Page last updated: 2024-12-11

n-(5-adamantane-1-yl-methoxy-pentyl)deoxynojirimycin

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Cross-References

ID SourceID
PubMed CID9822159
CHEMBL ID574645
SCHEMBL ID13777990
SCHEMBL ID17132950
MeSH IDM0480685

Synonyms (15)

Synonym
amp-dnm
n-(adamantanemethyloxypentyl)-deoxynojirimycin
CHEMBL574645 ,
bdbm50299749
(2r,3r,4r,5s)-1-[5-(adamantan-1-ylmethoxy)-pentyl]-2-hydroxymethyl-piperidine-3,4,5-triol
n-adamantanemethyloxypentyl-1-deoxynojirimycin
216758-20-2
3,4,5-piperidinetriol, 2-(hydroxymethyl)-1-[5-(tricyclo[3.3.1.13,7]dec-1-ylmethoxy)pentyl]-, (2r,3r,4r,5s)-
amp-deoxynojirimycin
SCHEMBL13777990
SCHEMBL17132950
AKOS030538164
J-014228
(2r,3r,4r,5s)-1-[5-(1-adamantylmethoxy)pentyl]-2-(hydroxymethyl)piperidine-3,4,5-triol
n-(5-adamantane-1-yl-methoxy)-pentyl-deoxynojirimycin

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" Four weeks of dosing resulted in decreased plasma triglycerides and reduced hepatic fat deposition."( Discovery and characterization of an inhibitor of glucosylceramide synthase.
Aay, N; Aoyama, R; Arcalas, A; Bentzien, F; Cancilla, B; Chan, V; Du, H; Finn, P; Galan, A; Hanel, A; Harrison, A; Kearney, P; Koltun, ES; Lamb, P; Larson, CJ; Mohan, R; Nachtigall, J; Nuss, J; Ogilvie, K; Plonowski, A; Qian, F; Richards, S; Rosen, J; Tam, D; Wang, T; Won, KA; Yakes, M; Zhang, J; Zhang, W, 2012
)
0.38
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (13)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Sucrase-isomaltase Mus musculus (house mouse)IC50 (µMol)0.50000.40000.75001.5000AID553255
Maltase-glucoamylase, intestinalHomo sapiens (human)IC50 (µMol)3.50000.04003.46529.0000AID1166042; AID466668
Ceramide glucosyltransferaseMus musculus (house mouse)IC50 (µMol)0.20000.20001.46674.0000AID553252; AID652571
Lysosomal acid glucosylceramidaseHomo sapiens (human)IC50 (µMol)0.15000.03002.35898.8000AID1166038; AID553253
Cytochrome P450 3A4Homo sapiens (human)IC50 (µMol)0.09000.00011.753610.0000AID626355
Lysosomal alpha-glucosidaseHomo sapiens (human)IC50 (µMol)0.40000.06002.28897.8000AID437995; AID466672
Sucrase-isomaltase, intestinalHomo sapiens (human)IC50 (µMol)0.55000.04902.72947.8000AID1166040; AID466667
Glycogen debranching enzymeHomo sapiens (human)IC50 (µMol)10.00008.40009.514310.0000AID466673
Lysosomal alpha-glucosidaseMus musculus (house mouse)IC50 (µMol)4.00004.00007.00009.0000AID553257
Ceramide glucosyltransferaseHomo sapiens (human)IC50 (µMol)5.58830.09000.13250.2000AID1166037; AID466666; AID626355; AID626356; AID699202; AID699203
Non-lysosomal glucosylceramidaseHomo sapiens (human)IC50 (µMol)0.00150.00030.08970.3000AID1166039; AID1596605; AID437994; AID466671; AID553254; AID700851; AID700852
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (118)

Processvia Protein(s)Taxonomy
maltose catabolic processMaltase-glucoamylase, intestinalHomo sapiens (human)
starch catabolic processMaltase-glucoamylase, intestinalHomo sapiens (human)
dextrin catabolic processMaltase-glucoamylase, intestinalHomo sapiens (human)
mitochondrion organizationLysosomal acid glucosylceramidaseHomo sapiens (human)
neuron projection developmentLysosomal acid glucosylceramidaseHomo sapiens (human)
glucosylceramide catabolic processLysosomal acid glucosylceramidaseHomo sapiens (human)
autophagyLysosomal acid glucosylceramidaseHomo sapiens (human)
lysosome organizationLysosomal acid glucosylceramidaseHomo sapiens (human)
cholesterol metabolic processLysosomal acid glucosylceramidaseHomo sapiens (human)
determination of adult lifespanLysosomal acid glucosylceramidaseHomo sapiens (human)
cellular response to starvationLysosomal acid glucosylceramidaseHomo sapiens (human)
response to pHLysosomal acid glucosylceramidaseHomo sapiens (human)
microglia differentiationLysosomal acid glucosylceramidaseHomo sapiens (human)
regulation of macroautophagyLysosomal acid glucosylceramidaseHomo sapiens (human)
antigen processing and presentationLysosomal acid glucosylceramidaseHomo sapiens (human)
lipid storageLysosomal acid glucosylceramidaseHomo sapiens (human)
cerebellar Purkinje cell layer formationLysosomal acid glucosylceramidaseHomo sapiens (human)
pyramidal neuron differentiationLysosomal acid glucosylceramidaseHomo sapiens (human)
respiratory electron transport chainLysosomal acid glucosylceramidaseHomo sapiens (human)
termination of signal transductionLysosomal acid glucosylceramidaseHomo sapiens (human)
