beta-1-C-ethyl-1-deoxymannojirimycin

Details

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Internal ID a41ea508-490c-494b-8156-5bd9d3161587
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name (2S,3R,4R,5R,6R)-2-ethyl-6-(hydroxymethyl)piperidine-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H17NO4/c1-2-4-6(11)8(13)7(12)5(3-10)9-4/h4-13H,2-3H2,1H3/t4-,5+,6+,7+,8+/m0/s1
InChI Key AFRPVDHJWCJLNM-SLBCVNJHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H17NO4
Molecular Weight 191.22 g/mol
Exact Mass 191.11575802 g/mol
Topological Polar Surface Area (TPSA) 93.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -2.19
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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BDBM50214378
beta-1-C-ethyl-1-deoxymannojirimycin

2D Structure

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2D Structure of beta-1-C-ethyl-1-deoxymannojirimycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6715 67.15%
Caco-2 - 0.9192 91.92%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4714 47.14%
OATP2B1 inhibitior - 0.8488 84.88%
OATP1B1 inhibitior + 0.9633 96.33%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9693 96.93%
P-glycoprotein inhibitior - 0.9638 96.38%
P-glycoprotein substrate - 0.8909 89.09%
CYP3A4 substrate - 0.7084 70.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4466 44.66%
CYP3A4 inhibition - 0.9674 96.74%
CYP2C9 inhibition - 0.9152 91.52%
CYP2C19 inhibition - 0.9539 95.39%
CYP2D6 inhibition - 0.9029 90.29%
CYP1A2 inhibition - 0.9263 92.63%
CYP2C8 inhibition - 0.9688 96.88%
CYP inhibitory promiscuity - 0.9770 97.70%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7679 76.79%
Eye corrosion - 0.9806 98.06%
Eye irritation - 0.9388 93.88%
Skin irritation - 0.7640 76.40%
Skin corrosion - 0.8994 89.94%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4898 48.98%
Micronuclear + 0.6400 64.00%
Hepatotoxicity - 0.7799 77.99%
skin sensitisation - 0.8541 85.41%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6582 65.82%
Acute Oral Toxicity (c) III 0.6775 67.75%
Estrogen receptor binding - 0.7558 75.58%
Androgen receptor binding - 0.7482 74.82%
Thyroid receptor binding - 0.6580 65.80%
Glucocorticoid receptor binding - 0.7421 74.21%
Aromatase binding - 0.7598 75.98%
PPAR gamma - 0.8165 81.65%
Honey bee toxicity - 0.9716 97.16%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity - 0.9733 97.33%

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 96.76% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.87% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.21% 97.25%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 87.31% 94.55%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.05% 96.61%
CHEMBL2581 P07339 Cathepsin D 85.61% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 84.82% 97.79%
CHEMBL226 P30542 Adenosine A1 receptor 82.90% 95.93%
CHEMBL255 P29275 Adenosine A2b receptor 81.89% 98.59%

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.
Ledebouria socialis

Cross-Links

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PubChem 14446759
NPASS NPC268922
LOTUS LTS0048997
wikiData Q104911454