1-Piperidin-1-yltetradeca-2,4,6,12-tetraen-8,10-diyn-1-one

Details

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Internal ID 13dafae4-3770-4986-890f-79c315ed9b81
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 1-piperidin-1-yltetradeca-2,4,6,12-tetraen-8,10-diyn-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/h2-3,8-11,13,16H,12,14-15,17-18H2,1H3
InChI Key MCTACVMSLNVLIA-UHFFFAOYSA-N
Popularity 2 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 4.10
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Piperidin-1-yltetradeca-2,4,6,12-tetraen-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 + 0.9713 97.13%
Caco-2 + 0.6724 67.24%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.4511 45.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9234 92.34%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.6612 66.12%
P-glycoprotein inhibitior - 0.8555 85.55%
P-glycoprotein substrate - 0.8383 83.83%
CYP3A4 substrate - 0.5245 52.45%
CYP2C9 substrate - 0.6083 60.83%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9211 92.11%
CYP2C9 inhibition - 0.7413 74.13%
CYP2C19 inhibition + 0.5853 58.53%
CYP2D6 inhibition - 0.9485 94.85%
CYP1A2 inhibition - 0.6538 65.38%
CYP2C8 inhibition - 0.9316 93.16%
CYP inhibitory promiscuity - 0.7127 71.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5181 51.81%
Eye corrosion - 0.7230 72.30%
Eye irritation - 0.7238 72.38%
Skin irritation + 0.6505 65.05%
Skin corrosion - 0.7239 72.39%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6737 67.37%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.7519 75.19%
skin sensitisation - 0.8680 86.80%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5575 55.75%
Acute Oral Toxicity (c) III 0.6077 60.77%
Estrogen receptor binding + 0.6003 60.03%
Androgen receptor binding - 0.5578 55.78%
Thyroid receptor binding + 0.6047 60.47%
Glucocorticoid receptor binding - 0.6399 63.99%
Aromatase binding + 0.7149 71.49%
PPAR gamma - 0.5320 53.20%
Honey bee toxicity - 0.9137 91.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.8173 81.73%

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
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 96.72% 83.57%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.65% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.30% 98.95%
CHEMBL3012 Q13946 Phosphodiesterase 7A 82.63% 99.29%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.74% 93.10%
CHEMBL4208 P20618 Proteasome component C5 81.18% 90.00%
CHEMBL5028 O14672 ADAM10 80.35% 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 grandifolia

Cross-Links

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PubChem 73823905
LOTUS LTS0059465
wikiData Q105161423