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TargetMol | Compound Library

Bioactive Compounds Library Max

Catalog No. L4010

Bioactive Compound Library Max is a collection of 26421 compounds with biological activity that elicit biological responses in cells, tissues and even individuals. It includes drug molecules that are in preclinical studies, clinical-phase studies and those that are already on the market. With clear targets and comprehensive information, it is ideal for drug repurposing, cell induction and differentiation, and protein target identification in biochemical mechanistic studies.

Because of the clear activity and known targets, many scientists will select small molecules from the Bioactive Compound Library that can be used for cell induction and differentiation. By the combined actions of a single or several small molecules, molecules capable of inducing various somatic cells into induced pluripotent stem cells, neural precursor cells, cardiomyocytes, etc. have been screened; there have even been successful trials of induced differentiation in vivo using combinations of small molecules.

The Bioactive Compound Library Max is a more extensive version of the Bioactive Compound Library (L4000), with the addition of TargetMol's unique and novel compounds (Part B), all of which have clear targets and have been tested for activity at the cellular level. Therefore, it has more novel structures than approved drug libraries and leads to easier active compounds discovery than drug-like compound libraries.

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

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Catalog No. L4010

Bioactive Compounds Library Max

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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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.

Product Description Product Description

  • A collection of 26421 bioactive compounds for high-throughput screening, high-content screening, cell induction and target identification.
  • All compounds are described with corresponding target information, which makes activity studies more evidence-based.
  • An effective tool for drug repurposing and cell-induced target screening.
  • Covers multiple areas of disease studies, such as cancer, metabolism, immune system and cardiovascular system.
  • Detailed instructions, compound structures, target information, activity descriptions, etc.
  • Structural diversity, significant drug potency and cell penetration.

Advantages Introduction Advantages Introduction

High-Standard Entry Criteria

TargetMol's Bioactive Compounds Library Max is established upon rigorous entry standards to ensure that every compound included is structurally well-defined and of exceptional purity, verified through multiple analytical techniques such as NMR, HPLC, and LC-MS. Our multi-layered screening mechanism effectively eliminates compounds with ambiguous structures, such as mixtures and polymers. Moreover, we specifically exclude substances like sunscreens, contrast agents, dyes, fragrances, plastic additives, and intermediates—compounds typically lacking biological activity due to their specificity and stability, which generally prevent interactions with biological systems. This meticulous curation reduces time and resource waste caused by ineffective screenings. To further enhance hit rates in activity screening, we have introduced TargetMol’s exclusive novel compounds (Part B), all of which have well-defined targets and have undergone activity testing at both cellular and protein levels.

Significant Structural Diversity

TargetMol’s Bioactive Compounds Library Max features extensive scaffold diversity and structural complexity, offering a substantial advantage in drug discovery. Based on the Bemis-Murcko scaffold classification, our library is categorized into 15,111 unique classes, each representing a distinct molecular scaffold, thereby extensively covering a broad chemical space. The compounds range from simple to highly complex structures, providing a diverse foundation for identifying lead compounds with strong affinity and specificity toward target proteins. This structural richness significantly advances pharmaceutical innovation. Whether targeting traditional drug targets or emerging, more challenging ones, our Bioactive Compounds Library Max offers a wealth of candidate molecules to accelerate the drug development process.

 Bioactive Compounds Library Max
Library Diversity Analysis

Superior Drug-Like Properties

73% of the compounds in TargetMol's Bioactive Compounds Library Max comply with Lipinski’s "Rule of Five" (Ro5), indicating excellent bioavailability and permeability.

 Bioactive Compounds Library Max  Bioactive Compounds Library Max
 Bioactive Compounds Library Max  Bioactive Compounds Library Max
 Bioactive Compounds Library Max  Bioactive Compounds Library Max

Multidimensional Pharmacokinetic Analysis

A multidimensional evaluation is conducted on TargetMol’s Bioactive Compounds Library Max, which systematically analyzes three key pharmacological parameters: blood-brain barrier permeability, cardiotoxicity (HERG K+ channel inhibition), and oral absorption performance.

 Bioactive Compounds Library Max  Bioactive Compounds Library Max  Bioactive Compounds Library Max

15% of the compounds can cross the blood-brain barrier, while 85% cannot.
58% of the compounds exhibit cardiotoxicity, while 42% do not.
60% of the compounds are highly orally absorbable, 28% are orally absorbable, and 12% are poorly orally absorbable.

