Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • ADC Linker
    (47)
  • Endogenous Metabolite
    (26)
  • Antibacterial
    (21)
  • Antibiotic
    (12)
  • Apoptosis
    (12)
  • Autophagy
    (11)
  • Epigenetic Reader Domain
    (9)
  • Antifungal
    (7)
  • COX
    (6)
  • Others
    (2211)
Filter
Search Result
Results for "

chemical

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    2627
    TargetMol | Inhibitors_Agonists
  • Compound Libraries
    34
    TargetMol | Compound_Libraries
  • Peptide Products
    50
    TargetMol | Peptide_Products
  • Inhibitory Antibodies
    1
    TargetMol | Inhibitory_Antibodies
  • Dye Reagents
    76
    TargetMol | Dye_Reagents
  • PROTAC Products
    88
    TargetMol | PROTAC
  • Natural Products
    201
    TargetMol | Natural_Products
  • Reagent Kits
    9
    TargetMol | Reagent_Kits
  • Recombinant Protein
    17
    TargetMol | Recombinant_Protein
  • Isotope Products
    18
    TargetMol | Isotope_Products
  • Antibody Products
    1
    TargetMol | Antibody_Products
  • Disease Modeling
    2
    TargetMol | Disease_Modeling_Products
HEPES
T85497365-45-9
HEPES is a zwitterionic sulfonic acid buffering agent, commonly used to uphold a neutral pH of basal medium within cell cultures.HEPES is a potent inducer of lysosome biogenesis.
  • Inquiry Price
Size
QTY
Chemical phosphorylation amidite
T89735202284-84-2
Chemical phosphorylation amidite is a potent chemoselective reagent characterized by its azide groups. Chemoselectivity denotes a powerful chemical reaction that showcases excellent biocompatibility, rapidity, and high specificity within biological environments.
  • Inquiry Price
10-14 weeks
Size
QTY
Valspodar
PSC 833
T17216121584-18-7
Valspodar (PSC 833), a specific P-glycoprotein inhibitor and MDR regulator, is commonly used as a chemical sensitizer in the study of advanced epithelial ovarian cancer.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Hot
4-((benzo[g]quinolin-4-yl(methyl)amino)methyl)-N,N-dimethylbenzenesulfonamide
T9440313528-19-7In house
4-((benzo[g]quinolin-4-yl(methyl)amino)methyl)-N,N-dimethylbenzenesulfonamide is a chemical agent.
  • Inquiry Price
Size
QTY
2,4,5-Trichloro-7H-pyrrolo[2,3-d]pyrimid
T95711053228-28-6In house
2,4,5-Trichloro-7H-pyrrolo[2,3-d]pyrimid is a chemical agent.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
Methylseleno carboxyethylglutamine
Peptiselene
T3335526046-89-9In house
Methylseleno carboxyethylglutamine is a bioactive chemical.
  • Inquiry Price
Size
QTY
11β-HSD1-IN-11
T60149859721-81-6In house
11β-HSd1-in-11 is a potent and competitive inhibitor of 11-β-hydroxysteroid dehydrogenase 1 (11β-HSD1) IN rats and humans with IC50 values of 0.34 μM and 0.13 μM, respectively. 11β-Hsvd1-in-11 is a compound used as a chemical compound. 11β-HSD1-IN-11 is a hormone involved in regulating various physiological processes, such as metabolism, inflammation, and stress responses. 11β-Hd1-in-11 is a potential compound for the treatment of metabolic disorders, obesity, and certain inflammatory conditions.
  • Inquiry Price
Size
QTY
Bis(2-methoxy-5-((Z)-3,4,5-trimethoxystyryl)phenyl) hydrogen phosphate
T67906735261-22-0In house
Phenol, 2-methoxy-5-[(1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]-, 1,1'-(hydrogen phosphate) is a chemical compound that is a phosphate derivative of the statin class.
  • Inquiry Price
6-8weeks
Size
QTY
TargetMol | Inhibitor Sale
SB-747651A Dihydrochloride
T96521781882-72-1In house
SB-747651A dihydrochloride is a chemical compound that serves as an ATP-competitive inhibitor for mitogen- and stress-activated kinase 1 (MSK1), featuring an IC50 of 11 nM. Additionally, this compound effectively inhibits PRK2, RSK1, p70S6K, and ROCK-II, showcasing its potential in inflammation research [1].
  • Inquiry Price
6-8 weeks
Size
QTY
BAY-678
T10473675103-36-3In house
BAY-678 is a human neutrophil elastase (HNE; IC50: 20 nM) inhibitor with oral bioactivity, potency and selectivity.BAY-678 is a chemical probe recommended by the Structural Genomics Consortium (SGC).
  • Inquiry Price
8-10weeks
Size
QTY
JNJ-65355394
T677602230598-99-7In house
JNJ-65355394 is an effective O-GlcNAc hydrolase (OGA) inhibitor and an OGA chemical probe.