lipid glycosylationLysosomal acid glucosylceramidaseHomo sapiens (human)
negative regulation of protein-containing complex assemblyLysosomal acid glucosylceramidaseHomo sapiens (human)
regulation of TOR signalingLysosomal acid glucosylceramidaseHomo sapiens (human)
positive regulation of proteasomal ubiquitin-dependent protein catabolic processLysosomal acid glucosylceramidaseHomo sapiens (human)
negative regulation of interleukin-6 productionLysosomal acid glucosylceramidaseHomo sapiens (human)
T cell differentiation in thymusLysosomal acid glucosylceramidaseHomo sapiens (human)
response to testosteroneLysosomal acid glucosylceramidaseHomo sapiens (human)
positive regulation of protein dephosphorylationLysosomal acid glucosylceramidaseHomo sapiens (human)
proteasome-mediated ubiquitin-dependent protein catabolic processLysosomal acid glucosylceramidaseHomo sapiens (human)
positive regulation of protein-containing complex disassemblyLysosomal acid glucosylceramidaseHomo sapiens (human)
negative regulation of MAP kinase activityLysosomal acid glucosylceramidaseHomo sapiens (human)
negative regulation of neuron apoptotic processLysosomal acid glucosylceramidaseHomo sapiens (human)
response to estrogenLysosomal acid glucosylceramidaseHomo sapiens (human)
sphingosine biosynthetic processLysosomal acid glucosylceramidaseHomo sapiens (human)
ceramide biosynthetic processLysosomal acid glucosylceramidaseHomo sapiens (human)
cell maturationLysosomal acid glucosylceramidaseHomo sapiens (human)
brain morphogenesisLysosomal acid glucosylceramidaseHomo sapiens (human)
homeostasis of number of cellsLysosomal acid glucosylceramidaseHomo sapiens (human)
negative regulation of inflammatory responseLysosomal acid glucosylceramidaseHomo sapiens (human)
neuromuscular processLysosomal acid glucosylceramidaseHomo sapiens (human)
neuron apoptotic processLysosomal acid glucosylceramidaseHomo sapiens (human)
establishment of skin barrierLysosomal acid glucosylceramidaseHomo sapiens (human)
microglial cell proliferationLysosomal acid glucosylceramidaseHomo sapiens (human)
motor behaviorLysosomal acid glucosylceramidaseHomo sapiens (human)
cellular response to tumor necrosis factorLysosomal acid glucosylceramidaseHomo sapiens (human)
hematopoietic stem cell proliferationLysosomal acid glucosylceramidaseHomo sapiens (human)
response to dexamethasoneLysosomal acid glucosylceramidaseHomo sapiens (human)
lymphocyte migrationLysosomal acid glucosylceramidaseHomo sapiens (human)
response to thyroid hormoneLysosomal acid glucosylceramidaseHomo sapiens (human)
beta-glucoside catabolic processLysosomal acid glucosylceramidaseHomo sapiens (human)
positive regulation of protein lipidationLysosomal acid glucosylceramidaseHomo sapiens (human)
positive regulation of neuronal action potentialLysosomal acid glucosylceramidaseHomo sapiens (human)
positive regulation of autophagy of mitochondrion in response to mitochondrial depolarizationLysosomal acid glucosylceramidaseHomo sapiens (human)
autophagosome organizationLysosomal acid glucosylceramidaseHomo sapiens (human)
regulation of lysosomal protein catabolic processLysosomal acid glucosylceramidaseHomo sapiens (human)
lipid hydroxylationCytochrome P450 3A4Homo sapiens (human)
lipid metabolic processCytochrome P450 3A4Homo sapiens (human)
steroid catabolic processCytochrome P450 3A4Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 3A4Homo sapiens (human)
steroid metabolic processCytochrome P450 3A4Homo sapiens (human)
cholesterol metabolic processCytochrome P450 3A4Homo sapiens (human)
androgen metabolic processCytochrome P450 3A4Homo sapiens (human)
estrogen metabolic processCytochrome P450 3A4Homo sapiens (human)
alkaloid catabolic processCytochrome P450 3A4Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 3A4Homo sapiens (human)
calcitriol biosynthetic process from calciolCytochrome P450 3A4Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 3A4Homo sapiens (human)
vitamin D metabolic processCytochrome P450 3A4Homo sapiens (human)
vitamin D catabolic processCytochrome P450 3A4Homo sapiens (human)
retinol metabolic processCytochrome P450 3A4Homo sapiens (human)
retinoic acid metabolic processCytochrome P450 3A4Homo sapiens (human)
long-chain fatty acid biosynthetic processCytochrome P450 3A4Homo sapiens (human)
aflatoxin metabolic processCytochrome P450 3A4Homo sapiens (human)
