3-Epi-fagomine

Details

Top
Internal ID 799afff8-5889-4d2b-87bc-ed8be1e2ec87
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name (2R,3R,4S)-2-(hydroxymethyl)piperidine-3,4-diol
SMILES (Canonical) C1CNC(C(C1O)O)CO
SMILES (Isomeric) C1CN[C@@H]([C@H]([C@H]1O)O)CO
InChI InChI=1S/C6H13NO3/c8-3-4-6(10)5(9)1-2-7-4/h4-10H,1-3H2/t4-,5+,6-/m1/s1
InChI Key YZNNBIPIQWYLDM-NGJCXOISSA-N
Popularity 8 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H13NO3
Molecular Weight 147.17 g/mol
Exact Mass 147.08954328 g/mol
Topological Polar Surface Area (TPSA) 72.70 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.94
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

Top
3-Epifagomine
CHEMBL456583
(2R,3R,4S)-2-(hydroxymethyl)piperidine-3,4-diol
156639-77-9
CHEBI:132399
DTXSID001317313
BDBM50292389
AKOS006352899
Q27225561

2D Structure

Top
2D Structure of 3-Epi-fagomine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6892 68.92%
Caco-2 - 0.9270 92.70%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7186 71.86%
OATP2B1 inhibitior - 0.8479 84.79%
OATP1B1 inhibitior + 0.9644 96.44%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9489 94.89%
P-glycoprotein inhibitior - 0.9803 98.03%
P-glycoprotein substrate - 0.9120 91.20%
CYP3A4 substrate - 0.6610 66.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4714 47.14%
CYP3A4 inhibition - 0.9920 99.20%
CYP2C9 inhibition - 0.9440 94.40%
CYP2C19 inhibition - 0.9536 95.36%
CYP2D6 inhibition - 0.9221 92.21%
CYP1A2 inhibition - 0.9093 90.93%
CYP2C8 inhibition - 0.9820 98.20%
CYP inhibitory promiscuity - 0.9909 99.09%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7200 72.00%
Eye corrosion - 0.8993 89.93%
Eye irritation - 0.6357 63.57%
Skin irritation - 0.6491 64.91%
Skin corrosion - 0.8684 86.84%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5923 59.23%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5139 51.39%
skin sensitisation - 0.8654 86.54%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5622 56.22%
Acute Oral Toxicity (c) III 0.6909 69.09%
Estrogen receptor binding - 0.8999 89.99%
Androgen receptor binding - 0.7817 78.17%
Thyroid receptor binding - 0.7939 79.39%
Glucocorticoid receptor binding - 0.8251 82.51%
Aromatase binding - 0.8320 83.20%
PPAR gamma - 0.8318 83.18%
Honey bee toxicity - 0.9400 94.00%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.9928 99.28%

Targets

Top

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 96.28% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.64% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.00% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 91.83% 95.93%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 90.84% 94.55%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 85.54% 96.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.78% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.51% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.86% 96.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.74% 100.00%

Plants that contains it

Top

Cross-Links

Top
PubChem 10290867
NPASS NPC290106
ChEMBL CHEMBL456583
LOTUS LTS0252876
wikiData Q27225561