Home >> Signaling Pathways >> Immunology/Inflammation >> Apoptosis

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. GC72511 L-Cystathionine dihydrochloride L-Cystathionine dihydrochloride是一种非蛋白硫醚,是与含硫氨基酸代谢状态相关的关键氨基酸。
  3. GC72575 L-Glutamic acid monosodium (hydrate) L-Glutamic acid monosodium (hydrate)是一种营养添加剂和调味剂。
  4. GC64352 L-Glutamic acid-15N

    L-谷氨酸 15N

    L-Glutamic acid-15N 是一种 15N 标记的 L-Glutamic acid。L-Glutamic acid 作为一种兴奋性氨基酸神经递质,为谷氨酸盐受体所有亚型(代谢型红藻氨酸、NMDA 和 AMPA)的激动剂。对 DA 从多巴胺能神经末梢释放的过程有激动作用。
  5. GC65095 L-Glutamic acid-d5

    L-谷氨酸 d5

    L-Glutamic acid-d5 是 L-Glutamic acid 的氘代物。L-Glutamic acid 作为一种兴奋性氨基酸神经递质,为谷氨酸盐受体所有亚型(代谢型红藻氨酸、NMDA 和 AMPA)的激动剂。对 DA 从多巴胺能神经末梢释放的过程有激动作用。
  6. GC44085 L-Sulforaphene

    莱菔素

    A natural isothiocyanate
  7. GC69405 L-Theanine-d5

    L-Glutamic Acid γ-ethyl amide-d5; Nγ-Ethyl-L-glutamine-d5

    L-Theanine-d5 是 L-Theanine 的氘代物。L-Theanine (L-Glutamic Acid γ-ethyl amide)是一种存在绿茶叶片中的非蛋白氨基酸物质, 能阻断大脑中谷氨酸与谷氨酸受体结合,具有神经保护和抗氧化活性。 能通过口服 L-Theanine (L-Glutamic Acid γ-ethyl amide) 抑制皮层神经元兴奋从而产生抗应激作用 。
  8. GC44087 L-threo-PPMP (hydrochloride)

    L-threo-1-phenyl-2-Palmitoylamino-3-morpholino-1-propanol

    An inhibitor of glucosylceramide synthetase
  9. GC60221 Lactoferrin (17-41) (acetate)

    Lactoferricin B acetate; Lfcin B acetate

    Lactoferrin 17-41 (Lactoferricin B) acetate 对应于牛乳铁蛋白的残基 17-41,对革兰氏阳性和革兰氏阴性细菌、病毒、原生动物和真菌等多种微生物具有抗菌活性。Lactoferrin 17-41 acetate 具有抗肿瘤活性。
  10. GC40222 Lapatinib-d4 (tosylate) An internal standard for the quantification of lapatinib
  11. GC39209 LCH-7749944

    GNF-PF-2356

    LCH-7749944 (GNF-PF-2356) is a novel and potent p21-activated kinase 4 (PAK4) inhibitor with an IC50 of 14.93 μM and has less potently inhibitory effect against PAK1, PAK5 and PAK6. LCH-7749944 causes successful inhibition of EGFR activity due to its inhibitory effect on PAK4.
  12. GC63592 LCS-1

    4,5-二氯-2-(3-甲苯基)哒嗪-3-酮

    An inhibitor of SOD1
  13. GC49753 LCS3 An inhibitor of glutathione reductase and thioredoxin reductase
  14. GC69364 LDCA LDCA 是一种双重打击代谢调节剂,可抑制 LDH-A 酶活性,刺激恶性群体的凋亡。LDCA 可用于致癌进展的研究。
  15. GC64325 Ligustilide

    蒿本内酯

    Ligustilide is the most abundant bioactive ingredient in Rhizoma Chuanxiong, a Chinese medicinal herb commonly used for the treatment of cardiovascular ailments. Solutions are best fresh-prepared.
  16. GC69379 Lipid 8 Lipid 8 是一种可电离的氨基脂质,可用于合成脂质纳米颗粒。
  17. GC69380 Lirentelimab

    AK002; Anti-Siglec-8 Reference Antibody (lirentelimab)