oxidative demethylationCytochrome P450 3A4Homo sapiens (human)
lactose catabolic processLactase-phlorizin hydrolaseHomo sapiens (human)
glycosylceramide catabolic processLactase-phlorizin hydrolaseHomo sapiens (human)
quercetin catabolic processLactase-phlorizin hydrolaseHomo sapiens (human)
cellobiose catabolic processLactase-phlorizin hydrolaseHomo sapiens (human)
maltose metabolic processLysosomal alpha-glucosidaseHomo sapiens (human)
regulation of the force of heart contractionLysosomal alpha-glucosidaseHomo sapiens (human)
diaphragm contractionLysosomal alpha-glucosidaseHomo sapiens (human)
heart morphogenesisLysosomal alpha-glucosidaseHomo sapiens (human)
glycogen catabolic processLysosomal alpha-glucosidaseHomo sapiens (human)
sucrose metabolic processLysosomal alpha-glucosidaseHomo sapiens (human)
glucose metabolic processLysosomal alpha-glucosidaseHomo sapiens (human)
lysosome organizationLysosomal alpha-glucosidaseHomo sapiens (human)
locomotory behaviorLysosomal alpha-glucosidaseHomo sapiens (human)
tissue developmentLysosomal alpha-glucosidaseHomo sapiens (human)
aorta developmentLysosomal alpha-glucosidaseHomo sapiens (human)
vacuolar sequesteringLysosomal alpha-glucosidaseHomo sapiens (human)
muscle cell cellular homeostasisLysosomal alpha-glucosidaseHomo sapiens (human)
neuromuscular process controlling postureLysosomal alpha-glucosidaseHomo sapiens (human)
neuromuscular process controlling balanceLysosomal alpha-glucosidaseHomo sapiens (human)
cardiac muscle contractionLysosomal alpha-glucosidaseHomo sapiens (human)
glycophagyLysosomal alpha-glucosidaseHomo sapiens (human)
sucrose catabolic processSucrase-isomaltase, intestinalHomo sapiens (human)
polysaccharide digestionSucrase-isomaltase, intestinalHomo sapiens (human)
glycogen biosynthetic processGlycogen debranching enzymeHomo sapiens (human)
glycogen catabolic processGlycogen debranching enzymeHomo sapiens (human)
response to nutrientGlycogen debranching enzymeHomo sapiens (human)
response to glucocorticoidGlycogen debranching enzymeHomo sapiens (human)
protein lipidationCeramide glucosyltransferaseHomo sapiens (human)
glucosylceramide biosynthetic processCeramide glucosyltransferaseHomo sapiens (human)
glycosphingolipid biosynthetic processCeramide glucosyltransferaseHomo sapiens (human)
epidermis developmentCeramide glucosyltransferaseHomo sapiens (human)
regulation of signal transductionCeramide glucosyltransferaseHomo sapiens (human)
cell differentiationCeramide glucosyltransferaseHomo sapiens (human)
keratinocyte differentiationCeramide glucosyltransferaseHomo sapiens (human)
leptin-mediated signaling pathwayCeramide glucosyltransferaseHomo sapiens (human)
neuron developmentCeramide glucosyltransferaseHomo sapiens (human)
establishment of skin barrierCeramide glucosyltransferaseHomo sapiens (human)
intestinal lipid absorptionCeramide glucosyltransferaseHomo sapiens (human)
cornified envelope assemblyCeramide glucosyltransferaseHomo sapiens (human)
carbohydrate metabolic processNon-lysosomal glucosylceramidaseHomo sapiens (human)
glucosylceramide catabolic processNon-lysosomal glucosylceramidaseHomo sapiens (human)
cholesterol metabolic processNon-lysosomal glucosylceramidaseHomo sapiens (human)
bile acid metabolic processNon-lysosomal glucosylceramidaseHomo sapiens (human)
glycoside catabolic processNon-lysosomal glucosylceramidaseHomo sapiens (human)
central nervous system neuron developmentNon-lysosomal glucosylceramidaseHomo sapiens (human)
lipid glycosylationNon-lysosomal glucosylceramidaseHomo sapiens (human)
regulation of actin filament polymerizationNon-lysosomal glucosylceramidaseHomo sapiens (human)
regulation of microtubule polymerizationNon-lysosomal glucosylceramidaseHomo sapiens (human)
glycosphingolipid catabolic processNon-lysosomal glucosylceramidaseHomo sapiens (human)
regulation of membrane lipid distributionNon-lysosomal glucosylceramidaseHomo sapiens (human)
central nervous system developmentNon-lysosomal glucosylceramidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (52)

Processvia Protein(s)Taxonomy
catalytic activityMaltase-glucoamylase, intestinalHomo sapiens (human)
glucan 1,4-alpha-glucosidase activityMaltase-glucoamylase, intestinalHomo sapiens (human)
alpha-1,4-glucosidase activityMaltase-glucoamylase, intestinalHomo sapiens (human)
protein bindingMaltase-glucoamylase, intestinalHomo sapiens (human)
