1-Piperidin-1-yltetradeca-2,4-dien-8,10,12-triyn-1-one

Details

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Internal ID 84588dfc-69d0-4b55-925d-87e72a673baf
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 1-piperidin-1-yltetradeca-2,4-dien-8,10,12-triyn-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H21NO/c1-2-3-4-5-6-7-8-9-10-11-13-16-19(21)20-17-14-12-15-18-20/h10-11,13,16H,8-9,12,14-15,17-18H2,1H3
InChI Key ATLZTZPDWRYMJQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H21NO
Molecular Weight 279.40 g/mol
Exact Mass 279.162314293 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.92
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-Piperidin-1-yltetradeca-2,4-dien-8,10,12-triyn-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 + 0.9693 96.93%
Caco-2 + 0.6779 67.79%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5207 52.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9182 91.82%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior - 0.7834 78.34%
P-glycoprotein inhibitior - 0.8938 89.38%
P-glycoprotein substrate - 0.8344 83.44%
CYP3A4 substrate + 0.5053 50.53%
CYP2C9 substrate - 0.6083 60.83%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9508 95.08%
CYP2C9 inhibition - 0.7970 79.70%
CYP2C19 inhibition + 0.5781 57.81%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.7135 71.35%
CYP2C8 inhibition - 0.9025 90.25%
CYP inhibitory promiscuity - 0.7006 70.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5301 53.01%
Eye corrosion - 0.8638 86.38%
Eye irritation - 0.6159 61.59%
Skin irritation + 0.6088 60.88%
Skin corrosion - 0.6809 68.09%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5306 53.06%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8523 85.23%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5252 52.52%
Acute Oral Toxicity (c) III 0.6347 63.47%
Estrogen receptor binding - 0.7233 72.33%
Androgen receptor binding + 0.5831 58.31%
Thyroid receptor binding - 0.5062 50.62%
Glucocorticoid receptor binding - 0.7301 73.01%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.5400 54.00%
Honey bee toxicity - 0.9417 94.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.8189 81.89%

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 96.79% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.99% 83.57%
CHEMBL2581 P07339 Cathepsin D 88.20% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.82% 85.14%
CHEMBL230 P35354 Cyclooxygenase-2 83.23% 89.63%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 82.29% 97.47%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.34% 90.24%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.81% 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 spinulifolia

Cross-Links

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PubChem 73823904
LOTUS LTS0021021
wikiData Q104918531