    Lirentelimab (AK002) 是一种人源化 IgG1 单克隆抗体,靶向唾液酸结合的 Ig 样凝集素 8 (SIGLEC8)。Lirentelimab 诱导 IL-5 激活的嗜酸性粒细胞细胞凋亡并抑制 IL-5 介导的肥大细胞激活。Lirentelimab 可用于嗜酸性胃炎、十二指肠炎的研究。
  18. GC60997 Lixisenatide acetate Lixisenatideacetate是胰高血糖素样肽1受体(GLP-1R)的激动剂,可用于2型糖尿病的研究。
  19. GC49177 Loliolide

    地芰普内酯

    A monoterpene lactone with diverse biological activities
  20. GC39820 Lometrexol hydrate

    洛美曲索水合物,DDATHF hydrate

    A GART inhibitor
  21. GC40909 Lonicerin

    忍冬苦苷

    A flavonoid with diverse biological activities
  22. GC67936 Lupiwighteone

    黄羽扇豆魏特酮; 8-prenylgenistein

    Lupiwighteone 是一种广泛存在于野生植物中的异黄酮,具有抗氧化、抗菌和抗癌作用。Lupiwighteone 通过抑制 PI3K/Akt/mTOR 通路,诱导人乳腺癌细胞 caspase 依赖性和非依赖性凋亡 (Apoptosis)。
  23. GC50009 LY 294002 hydrochloride Prototypical PI 3-kinase inhibitor; also inhibits other kinases
  24. GC44096 LY293111

    Etalocib; VML 295

    A LTB4 receptor antagonist
  25. GC38967 Lycorine

    石蒜碱

    An alkaloid with diverse biological activities
  26. GC18241 Lysophosphatidylcholines

    L-溶血卵磷脂,Lyso-Lecithins (egg)

    A glycerophospholipid
  27. GC90483 Magainin 1 (trifluoroacetate salt)

    MG1

    一种抗微生物阳离子肽。

  28. GC61021 Malachite green oxalate

    孔雀石绿草酸盐

    Malachite green (Aniline green, Basic green 4, Diamond green B, Victoria green B) is a synthetic dyestuff and antimicrobial with potential carcinogenicity.
  29. GC40007 Malformin A

    Malformin A1

    A cyclopentapeptide fungal metabolite with diverse biological activities
  30. GC63058 Malvidin-3-galactoside chloride

    氯化锦葵色素-3-O-半乳糖苷

    Malvidin-3-galactoside chloride 是一种花青素单体,可诱导肝细胞癌 (HCC) 细胞周期停滞和凋亡。Malvidin-3-galactoside chloride 抑制 ROS 的产生和积累。Malvidin-3-galactoside chloride 具有抗肿瘤功能。
  31. GC18363 Mca-DEVDAPK(Dnp)-OH

    Caspase-3 Fluorogenic Substrate III, CPP32 Fluorogenic Substrate III, 7-Methoxycoumarin-4-acetyl-DEVDAPK(Dnp)-OH, Mca-Asp-Glu-Val-Asp-Ala-Pro-Lys(Dnp)-OH

    A caspase-3 fluorogenic substrate
  32. GC44135 Mca-VDQMDGW-K(Dnp)-NH2 (ammonium salt)

    Caspase-3 Fluorogenic Substrate V

    A caspase-3 fluorogenic substrate
  33. GC62252 Mefuparib hydrochloride

    MPH

    Mefuparib hydrochloride (MPH) 是一种具有口服活性的,底物竞争性和选择性的 PARP1/2 抑制剂,IC50 分别为 3.2 nM 和 1.9 nM。Mefuparib hydrochloride 诱导细胞凋亡 (apoptosis),并在体内外具有显着的抗癌活性。
  34. GC60241 Melatonin D5

    褪黑素 D5; N-Acetyl-5-methoxytryptamine-d4

    An internal standard for the quantification of melatonin
  35. GC71607 Melatonin-d7 Melatonin-d7是氘标记的褪黑素。
  36. GC40065 Meloxicam-d3

    美洛昔康 d3

    An internal standard for the quantification of meloxicam
  37. GC71632 Meloxicam-d3-1 Meloxicam-d3-1是氘标记的美洛昔康。
  38. GC47620 Mensacarcin A bacterial metabolite with anticancer activity
  39. GC61041 Mepazine hydrochloride

    哌卡嗪盐酸盐,Pecazine hydrochloride

    Mepazinehydrochloride(Pecazinehydrochloride)是一种有效的选择性MALT1蛋白酶抑制剂。Mepazinehydrochloride抑制全长GSTMALT1和GSTMALT1325-760段的IC50分别为0.83和0.42μM。Mepazinehydrochloride通过增强细胞凋亡(apoptosis)来影响ABC-DLBCL细胞的生存能力。
  40. GC48907 Metaxalone-d6