amylase activityMaltase-glucoamylase, intestinalHomo sapiens (human)
carbohydrate bindingMaltase-glucoamylase, intestinalHomo sapiens (human)
maltose alpha-glucosidase activityMaltase-glucoamylase, intestinalHomo sapiens (human)
galactosylceramidase activityLysosomal acid glucosylceramidaseHomo sapiens (human)
glucosylceramidase activityLysosomal acid glucosylceramidaseHomo sapiens (human)
signaling receptor bindingLysosomal acid glucosylceramidaseHomo sapiens (human)
scavenger receptor bindingLysosomal acid glucosylceramidaseHomo sapiens (human)
protein bindingLysosomal acid glucosylceramidaseHomo sapiens (human)
glucosyltransferase activityLysosomal acid glucosylceramidaseHomo sapiens (human)
steryl-beta-glucosidase activityLysosomal acid glucosylceramidaseHomo sapiens (human)
monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
steroid bindingCytochrome P450 3A4Homo sapiens (human)
iron ion bindingCytochrome P450 3A4Homo sapiens (human)
protein bindingCytochrome P450 3A4Homo sapiens (human)
steroid hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
retinoic acid 4-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
oxidoreductase activityCytochrome P450 3A4Homo sapiens (human)
oxygen bindingCytochrome P450 3A4Homo sapiens (human)
enzyme bindingCytochrome P450 3A4Homo sapiens (human)
heme bindingCytochrome P450 3A4Homo sapiens (human)
vitamin D3 25-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
caffeine oxidase activityCytochrome P450 3A4Homo sapiens (human)
quinine 3-monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
testosterone 6-beta-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
1-alpha,25-dihydroxyvitamin D3 23-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 8,9 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 11,12 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 14,15 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
aromatase activityCytochrome P450 3A4Homo sapiens (human)
vitamin D 24-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
estrogen 16-alpha-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
estrogen 2-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
1,8-cineole 2-exo-monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
lactase activityLactase-phlorizin hydrolaseHomo sapiens (human)
galactosylceramidase activityLactase-phlorizin hydrolaseHomo sapiens (human)
glucosylceramidase activityLactase-phlorizin hydrolaseHomo sapiens (human)
beta-glucosidase activityLactase-phlorizin hydrolaseHomo sapiens (human)
glycosylceramidase activityLactase-phlorizin hydrolaseHomo sapiens (human)
protein homodimerization activityLactase-phlorizin hydrolaseHomo sapiens (human)
cellobiose glucosidase activityLactase-phlorizin hydrolaseHomo sapiens (human)
phlorizin hydrolase activityLactase-phlorizin hydrolaseHomo sapiens (human)
alpha-1,4-glucosidase activityLysosomal alpha-glucosidaseHomo sapiens (human)
carbohydrate bindingLysosomal alpha-glucosidaseHomo sapiens (human)
maltose alpha-glucosidase activityLysosomal alpha-glucosidaseHomo sapiens (human)
alpha-glucosidase activityLysosomal alpha-glucosidaseHomo sapiens (human)
oligo-1,6-glucosidase activitySucrase-isomaltase, intestinalHomo sapiens (human)
sucrose alpha-glucosidase activitySucrase-isomaltase, intestinalHomo sapiens (human)
protein bindingSucrase-isomaltase, intestinalHomo sapiens (human)
carbohydrate bindingSucrase-isomaltase, intestinalHomo sapiens (human)
alpha-1,4-glucosidase activitySucrase-isomaltase, intestinalHomo sapiens (human)
glycogen debranching enzyme activityGlycogen debranching enzymeHomo sapiens (human)
4-alpha-glucanotransferase activityGlycogen debranching enzymeHomo sapiens (human)
amylo-alpha-1,6-glucosidase activityGlycogen debranching enzymeHomo sapiens (human)
protein bindingGlycogen debranching enzymeHomo sapiens (human)
polysaccharide bindingGlycogen debranching enzymeHomo sapiens (human)
polyubiquitin modification-dependent protein bindingGlycogen debranching enzymeHomo sapiens (human)
beta-maltose 4-alpha-glucanotransferase activityGlycogen debranching enzymeHomo sapiens (human)
protein bindingCeramide glucosyltransferaseHomo sapiens (human)
ceramide glucosyltransferase activityCeramide glucosyltransferaseHomo sapiens (human)
dihydroceramide glucosyltransferase activityCeramide glucosyltransferaseHomo sapiens (human)
galactosylceramidase activityNon-lysosomal glucosylceramidaseHomo sapiens (human)
