1-Piperidin-2-ylbutan-2-ol

Details

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Internal ID 273503d8-b24f-4b66-9061-a328eeac6881
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 1-piperidin-2-ylbutan-2-ol
SMILES (Canonical) CCC(CC1CCCCN1)O
SMILES (Isomeric) CCC(CC1CCCCN1)O
InChI InChI=1S/C9H19NO/c1-2-9(11)7-8-5-3-4-6-10-8/h8-11H,2-7H2,1H3
InChI Key ZRXAUOSECWYDMA-UHFFFAOYSA-N
Popularity 0 references 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 1.30
Atomic LogP (AlogP) 1.29
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Piperidin-2-ylbutan-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9804 98.04%
Caco-2 + 0.7619 76.19%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.6420 64.20%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.9505 95.05%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8950 89.50%
P-glycoprotein inhibitior - 0.9736 97.36%
P-glycoprotein substrate - 0.7914 79.14%
CYP3A4 substrate - 0.6870 68.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5555 55.55%
CYP3A4 inhibition - 0.9833 98.33%
CYP2C9 inhibition - 0.9123 91.23%
CYP2C19 inhibition - 0.9563 95.63%
CYP2D6 inhibition - 0.6370 63.70%
CYP1A2 inhibition - 0.8180 81.80%
CYP2C8 inhibition - 0.9322 93.22%
CYP inhibitory promiscuity - 0.9647 96.47%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7187 71.87%
Eye corrosion + 0.5543 55.43%
Eye irritation + 0.8716 87.16%
Skin irritation + 0.5174 51.74%
Skin corrosion - 0.5548 55.48%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6664 66.64%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.6909 69.09%
skin sensitisation - 0.7973 79.73%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8123 81.23%
Acute Oral Toxicity (c) III 0.6465 64.65%
Estrogen receptor binding - 0.8011 80.11%
Androgen receptor binding - 0.7119 71.19%
Thyroid receptor binding - 0.7505 75.05%
Glucocorticoid receptor binding - 0.8296 82.96%
Aromatase binding - 0.8666 86.66%
PPAR gamma - 0.8817 88.17%
Honey bee toxicity - 0.9787 97.87%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9623 96.23%

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 97.51% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.69% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.09% 97.09%
CHEMBL2581 P07339 Cathepsin D 93.75% 98.95%
CHEMBL213 P08588 Beta-1 adrenergic receptor 87.56% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.54% 96.95%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 86.04% 92.88%
CHEMBL237 P41145 Kappa opioid receptor 84.66% 98.10%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.87% 98.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.65% 93.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.19% 94.45%
CHEMBL206 P03372 Estrogen receptor alpha 82.84% 97.64%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.05% 92.62%
CHEMBL268 P43235 Cathepsin K 81.58% 96.85%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.75% 97.50%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.31% 96.47%

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.
Andrachne aspera
Sedum fusiforme

Cross-Links

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PubChem 73812584
LOTUS LTS0052956
wikiData Q105382302