4-Methylpiperidine

Details

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Internal ID 362e580f-37f2-4310-82eb-b2ebbae051c6
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 4-methylpiperidine
SMILES (Canonical) CC1CCNCC1
SMILES (Isomeric) CC1CCNCC1
InChI InChI=1S/C6H13N/c1-6-2-4-7-5-3-6/h6-7H,2-5H2,1H3
InChI Key UZOFELREXGAFOI-UHFFFAOYSA-N
Popularity 216 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13N
Molecular Weight 99.17 g/mol
Exact Mass 99.104799419 g/mol
Topological Polar Surface Area (TPSA) 12.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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626-58-4
4-Pipecoline
Piperidine, 4-methyl-
4-methylpiperidin
gamma-Pipecoline
4-Methyl-piperidine
.gamma.-Pipecoline
MFCD00006005
EV6HN6HDP8
4-Methylpiperidine--d4
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methylpiperidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 + 0.7753 77.53%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.9413 94.13%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9716 97.16%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.9753 97.53%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9482 94.82%
CYP3A4 substrate - 0.7517 75.17%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate + 0.4793 47.93%
CYP3A4 inhibition - 0.9815 98.15%
CYP2C9 inhibition - 0.9680 96.80%
CYP2C19 inhibition - 0.9547 95.47%
CYP2D6 inhibition - 0.8543 85.43%
CYP1A2 inhibition - 0.8133 81.33%
CYP2C8 inhibition - 0.9936 99.36%
CYP inhibitory promiscuity - 0.9857 98.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7273 72.73%
Eye corrosion + 0.9898 98.98%
Eye irritation + 0.9889 98.89%
Skin irritation + 0.8984 89.84%
Skin corrosion + 0.9720 97.20%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6880 68.80%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.6542 65.42%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5926 59.26%
Acute Oral Toxicity (c) II 0.5349 53.49%
Estrogen receptor binding - 0.9406 94.06%
Androgen receptor binding - 0.9161 91.61%
Thyroid receptor binding - 0.8815 88.15%
Glucocorticoid receptor binding - 0.9294 92.94%
Aromatase binding - 0.8409 84.09%
PPAR gamma - 0.9147 91.47%
Honey bee toxicity - 0.9340 93.40%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.7650 76.50%

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 97.70% 97.09%
CHEMBL4072 P07858 Cathepsin B 94.42% 93.67%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.62% 97.25%
CHEMBL228 P31645 Serotonin transporter 93.20% 95.51%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 90.19% 94.55%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 86.77% 95.58%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.08% 96.09%
CHEMBL222 P23975 Norepinephrine transporter 83.57% 96.06%
CHEMBL206 P03372 Estrogen receptor alpha 82.93% 97.64%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.29% 99.18%

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.
Spatholobus suberectus

Cross-Links

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PubChem 69381
NPASS NPC203203