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TargetMol | Tags By Target
  • Apoptosis
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  • Beta Amyloid
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  • Estrogen Receptor/ERR
    (1)
  • Estrogen/progestogen Receptor
    (2)
  • Gamma-secretase
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Results for "

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  • Inhibitors & Agonists
    13
    TargetMol | Activity
ACES
N-(2-Acetamido)-2-aminoethanesulfonic acid
T408517365-82-4
ACES, or N-(2-Acetamido)-2-aminoethanesulfonic acid, is a zwitterionic buffer compound. It offers an effective pH range of 6.8-7.2 for various applications.
  • Inquiry Price
7-10 days
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Acesulfame Potassium
T094055589-62-3
Acesulfame potassium is a non-nutritive sweetener.
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TargetMol | Inhibitor Sale
Crenigacestat
LY3039478
T36331421438-81-4
Crenigacestat (LY3039478) is an orally bioavailable Notch inhibitor with an IC50 of ~1 nM in most tumor cell lines tested. It effectively inhibits mutant Notch receptor activity and, in a xenograft tumor model, inhibits the expression of Notch-regulated genes and N1ICD cleavage in the tumor microenvironment.
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TargetMol | Citations Cited
Elacestrant
RAD1901
T13674722533-56-4
Elacestrant (RAD1901) with IC50s of 48 and 870 nM for ERα and ERβ, respectively.Elacestrant  is an orally available selective estrogen receptor degrader .
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Semagacestat
LY450139
T6125425386-60-3
Semagacestat (LY450139) (LY450139) is a γ-secretase blocker for Aβ42 Aβ40 Aβ38 (IC50: 10.9 12.1 12.0 nM) and also inhibits Notch signaling (IC50: 14.1 nM).
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Avagacestat
BMS-708163
T62491146699-66-2
Avagacestat (BMS-708163) (BMS-708163) is a potent, selective, orally bioavailable γ-secretase inhibitor of Aβ40 and Aβ42 with IC50 of 0.3 nM and 0.27 nM, demonstrating a 193-fold selectivity against Notch. Phase 2.
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Elacestrant dihydrochloride
RAD1901 dihydrochloride
T136751349723-93-8
Elacestrant dihydrochloride (DA-DKRAD1901 dihydrochloride) is an orally available selective estrogen receptor degrader with IC50s of 48 for ERα and 870 nM for ERβ, respectively.
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Elacestrant S enantiomer
RAD1901 S enantiomer
T11173
Elacestrant S enantiomer is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively.
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Nirogacestat dihydrobromide
T382661962925-29-6
Potent γ-secretase inhibitor (IC50 values are 1.2 and 6.2 nM in whole cell and cell-free assays, respectively). Reduces Aβ in brain, CSF and plasma in mice and guinea pigs. Lanz et al (2010) Pharmacodynamics and pharmacokinetics of the gamma-secretase inhibitor PF-3084014. J.Pharmacol.Exp.Ther. 334 269 PMID:20363853
  • Inquiry Price
8-10 weeks
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Aspartame acesulfame
Aspartame acesulfame salt,Acesulfame mixture with aspartame
T30172106372-55-8
Aspartame acesulfame, as an artificial sweetener, is 350 times sweeter than sucrose.
  • Inquiry Price
6-8 weeks
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QTY
Begacestat
GSI-953
T14525769169-27-9
Begacestat is a selective thiophene sulfonamide amyloid precursor protein gamma-secretase inhibitor (Aβ40,IC50=15 nM),and for the treatment of Alzheimer's disease.
  • Inquiry Price
7-10 days
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Elacestrant S enantiomer dihydrochloride
RAD1901 S enantiomer dihydrochloride,RAD-1901 S enantiomer dihydrochloride,RAD 1901 S enantiomer dihydrochloride
T11173L
Elacestrant (RAD1901) dihydrochloride is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively. Elacestrant S enantiomer dihydrochloride is an low activity enantiomer of elacestrant dihydrochloride.
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Nirogacestat
PF-03084014,PF-3084014,PF03084014,PF 03084014
T69351290543-63-3
Nirogacestat (PF 03084014) is a specific γ-secretase inhibitor (IC50: 6.2 nM, in a cell-free assay).
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