glucosylceramidase activityNon-lysosomal glucosylceramidaseHomo sapiens (human)
beta-glucosidase activityNon-lysosomal glucosylceramidaseHomo sapiens (human)
glucosyltransferase activityNon-lysosomal glucosylceramidaseHomo sapiens (human)
steryl-beta-glucosidase activityNon-lysosomal glucosylceramidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (29)

Processvia Protein(s)Taxonomy
plasma membraneMaltase-glucoamylase, intestinalHomo sapiens (human)
apical plasma membraneMaltase-glucoamylase, intestinalHomo sapiens (human)
extracellular exosomeMaltase-glucoamylase, intestinalHomo sapiens (human)
tertiary granule membraneMaltase-glucoamylase, intestinalHomo sapiens (human)
ficolin-1-rich granule membraneMaltase-glucoamylase, intestinalHomo sapiens (human)
lysosomeLysosomal acid glucosylceramidaseHomo sapiens (human)
lysosomal membraneLysosomal acid glucosylceramidaseHomo sapiens (human)
endoplasmic reticulumLysosomal acid glucosylceramidaseHomo sapiens (human)
Golgi apparatusLysosomal acid glucosylceramidaseHomo sapiens (human)
trans-Golgi networkLysosomal acid glucosylceramidaseHomo sapiens (human)
lysosomal lumenLysosomal acid glucosylceramidaseHomo sapiens (human)
extracellular exosomeLysosomal acid glucosylceramidaseHomo sapiens (human)
cytoplasmCytochrome P450 3A4Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 3A4Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 3A4Homo sapiens (human)
plasma membraneLactase-phlorizin hydrolaseHomo sapiens (human)
external side of apical plasma membraneLactase-phlorizin hydrolaseHomo sapiens (human)
lysosomeLysosomal alpha-glucosidaseHomo sapiens (human)
lysosomal membraneLysosomal alpha-glucosidaseHomo sapiens (human)
plasma membraneLysosomal alpha-glucosidaseHomo sapiens (human)
membraneLysosomal alpha-glucosidaseHomo sapiens (human)
azurophil granule membraneLysosomal alpha-glucosidaseHomo sapiens (human)
lysosomal lumenLysosomal alpha-glucosidaseHomo sapiens (human)
intracellular membrane-bounded organelleLysosomal alpha-glucosidaseHomo sapiens (human)
extracellular exosomeLysosomal alpha-glucosidaseHomo sapiens (human)
tertiary granule membraneLysosomal alpha-glucosidaseHomo sapiens (human)
ficolin-1-rich granule membraneLysosomal alpha-glucosidaseHomo sapiens (human)
autolysosome lumenLysosomal alpha-glucosidaseHomo sapiens (human)
Golgi apparatusSucrase-isomaltase, intestinalHomo sapiens (human)
plasma membraneSucrase-isomaltase, intestinalHomo sapiens (human)
brush borderSucrase-isomaltase, intestinalHomo sapiens (human)
apical plasma membraneSucrase-isomaltase, intestinalHomo sapiens (human)
extracellular exosomeSucrase-isomaltase, intestinalHomo sapiens (human)
extracellular regionGlycogen debranching enzymeHomo sapiens (human)
nucleusGlycogen debranching enzymeHomo sapiens (human)
cytoplasmGlycogen debranching enzymeHomo sapiens (human)
cytosolGlycogen debranching enzymeHomo sapiens (human)
inclusion bodyGlycogen debranching enzymeHomo sapiens (human)
sarcoplasmic reticulumGlycogen debranching enzymeHomo sapiens (human)
secretory granule lumenGlycogen debranching enzymeHomo sapiens (human)
ficolin-1-rich granule lumenGlycogen debranching enzymeHomo sapiens (human)
isoamylase complexGlycogen debranching enzymeHomo sapiens (human)
Golgi membraneCeramide glucosyltransferaseHomo sapiens (human)
membraneCeramide glucosyltransferaseHomo sapiens (human)
Golgi membraneNon-lysosomal glucosylceramidaseHomo sapiens (human)
endoplasmic reticulum membraneNon-lysosomal glucosylceramidaseHomo sapiens (human)
smooth endoplasmic reticulumNon-lysosomal glucosylceramidaseHomo sapiens (human)
cytosolNon-lysosomal glucosylceramidaseHomo sapiens (human)
plasma membraneNon-lysosomal glucosylceramidaseHomo sapiens (human)
membraneNon-lysosomal glucosylceramidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (70)

Assay IDTitleYearJournalArticle
AID466856Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as reduction in HbA1c at 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466668Inhibition of maltase by HPLC2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466863Mean residence time in ZDE/Crl-leprfa rat at 3 mg/kg, iv2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID437998Inhibition of Bacillus stearothermophilus alpha glucosidase2009Bioorganic & medicinal chemistry letters, Dec-01, Volume: 19, Issue:23
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors.
