Piperidine

Details

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Internal ID 3eba0110-2743-4dec-8b4d-abd5d0fac360
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name piperidine
SMILES (Canonical) C1CCNCC1
SMILES (Isomeric) C1CCNCC1
InChI InChI=1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2
InChI Key NQRYJNQNLNOLGT-UHFFFAOYSA-N
Popularity 16,982 references in papers

Physical and Chemical Properties

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Molecular Formula C5H11N
Molecular Weight 85.15 g/mol
Exact Mass 85.089149355 g/mol
Topological Polar Surface Area (TPSA) 12.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.76
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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110-89-4
Hexahydropyridine
Cyclopentimine
Azacyclohexane
Piperidin
Cypentil
Hexazane
Pentamethyleneimine
Pentamethylenimine
Perhydropyridine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Piperidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9762 97.62%
Caco-2 + 0.7139 71.39%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.8708 87.08%
OATP2B1 inhibitior - 0.8638 86.38%
OATP1B1 inhibitior + 0.9777 97.77%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6750 67.50%
BSEP inhibitior - 0.9737 97.37%
P-glycoprotein inhibitior - 0.9875 98.75%
P-glycoprotein substrate - 0.9884 98.84%
CYP3A4 substrate - 0.8413 84.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5330 53.30%
CYP3A4 inhibition - 0.9814 98.14%
CYP2C9 inhibition - 0.9696 96.96%
CYP2C19 inhibition - 0.9575 95.75%
CYP2D6 inhibition - 0.7413 74.13%
CYP1A2 inhibition - 0.6039 60.39%
CYP2C8 inhibition - 0.9966 99.66%
CYP inhibitory promiscuity - 0.9796 97.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7146 71.46%
Eye corrosion + 0.9972 99.72%
Eye irritation + 0.9948 99.48%
Skin irritation + 0.9219 92.19%
Skin corrosion + 0.9719 97.19%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6770 67.70%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.7700 77.00%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.4877 48.77%
Acute Oral Toxicity (c) II 0.7407 74.07%
Estrogen receptor binding - 0.9385 93.85%
Androgen receptor binding - 0.9004 90.04%
Thyroid receptor binding - 0.8814 88.14%
Glucocorticoid receptor binding - 0.9230 92.30%
Aromatase binding - 0.8378 83.78%
PPAR gamma - 0.9294 92.94%
Honey bee toxicity - 0.9161 91.61%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.9389 93.89%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 92.59% 97.09%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 90.46% 94.55%
CHEMBL228 P31645 Serotonin transporter 84.96% 95.51%
CHEMBL4630 O14757 Serine/threonine-protein kinase Chk1 84.69% 97.03%
CHEMBL3012 Q13946 Phosphodiesterase 7A 83.75% 99.29%

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.
Cannabis sativa
Piper longum
Piper nigrum

Cross-Links

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PubChem 8082
NPASS NPC21157
LOTUS LTS0191209
wikiData Q410234