1-Pyrrolidin-1-yltetradeca-2,4-dien-8,10-diyn-1-one

Details

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Internal ID 7c4badf1-8700-4362-8916-b98486c2afb2
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-yltetradeca-2,4-dien-8,10-diyn-1-one
SMILES (Canonical) CCCC#CC#CCCC=CC=CC(=O)N1CCCC1
SMILES (Isomeric) CCCC#CC#CCCC=CC=CC(=O)N1CCCC1
InChI InChI=1S/C18H23NO/c1-2-3-4-5-6-7-8-9-10-11-12-15-18(20)19-16-13-14-17-19/h10-12,15H,2-3,8-9,13-14,16-17H2,1H3
InChI Key LBTCUMZRXYUDKA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H23NO
Molecular Weight 269.40 g/mol
Exact Mass 269.177964357 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

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-8,10-diyn-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 + 0.9815 98.15%
Caco-2 + 0.8582 85.82%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Plasma membrane 0.4288 42.88%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6164 61.64%
BSEP inhibitior - 0.6233 62.33%
P-glycoprotein inhibitior - 0.8881 88.81%
P-glycoprotein substrate - 0.7843 78.43%
CYP3A4 substrate - 0.5276 52.76%
CYP2C9 substrate - 0.6083 60.83%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.7238 72.38%
CYP2C19 inhibition + 0.5090 50.90%
CYP2D6 inhibition - 0.8233 82.33%
CYP1A2 inhibition - 0.6144 61.44%
CYP2C8 inhibition - 0.9248 92.48%
CYP inhibitory promiscuity - 0.6520 65.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.4655 46.55%
Eye corrosion - 0.7672 76.72%
Eye irritation + 0.7336 73.36%
Skin irritation - 0.5215 52.15%
Skin corrosion - 0.6423 64.23%
Ames mutagenesis - 0.7278 72.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6527 65.27%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8786 87.86%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5460 54.60%
Acute Oral Toxicity (c) III 0.5514 55.14%
Estrogen receptor binding - 0.6866 68.66%
Androgen receptor binding - 0.4817 48.17%
Thyroid receptor binding + 0.6860 68.60%
Glucocorticoid receptor binding - 0.5414 54.14%
Aromatase binding - 0.5714 57.14%
PPAR gamma + 0.6577 65.77%
Honey bee toxicity - 0.9623 96.23%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.6348 63.48%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.08% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 95.81% 89.63%
CHEMBL2581 P07339 Cathepsin D 91.02% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 89.78% 83.57%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 85.96% 97.34%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.04% 96.61%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.45% 96.38%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 83.54% 97.47%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 83.14% 93.90%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.79% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 81.66% 90.17%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.04% 90.24%

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 erba-rotta

Cross-Links

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PubChem 163031463
LOTUS LTS0024705
wikiData Q105149639