 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pyrrolidin-1-yltetradeca-2,4-dien-8-yn-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 + 0.9842 98.42%
Caco-2 + 0.8672 86.72%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Plasma membrane 0.4312 43.12%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.8970 89.70%
OATP1B3 inhibitior + 0.9437 94.37%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.5535 55.35%
P-glycoprotein inhibitior - 0.8690 86.90%
P-glycoprotein substrate - 0.7618 76.18%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.8866 88.66%
CYP3A4 inhibition - 0.9600 96.00%
CYP2C9 inhibition - 0.7672 76.72%
CYP2C19 inhibition + 0.5219 52.19%
CYP2D6 inhibition - 0.8027 80.27%
CYP1A2 inhibition - 0.6027 60.27%
CYP2C8 inhibition - 0.8209 82.09%
CYP inhibitory promiscuity - 0.7727 77.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5127 51.27%
Eye corrosion - 0.7691 76.91%
Eye irritation + 0.8484 84.84%
Skin irritation - 0.5456 54.56%
Skin corrosion - 0.5785 57.85%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6699 66.99%
skin sensitisation - 0.8947 89.47%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5830 58.30%
Acute Oral Toxicity (c) III 0.6389 63.89%
Estrogen receptor binding - 0.5864 58.64%
Androgen receptor binding + 0.5265 52.65%
Thyroid receptor binding + 0.6164 61.64%
Glucocorticoid receptor binding - 0.6641 66.41%
Aromatase binding - 0.6096 60.96%
PPAR gamma + 0.6097 60.97%
Honey bee toxicity - 0.9808 98.08%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6118 61.18%
Fish aquatic toxicity + 0.7593 75.93%

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 98.95% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.27% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.15% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.15% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 90.64% 91.81%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.69% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.30% 99.17%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 83.18% 93.90%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.68% 90.24%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 81.25% 96.25%
CHEMBL221 P23219 Cyclooxygenase-1 81.14% 90.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.83% 94.33%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 80.67% 97.47%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.29% 86.33%

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.
Achillea ageratifolia

Cross-Links

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PubChem 162952287
LOTUS LTS0000698
wikiData Q105180381