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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. GC49403 Benzarone

    苯扎隆,Fragivix

    An active metabolite of benzbromarone
  3. GC70742 Betamethasone-d5-1 βmethasone-d5-1氘标记为倍他米松。
  4. GC73940 BFC1108 BFC1108是一种小分子Bcl-2功能转换器。
  5. GC68757 BH3 hydrochloride BH3 hydrochloride 是能透过血脑屏障的多肽,通过直接激活促凋亡 Bax/Bak 或通过中和抗凋亡 Bcl-2 蛋白 (Bcl-2、Bcl-XL、Bcl-w、mcl1和A-1)来诱导细胞凋亡,通过与BH3 结构域结合。
  6. GC60076 Bigelovin

    锦菊素

    Bigelovin是可从海百合中分离得到的一种倍半萜内酯,是选择性的视黄素X受体α(retinoidXreceptorα)的激动剂。Bigelovin可通过诱导凋亡和自噬来发挥抗肿瘤活性。Bigelovin通过抑制ROS的生成来调节mTOR信号通路。
  7. GC49513 Bim/BOD (IN) Polyclonal Antibody For immunodetection of Bim-related proteins
  8. GC52355 BimS BH3 (51-76) (human) (trifluoroacetate salt)

    DMRPEIWIAQELRRIGDEFNAYYARR-OH, Bims (51-76)

    A Bim-derived peptide
  9. GC68769 Biotin-COG1410 TFA Biotin-COG1410 TFA 是生物素化的 COG1410 。COG1410 是一种载脂蛋白 E 的衍生肽和凋亡 (apoptosis) 抑制剂。COG1410 在小鼠颅脑损伤 (TBI) 模型中发挥神经保护和抗炎作用。COG1410 可用于神经系统疾病的研究。
  10. GC40155 Biotin-DEVD-CHO (trifluoroacetate salt)

    Biotin-Asp-Glu-Val-Asp-CHO

    A biotinylated caspase-3 and -7 inhibitor
  11. GC68308 Bisdemethoxycurcumin-d8

    Curcumin III-d8; Didemethoxycurcumin-d8

    Bisdemethoxycurcumin-d8 (Curcumin III-d8) 是 Bisdemethoxycurcumin 的氘代物。Bisdemethoxycurcumin 是姜黄素衍生物,具有抗炎症和抗癌活性。
  12. GC68774 Bleomycin A5

    Pingyangmycin

    Bleomycin A5 (Pingyangmycin) 是糖肽类抗生素,具有口服活性。Bleomycin A5 具有抗肿瘤剂、细胞凋亡诱导剂和细菌代谢物的作用。
  13. GC65428 BLM-IN-1 BLM-IN-1 (compound 29) 是有效的、布鲁姆综合征蛋白 (BLM) 的抑制剂,对BLM的KD 值为1.81 μM,IC50 值为0.95 μM。可诱导DNA损伤反应,癌细胞的凋亡和增殖抑制。
  14. GC73893 BLU-222 BLU-222是一种口服活性高选择性CDK2抑制剂。
  15. GC39483 BO-264 A TACC3 inhibitor
  16. GC40149 Boc-AEVD-CHO (trifluoroacetate salt)

    Boc-Ala-Glu-Val-Asp-CHO

    An inhibitor of caspase-8
  17. GC46942 Bortezomib-d15

    LDP-341-d15, MG-341-d15, PS-341-d15

    A neuropeptide with diverse biological activities
  18. GC65010 Bortezomib-d8

    PS-341-d8; LDP-341-d8; NSC 681239-d8

    Bortezomib-d8 (PS-341-d8) 是 Bortezomib 的氘代物。Bortezomib (PS-341) 是一种可逆性和选择性的蛋白酶体 (proteasome) 抑制剂,通过靶向苏氨酸残基有效抑制 20S 蛋白酶体 (Ki=0.6 nM)。Bortezomib 破坏细胞周期、诱导细胞凋亡以及抑制核因子 NF-κB。Bortezomib 是第一种蛋白酶体抑制剂,具有抗癌活性。
  19. GC40009 Bostrycin

    Rhodosporin

    An anthraquinone with diverse biological activities
  20. GC74024 BPU BPU在亚g1期阻止细胞周期进程。
  21. GC42969 bpV(phen) (potassium hydrate)

    Bisperoxovanadium(phen), Potassium Bisperoxo(1,10phenanthroline) oxovanadate (V)

    An inhibitor of phosphatases
  22. GC39551 BRD3308 An HDAC3 inhibitor
  23. GC62536 Bromelain

    菠萝蛋白酶

    A mixture of proteolytic enzymes
  24. GC70853 Broussochalcone A Broussochalcone A是黄嘌呤氧化酶的抗氧化剂和抑制剂(IC50=2.21 μM),具有清除自由基的活性。
  25. GC39355 BTSA1 BTSA1 is a pharmacologically optimized BAX activator that binds with high affinity and specificity to the N-terminal activation site and induces conformational changes to BAX leading to BAX-mediated apoptosis. It effectively promotes apoptosis in leukemia cell lines and patient samples while sparing healthy cells.
  26. GC46962 Busulfan-d8

    白消安 d8

    An internal standard for the quantification of busulfan
  27. GC73237 BWA-522 BWA-522是一种口服小分子蛋白靶向嵌合体(PROTACs),对AR-FL和AR-V7具有显著的降解作用。
  28. GC48433 BX-320

