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Results for "

T1411

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    9
    TargetMol | All_Pathways
  • Dye Reagents
    1
    TargetMol | All_Dye_Reagents
  • PROTAC Products
    4
    TargetMol | PROTAC
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    TargetMol | Natural_Products
Terbinafine hydrochloride
Terbinafine HCl, TDT 067 hydrochloride, KWD 2019
T141178628-80-5
Terbinafine hydrochloride (KWD 2019) is a synthetic allylamine derivative structurally related to naftifine. Terbinafine is active against dermatophytes.
  • $32
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Acoziborole
SCYX-7158, AN5568
T141151266084-51-8In house
Acoziborole (SCYX-7158), a derivative of benzoxaborole, is a safe, effective and structurally novel antigen-worm agent for human African trypanosomiasis (HAT) studies. The MIC value of Acoziborole for T. b. brucei S427 was 0.6 µg/mL.
  • $987
7-10 days
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QTY
Acid-PEG5-TEMPO
T141102055040-79-2
Acid-PEG5-TEMPO is a PEG-based linker for PROTACs, joining two essential ligands crucial for PROTAC molecule formation, and facilitates selective protein degradation using the ubiquitin-proteasome system within cells.
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Acid-PEG6-C2-Boc
T141112093153-84-3
Acid-PEG6-C2-Boc is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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Acid-PEG6-mono-methyl ester
T141121807512-38-4
Acid-PEG6-mono-methyl ester is a polyethylene glycol (PEG)-based PROTAC linker suitable for the synthesis of PROTACs [1].
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Acid-PEG9-NHS ester
T141131895916-27-4
Acid-PEG9-NHS ester is a PEG-based linker for PROTACs [proteolysis-targeting chimeras], facilitating the conjugation of two essential ligands, essential for PROTAC molecule formation, and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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Acivicin
U-42126, U42126, U 42126, AT-125, AT125, AT 125
T1411442228-92-2
Acivicin (AT-125), a chlorinated amino acid antibiotic produced by Streptomyces porcineus, is a γ-glutamyl transpeptidase (GGT) inhibitor that crosses the blood-brain barrier, exhibits anticancer and antiparasitic activity, and is used in the study of visceral leishmaniasis.
  • $178
35 days
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ACP-105
T14116899821-23-9
ACP-105 is a novel and potent nonsteroidal selective androgen receptor modulator (SARM) with partial agonist activity relative to the natural androgen testosterone.
  • $32
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ACT-678689
Compound Example 1.53.4
T141191783256-96-1
ACT-678689 (Compound Example 1.53.4) is a tryptophan hydroxylase (TPH) inhibitor with an IC50 of 8 nM[1].
  • $115
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