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Apoptosis(凋亡)

FKBP (FK506-binding protein) is one of two major immunophilins and most of FKBP family members bind FK506 and show peptidylprolyl cis/trans isomerase (PPIase) activity. Small size FKBP family members contain only FK506-binding domain, while FKBPs with large molecular weights possess extra domains such as tetratricopeptide repeat domains, calmodulin binding and transmembrane motifs. FKBPs are involved in several biochemical processes including protein folding, receptor signaling, protein trafficking and transcription. FKBP family proteins play important functional roles in the T-cell activation, when complexed with their ligands.

FK506-binding proteins 1a and 1b (FKBP1a/1b) are immunophilin proteins that bind the immunosuppressant agent FK506 and AY 22989. FKBP12 is a ubiquitous abundant protein that acts as a receptor for FK506, binds tightly to intracellular calcium release channels and to the transforming growth factor β (TGF-β) type I receptor.

Products for  Apoptosis

  1. Cat.No. 产品名称 Information
  2. GC39022 Tetramethylcurcumin

    四甲基姜黄素; FLLL31

    Tetramethylcurcumin (FLLL31), a small-molecule signal transducer and activator of transcription 3 (STAT3) inhibitor derived from curcumin, binds selectively to Janus kinase 2 and the STAT3 Src homology-2 domain, which serve crucial roles in STAT3 dimerization and signal transduction.
  3. GC64373 Tezacitabine

    替扎西他滨

    Tezacitabine 是一种具有细胞生长抑制和细胞毒性的抗代谢药,是一种核苷类似物。Tezacitabine 不可逆地抑制核糖核苷酸还原酶 (ribonucleotide reductase) 并干扰 DNA 复制和修复。Tezacitabine 有效诱导细胞凋亡 (apoptotic),可用于白血病和实体瘤的研究。
  4. GC73212 TH-6 TH-6是一种强效的HDAC抑制剂,HDAC1、HDAC2、HDAC3、HDAC6、HDAC8的IC50分别为0.115、0.135、0.242、0.138、2.120µM。
  5. GC73599 TH9619 TH9619是MTHFD1和MTHFD2中去磷酸根酶和环磷酸根酶活性的有效抑制剂,IC50值为47nM,并选择性杀死癌症细胞。
  6. GC60364 Thienopyridone Thienopyridone 是一种有效的选择性的肝再生磷酸酶 (PRL) 磷酸酶抑制剂,对于 PRL-1,PRL-2 和 PRL-3,IC50 值分别为 173 nM,277 nM 和 128 nM。Thienopyridone 对其他磷酸酶的影响很小。Thienopyridone 可诱导 p130Cas 裂解和细胞凋亡 (apoptosis),并具有抗癌作用。
  7. GC45039 Thiocolchicine

    硫代秋水仙碱

    An inhibitor of microtubule assembly
  8. GC39094 Thonningianin A Thonningianin A 是一种鞣花素,从非洲草药通宁宁的甲醇提取物中分离得到。Thonningianin A 的抗氧化特性包括自由基清除、抗超氧物生成和金属螯合作用。具有抗癌活性。
  9. GC70026 Thymidine 3',5'-diphosphate tetrasodium

    Deoxythymidine 3′,5′-diphosphate tetrasodium; pdTp tetrasodium

    Thymidine 3',5'-diphosphate (Deoxythymidine 3′,5′-diphosphate) tetrasodium 是葡萄球菌核酸酶和含有 1 的都铎结构域 (SND1,MicroRNA 调控复合体 RISC 亚基) 与 [3,5-2H2] 酪氨酸核酸酶 ( [3,5-2H2] tyrosyl nuclease) 的选择性抑制剂。Thymidine 3',5'-diphosphate tetrasodium 具有抗肿瘤活性,在生化反应也可用作催化剂。
  10. GC70242 Thymocartin TFA Thymocartin TFA是胸腺素的TFA盐形式。
  11. GC74630 TI17 TI17是甲状腺激素受体相互作用蛋白Trip13的抑制剂,具有抗癌活性。
  12. GC74477 Tigatuzumab

    替加组单抗; CS-1008; Anti-Human TRAIL-R2 Recombinant Antibody

    Tigatuzumab(CS-1008)是一种靶向死亡受体5(DR5)的人源化IgG1单克隆抗体。
  13. GC62676 TJ191 TJ191 is a selective anti-cancer small molecule that targets low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.
  14. GC74684 Topoisomerase II inhibitor 14 Topoisomerase II inhibitor 14(化合物2f)是拓扑异构酶II的强效抑制剂,具有抗癌活性。
  15. GC61896 trans-Chalcone