Diverse Compound Collection

TargetMol’s Bioactive Compounds Library Max encompasses a wide range of molecule types with diverse biological activities. This includes approved drugs, clinical trial candidates, literature-reported bioactive compounds, and molecules capable of eliciting responses at the cellular, tissue, or even whole-organism level. The library covers not only major signaling pathways and targets but also many emerging therapeutic targets. The Bioactive Compounds Library Max (L4010) is established upon the classic L4000 library by adding approximately 300 new targets, bringing the total to nearly 900 targets across about 4,000 receptors. This significantly enhances the likelihood of successful screening hits. The library spans a broad spectrum of therapeutic areas, including cancer, cardiovascular diseases, and neurological disorders.

 Bioactive Compounds Library Max  Bioactive Compounds Library Max
 Bioactive Compounds Library Max  Bioactive Compounds Library Max

Regular Updates to Compound Libraries

We ensure our compound libraries remain at the forefront of scientific research by regularly updating our database with compounds mentioned in cutting-edge literature and newly custom-synthesized compounds.

Flexible Packaging Options

We offer a variety of standard packaging sizes (e.g., 30 μL, 50 μL, 100 μL, 250 μL, 1 mg), and we can customize packaging solutions to meet specific needs.

Customized Services

To support specific needs, we offer tailored screening services, including the design and synthesis of customized compound libraries and the execution of personalized screening projects. Our highly flexible service model is designed to efficiently meet unique needs of scientists and accelerate breakthrough discoveries.

