6-Ethyl-2-(hydroxymethyl)piperidine-3,4-diol

Details

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Internal ID ed2eef9f-dd37-4e31-a502-e0a8a104f6bf
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 6-ethyl-2-(hydroxymethyl)piperidine-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H17NO3/c1-2-5-3-7(11)8(12)6(4-10)9-5/h5-12H,2-4H2,1H3
InChI Key QWEWPBRDYZVGBR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H17NO3
Molecular Weight 175.23 g/mol
Exact Mass 175.12084340 g/mol
Topological Polar Surface Area (TPSA) 72.70 Ų
XlogP -0.40
Atomic LogP (AlogP) -1.16
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Ethyl-2-(hydroxymethyl)piperidine-3,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8878 88.78%
Caco-2 - 0.8667 86.67%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5354 53.54%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.9537 95.37%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9593 95.93%
P-glycoprotein inhibitior - 0.9758 97.58%
P-glycoprotein substrate - 0.7348 73.48%
CYP3A4 substrate - 0.6311 63.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4466 44.66%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9305 93.05%
CYP2C19 inhibition - 0.9401 94.01%
CYP2D6 inhibition - 0.9135 91.35%
CYP1A2 inhibition - 0.9402 94.02%
CYP2C8 inhibition - 0.9528 95.28%
CYP inhibitory promiscuity - 0.9785 97.85%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7363 73.63%
Eye corrosion - 0.9772 97.72%
Eye irritation - 0.8138 81.38%
Skin irritation - 0.7577 75.77%
Skin corrosion - 0.8909 89.09%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4655 46.55%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5300 53.00%
skin sensitisation - 0.8484 84.84%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6515 65.15%
Acute Oral Toxicity (c) III 0.6861 68.61%
Estrogen receptor binding - 0.7185 71.85%
Androgen receptor binding - 0.7234 72.34%
Thyroid receptor binding - 0.6811 68.11%
Glucocorticoid receptor binding - 0.7483 74.83%
Aromatase binding - 0.7322 73.22%
PPAR gamma - 0.7953 79.53%
Honey bee toxicity - 0.9405 94.05%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.9769 97.69%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.32% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.29% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.46% 97.25%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 91.95% 94.55%
CHEMBL226 P30542 Adenosine A1 receptor 90.22% 95.93%
CHEMBL2996 Q05655 Protein kinase C delta 88.17% 97.79%
CHEMBL206 P03372 Estrogen receptor alpha 87.64% 97.64%
CHEMBL2581 P07339 Cathepsin D 85.86% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.45% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.95% 96.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.36% 100.00%

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.
Adenophora triphylla var. japonica

Cross-Links

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PubChem 75022977
LOTUS LTS0219739
wikiData Q105229135