1-Pyrrolidin-1-yltetradeca-2,4,12-trien-8,10-diyn-1-one

Details

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Internal ID c19805fe-4bb3-4b8d-90e3-9370911a54b2
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-acylpyrrolidines
IUPAC Name 1-pyrrolidin-1-yltetradeca-2,4,12-trien-8,10-diyn-1-one
SMILES (Canonical) CC=CC#CC#CCCC=CC=CC(=O)N1CCCC1
SMILES (Isomeric) CC=CC#CC#CCCC=CC=CC(=O)N1CCCC1
InChI InChI=1S/C18H21NO/c1-2-3-4-5-6-7-8-9-10-11-12-15-18(20)19-16-13-14-17-19/h2-3,10-12,15H,8-9,13-14,16-17H2,1H3
InChI Key XKCLCATWJFCVNH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H21NO
Molecular Weight 267.40 g/mol
Exact Mass 267.162314293 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pyrrolidin-1-yltetradeca-2,4,12-trien-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 + 0.9707 97.07%
Caco-2 + 0.8246 82.46%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.4461 44.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8864 88.64%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5414 54.14%
BSEP inhibitior - 0.5942 59.42%
P-glycoprotein inhibitior - 0.9193 91.93%
P-glycoprotein substrate - 0.7642 76.42%
CYP3A4 substrate + 0.5225 52.25%
CYP2C9 substrate - 0.6083 60.83%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9635 96.35%
CYP2C9 inhibition - 0.7507 75.07%
CYP2C19 inhibition + 0.6127 61.27%
CYP2D6 inhibition - 0.8170 81.70%
CYP1A2 inhibition - 0.7232 72.32%
CYP2C8 inhibition - 0.8691 86.91%
CYP inhibitory promiscuity - 0.6024 60.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4173 41.73%
Eye corrosion - 0.6596 65.96%
Eye irritation - 0.4865 48.65%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.6107 61.07%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5987 59.87%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8945 89.45%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5572 55.72%
Acute Oral Toxicity (c) III 0.6249 62.49%
Estrogen receptor binding + 0.5464 54.64%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5542 55.42%
Glucocorticoid receptor binding - 0.5792 57.92%
Aromatase binding - 0.5473 54.73%
PPAR gamma + 0.6498 64.98%
Honey bee toxicity - 0.9229 92.29%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.8486 84.86%

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 96.38% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.49% 83.57%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 86.64% 97.47%
CHEMBL2581 P07339 Cathepsin D 85.33% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.31% 85.14%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 83.17% 96.38%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.30% 90.24%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.27% 98.75%
CHEMBL4208 P20618 Proteasome component C5 81.09% 90.00%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 80.85% 93.90%
CHEMBL5028 O14672 ADAM10 80.53% 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.
Achillea erba-rotta

Cross-Links

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PubChem 163026154
LOTUS LTS0176894
wikiData Q105329408