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TargetMol | Compound Library

Bioactive Compounds Library Max

Catalog No. L4010

Bioactive Compound Library Max is a collection of 27302 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 27302 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
Parasite
Antifungal
DNA/RNA Synthesis
AChR
NF-κB
Adrenergic Receptor
COX
Reactive Oxygen Species
Calcium Channel
Dopamine Receptor
Potassium Channel
CDK
HIV Protease
Cytochromes P450
PI3K
Ras
Antioxidant
EGFR
Dehydrogenase
Sodium Channel
Histamine Receptor
Epigenetic Reader Domain
PDE
GABA Receptor
VEGFR
Akt
TNF
p38 MAPK
Influenza Virus
Caspase
Virus Protease
PPAR
iGluR
Cholinesterase (ChE)
GluR
ERK
TRP/TRPV Channel
Microtubule Associated
Histone Methyltransferase
HDAC
SARS-CoV
Nucleoside Antimetabolite/Analog
JAK
mTOR
GPCR
Phosphatase
Bcl-2 Family
Wnt/beta-catenin
PARP
NO Synthase
Prostaglandin Receptor
Interleukin
Topoisomerase
STAT
Ferroptosis
Estrogen Receptor/ERR
Drug Metabolite
AMPK
MMP
Src
PKC
HCV Protease
IL Receptor
Anti-infection
Antiviral
Estrogen/progestogen Receptor
Opioid Receptor
FLT
ROS
Adenosine Receptor
NMDAR
RAAS
Androgen Receptor
GSK-3
Mitochondrial Metabolism
PDGFR
HIF/HIF Prolyl-Hydroxylase
TGF-beta/Smad
Beta Amyloid
FGFR
TLR
Glucocorticoid Receptor
HSP
Monoamine Oxidase
Nrf2
Raf
c-Met/HGFR
Proteasome
Lipoxygenase
MAO
MDM-2/p53
Phospholipase
MAPK
HBV
JNK
Tyrosinase
c-Kit
Cannabinoid Receptor
ALK
ATPase
HSV
Bcr-Abl
Sirtuin
Amino Acids and Derivatives
Serine Protease
Histone Demethylase
E1/E2/E3 Enzyme
Transferase
Glucosidase
Integrin
DUB
PKA
Immunology/Inflammation related
LPL Receptor
Kras
Mitophagy
PROTACs
Aurora Kinase
Casein Kinase
Antifection
Carbonic Anhydrase
P-gp
CCR
NOS
IκB/IKK
Tyrosine Kinases
Reductase
ROCK
p53
Reverse Transcriptase
Serotonin Transporter
MEK
Gamma-secretase
IGF-1R
Angiotensin-converting Enzyme (ACE)
HIF
Serine/threonin kinase
Cysteine Protease
NOD-like Receptor (NLR)
Retinoid Receptor
Histone Acetyltransferase
CXCR
Neurokinin receptor
Norepinephrine
Proton pump
S1P Receptor
RIP kinase
FAK
PERK
CaMK
P2X Receptor
Sigma receptor
c-RET
Leukotriene Receptor
S6 Kinase
Aryl Hydrocarbon Receptor
NADPH
NOD
Hedgehog/Smoothened
Acyltransferase
Ligand for E3 Ligase
Fatty Acid Synthase
DNA-PK
Molecular Glues
c-Fms
TAM Receptor
Chloride channel
transporter
Trk receptor
FAAH
ATM/ATR
Glucokinase
CFTR
Syk
DNA Methyltransferase
Progesterone Receptor
Glutathione Peroxidase
Smo
PD-1/PD-L1
HER
ribosome
Hydroxylase
Thyroid hormone receptor(THR)
Pim
P2Y Receptor
DPP-4
PLK
HMG-CoA Reductase
Thrombin
Glucagon Receptor
Chk
Mdm2
c-Myc
cAMP
DNA
DNA Alkylator/Crosslinker
FXR
DHFR
Cholecystokinin Receptor
IRAK
Complement System
Protease-activated Receptor
Kinesin
DYRK
Endothelin Receptor
ROS Kinase
AhR
ADC Cytotoxin
Rho
LTR
YAP
ROR
Factor Xa
Xanthine Oxidase
IDO
Indoleamine 2,3-Dioxygenase (IDO)
PGE Synthase
STING
Lipid
LPA Receptor
PDK
Lipase
BTK
Melanocortin Receptor