    N1-[3-[[5-溴-2-[[3-[(1-吡咯烷基羰基)氨基]苯基]氨基]-4-嘧啶基]氨基]丙基]-2,2-二甲基丙烷二酰胺

    An inhibitor of PDK1
  29. GC46989 C18 dihydro Ceramide-d3 (d18:0/18:0-d3)

    N-octadecanoyl-D-erythro-Dihydrosphingosine-d3

    An internal standard for the quantification of C18 dihydro ceramide
  30. GC40141 C18 Phytoceramide-d3 (t18:0/18:0-d3)

    Cer(t18:0/18:0) - d3, Ceramide (t18:0/18:0)- d3, N-Octadecanoyl Phytosphingosine- d3, C18:0 Phytoceramide- d3, N-Stearoyl Phytosphingosine- d3

    An internal standard for the quantification of C18 phytoceramide
  31. GC43105 C8 Ceramide (d18:1.8:0)

    N-辛酰基-D-神经鞘氨醇; N-Octanoyl-D-erythro-sphingosine

    A cell-permeable ceramide analog
  32. GC47016 Cabergoline-d6

    FCE-21336-d6

    A neuropeptide with diverse biological activities
  33. GC60668 Calcimycin hemimagnesium

    CALIMYCIN半镁盐,A-23187 hemimagnesium; Antibiotic A-23187 hemimagnesium

    Calcimycin(A-23187)hemimagnesium是一种抗生素和独特的二价阳离子离子载体(divalentcationionophore),如钙离子和镁离子。Calcimycinhemimagnesium通过增加细胞内钙浓度诱导Ca2+依赖性细胞死亡。Calcimycinhemimagnesium抑制革兰氏阳性细菌和一些真菌的生长,还抑制ATP酶的活性并解耦哺乳动物细胞的氧化磷酸化(OXPHOS),诱导细胞凋亡(apoptosis)。
  34. GC65081 CALP1 TFA CALP1 TFA 是一种钙调蛋白 (CaM) 激动剂 (Kd 为 88 µM),与 CaM EF-hand/Ca2+ 结合位点结合。CALP1 TFA 通过抑制钙通道 (calcium channel) 的开放来阻止钙的流入和凋亡 (IC50 为 44.78 µM)。CALP1 TFA 阻止谷氨酸受体 ( glutamate receptor channels) 通道,并阻止存储操作的非选择性阳离子通道。CALP1 TFA 激活 CaM 依赖性磷酸二酯酶 (phosphodiesterase) 活性。
  35. GC18315 Calpain Inhibitor VI

    SJA6017

    A calpain and cathepsin inhibitor
  36. GC68826 Cantrixil

    TRX-E-002-1

    Cantrixil (TRX-E-002-1) 是 TRX-E-002 的活性对映异构体,是第二代超级苯并吡喃 (SBP) 化合物。Cantrixil 增加磷酸化 c-Jun 水平,导致卵巢癌细胞中半胱天冬酶介导的细胞凋亡。Cantrixil 对广泛的癌症表型具有有效的抗癌活性。
  37. GC49415 Capsorubin

    辣椒紫紅素

    A carotenoid with diverse biological activities
  38. GC18449 Cardanol monoene

    腰果酚(C15:1),Cardanol C15

    An inhibitor of tyrosinase with anticancer properties
  39. GC43144 Carfilzomib Impurity 13 (hydrochloride) A potential impurity found in commercial carfilzomib preparations
  40. GC64110 Carubicin hydrochloride

    盐酸洋红霉素,Carminomycin hydrochloride; Carminomicin I hydrochloride

    An anthracycline with anticancer activity
  41. GC62442 Casein Kinase inhibitor A51 Casein Kinase inhibitor A51 是一种有效且具有口服活性的酪蛋白激酶 1α (CK1α) 抑制剂。Casein Kinase inhibitor A51 可诱导白血病细胞凋亡 (apoptosis),并具有有效的抗白血病活性。
  42. GC73417 CASP8-IN-1 CASP8-IN-1(化合物63-R)是胱天蛋白酶8(CASP8)的选择性抑制剂,IC50为0.7μM。
  43. GC43146 Caspase-9 Inhibitor III (trifluoroacetate salt)

    Ac-LEHD-CMK

    A caspase-9 inhibitor
  44. GC43149 CAY10404 A COX-2 inhibitor
  45. GC18530 CAY10616

    顺式3,4',5-三甲氧基-3'-羟基二苯乙烯

    Pro-apoptotic analog of resveratrol
  46. GC48392 CAY10747 An inhibitor of the Hsp90-Cdc37 protein-protein interaction
  47. GC49080 CAY10786

    GPR52-IN-43

    A GPR52 antagonist
  48. GC52245 CAY10792 An anticancer agent
  49. GC61532 CCI-007

    2-(4-((2-氨基-4-氧代噻唑-5(4H)-亚基)甲基)-2-甲氧基苯氧基)乙酸乙酯

    CCI-007 is a novel small molecule with cytotoxic activity against infant leukemia with MLL rearrangements.
  50. GC39555 CDDO-2P-Im CDDO-2P-Im 是 CDDO 咪唑胺类似物,具有化学预防作用。CDDO-2P-Im 可降低小鼠肺癌模型肺肿瘤的大小和严重程度。
  51. GC39556 CDDO-3P-Im CDDO-3P-Im 是 CDDO 咪唑胺类似物,具有化学预防作用。CDDO-3P-Im 可降低小鼠肺癌模型肺肿瘤的大小和严重程度。

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