  • Inquiry Price
Size
QTY
Gevotroline
T68080107266-06-8In house
Gevotroline, a chemical in palm wine that can be used to treat psychosis, is a 5-HT2 receptor antagonist that can be used to study behavioral disorders.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
1-(2-fluorophenyl)-3-[5-(2-methoxyphenyl)
T67696426242-86-6In house
1-(2-fluorophenyl)-3-[5-(2-methoxyphenyl)-1,3,4-thiadiazol-2-yl]urea is a chemical compound.
  • Inquiry Price
8-10weeks
Size
QTY
TargetMol | Inhibitor Sale
(+)-ORM-10921
T28267L610782-83-7In house
(+)-ORM-10921 is a conformation of ORM-10921 and can be used in chemical synthesis studies.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
Cpd.4
T9547 In house
Cpd.4 is a chemical agent.
  • Inquiry Price
Size
QTY
Vutiglabridin
HSG4112
T612681800188-47-9In house
Vutiglabridin (HSG4112) is a novel and safe modulator of PON2, a racemic compound. vutiglabridin is an optimized structural analogue of Glabridin and is superior to Glabridin in terms of weight loss and chemical stability. vutiglabridin ameliorates mptp-induced neurodegeneration in Parkinson's disease mice by targeting mitochondrial paraoxonase-2. Vutiglabridin is a clinical phase 2 drug for the treatment of obesity and has therapeutic effects on p-mitochondrial PON2 in a PD model. vutiglabridin penetrates the brain, binds PON2, and restores 1-methyl-4-phenylpyridine (MPP*)-induced neuroblastoma in SH-SY5Y Vutiglabridin significantly attenuated 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced dyskinesia and dopaminergic neuronal damage in mice modeled with PD in mouse experiments.
  • Inquiry Price
6-8weeks
Size
QTY
TargetMol | Inhibitor Sale
ALX-1393
T14198949164-09-4In house
ALX-1393 is a selective GlyT2 inhibitor that effectively reduces neuronal action potential activity in a concentration-dependent manner and inhibits the activity of spontaneous networks by inducing glycinergic tetanic currents in the abdominal horn of the spinal cord. Antiinjurious effects on thermal, mechanical and chemical stimuli in rat models of acute pain.
  • Inquiry Price
6-8weeks
Size
QTY
4-((benzo[g]quinolin-4-ylamino)methyl)benzenesulfonamide
T94392803465-12-3In house
4-((benzo[g]quinolin-4-ylamino)methyl)benzenesulfonamide is a chemical agent.
  • Inquiry Price
Size
QTY
Anticonvulsant agent 1
4-(2,2-Difluoroethenyl)-α-ethyl-2-oxo-1-pyrrolidineacetamide
T10027357336-17-5In house
Anticonvulsant agent 1 is a chemical compound with potent anticonvulsant properties.
  • Inquiry Price
3-6 months
Size
QTY
Estredox
IDR-90104, IDR 90104, E-2-CDS, E-2CDS, E2 CDS, E 2CDS
T27287103562-82-9In house
Estredox (E2 CDS) is a redox-based estradiol (E2) chemical delivery system.E2-CDS provides sustained and brain-selective delivery of estradiol.
  • Inquiry Price
6-8 weeks
Size
QTY
6-Chloropurine
6-Chloro-9H-purine
T747087-42-3
6-Chloropurine (6-Chloro-9H-purine) is a building block in chemical synthesis,with Antitumor activities.
  • Inquiry Price
Size
QTY
TargetMol | Inhibitor Sale
2-(propan-2-yldisulfanyl)propane
Isopropyl disulfid
T2038764253-89-8
2-(propan-2-yldisulfanyl)propane is an organic sulfide, with a special odor, commonly used in chemical synthesis and preparation of fragrances, can be used as an organic synthesis intermediate for the preparation of other compounds.
  • Inquiry Price
Size
QTY
Flavonol
3-Hydroxyflavone, 3-HF, Flavon-3-ol, 3-Hydroxy-2-phenylchromone
T2910577-85-5
Flavonol (3-Hydroxyflavone) is a member of the class of compounds known as flavonols. 3-hydroxyflavone can be found in a number of food items such as brassicas, pomegranate, red raspberry, and fenugreek. 3-hydroxyflavone is a chemical compound. It is the backbone of all flavonols, a type of flavonoid. It serves as a model molecule as it possesses an excited-state intramolecular proton transfer (ESIPT) effect to serve as a fluorescent probe to study membranes for example or intermembrane proteins.
  • Inquiry Price
Size
QTY
Acetazolamide
Diamox
T081359-66-5
Acetazolamide (Diamox) is a Carbonic Anhydrase Inhibitor. The mechanism of action of acetazolamide is as a Carbonic Anhydrase Inhibitor. The chemical classification of acetazolamide is Sulfonamides.
  • Inquiry Price
Size
QTY