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Results for "

T7395

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Dye Reagents
    1
    TargetMol | All_Dye_Reagents
  • PROTAC Products
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    TargetMol | PROTAC
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Lys-CoA TFA
T73951
Lys-CoA TFA, a selective p300 histone acetyltransferase (HAT) inhibitor (IC 50 =50-500 nM), exhibits a specificity that exceeds 100-fold over PCAF (IC 50 =200 μM). This compound effectively suppresses transcriptional activation dependent on p300 HAT activity [1] [2].
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Neomycin C
T7395366-86-4
Neomycin C, an isomeric component of the Neomycin complex, is a 2-DOS-containing aminoglycoside that comprises neomycin A, B, and C. It is notably less potent, exhibiting approximately half the activity of neomycin B [1] [2].
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Leucinostatin (mixture of A&B)
T73954
Leucinostatin, a mixture of components A and B, constitutes the primary elements of a unique nonapeptide complex synthesized by Paecilomyces lilacinus, functioning as antibiotics [1].
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Potassium clavulanate mixture with silicon dioxide (1:1)
T73955
Potassium Clavulanate Mixture with Silicon Dioxide (1:1) is a compound consisting of an equal parts ratio, specifically one part Potassium Clavulanate to one part Silicon Dioxide, presented in a powdered form [1].
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Amoxicillin trihydrate mixture with potassium clavulanate (4:1)
T73956
Amoxicillin (trihydrate) mixed with potassium clavulanate (4:1) is a broad-spectrum antibiotic that exhibits strong oral absorption. It functions by inhibiting the biosynthesis of polypeptides in bacterial cell walls, which effectively halts cell growth, demonstrating its antimicrobial activity [1] [2] [3].
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PROTAC Bcl-xL degrader-1
T73957
PROTAC Bcl-xL degrader-1 is a potent PROTAC composed of a Bcl-xL (Bcl-2 family member) ligand-binding group, a linker, and an IAP E3 ligases binding group, demonstrating effectiveness as a Bcl-xL degrader. It exhibits toxicity towards human platelets and MyLa 1929 cells, with IC50 values of 62 nM and 8.5 μM, respectively [1].
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