AID626356Inhibition of GCS activity in human A549 cells assessed as amount of GM1 on the cell membrane after 72 hrs by FL-CTB-based fluorescent microscopy2011Bioorganic & medicinal chemistry letters, Nov-15, Volume: 21, Issue:22
Discovery of a new class of glucosylceramide synthase inhibitors.
AID466860AUC (infinity) in ZDE/Crl-leprfa rat at 3 mg/kg, iv2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID437999Inhibition of sweet almond beta glucosidase2009Bioorganic & medicinal chemistry letters, Dec-01, Volume: 19, Issue:23
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors.
AID466853Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as reduction in blood insulin at 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID437996Inhibition of rice alpha glucosidase2009Bioorganic & medicinal chemistry letters, Dec-01, Volume: 19, Issue:23
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors.
AID699186Inhibition of GCS in C57/B6 mouse assessed as decrease in liver GM3 level at 25 mg/kg, po qd for 4 days measured 4 hrs post last dose by HPLC analysis2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Discovery and characterization of an inhibitor of glucosylceramide synthase.
AID466858Dose normalized Cmax in ZDE/Crl-leprfa rat at 3 mg/kg, iv2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466868Antidiabetic activity in ZDF rat assessed as improvement in HbA1c levels at 20 to 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID1596612Cytotoxicity against human CuFi1 cells assessed as reduction in cell viability incubated for 48 hrs by Muse cell analyser method2019European journal of medicinal chemistry, Aug-01, Volume: 175Exploring the effect of chirality on the therapeutic potential of N-alkyl-deoxyiminosugars: anti-inflammatory response to Pseudomonas aeruginosa infections for application in CF lung disease.
AID466666Inhibition of GCS by cell-based assay2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID1596606Inhibition of NLGase in human SH-SY5Y cells at 1 nM to 1 mM using MUG-Gluc as fluorogenic substrate preincubated for 30 mins followed by substrate addition and measured after 2 hrs in presence of AMP-DNM by fluorescence based assay relative to control2019European journal of medicinal chemistry, Aug-01, Volume: 175Exploring the effect of chirality on the therapeutic potential of N-alkyl-deoxyiminosugars: anti-inflammatory response to Pseudomonas aeruginosa infections for application in CF lung disease.
AID553253Inhibition of recombinant GBA1 preincubated with compound for 30 mins using 4-methylumbelliferyl-B-glucoside substrate by fluorimetric assay2011ACS medicinal chemistry letters, Feb-10, Volume: 2, Issue:2
Identification of potent and selective glucosylceramide synthase inhibitors from a library of N-alkylated iminosugars.
AID1596608Anti-inflammatory activity in human CuFi1 cells assessed as reduction in Pseudomonas aeruginosa PAO1-induced IL-8 mRNA expression level pretreated for 1 hr followed by Pseudomonas aeruginosa PAO1 challenge and measured after 4 hrs by RT-PCR analysis2019European journal of medicinal chemistry, Aug-01, Volume: 175Exploring the effect of chirality on the therapeutic potential of N-alkyl-deoxyiminosugars: anti-inflammatory response to Pseudomonas aeruginosa infections for application in CF lung disease.
AID466852Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as reduction in blood glucose at 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466870Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as blood glucose AUC at 100 mg/kg/day, po treated for 6 weeks administered 1 g/kg sucrose treatment at end of week 4 followed by 0.5 g/kg glucose treatment at end of week 6 measured2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466869Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as blood glucose AUC at 100 mg/kg/day, po treated for 4 weeks followed by 1 g/kg sucrose treatment after last dose measured after 1 hr after sucrose challenge (Rvb=1325+/-210 mM.min2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466670Inhibition of GBA1 by HPLC2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID437994Inhibition of human GBA22009Bioorganic & medicinal chemistry letters, Dec-01, Volume: 19, Issue:23
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors.
AID437995Inhibition of human lysosomal alpha glucosidase2009Bioorganic & medicinal chemistry letters, Dec-01, Volume: 19, Issue:23
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors.
AID553255Inhibition of sucrase in mouse intestinal input by glucose release assay2011ACS medicinal chemistry letters, Feb-10, Volume: 2, Issue:2
Identification of potent and selective glucosylceramide synthase inhibitors from a library of N-alkylated iminosugars.
