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TargetMol | Compound Library

High-Efficiency Gene Editing Small Molecule Library

Catalog No. L3910

In modern biomedical research, CRISPR-Cas technology has emerged as a mainstream tool for gene editing. Its high efficiency and programmability have enabled broad applications in gene therapy, crop improvement, functional genomics, and disease model development. However, several key challenges remain in practical applications of the CRISPR-Cas system, including off-target effects and limited editing efficiency. In particular, the low efficiency of homology-directed repair (HDR) in mammalian cells significantly hampers the implementation of precise gene edits, such as point mutations or gene knock-ins.
To address these limitations, researchers have been actively developing auxiliary tools to enhance the performance of the CRISPR-Cas system. This library includes a wide range of known DNA repair pathway modulators and potential regulatory molecules, particularly small molecules that inhibit the non-homologous end joining (NHEJ) pathway or promote the HDR pathway. Representative compounds include DNA-PK inhibitors, DNA ligase IV inhibitors, and RAD51 activators. The library features a diverse collection of synthetic compounds, natural products, and approved/clinical drugs, offering broad potential for application across various research and therapeutic contexts.

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

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Catalog No. L3910

High-Efficiency Gene Editing Small Molecule Library

size

  • 1 mg
  • 10 µL x 10 mM (in DMSO)
  • 20 µL x 10 mM (in DMSO)
  • 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

  • Offers 910 small molecules that enhance gene editing efficiency, suitable for high- throughput screening (HTS) and high- content screening (HCS);
  • The targets include DNA- PK、DNA ligase IV、RAD51 and others;
  • Structurally diverse, medicinally active, and cell permeable;
  • Rich documentation with structure, target, IC50 value and biological activity description;
  • NMR and HPLC/LCMS validated to ensure high purity.

Packaging And Storage Packaging And Storage

  • Powder or pre-dissolved DMSO solutions in 96/384 well plate with optional 2D barcode
  • Shipped with blue ice
  • This compound library is provided at a concentration of 10 mM in DMSO. A small number of compounds may be provided in different solvents or concentrations due to solubility or stability requirements. Please refer to the specific product information for details.

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Library Customization | TargetMol Library Composition

CDK
Apoptosis
HDAC
Histone Methyltransferase
Microtubule Associated
PARP
Autophagy
Sirtuin
DNA-PK
ATM/ATR
PI3K
DNA Methyltransferase
GSK-3
mTOR
Epigenetic Reader Domain
Caspase
Wnt/beta-catenin
Ras
Endogenous Metabolite
Antibacterial
Bcl-2 Family
HIV Protease
Parasite
ERK
DNA/RNA Synthesis
VEGFR
Src
JAK
FLT
Aurora Kinase
Virus Protease
PROTACs
DYRK
ROS
Chk
MAPK
NF-κB
CRISPR/Cas9
PKC
Casein Kinase
Mitophagy
PKA
Akt
Reactive Oxygen Species
Antibiotic
p38 MAPK
MDM-2/p53
Gamma-secretase
p53
Histone Demethylase
Beta Amyloid
S6 Kinase
Bcr-Abl
Kinesin
HIF/HIF Prolyl-Hydroxylase
Serine/threonin kinase
PDE
AChR
EGFR
Histone Acetyltransferase
Molecular Glues
Influenza Virus
FGFR
PPAR
Phosphatase
Topoisomerase
Nrf2
Tyrosine Kinases
HSV
Interleukin
AMPK
GABA Receptor
TNF
ADC Cytotoxin
Dehydrogenase
Pim
Adrenergic Receptor
Arp2/3 Complex
Cytochromes P450
STAT
SGK
IL Receptor
Trk receptor
PLK
Aryl Hydrocarbon Receptor
LRRK2
NO Synthase
Nucleoside Antimetabolite/Analog
Histamine Receptor
Cholecystokinin Receptor
Calcium Channel
DNA Alkylation
SARS-CoV
IκB/IKK
c-RET
c-Myc
HIF
Raf
COX
PDK
Anti-infection
PYK2
FAK
Antifungal
Serine Protease
Angiotensin-converting Enzyme (ACE)
MMP
DUB
c-Fms
PI4K
Potassium Channel
OXPHOS
P-gp
Tyrosinase
Carbonic Anhydrase
Antioxidant
HBV
NR4A
PDGFR
JNK
c-Met/HGFR
Adenosine Receptor
Reverse Transcriptase
Sodium Channel
NOD
IRAK
ROCK
Antiviral
5-HT Receptor
MEK
Amino Acids and Derivatives
Ligands for Target Protein for PROTAC
LIM Kinase
Immunology/Inflammation related
PAFR
Haspin Kinase
Glucagon Receptor
NMDAR
Syk
NOS
HCV Protease
MyD88
DNA Alkylator/Crosslinker
STING
TLR
Free radical scavengers
Pyroptosis
Retinoid Receptor
MLK
ATPase
PERK
IAP
Endonuclease
Monoamine Transporter
PROTAC Linker
CCR
Cholinesterase (ChE)
glycosidase
IGF-1R
CFTR
HER
Proteasome
RAAS
TOPK
Glucosidase
Hedgehog/Smoothened
TGF-beta/Smad
HSP
Phospholipase
Mdm2
Ferroptosis
Rho
Liver X Receptor
PAK
Lipoxygenase
ALK
MELK
Carboxypeptidase
PD-1/PD-L1
Transferase
BACE
IDO
Telomerase
c-Kit
Estrogen/progestogen Receptor
Antifolate
Adenylate cyclase
RIP kinase
UGT
Drug Metabolite
Antifection
Fatty Acid Synthase
PAD
Indoleamine 2,3-Dioxygenase (IDO)
Aminopeptidase
Methionine Adenosyltransferase (MAT)
DAPK
Drug-Linker Conjugates for ADC

Keywords