    反-查耳酮

    Trans-Chalcone, the backbone of flavonoids, also is a potent fatty acid synthase (FAS) with IC50 of 17.1 μg/mL, and α-amylase inhibitor, causes cellcycle arrest and induces apoptosis in the breastcancer cell line MCF-7, exerting antifungal and anticancer activities.
  16. GC61349 Tributyrin

    甘油三丁酸酯,Glyceryl tributyrate

    Glycerol tributyrate (Tributyrin) is a triglyceride that may inhibit cell growth and induce cell differentiation.
  17. GC64862 Tricetin

    三粒小麦黄酮

    Tricetin 是一种有效的竞争性 Keap1-Nrf2 蛋白相互作用 (PPI) 抑制剂。Tricetin 作用于帕金森病模型,通过激活 Nrf2/HO-1 信号通路和阻止线粒体依赖性细胞凋亡 (apoptosis) 通路来保护 6-OHDA 诱导的神经毒性。
  18. GC49137 Triclabendazole-13C-d3

    CGA89317-13C,d3

    An internal standard for the quantification of triclabendazole
  19. GC61352 Triglycidyl isocyanurate

    1,3,5-三缩水甘油-S-三嗪三酮,TGIC; Teroxirone

    Triglycidyl Isocyanurate (Teroxirone, Tris(2,3-epoxypropyl) Isocyanurate, TGI, TGIC) is a triazene triepoxide with antineoplastic activity. It inhibits growth of human non-small cell lung cancer cells by activating p53. Triglycidyl Isocyanurate alkylates and cross-links DNA, thereby inhibiting DNA replication. Triglycidyl Isocyanurate is also used in various polyester powder coatings in the metal finishing industry.
  20. GC73760 Trilexium

    TRX-E-009-1

    Trilexium (TRX-E-009-1)是与TRX-E-002-1结构相关的第三代苯并吡喃。
  21. GC72251 Tripeptide-32 Tripeptide-32是一种具有抗衰老作用的生物活性肽,已被报道用作化妆品成分。
  22. GC91977 TrkB Agonist Prodrug R13

    TrkB-IN-1; Tropomyosin-related Kinase B Agonist Prodrug R13; Tropomyosin-related Kinase B Inhibitor 1

    TrkB Agonist Prodrug R13(R13)是原肌球蛋白相关激酶B(TrkB)激活剂7,8-二羟基黄酮的前药形式。
  23. GC45829 Troglitazone-d4

    CS-045-d4

    Troglitazone-d4 是氘标记的曲格列酮。 Troglitazone 是一种 PPARγ 激动剂,对人和鼠 PPARγ 受体的 EC50 分别为 550 nM 和 780 nM。
  24. GC48442 Tryptoquivaline D

    Nortryptoquivaline, NSC 292204

    A fungal metabolite with anticancer activity
  25. GC74001 TS-24 TS-24是组织蛋白酶S的抑制剂,IC50为4.3μM。
  26. GC73571 Tubulin polymerization-IN-56 Tubulin polymerization-IN-56吲唑衍生物是一种强效的微管蛋白聚合抑制剂,通过与秋水仙素位点相互作用,导致细胞周期阻滞和细胞凋亡。
  27. GC61361 Tubuloside B

    管花苷B

    TubulosideB是可从Cistanchesalsa茎中分离出的天然产物,可抑制TNFα诱导的细胞凋亡。TubulosideB还具有抗氧化活性。
  28. GC73166 U7D-1 U7D-1是一流的有效和选择性USP7(泛素特异性蛋白酶7)PROTAC降解剂,在RS4;11细胞中的DC50为33 nM。
  29. GC71119 UBX1325 UBX1325是一种促进衰老细胞凋亡的Bcl-xL抑制剂。
  30. GC60376 UC2288 UC2288 is a novel, cell-permeable, and orally active p21 attenuator, decreases p21 mRNA expression independently of p53, and attenuates p21 protein levels with minimal effect on p21 protein stability.
  31. GC72878 UCD38B hydrochloride UCD38B hydrochloride是一种细胞渗透的竞争性酶促uPA抑制剂,IC50值为7 μM。
  32. GC73601 UCM-1336 UCM-1336是一种有效的ICMT抑制剂,IC50为2μM。
  33. GC18308 UNC569 A TAM family kinase inhibitor
  34. GC49308 Ungeremine