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Apoptosis
Antibacterial
Endogenous Metabolite
Autophagy
Antibiotic
5-HT Receptor
AChR
Antifungal
Adrenergic Receptor
Parasite
DNA/RNA Synthesis
NF-κB
COX
Dopamine Receptor
CDK
Calcium Channel
Potassium Channel
HIV Protease
Antioxidant
PI3K
EGFR
Histamine Receptor
Cytochromes P450
Dehydrogenase
Epigenetic Reader Domain
Sodium Channel
PDE
GABA Receptor
Reactive Oxygen Species
VEGFR
GluR
Histone Methyltransferase
PPAR
TRP/TRPV Channel
Influenza Virus
Microtubule Associated
HDAC
TNF
Wnt/beta-catenin
Cholinesterase (ChE)
Phosphatase
JAK
Akt
Topoisomerase
GPCR
mTOR
p38 MAPK
Prostaglandin Receptor
Estrogen/progestogen Receptor
SARS-CoV
Antiviral
ERK
Ferroptosis
Src
NMDAR
PKC
FLT
HCV Protease
IL Receptor
RAAS
Estrogen Receptor/ERR
PARP
Adenosine Receptor
STAT
Nucleoside Antimetabolite/Analog
iGluR
Caspase
PDGFR
AMPK
Opioid Receptor
FGFR
MMP
Glucocorticoid Receptor
NO Synthase
Virus Protease
Androgen Receptor
Bcl-2 Family
GSK-3
ROS
Raf
MAO
Lipoxygenase
TLR
c-Kit
HSP
ATPase
Cannabinoid Receptor
Bcr-Abl
ALK
Beta Amyloid
c-Met/HGFR
Phospholipase
HBV
Proteasome
TGF-beta/Smad
Tyrosinase
Mitochondrial Metabolism
Sirtuin
MAPK
Drug Metabolite
HSV
Nrf2
HIF/HIF Prolyl-Hydroxylase
Anti-infection
Histone Demethylase
Ras
DUB
Integrin
NOS
JNK
p53
Aurora Kinase
Antifection
Mitophagy
PKA
Tyrosine Kinases
CCR
E1/E2/E3 Enzyme
P-gp
PROTACs
ROCK
Transferase
MEK
Carbonic Anhydrase
Casein Kinase
Gamma-secretase
HIF
Immunology/Inflammation related
IκB/IKK
Monoamine Oxidase
Cysteine Protease
Reverse Transcriptase
Interleukin
Retinoid Receptor
S1P Receptor
Norepinephrine
CXCR
RIP kinase
Serotonin Transporter
P2X Receptor
Serine/threonin kinase
Reductase
Serine Protease
Glucosidase
IGF-1R
c-RET
Neurokinin receptor
FAK
LPL Receptor
DNA-PK
Hedgehog/Smoothened
NOD
Histone Acetyltransferase
TAM Receptor
Sigma receptor
ATM/ATR
CaMK
FAAH
Fatty Acid Synthase
Glucokinase
S6 Kinase
PERK
Trk receptor
HER
transporter
c-Fms
Chloride channel
NADPH
Progesterone Receptor
Proton pump
ribosome
Amino Acids and Derivatives
CFTR
DPP-4
PLK
Syk
Acyltransferase
HMG-CoA Reductase
Pim
DNA Methyltransferase
Endothelin Receptor
Mdm2
Thrombin
Chk
DNA
Glucagon Receptor
Protease-activated Receptor
Rho
cAMP
Kinesin
LTR
AhR
Aryl Hydrocarbon Receptor
DHFR
Neuropeptide Y Receptor
P2Y Receptor
Cholecystokinin Receptor
DNA Alkylator/Crosslinker
FXR
IRAK
PD-1/PD-L1
ROR
Smo
STING
Thyroid hormone receptor(THR)
Leukotriene Receptor
Lipase
LPA Receptor
ADC Cytotoxin
BACE
Complement System
Hydroxylase
LRRK2
MRP
PDK
SGLT
Xanthine Oxidase
YAP
BTK
DYRK
Factor Xa
Glutathione Peroxidase
Guanylate cyclase
Indoleamine 2,3-Dioxygenase (IDO)
OX Receptor
c-Myc
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Epoxide Hydrolase
Platelet aggregation
Vasopressin Receptor
Liver X Receptor
Kras
Aromatase
IAP
PAK
RSV
Ephrin Receptor
IRE1
Ligand for E3 Ligase
NOD-like Receptor (NLR)
PGE Synthase
ROS Kinase
Antifolate
GTPase
Myosin
ABC Transporter
Bradykinin Receptor
CSF-1R
GHSR
LDL
Melanocortin Receptor
Molecular Glues
PI4K
Telomerase
Acetyl-CoA Carboxylase
Beta-Secretase
GPCR19
Lipid
Monoamine Transporter
Neurotensin Receptor
Aminopeptidase
Free radical scavengers
MicroRNA
Monocarboxylate transporter
NADPH-oxidase
PAI-1
Discoidin Domain Receptor (DDR)
DNA gyrase
Glutaminase
GNRH Receptor
IDO
PAFR
Somatostatin
Stearoyl-CoA Desaturase (SCD)
Arrestin
CaSR
CETP
GPX
GRK
IFNAR
Isocitrate Dehydrogenase (IDH)
Ligands for Target Protein for PROTAC
MNK
NAMPT
Phosphorylase
PKM
BCRP
Imidazoline Receptor
Melatonin Receptor
MLK
Neprilysin
OAT
UGT
Angiotensin-converting Enzyme (ACE)
Arginase
ATP Citrate Lyase
Dynamin
LIM Kinase
MT Receptor
Porcupine
SGK
Wee1
AAK1
Adenylyl Cyclase
APC/C
Apelin receptor
ASK
Bombesin Receptor
Carboxypeptidase
Gap Junction Protein
GlyT
GST
Na+/Ca2+ Exchanger
OCT
PAD
Protease
PTEN
SIK
Tie-2
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cGAS
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CRFR
MAGL
Melanin-concentrating Hormone Receptor (MCHR)
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MyD88
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p97
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MTH1
NEDD8
RAR/RXR
Adiponectin Receptor
Advanced Glycation End Products
AIM2
CD38
FOXO3
Galectin
gp120/CD4
Hck
Hexokinase
NPC1L1
RANKL/RANK
Thrombopoietin Receptor
VDAC
Vitamin
CPT
FABP
GluCls
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Haspin Kinase
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KLF
KSP
Liposome
Na-K-Cl cotransporter
Necroptosis
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Transaminase
ADC Linker
ATTECs
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EBI2/GPR183
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FKBP
FOXO1
Glutaminyl Cyclase
Glyoxalase
GSNOR
hCE
Huntingtin
Integrase
Lysosomal Autophagy
NUDIX hydrolase
PACAP
Piezo Channel
Prolyl Endopeptidase (PREP)
PROTAC Linker
RXFP receptor
Taste receptor
Transketolase
VDA
OLIG2
PGK1
Aconitase
Anion Exchanger
Cuproptosis
CYP19A1
Endonuclease
Fer/FerT kinase
glycosidase
MAP3K
MDM-2/p53
Motilin Receptor
Mucin
N-Acetylglucosaminyltransferase
NEDD4-1
Neuropeptide W
NMU2R
Procollagen C Proteinase
REV-ERB
Stemness kinase
stilbene oxidase
Thioredoxin
Ferroportin
IGF-2R
PARG(Poly(ADP-ribose) Glycohydrolase)
PGC-1α
Sodium-dependent phosphate transporter
Poly(ADP-ribose) Glycohydrolase (PARG)