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  • Apoptosis
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Results for "

fas/fasl

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    9
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    1
    TargetMol | Peptide_Products
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    TargetMol | Inhibitors_Agonists
Araloside A
Chikusetsusaponin IV
T4S02907518-22-1
Araloside A (Chikusetsusaponin IV) might relieve cutaneous symptoms caused by excessive apoptotic cell death in the skin through the Fas/FasL pathway.
  • $31
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TargetMol | Citations Cited
KR-33493
KR-33494, KM-819
TQ02201021497-97-1
KR-33493 is a FAS-associated factor 1 (FAF1) inhibitor and can be used in studies about Parkinson's disease.
  • $34
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Marginatoxin
TN44961422536-56-8
Marginatoxin may be a promising chemopreventive agent for treating hepatocellular carcinoma, it induces human hepatoma BEL-7402 cells apoptosis in vitro and in vivo via activation of Fas/FasL-mediated apoptotic pathway.
  • $700
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PaPE-1
pathway Preferential Estrogen, PaPE1, PaPE 1
T2023972107327-36-4
PaPE-1 is a pathway-preferential estrogen that activates extracellular nuclear signaling pathways without affecting nuclear signaling pathways. It exerts anti-apoptotic effects by inhibiting Aβ-induced caspase activity and reducing chromatin condensation associated with apoptosis, thereby preventing neuronal cell death. Additionally, post-treatment with PaPE-1 decreases the mRNA expression of apoptosis-specific factors (such as Bax, Gsk3b, Fas, and Fasl) under Aβ influence, while upregulating Bcl2 expression.
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10-14 weeks
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Fenvalerate
Phenvalerate, Evercide 2362
T2541651630-58-1
Fenvalerate (Evercide 2362) is a inhibitor of protein phosphatase 2B (calcineurin), a synthetic pyrethroid insecticide, and inhibits PP2B-Aα.High doses of Fenvalerate impair cognitive and behavioral development.Fenvalerate induces, through the Fas/FasL signaling pathway, the induction of Fenvalerate induces germ cell apoptosis in mouse testis through the Fas/FasL signaling pathway.
  • $40
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(Rac)-Indoximod
T6026626988-72-7
(Rac)-Indoximod (1-Methyl-DL-tryptophan) is a potent inhibitor of indoleamine 2,3-dioxygenase (IDO). Combined treatment with IFN-γ and (Rac)-Indoximod significantly suppresses the activity of α-SMA-expressing human cardiac myofibroblasts (hCMs) and promotes apoptosis by up-regulating the genes IRF-1, Fas, and FasL, effectively improving cardiac fibrosis[1].
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6-8 weeks
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Fenvalerate (Standard)
TMSM-118251630-58-1
Fenvalerate (Standard) is the standard substance of Fenvalerate, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Fenvalerate (Evercide 2362) is a inhibitor of protein phosphatase 2B (calcineurin), a synthetic pyrethroid insecticide, and inhibits PP2B-Aα.High doses of Fenvalerate impair cognitive and behavioral development.Fenvalerate induces, through the Fas/FasL signaling pathway, the induction of Fenvalerate induces germ cell apoptosis in mouse testis through the Fas/FasL signaling pathway.
  • $30
7-10 days
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Kp7-6
TP2594629628-53-1
Kp7-6, functioning as a Fas/FasL antagonist, is a Fas mimetic peptide that shields cells from Fas-mediated apoptosis and protects mice from Fas-mediated hepatic injury [1] [2].
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IP3RCYT
TP3028
IP3RCYT is an inhibitory peptide of IP3R that can prevent cytochrome C from binding with IP3R, with an IC50 of approximately 100 nM. It regulates intracellular calcium signaling. Additionally, IP3RCYT inhibits apoptosis in HeLa and Jurkat cells treated with staurosporine or membrane-bound Fas ligand (FasL).
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