Guanylate cyclase
OXPHOS
LRRK2
Antifolate
OX Receptor
Liver X Receptor
PAK
Platelet aggregation
IAP
MAGL
Neuropeptide Y Receptor
SGLT
MRP
GNRH Receptor
BACE
IFNAR
RSV
Isocitrate Dehydrogenase (IDH)
Vasopressin Receptor
Aromatase
Epoxide Hydrolase
Myosin
DNA Alkylation
Glutaminase
Aminopeptidase
Ephrin Receptor
Bradykinin Receptor
Beta-Secretase
Telomerase
Ligands for Target Protein for PROTAC
Photosensitizer
Monoamine Transporter
Pyroptosis
Acetyl-CoA Carboxylase
Stearoyl-CoA Desaturase (SCD)
PAFR
GPCR19
PI4K
GTPase
PAI-1
GST
IRE1
LDL
CaSR
ABC Transporter
CSF-1R
MicroRNA
Neurotensin Receptor
Monocarboxylate transporter
Arrestin
Necroptosis
Somatostatin
Liposome
GHSR
PTEN
NADPH-oxidase
ATG
DNA gyrase
Free radical scavengers
Tie-2
Phosphorylase
BCRP
Survivin
Discoidin Domain Receptor (DDR)
NR4A
MyD88
Melatonin Receptor
FKBP
IKZF
Bcl-6
MLK
PKM
Apelin receptor
MNK
UGT
Na+/Ca2+ Exchanger
NAMPT
GPX
Dynamin
OAT
MIF
Imidazoline Receptor
Arginase
CRFR
Gap Junction Protein
Porcupine
FLAP
Neprilysin
OCT
GRK
Bombesin Receptor
PYK2
GlyT
Wee1
Methionine Adenosyltransferase (MAT)
SGK
Carboxypeptidase
ATP Citrate Lyase
CRISPR/Cas9
Amylase
Prolyl Endopeptidase (PREP)
SIK
FOXO
Annexin A
MT Receptor
LIM Kinase
CRM1
PAD
DAPK
p97
Oxytocin Receptor
cGAS
p62
CGRP Receptor
Melanin-concentrating Hormone Receptor (MCHR)
E3 Ligase Ligand-Linker Conjugate
Protease
Adenylyl Cyclase
Thrombopoietin Receptor
ASK
APC/C
CAT
HCN Channel
TSH Receptor
AAK1
Neuropeptide FF Receptor
RANKL/RANK
Cell Cycle Arrest
Aquaporin
MELK
REV-ERB
NEDD8
Vitamin
RAR/RXR
MALT
MTP
Succinate Receptor 1 (SUCNR1)
TOPK
Decarboxylase
Adenosine Deaminase
CETP
Arp2/3 Complex
Na-K-Cl cotransporter
PSMA
Galectin
KLF
BMI-1
ADC Linker
FOXO3
AIM2
CD38
VDAC
CD73
Hippo pathway
DprE1
MRGPR
LDLR
Cell wall
ACK1
MTH1
ASBT
Cuproptosis
gp120/CD4
ASCT
CPT
Adiponectin Receptor
PROTAC Linker
Cadherin
Taste receptor
NPC1L1
Advanced Glycation End Products
Hck
AAK1 (AP2 associated kinase 1)
Haspin Kinase
Hexokinase
Orphan Receptor
PGK1
EBI2/GPR183
Factor VIIa
Endonuclease
FABP
KSP
Huntingtin
GluCls
Kisspeptin
Glutathione reductase
HuR
NEDD4-1
Transaminase
Mucin
GSNOR
Y Box Binding Protein 1
GDNF
VDA
PARG(Poly(ADP-ribose) Glycohydrolase)
Photosystem (PS)
Transketolase
glycosidase
PACAP
RXFP receptor
Aconitase
Integrase
Piezo Channel
NUDIX hydrolase
Fas/FasL
hCE
TMV
Lysosomal Autophagy
ATTECs
Glyoxalase
HCAR
Drug-Linker Conjugates for ADC
Glutaminyl Cyclase
OLIG2
LHRH
stilbene oxidase
N-Acetylglucosaminyltransferase
Anion Exchanger
CD74
Neuropeptide W
Motilin Receptor
Thioredoxin
Procollagen C Proteinase
Stemness kinase
Early 2 Factor (E2F)
Poly(ADP-ribose) Glycohydrolase (PARG)
Enteropeptidase (EP)
MAP3K
CYP19A1
B7
Target Protein Ligand-Linker Conjugate
AUTACs
Fer/FerT kinase
Tight Junction Protein
Urea Transporter
Chemerin Receptor
Ferroportin
IGF-2R
Sodium-dependent phosphate transporter
PGC-1α
NMU2R
NMUR

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