    石蒜碱内铵盐

    A betaine-type alkaloid with diverse biological activities
  35. GC74047 UR778Br UR778Br靶向IQGAP1蛋白的GTP酶激活蛋白相关结构域(GRD结构域)。
  36. GC60377 Urolithin C

    尿石素C

    UrolithinC,是鞣花酸的多酚类肠道微生物代谢产物,是胰岛素分泌(insulinsecretion)的葡萄糖依赖性激活剂。UrolithinC是一种L型Ca2+通道开放剂,可增强Ca2+的流入。UrolithinC通过线粒体介导的途径诱导细胞凋亡(apoptosis),并刺激活性氧(ROS)的形成。
  37. GC62457 UZH1 UZH1 是 UZH1a 和 UZH1b 的外消旋体。UZH1a 是一种有效和选择性的 METTL3 抑制剂,IC50 值为 280 nM。UZH1b (IC50=28 µM) 基本无活性。UZH1 可用于细胞进程的转录组调控。UZH1 具有抗肿瘤活性。UZH1 也可用作研究 METTL3 的化学探针。
  38. GC62652 UZH1a UZH1a 是一种有效和选择性的 METTL3 抑制剂,IC50 值为 280 nM。UZH1a 可用于细胞进程的转录组调控。UZH1a 具有抗肿瘤活性。UZH1a 也可用作研究 METTL3 的化学探针。
  39. GC39232 Valepotriate

    戊曲酯,Valtrate

    A valepotriate with diverse biological activities
  40. GC63986 VAS 3947 VAS 3947 是一种特异的 NADPH 氧化酶 (NOX) 抑制剂,具有强大的抗血小板作用。VAS 3947 通过 UPR 激活,主要由于蛋白质聚集和错误折叠,独立于抗 NOX 活性诱导细胞凋亡 (apoptosis)。
  41. GC48247 Verrucarin A

    疣孢菌素,Muconomycin A

    A macrocyclic trichothecene with diverse biological activities
  42. GC52364 Vimentin (139-159)-biotin Peptide

    VIM (139-159)-biotin

    A biotinylated vimentin peptide
  43. GC52371 Vimentin (G146R) (139-159)-biotin Peptide

    Biotin-GQGKSRLRDLYEEEMRELRRQ, Biotin-GQGKSRLRDLYEEEMRELRRQ (X=Citrulline), VIM (G146R) (139-159)-biotin

    A biotinylated mutant vimentin peptide
  44. GC72365 Visilizumab Visilizumab(抗人CD3E重组抗体)是一种人源化低Fc受体结合的抗CD3单克隆IgG2抗体。
  45. GC49168 Visnagin

    齿阿米素

    A furanochromone with diverse biological activities
  46. GC73136 VPC-70063 VPC-70063是一种强效的Myc-Max抑制剂,抑制Myc-Max转录活性的IC50值为8.9μM。
  47. GC64040 VTP50469 fumarate VTP50469 fumarate 是一种有效的,高选择性和口服活性的 Menin-MLL 相互作用抑制剂,Ki 为 104 pM。VTP50469 fumarate 具有高效的抗白血病活性。
  48. GC73868 WD6305 TFA WD6305 TFA是一种有效的mettl3靶向PROTAC降解剂。
  49. GC62558 WDR5-IN-1 WDR5-IN-1 是一种有效的选择性 WD 重复结构域 5 (WDR5) 抑制剂,Kd 为 <0.02 nM。WDR5-IN-1 抑制 MLL1 组蛋白甲基转移酶活性 (HMT),IC50为 2.2 nM。WDR5-IN-1 减少 WDR5 移位基因的 MYC 募集,并在 CHP-134 (神经母细胞瘤) 和 Ramos (Burkitt淋巴瘤) 细胞系中显示出有效的抗增殖作用。
  50. GC62641 WEHI-9625 WEHI-9625 是一种首创的,三环砜小分子凋亡抑制剂,EC50 值为 69 nM。WEHI-9625 与 VDAC2 结合可促进其抑制小鼠 BAK 诱导的细胞凋亡的能力,但对人 BAK 和与凋亡效应密切相关的 BAX 因子均完全无效。
  51. GC73932 WK369 WK369是一种新型的BCL6小分子抑制剂,具有良好的抗卵巢癌生物活性,可诱导细胞周期阻滞和细胞凋亡。

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