1-Pyrrolidin-1-yltetradeca-2,4,10-trien-8-yn-1-one

Details

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Internal ID b25b9161-ea44-4e75-8bd2-493f2be0c1f5
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-yltetradeca-2,4,10-trien-8-yn-1-one
SMILES (Canonical) CCCC=CC#CCCC=CC=CC(=O)N1CCCC1
SMILES (Isomeric) CCCC=CC#CCCC=CC=CC(=O)N1CCCC1
InChI InChI=1S/C18H25NO/c1-2-3-4-5-6-7-8-9-10-11-12-15-18(20)19-16-13-14-17-19/h4-5,10-12,15H,2-3,8-9,13-14,16-17H2,1H3
InChI Key JWHBEVMAHPNUBJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H25NO
Molecular Weight 271.40 g/mol
Exact Mass 271.193614421 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.86
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pyrrolidin-1-yltetradeca-2,4,10-trien-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 + 0.9815 98.15%
Caco-2 + 0.8465 84.65%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Plasma membrane 0.4288 42.88%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9087 90.87%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6164 61.64%
BSEP inhibitior - 0.4686 46.86%
P-glycoprotein inhibitior - 0.8477 84.77%
P-glycoprotein substrate - 0.7666 76.66%
CYP3A4 substrate + 0.5099 50.99%
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 - 0.8466 84.66%
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 + 0.6308 63.08%
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 - 0.6364 63.64%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.6806 68.06%
skin sensitisation - 0.8786 87.86%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5667 56.67%
Acute Oral Toxicity (c) III 0.5514 55.14%
Estrogen receptor binding - 0.4938 49.38%
Androgen receptor binding - 0.6413 64.13%
Thyroid receptor binding + 0.6467 64.67%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.6063 60.63%
PPAR gamma + 0.6436 64.36%
Honey bee toxicity - 0.9295 92.95%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6300 63.00%
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 96.27% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 91.34% 89.63%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.39% 96.38%
CHEMBL221 P23219 Cyclooxygenase-1 88.03% 90.17%
CHEMBL2581 P07339 Cathepsin D 86.94% 98.95%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.79% 96.61%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.27% 83.57%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 82.72% 97.47%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.61% 98.75%
CHEMBL3691 Q13822 Autotaxin 80.19% 96.39%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.16% 94.33%

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 erba-rotta
Mutisia friesiana

Cross-Links

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PubChem 73823902
LOTUS LTS0207562
wikiData Q105021658