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Apoptosis

Apoptosis

Cell membrane blebbing, chromatin condensation, genomic DNA fragmentation, and the exposure of particular phagocytosis signaling molecules on the cell surface are just a few of the distinctive morphological and biochemical features of the cell death process known as apoptosis. Apoptosis-initiated cell death is distinct from necrosis-induced cell death. Apoptotic death, in contrast, is silent and orderly. Necrotic cells are typically recognized as a danger signal by the immune system, which causes inflammation.

There are two main methods for inducing apoptotic cell death: The intrinsic pathway, also known as the Bcl-2-regulated or mitochondrial pathway, is strictly regulated by the BCL-2 family of proteins and is activated by a variety of developmental cues or cytotoxic insults, such as viral infection, DNA damage, and growth-factor deprivation.The tumor necrosis factor (TNF) receptor family members, such as Fas or TNF receptor-1 (TNFR1), which contain an intracellular death domain and can recruit and activate caspase-8 through the adaptor protein Fas-associated death domain (FADD; also known as MORT1) at the cell surface, are what initiate the extrinsic or death-receptor pathway. Without the involvement of the BCL-2 family, this recruitment results in the subsequent activation of downstream (effector) caspases like caspase-3, -6, or -7.

Numerous human diseases, including cancer, viral infections, autoimmune diseases, neurodegenerative disorders, and AIDS (acquired immunodeficiency syndrome), may be influenced by changes in cell survival, according to studies. Some of these diseases may not progress naturally unless specific therapies that change the apoptotic threshold are used.

Apoptosis related products

Structure Cat No. Product Name CAS No. Product Description
LDC7559 V51876 LDC7559 2407782-01-6 LDC7559 is an inhibitor (blocker/antagonist) of desmin D (GSDMD) and acts by inhibiting late stages of the neutrophil extracellular bactericidal network (NET).
LEESGGGLVQPGGSMK V35003 LEESGGGLVQPGGSMK 2096980-79-7 LEESGGGLVQPGGSMK, a proteolytic peptide that is a component of Infliximab, can be used for quantitative analysis of Infliximab.
LEI-515 V85863 LEI-515
Lenercept (p55TNF-R:Ig; Ro 45-2081; TNFR55-IgG1) V51873 Lenercept (p55TNF-R:Ig; Ro 45-2081; TNFR55-IgG1) 156679-34-4 Lenercept (Ro 45-2081) is a recombinant fusion protein consisting of a soluble TNF-receptor (p55) linked to the Fc portion of human IgG1.
Lepadin E V54978 Lepadin E 444914-19-6 Lepadin E is a ferroptosis inducer with significant cytotoxic effect and induces ferroptosis through the classic p53-SLC7A11-GPX4 pathway.
Lepadin H V56453 Lepadin H 412328-25-7 Lepadin H is a marine alkaloid and ferroptosis inducer.
Lepidozin G V54840 Lepidozin G 2869125-43-7 Lepidozin G can suppress the growth of cancer cell lines with IC50s ranging from 4.2 ± 0.2 to 5.7 ± 0.5 μM.
LG308 V54886 LG308 1428341-65-4 LG308 is a novel synthetic compound with antimicrotubule activity.
Licofelone-d6 (ML-3000-d6) V56406 Licofelone-d6 (ML-3000-d6) 1178549-81-9 Licofelone-d6 is the deuterium labelled form of Licofelone.
Lidocaine-d10 (利多卡因 d10) V52609 Lidocaine-d10 (lidocaine d10) 851528-09-1 Lidocaine-d10 is the deuterium labelled form of Lidocaine.
Lidocaine-d10 hydrochloride (盐酸利多卡因 d10 (盐酸盐)) V56402 Lidocaine-d10 hydrochloride (lidocaine d10 hydrochloride (hydrochloride)) 1189959-13-4 Lidocaine-d10 ( HCl) is the deuterated form of Lidocaine HCl.
Liproxstatin-1 hydrochloride V51856 Liproxstatin-1 hydrochloride 2250025-95-5 Liproxstatin-1 HCl is a potent ferroptosis inhibitor that can suppress ferroptotic cell death (IC50=22 nM).
Liriodenine (Spermatheridine; VLT045) V51854 Liriodenine (Spermatheridine; VLT045) 475-75-2 Liriodenine (Spermatheridine; VLT045) is extracted from the plant Mitrephora sirikitiae and has anti-neoplastic activity.
Lithium chloride hydrate (hydrate/monohydrateortrihydrate) V34788 Lithium chloride hydrate (hydrate/monohydrateortrihydrate) 85144-11-2 Lithium chloride hydrate is an orally bioactive mood stabilizer that is a potent viral inhibitor and immune modulator.
Lithocholic acid-d4 (3α-Hydroxy-5β-cholanic acid-d4) V34751 Lithocholic acid-d4 (3α-Hydroxy-5β-cholanic acid-d4) 83701-16-0 Lithocholic acid-d4 is deuterium-labeled lithocholic acid, a toxic secondary bile acid.
Lobetyol V51853 Lobetyol 136171-87-4 Lobetyol is a natural compound extracted from Lobelia chinensis.
LPd peroxida probe (脂质过氧化绿色探针) V6203 LPd peroxida probe (lipid peroxidation green probe) 1448846-35-2 The LPd peroxida probe, a marker of ferroptosis, is a useful fluorescent probe for studying the role of lipid peroxidation in various cellular pathophysiology.
Lusianthridin V51837 Lusianthridin 87530-30-1 Lusianthridin is a natural compound from Dendrobium venustum that has anti-migration effects.
Luxeptinib (CG-806) V51836 Luxeptinib (CG-806) 1616428-23-9 Luxeptinib (CG-806) is an orally bioactive, reversible, first-in-class, non-covalent, potent pan-FLT3/pan-BTK inhibitor.
m-Se3 V54943 m-Se3 2829939-44-6 m-Se3 is a potent and specific c-MYC transcription inhibitor that can inhibit tumor growth and has anti-cancer activity.
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