2-Methyl-3,4,5-piperidinetriol

Details

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Internal ID 5ff511d9-6b0c-4bd8-8400-d6c422487fac
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 2-methylpiperidine-3,4,5-triol
SMILES (Canonical) CC1C(C(C(CN1)O)O)O
SMILES (Isomeric) CC1C(C(C(CN1)O)O)O
InChI InChI=1S/C6H13NO3/c1-3-5(9)6(10)4(8)2-7-3/h3-10H,2H2,1H3
InChI Key VYOCYWDJTQRZLC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO3
Molecular Weight 147.17 g/mol
Exact Mass 147.08954328 g/mol
Topological Polar Surface Area (TPSA) 72.70 Ų
XlogP -1.90
Atomic LogP (AlogP) -1.94
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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NSC649690
2-methylpiperidine-3,4,5-triol
2-Methyl-3,4,5-piperidinetriol
SCHEMBL1867289
NSC-649690
FT-0624513

2D Structure

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2D Structure of 2-Methyl-3,4,5-piperidinetriol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7411 74.11%
Caco-2 - 0.9041 90.41%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5196 51.96%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9697 96.97%
OATP1B3 inhibitior + 0.9584 95.84%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9739 97.39%
P-glycoprotein inhibitior - 0.9792 97.92%
P-glycoprotein substrate - 0.8974 89.74%
CYP3A4 substrate - 0.7003 70.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3942 39.42%
CYP3A4 inhibition - 0.9958 99.58%
CYP2C9 inhibition - 0.9655 96.55%
CYP2C19 inhibition - 0.9622 96.22%
CYP2D6 inhibition - 0.9558 95.58%
CYP1A2 inhibition - 0.9711 97.11%
CYP2C8 inhibition - 0.9891 98.91%
CYP inhibitory promiscuity - 0.9935 99.35%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6708 67.08%
Eye corrosion - 0.9778 97.78%
Eye irritation - 0.9291 92.91%
Skin irritation - 0.6978 69.78%
Skin corrosion - 0.7593 75.93%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6715 67.15%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8377 83.77%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8102 81.02%
Acute Oral Toxicity (c) III 0.6724 67.24%
Estrogen receptor binding - 0.8699 86.99%
Androgen receptor binding - 0.9301 93.01%
Thyroid receptor binding - 0.7667 76.67%
Glucocorticoid receptor binding - 0.8510 85.10%
Aromatase binding - 0.8686 86.86%
PPAR gamma - 0.9158 91.58%
Honey bee toxicity - 0.9353 93.53%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.9908 99.08%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4176 P04066 Alpha-L-fucosidase I 10 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.34% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.50% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.54% 97.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 86.94% 95.58%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.49% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.60% 91.11%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 81.79% 94.55%

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.
Angylocalyx pynaertii

Cross-Links

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PubChem 373419
LOTUS LTS0139042
wikiData Q105299109