AID466864Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as reduction in liver glycosphingolipids at 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466673Inhibition of glycogen glycogen de-branching enzyme by HPLC2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466867Antidiabetic activity in ZDF rat assessed as improvement in blood glucose concentration at 20 to 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID1596611Induction of apoptosis in human CuFi1 cells incubated for 48 hrs by Muse Annexin V based cell counter assay2019European journal of medicinal chemistry, Aug-01, Volume: 175Exploring the effect of chirality on the therapeutic potential of N-alkyl-deoxyiminosugars: anti-inflammatory response to Pseudomonas aeruginosa infections for application in CF lung disease.
AID466862Bioavailability in ZDE/Crl-leprfa rat at 3 mg/kg, iv2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466674Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as reduction in plasma glycosphingolipids at 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466672Inhibition of lysosomal alpha-glucosidase by HPLC2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID1166039Inhibition of GBA2 (unknown origin)2014Journal of medicinal chemistry, Nov-13, Volume: 57, Issue:21
Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors.
AID699187Inhibition of GCS in C57/B6 mouse assessed as decrease in liver lactosylceramide level at 25 mg/kg, po qd for 4 days measured 4 hrs post last dose by HPLC analysis2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Discovery and characterization of an inhibitor of glucosylceramide synthase.
AID466859Half life in ZDE/Crl-leprfa rat at 3 mg/kg, iv2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID553256Inhibition of lactase in mouse intestinal input by glucose release assay2011ACS medicinal chemistry letters, Feb-10, Volume: 2, Issue:2
Identification of potent and selective glucosylceramide synthase inhibitors from a library of N-alkylated iminosugars.
AID699189Inhibition of GCS in C57/B6 mouse assessed as decrease in liver ceramide level at 25 mg/kg, po qd for 4 days measured 4 hrs post last dose by HPLC analysis2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Discovery and characterization of an inhibitor of glucosylceramide synthase.
AID699203Inhibition of GCS assessed as amount of UDP glucose after 3 hrs by Fluorometry analysis2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Discovery and characterization of an inhibitor of glucosylceramide synthase.
AID466855Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as insulin resistance at 100 mg/kg/day for 4 weeks by HOMA-IR analysis2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID553254Inhibition of recombinant GBA2 preincubated with compound for 30 mins using 4-methylumbelliferyl-B-glucoside substrate by fluorimetric assay2011ACS medicinal chemistry letters, Feb-10, Volume: 2, Issue:2
Identification of potent and selective glucosylceramide synthase inhibitors from a library of N-alkylated iminosugars.
AID466667Inhibition of sucrase by HPLC2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID1596603Inhibition of GCase in human SH-SY5Y cells using MUG-Gluc as fluorogenic substrate preincubated for 30 mins followed by substrate addition and measured after 2 hrs in presence of conduritol B epoxide by fluorescence based assay2019European journal of medicinal chemistry, Aug-01, Volume: 175Exploring the effect of chirality on the therapeutic potential of N-alkyl-deoxyiminosugars: anti-inflammatory response to Pseudomonas aeruginosa infections for application in CF lung disease.
AID626355Inhibition of GCS assessed as amount of UDP-glucose consumed during enzyme-catalyzed reaction2011Bioorganic & medicinal chemistry letters, Nov-15, Volume: 21, Issue:22
Discovery of a new class of glucosylceramide synthase inhibitors.
AID1596605Inhibition of NLGase in human SH-SY5Y cells using MUG-Gluc as fluorogenic substrate preincubated for 30 mins followed by substrate addition and measured after 2 hrs in presence of AMP-DNM by fluorescence based assay2019European journal of medicinal chemistry, Aug-01, Volume: 175Exploring the effect of chirality on the therapeutic potential of N-alkyl-deoxyiminosugars: anti-inflammatory response to Pseudomonas aeruginosa infections for application in CF lung disease.
AID700849Activation of Beta-glucocerebrosidase G202R mutant in cell based assay2011European journal of medicinal chemistry, Jun, Volume: 46, Issue:6
The many faces of the adamantyl group in drug design.
AID1166041Inhibition of intestinal lactase (unknown origin)2014Journal of medicinal chemistry, Nov-13, Volume: 57, Issue:21
Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors.
AID699188Inhibition of GCS in C57/B6 mouse assessed as decrease in liver glucosylceramide level at 25 mg/kg, po qd for 4 days measured 4 hrs post last dose by HPLC analysis2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Discovery and characterization of an inhibitor of glucosylceramide synthase.
AID652572Inhibition of recombinant glucosylceramidase 1 using 4-methylumbelliferyl-B-glucoside as substrate by fluorimetric analysis2011ACS medicinal chemistry letters, Jul-14, Volume: 2, Issue:7
Assessment of partially deoxygenated deoxynojirimycin derivatives as glucosylceramide synthase inhibitors.
AID1166037Inhibition of glucosylceramide synthase (unknown origin) assessed as catabolism of NBD-glucosylceramide2014Journal of medicinal chemistry, Nov-13, Volume: 57, Issue:21
Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors.
