3alpha,4beta,5beta-Piperidinetriol

Details

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Internal ID a2a105e0-85c1-468e-9e02-4f30073bfbe6
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name (3S,5S)-piperidine-3,4,5-triol
SMILES (Canonical) C1C(C(C(CN1)O)O)O
SMILES (Isomeric) C1[C@@H](C([C@H](CN1)O)O)O
InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4-/m0/s1
InChI Key RMCNETIHECSPMZ-IMJSIDKUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H11NO3
Molecular Weight 133.15 g/mol
Exact Mass 133.07389321 g/mol
Topological Polar Surface Area (TPSA) 72.70 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.33
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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3alpha,4beta,5beta-Piperidinetriol
AKOS006353436

2D Structure

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2D Structure of 3alpha,4beta,5beta-Piperidinetriol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6064 60.64%
Caco-2 - 0.8817 88.17%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5598 55.98%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9808 98.08%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9590 95.90%
P-glycoprotein inhibitior - 0.9795 97.95%
P-glycoprotein substrate - 0.9607 96.07%
CYP3A4 substrate - 0.7661 76.61%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate + 0.4078 40.78%
CYP3A4 inhibition - 0.9927 99.27%
CYP2C9 inhibition - 0.9488 94.88%
CYP2C19 inhibition - 0.9470 94.70%
CYP2D6 inhibition - 0.9404 94.04%
CYP1A2 inhibition - 0.9577 95.77%
CYP2C8 inhibition - 0.9950 99.50%
CYP inhibitory promiscuity - 0.9948 99.48%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6828 68.28%
Eye corrosion - 0.9398 93.98%
Eye irritation + 0.6646 66.46%
Skin irritation - 0.6062 60.62%
Skin corrosion - 0.6330 63.30%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5833 58.33%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.6101 61.01%
skin sensitisation - 0.8306 83.06%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7205 72.05%
Acute Oral Toxicity (c) III 0.6540 65.40%
Estrogen receptor binding - 0.9150 91.50%
Androgen receptor binding - 0.9188 91.88%
Thyroid receptor binding - 0.7877 78.77%
Glucocorticoid receptor binding - 0.7813 78.13%
Aromatase binding - 0.8615 86.15%
PPAR gamma - 0.8664 86.64%
Honey bee toxicity - 0.8662 86.62%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.9952 99.52%

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 92.26% 97.09%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 91.02% 94.55%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.97% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.90% 91.11%
CHEMBL222 P23975 Norepinephrine transporter 83.18% 96.06%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.93% 97.25%

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.
Citrus aurantiifolia
Eupatorium fortunei
Lysimachia clethroides
Senna sophera

Cross-Links

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PubChem 10080444
NPASS NPC48814