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Results for "

T7470

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    9
    TargetMol | All_Pathways
  • PROTAC Products
    1
    TargetMol | PROTAC
  • Cell Research
    1
    TargetMol | Cell_Research_Reagents
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    1
    TargetMol | All_Pathways
  • Oligonucleotides
    5
    TargetMol | All_Pathways
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.
  • $29
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TargetMol | Inhibitor Sale
Mal-VC-PAB-(N-Me-amide-C3)-ADU-S100 triethylamine
T747002249935-19-9
Mal-VC-PAB-(N-Me-amide-C3)-ADU-S100 triethylamine is a linker–payload small molecule of an immune-stimulating antibody conjugate (ISAC), consisting of the STING agonist (ADU-S100) and a cleavable linker. Mal-VC-PAB-(N-Me-amide-C3)-ADU-S100 triethylamine can be used in cancer research.
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A18-Iso5-2DC18
T747012412492-09-0
A18-Iso5-2DC18 (compound A18), a lipidoid, enhances mRNA protein expression and induces a robust immune response [1].
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5'-ODMT cEt N-Bz A Phosphoramidite (Amidite)
T747021197033-19-4
5'-ODMT cEt N-Bz A Phosphoramidite Amidite, a locked nucleic acid (LNA) analogue, exhibits hybridization and mismatch discrimination capabilities similar to LNA, and shows resistance to exonuclease digestion [1].
  • $279
8-10 weeks
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QTY
5'-ODMT cEt G Phosphoramidite (Amidite)
T74703945628-66-0
5'-ODMT cEt G Phosphoramidite Amidite is a potent nucleic acid analog with exceptional safety and significant antisense activity, as demonstrated in studies [1] [2].
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5'-ODMT cEt N-Bzm5 C Phosphoramidite (Amidite)
T747041197033-17-2
5'-ODMT cEt N-Bzm5 C Phosphoramidite Amidite is a potent nucleic acid analog and a modified antisense oligonucleotide [1].
  • $279
8-10 weeks
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5'-ODMT cEt m5U Phosphoramidite (Amidite)
T747051197033-22-9
5'-ODMT cEt m5U Phosphoramidite Amidite, a locked nucleic acid (LNA) analog, demonstrates exceptional safety and antisense activity [1] [2].
  • $29
8-10 weeks
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PROTAC FLT3/CDK9 degrader-1
T74707
PROTAC FLT3/CDK9 degrader-1, a potent dual degrader of FLT3 and CDK9, effectively induces apoptosis and targets protein degradation of FLT3 and CDK9. This compound holds research potential for FLT3-ITD mutated AML [1].
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β2AR/M-receptor agonist-1
T747082230520-62-2
β2AR/M-receptor agonist-1 (example 131), a muscarinic antagonist and β2 adrenoceptor agonist (MABA), exhibits dual potency towards β2 adrenoceptor and muscarinic receptor, with an EC50 value of 9.2 nM for β2 adrenoceptor and a Ki value of 30.2 nM for the muscarinic receptor, and an EC50 value of 4.0 nM highlighting its MABA activity [1].
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