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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 986 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 986 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

Adrenergic Receptor
AChR
5-HT Receptor
Dopamine Receptor
Autophagy
PDE
Apoptosis
GABA Receptor
iGluR
Endogenous Metabolite
NMDAR
Beta Amyloid
AChE
Histamine Receptor
GSK-3
GluR
Gamma-secretase
PPAR
Potassium Channel
Antibacterial
Norepinephrine
Calcium Channel
Serotonin Transporter
Sodium Channel
HIV Protease
Adenosine Receptor
MAO
Influenza Virus
P450
Monoamine Oxidase
NF-κB
CDK
COX
BACE
Ferroptosis
Cannabinoid Receptor
Parasite
Beta-Secretase
TNF
Mitophagy
Reactive Oxygen Species
Nrf2
JNK
Antifungal
CaMK
Antibiotic
Microtubule Associated
Antioxidant
Virus Protease
Caspase
ERK
IL Receptor
P-gp
HDAC
Anti-infection
Src
Estrogen/progestogen Receptor
Transferase
Dehydrogenase
PKA
Wnt/beta-catenin
Drug Metabolite
Opioid Receptor
Epigenetic Reader Domain
Akt
HMG-CoA Reductase
NO Synthase
Phospholipase
c-Kit
Tyrosinase
Phosphatase
Amino Acids and Derivatives
PI3K
Estrogen Receptor/ERR
PARP
VEGFR
TRP/TRPV Channel
Glucocorticoid Receptor
Mitochondrial Metabolism
PKC
BCL
HSV
MMP
Lipoxygenase
EGFR
Sirtuin
CCR
Trk receptor
IκB/IKK
c-Fms
AMPK
MEK
FLT
Sigma receptor
HIF/HIF Prolyl-Hydroxylase
Imidazoline Receptor
Chloride channel
Carbonic Anhydrase
Histone Methyltransferase
RAAS
advanced glycation end products
p38 MAPK
Raf
MRP
CSF-1R
Immunology/Inflammation related
Monoamine Transporter
Guanylate cyclase
Aurora Kinase
Interleukin
TGF-beta/Smad
Acyltransferase
transporter
IGF-1R
mTOR
Antiviral
Prostaglandin Receptor
Histone Acetyltransferase
FGFR
Casein Kinase
Reverse Transcriptase
Retinoid Receptor
STAT
NOD
S6 Kinase
HER
Adenylyl cyclase
NOS
Transaminase
Monocarboxylate transporter
ROR
HCV Protease
DYRK
NADPH
Progesterone Receptor
Melatonin Receptor
ABC
Integrin
Na+/Ca2+ Exchanger
Histone Demethylase
Serine/threonin kinase
RANKL/RANK
IAP
Topoisomerase
Annexin A
Adiponectin receptor
UGT
Bcr-Abl
LDL
Rho
Hck
Cysteine Protease
Liver X Receptor
Nucleoside Antimetabolite/Analog
FXR
PAFR
GRK
MT Receptor
GlyT
BTK
Glucosidase
Stearoyl-CoA Desaturase (SCD)
Chk
Somatostatin
DNA/RNA Synthesis
SARS-CoV
TLR
Bombesin Receptor
PDGFR
PAD
Epoxide Hydrolase
Telomerase
MAPK
OAT
GluCls
ATM/ATR
GST
RSV
Aromatase
GPR
CRISPR/Cas9
HIF
Gap Junction Protein
Ras
FAK
NOD-like Receptor (NLR)
p53

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