AID466865Antidiabetic activity in ZDF rat assessed as reduction in plasma glycosphingolipids at 20 to 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID553258Selectivity index, ratio of IC50 for recombinant GBA1 to IC50 for glucosylceramide synthase in mouse RAW cells2011ACS medicinal chemistry letters, Feb-10, Volume: 2, Issue:2
Identification of potent and selective glucosylceramide synthase inhibitors from a library of N-alkylated iminosugars.
AID699202Inhibition of GCS in human A549 cells assessed as decrease in GM1 synthesis after 72 hrs by Fluorescence assay2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Discovery and characterization of an inhibitor of glucosylceramide synthase.
AID1166042Inhibition of intestinal maltase (unknown origin)2014Journal of medicinal chemistry, Nov-13, Volume: 57, Issue:21
Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors.
AID1596604Inhibition of GCase in human SH-SY5Y cells at 1 nM to 1 mM using MUG-Gluc as fluorogenic substrate preincubated for 30 mins followed by substrate addition and measured after 2 hrs in presence of conduritol B epoxide by fluorescence based assay relative to2019European journal of medicinal chemistry, Aug-01, Volume: 175Exploring the effect of chirality on the therapeutic potential of N-alkyl-deoxyiminosugars: anti-inflammatory response to Pseudomonas aeruginosa infections for application in CF lung disease.
AID466857Cmax in ZDE/Crl-leprfa rat at 3 mg/kg, iv2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466669Inhibition of lactase by HPLC2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID1166040Inhibition of intestinal sucrase (unknown origin)2014Journal of medicinal chemistry, Nov-13, Volume: 57, Issue:21
Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors.
AID466866Antidiabetic activity in ZDF rat assessed as reduction in liver glycosphingolipids at 20 to 100 mg/kg/day for 4 weeks2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID437993Inhibition of human GBA12009Bioorganic & medicinal chemistry letters, Dec-01, Volume: 19, Issue:23
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors.
AID437997Inhibition of Saccharomyces cerevisiae alpha glucosidase2009Bioorganic & medicinal chemistry letters, Dec-01, Volume: 19, Issue:23
Synthesis and evaluation of D-gluco-pyranocyclopropyl amines as potential glucosidase inhibitors.
AID700851Inhibition of non-lysosomal glucosylceramidase in cultured melanoma cells2011European journal of medicinal chemistry, Jun, Volume: 46, Issue:6
The many faces of the adamantyl group in drug design.
AID700850Activation of Beta-glucocerebrosidase N370S mutant in cell based assay2011European journal of medicinal chemistry, Jun, Volume: 46, Issue:6
The many faces of the adamantyl group in drug design.
AID466854Antidiabetic activity in obese, insulin resistant C57BL/6J mouse assessed as increase in glucose tolerance at 100 mg/kg/day for 4 weeks by OGTT2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID700852Inhibition of non-lysosomal glucosylceramidase2011European journal of medicinal chemistry, Jun, Volume: 46, Issue:6
The many faces of the adamantyl group in drug design.
AID1166038Inhibition of GBA1 (unknown origin) using beta-D-[1-14C]glucocerebroside assessed as 4-methylumbelliferrone by fluorimetry2014Journal of medicinal chemistry, Nov-13, Volume: 57, Issue:21
Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors.
AID553257Inhibition of maltase in mouse intestinal input by glucose release assay2011ACS medicinal chemistry letters, Feb-10, Volume: 2, Issue:2
Identification of potent and selective glucosylceramide synthase inhibitors from a library of N-alkylated iminosugars.
AID553252Inhibition of glucosylceramide synthase in mouse RAW cells preincubated with compound for 15 mins by in-situ enzyme inhibition assay2011ACS medicinal chemistry letters, Feb-10, Volume: 2, Issue:2
Identification of potent and selective glucosylceramide synthase inhibitors from a library of N-alkylated iminosugars.
AID652571Inhibition of glucosylceramide synthase in mouse RAW cells preincubated for 15 mins followed by substrate addition and measured after 1 hr by fluorescence scanner2011ACS medicinal chemistry letters, Jul-14, Volume: 2, Issue:7
Assessment of partially deoxygenated deoxynojirimycin derivatives as glucosylceramide synthase inhibitors.
AID466861Dose normalized AUC (infinity) in ZDE/Crl-leprfa rat at 3 mg/kg, iv2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID466671Inhibition of GBA2 by HPLC2010Journal of medicinal chemistry, Jan-28, Volume: 53, Issue:2
Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.
AID652573Inhibition of glucosylceramidase 2 from spleen of patient with gaucher's disease by fluorimetric analysis2011ACS medicinal chemistry letters, Jul-14, Volume: 2, Issue:7
Assessment of partially deoxygenated deoxynojirimycin derivatives as glucosylceramide synthase inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (11.11)29.6817
2010's8 (88.89)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.70

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.70 (24.57)
Research Supply Index2.30 (2.92)
Research Growth Index5.00 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.70)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (11.11%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (88.89%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]