2-Methyl-6-(2-hydroxypropyl)piperidine

Details

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Internal ID 52b55af2-77f4-4122-a34a-e8b3c99e1f3e
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 1-(6-methylpiperidin-2-yl)propan-2-ol
SMILES (Canonical) CC1CCCC(N1)CC(C)O
SMILES (Isomeric) CC1CCCC(N1)CC(C)O
InChI InChI=1S/C9H19NO/c1-7-4-3-5-9(10-7)6-8(2)11/h7-11H,3-6H2,1-2H3
InChI Key DVJHWTLBEYCZJZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C9H19NO
Molecular Weight 157.25 g/mol
Exact Mass 157.146664230 g/mol
Topological Polar Surface Area (TPSA) 32.30 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.29
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-6-(2-hydroxypropyl)piperidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9750 97.50%
Caco-2 + 0.7778 77.78%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5610 56.10%
OATP2B1 inhibitior - 0.8405 84.05%
OATP1B1 inhibitior + 0.9516 95.16%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9288 92.88%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.7759 77.59%
CYP3A4 substrate - 0.6667 66.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5555 55.55%
CYP3A4 inhibition - 0.9659 96.59%
CYP2C9 inhibition - 0.9029 90.29%
CYP2C19 inhibition - 0.9243 92.43%
CYP2D6 inhibition - 0.7854 78.54%
CYP1A2 inhibition - 0.7872 78.72%
CYP2C8 inhibition - 0.9815 98.15%
CYP inhibitory promiscuity - 0.9526 95.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7283 72.83%
Eye corrosion - 0.5994 59.94%
Eye irritation + 0.8541 85.41%
Skin irritation - 0.5973 59.73%
Skin corrosion - 0.5137 51.37%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7154 71.54%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5372 53.72%
skin sensitisation - 0.7270 72.70%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5172 51.72%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6341 63.41%
Acute Oral Toxicity (c) III 0.7604 76.04%
Estrogen receptor binding - 0.9027 90.27%
Androgen receptor binding - 0.8179 81.79%
Thyroid receptor binding - 0.6998 69.98%
Glucocorticoid receptor binding - 0.7746 77.46%
Aromatase binding - 0.8557 85.57%
PPAR gamma - 0.8615 86.15%
Honey bee toxicity - 0.9385 93.85%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.8526 85.26%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.40% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.53% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.96% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.37% 97.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 92.06% 97.23%
CHEMBL206 P03372 Estrogen receptor alpha 90.73% 97.64%
CHEMBL213 P08588 Beta-1 adrenergic receptor 90.69% 95.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.02% 96.47%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.90% 94.45%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.52% 93.03%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.72% 95.58%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.15% 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.
Pedicularis bracteosa
Picea glauca
Picea pungens

Cross-Links

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PubChem 427150
LOTUS LTS0010271
wikiData Q104990170