    AHR438-d6; NSC170959-d6

    An internal standard for the quantification of metaxalone
  41. GC61047 Methotrexate disodium

    甲氨蝶呤二钠盐,Amethopterin disodium; CL14377 disodium; WR19039 disodium

    Methotrexate sodium, an inhibitor of tetrahydrofolate dehydrogenase, is an antineoplastic antimetabolite with immunosuppressant properties.
  42. GC19959 Methylprednisolone acetate

    泼尼松龙EP杂质

    A synthetic glucocorticoid and an ester form of methylprednisolone
  43. GC67966 Methylstat Methylstat 是一种有效的组蛋白去甲基化酶 (histone demethylases) 抑制剂。Methylstat 具有抗增殖活性,低细胞毒性。Methylstat 诱导细胞凋亡 (Apoptosis) 和细胞周期停滞在 G0/G1 期。Methylstat 增加 p53 和 p21 蛋白水平的表达。Methylstat 抑制由各种细胞因子诱导的血管生成。Methylstat 可用作化学探针以解决其在血管生成中的作用。
  44. GC66462 MGH-CP1 MGH-CP1 is a potent and selective inhibitor of transcriptional enhanced associate domain (TEAD) palmitoylation. MGH-CP1 exhibits dose-dependent and potent inhibition of TEAD2/4 auto-palmitoylation in vitro with IC50 of 710 nM and 672 nM, respectively.
  45. GC62598 MI-1061 TFA MI-1061 TFA 是一种有效的,口服可生物利用的,化学稳定性的 MDM2 (MDM2-p53 互作) 抑制剂 (IC50=4.4 nM; Ki=0.16 nM)。MI-1061 TFA 激活小鼠 SJSA-1 异种移植瘤组织中 p53 并诱导凋亡,具有抗肿瘤活性。
  46. GC62621 Milademetan tosylate hydrate

    DS-3032b; DS-3032 tosylate hydrate

    Milademetan (DS-3032) tosylate hydrate 是特异性的、具有口服活性的 MDM2 抑制剂,用于急性髓系白血病和实体肿瘤的研究。Milademetan (DS-3032) tosylate hydrate 可诱导 G1 细胞周期阻滞、衰老和凋亡。
  47. GC68213 MitoBloCK-6 MitoBloCK-6 是一种有效的 Erv1/ALR 抑制剂,IC50 分别为 900 nM 和 700 nM。MitoBloCK-6 还抑制 Erv2 (IC50=1.4 μM)。MitoBloCK-6 可通过细胞色素 c 的释放诱导 hESCs 细胞凋亡。
  48. GC39814 Mitoguazone

    米托瓜酮; Methylglyoxal-bis(guanylhydrazone); MGBG; Methyl-GAG

    Mitoguazone (Methylglyoxal-bis(guanylhydrazone)) 是一种具有有效抗肿瘤活性的合成多羰基衍生物。Mitoguazone 是一种可透过血脑屏障的竞争性的 S-腺苷-蛋氨酸脱羧酶 (S-adenosyl-methionine decarboxylase) 抑制剂,可破坏多胺的生物合成。Mitoguazone 诱导细胞凋亡 (apoptosis),可抑制 HIV DNA 整合到单核细胞和巨噬细胞中的细胞 DNA 中。Mitoguazone 具可用于急性白血病,霍奇金淋巴瘤和非霍奇金淋巴瘤的研究。
  49. GC65143 MKC-1

    Ro-31-7453

    MKC-1 (Ro-31-7453) 是一种口服有效的细胞周期抑制剂,具有广泛的抗肿瘤活性。MKC-1 抑制 Akt/mTOR 通路。通过结合一系列不同的细胞蛋白,包括微管蛋白 (tubulin) 和导入蛋白 β (importin β) 家族成员,MKC-1 阻止细胞有丝分裂并诱导细胞凋亡 (apoptosis)。
  50. GC48676 Monascuspiloin

    Monascinol

    A fungal metabolite with anticancer activity
  51. GC61079 Monensin

    莫能菌素

    莫能菌素(蛋白质转运抑制剂)是一种离子载体,可破坏高尔基体,抑制细胞内蛋白质转运。

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