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Results for "

T7381

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    8
    TargetMol | All_Pathways
  • Peptide Products
    2
    TargetMol | Peptide_Products
  • PROTAC Products
    1
    TargetMol | PROTAC
  • Natural Products
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    TargetMol | Natural_Products
TCS 401
T7381243966-09-8
TCS 401 is a selective inhibitor of protein-tyrosine phosphatase 1B (PTP1B) with a Ki value of 0.29 μM.
  • $40
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H-Ile-Pro-Pro-OH hydrochloride
T738101208862-61-6
H-Ile-Pro-Pro-OH hydrochloride, a tripeptide derived from dairy products, consists of one isoleucine (Ile) and two prolines (Pro). H-Ile-Pro-Pro-OH hydrochloride inhibits angiotensin-converting enzyme (ACE) with an IC₅₀ of 5 μM. H-Ile-Pro-Pro-OH hydrochloride exhibits antihypertensive effects.
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Haemanthamine hydrochloride
T73813
Haemanthamine hydrochloride, a crinine-type alkaloid derived from Amaryllidaceae plants, exhibits potent anticancer properties. It acts by targeting ribosomes, thereby inhibiting protein biosynthesis during the translation elongation stage. Additionally, this compound demonstrates pro-apoptotic, antioxidant, antiviral, antimalarial, and anticonvulsant activities [1] [2].
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cis-Lomibuvir
T738141026785-59-0
Cis-Lomibuvir (cis-VX-222), a cis-isomer of Lomibuvir, is a selective non-nucleoside inhibitor of the hepatitis C virus (HCV) NS5B polymerase (RdRp), targeting thumb pocket 2 with a dissociation constant (Kd) of 17 nM. It exhibits an EC50 of 5.2 nM against the 1b/Con1 HCV subgenomic replicon, demonstrating a preference for inhibiting elongative RNA synthesis over de novo-initiated RNA synthesis.
  • $833
35 days
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TMC-205
T73815403646-00-4
TMC-205, a natural fungal metabolite, exhibits antiproliferative effects against cancer cell lines and functions as a transcriptional up-regulator of the SV40 promoter [1].
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Fusafungine
T738161393-87-9
Fusafungine, known commercially as Bioparox, Fusaloyos, and Locabiotal, serves as a potent antibiotic and anti-inflammatory agent effective in oral administration. It shows promise for research related to upper respiratory airways disease (URAD)[1][2].
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SLF TFA
T738172378802-47-0
SLF TFA, a synthetic ligand for FK506-binding protein (FKBP), exhibits affinity toward FKBP51 with a value of 3.1 μM and demonstrates an IC50 of 2.6 μM for FKBP12. This compound is utilized in the synthesis of PROTAC [1] [2] [3].
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Homocarnosine TFA
T738182991254-59-0
Homocarnosine TFA, a unique dipeptide of γ-aminobutyric acid (GABA) and histidine found in the brain, acts as an inhibitory neuromodulator synthesized from GABA within neurons. It exhibits anticonvulsant effects [1], and possesses antioxidant and anti-inflammatory properties, prevents DNA damage, and inhibits the formation of advanced glycation end-products [2].
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