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TargetMol | Compound Library

Anti-Alzheimer's Disease Compound Library

Catalog No. L9840

Alzheimer's disease (AD) is a progressive neurodegenerative disease with deficits in recent memory, wordfinding, and language difficulties, and gradually progresses to global cognitive impairment. The cognitive deficits are accompanied by a variety of abnormal neurological and psychiatric symptoms that increase in frequency and severity as the disease progresses. The cause of Alzheimer’s disease is unknown but the fifth-leading cause of death among those age 65 and older. The pathological features of AD mainly include cholinergic dysfunction, extracellular accumulation and deposition of Aβ peptides, intracellular neurofibrillary tangles, and other aberrant signaling pathways. Scientists have found that reducing brain Aβ levels, preventing the excessive phosphorylation of tau protein, rendering mitochondria resistant to damage, protecting neurons from apoptotic processes, controlling microglial activation, inhibiting the release of interleukin-2 and TNF-α, preventing oxidative stress damage; regulating the targets in cholinergic system, inhibiting the over activation of NMDA receptor to reduce the excitotoxicity can halt Alzheimer's disease.  Although Alzheimer’s disease (AD) is the world’s leading cause of dementia and the population of patients with AD continues to grow, no new therapies have been approved in more than a decade. Over the past decade, the focus of drug discovery and development efforts has shifted from symptom improving toward disease-modifying therapies for AD; that is, treatments whose aim is to affect the underlying disease process by impacting one or more of the many brain changes characteristic of AD. Many clinical trials of single-agent therapies have failed to affect disease progression or symptoms compared with placebo. The complex pathophysiology of AD may necessitate combination treatments rather than monotherapy. In addition, small molecules targeting neural stem cells (NSCs) regeneration represents a new drug discovery strategy. TargetMol’s Anti-Alzheimer’s Disease Compound Library, a collection of 1881 compounds with anti-AD activities or acting on main drug targets of AD, can be used for related drug discovery and pharmacology research.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.

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Catalog No. L9840

Anti-Alzheimer's Disease Compound Library

sizeIn stock

  • 1 mg
  • 30 μL x 10 mM (in DMSO)
  • 50 μL x 10 mM (in DMSO)
  • 100 μL x 10 mM (in DMSO)
  • 250 μL x 10 mM (in DMSO)
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Product Description Product Description

  • A unique collection of 1881 compounds with anti-AD activities or acting on main drug targets of AD can be used for HTS and HCS.
  • Targets include tau protein, γ Secretase, 5-HT Receptor, BACE, etc.
  • Some of them are FDA approved.?
  • Structurally diverse, medicinally active, and cell permeable;
  • Detailed information about compound structure, target, activity, IC50, etc.
  • NMR and HPLC/LCMS validated to ensure high purity and quality.

Packaging And Storage | TargetMol Packaging And Storage

  • Powder or pre-dissolved DMSO solutions in 96/384 well plate with optional 2D barcode
  • Shipped with blue ice

Library Customization | TargetMol Library Customization

Compound Library | TargetMol
Targetmol Compound Libraries
can be highly customized!
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Library Customization | TargetMol Library Composition

5-HT Receptor
AChR
Dopamine Receptor
PPAR
Wnt/beta-catenin
AChE
TNF
Apoptosis
Autophagy
GSK-3
AMPK
Histamine Receptor
TLR
Beta Amyloid
Adrenergic Receptor
Endogenous Metabolite
NF-κB
Gamma-secretase
Antibacterial
GABA Receptor
IL Receptor
COX
Serotonin Transporter
Norepinephrine
NOD
CDK
MAO
Parasite
Calcium Channel
Potassium Channel
BACE
P450
Sodium Channel
Antioxidant
Reactive Oxygen Species
Akt
Interleukin
Influenza Virus
Antibiotic
PARP
JAK
NO Synthase
p38 MAPK
Microtubule Associated
HIV Protease
ERK
iGluR
Beta-Secretase
PDE
TRP/TRPV Channel
Prostaglandin Receptor
NOD-like Receptor (NLR)
Monoamine Oxidase
Src
Ferroptosis
Virus Protease
GluR
STAT
Transferase
Antifungal
JNK
MMP
MAPK
Tyrosinase
NOS
Caspase
Drug Metabolite
Mitochondrial Metabolism
BCL
EGFR
transporter
Sigma receptor
PI3K
PKA
VEGFR
Lipoxygenase
CaMK
P-gp
SARS-CoV
Nrf2
HCV Protease
Dehydrogenase
Mitophagy
ABC
NMDAR
ROS
mTOR
Antiviral
Casein Kinase
Phospholipase
FGFR
Cannabinoid Receptor
FLT
Phosphatase
PKC
Immunology/Inflammation related
Bcr-Abl
P2X Receptor
Antifection
Molecular Glues
Opioid Receptor
Fatty Acid Synthase
PDGFR
CCR
Aurora Kinase
Epigenetic Reader Domain
DNA/RNA Synthesis
Porcupine
IκB/IKK
Ligand for E3 Ligase
HDAC
GPR
S6 Kinase
HER
Chloride channel
Adenylyl cyclase
DYRK
RAAS
Melatonin Receptor
HBV
Glucosidase
HSV
IGF-1R
TGF-beta/Smad
Sirtuin
MEK
HIF/HIF Prolyl-Hydroxylase
advanced glycation end products
Carbonic Anhydrase
Histone Methyltransferase
ADC Cytotoxin
MyD88
Adenosine Receptor
MRP
Cysteine Protease
Leukotriene Receptor
Glucocorticoid Receptor
Topoisomerase
E1/E2/E3 Enzyme
PAFR
LDL
MT Receptor
GlyT
Monoamine Transporter
Chk
cAMP
Lipid
Acyltransferase
Trk receptor
AIM2
ATM/ATR
Retinoid Receptor
c-Fms
c-Kit
p53
Melanin-concentrating Hormone Receptor (MCHR)
Proteasome
PROTACs
CAT
Transaminase
NPC1L1
DHFR
Piezo Channel
Dynamin
Integrin
Amino Acids and Derivatives
Estrogen/progestogen Receptor
YAP
Arginase
LTR
IFNAR
Arrestin
Histone Demethylase
PERK
Tie-2
gp120/CD4
GTPase
OCT
c-Myc
Estrogen Receptor/ERR
Tyrosine Kinases
Serine Protease
Hck
Serine/threonin kinase
FXR
Glucokinase
Amylase
Aryl Hydrocarbon Receptor
CSF-1R
SIK
Annexin A
FLAP
Raf
GRK
BTK
Bombesin Receptor
Stearoyl-CoA Desaturase (SCD)
PTEN
Somatostatin
Epoxide Hydrolase
ACK
DNA
Indoleamine 2,3-Dioxygenase (IDO)
Androgen Receptor
Telomerase
ATP Citrate Lyase
Huntingtin
Aminopeptidase
GluCls
PAI-1
RSV
Methionine Adenosyltransferase (MAT)
GST
Reverse Transcriptase
Aromatase
PDK
Hydroxylase
HIF
PLK
c-RET
Anti-infection
DNA Methyltransferase
NADPH-oxidase
cholecystokinin
Thrombin
FAK
CFTR
PKM

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