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
- Cat.No. 产品名称 Information
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GC49403
Benzarone
苯扎隆,Fragivix
An active metabolite of benzbromarone -
GC70742
Betamethasone-d5-1
βmethasone-d5-1氘标记为倍他米松。
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GC73940
BFC1108
BFC1108是一种小分子Bcl-2功能转换器。
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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。
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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。 -
GC49513
Bim/BOD (IN) Polyclonal Antibody
For immunodetection of Bim-
related proteins -
GC52355
BimS BH3 (51-76) (human) (trifluoroacetate salt)
DMRPEIWIAQELRRIGDEFNAYYARR-OH, Bims (51-76)
A Bim-derived peptide -
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。
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GC40155
Biotin-DEVD-CHO (trifluoroacetate salt)
Biotin-Asp-Glu-Val-Asp-CHO
A biotinylated caspase-3 and -7 inhibitor -
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。 -
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。 -
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。
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GC73893
BLU-222
BLU-222是一种口服活性高选择性CDK2抑制剂。
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GC39483
BO-264
A TACC3 inhibitor
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GC40149
Boc-AEVD-CHO (trifluoroacetate salt)
Boc-Ala-Glu-Val-Asp-CHO
An inhibitor of caspase-8 -
GC46942
Bortezomib-d15
LDP-341-d15, MG-341-d15, PS-341-d15
A neuropeptide with diverse biological activities -
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。 -
GC40009
Bostrycin
Rhodosporin
An anthraquinone with diverse biological activities -
GC74024
BPU
BPU在亚g1期阻止细胞周期进程。
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GC42969
bpV(phen) (potassium hydrate)
Bisperoxovanadium(phen), Potassium Bisperoxo(1,10phenanthroline) oxovanadate (V)
An inhibitor of phosphatases -
GC39551
BRD3308
An HDAC3 inhibitor
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GC62536
Bromelain
菠萝蛋白酶
A mixture of proteolytic enzymes -
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。
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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.
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GC46962
Busulfan-d8
白消安 d8
An internal standard for the quantification of busulfan -
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。
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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 -
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 -
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 -
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 -
GC47016
Cabergoline-d6
FCE-21336-d6
A neuropeptide with diverse biological activities -
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)。 -
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。
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GC18315
Calpain Inhibitor VI
SJA6017
A calpain and cathepsin inhibitor -
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。 -
GC49415
Capsorubin
辣椒紫紅素
A carotenoid with diverse biological activities -
GC18449
Cardanol monoene
腰果酚(C15:1),Cardanol C15
An inhibitor of tyrosinase with anticancer properties -
GC43144
Carfilzomib Impurity 13 (hydrochloride)
A potential impurity found in commercial carfilzomib preparations
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GC64110
Carubicin hydrochloride
盐酸洋红霉素,Carminomycin hydrochloride; Carminomicin I hydrochloride
An anthracycline with anticancer activity -
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。
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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。
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GC43146
Caspase-9 Inhibitor III (trifluoroacetate salt)
Ac-LEHD-CMK
A caspase-9 inhibitor -
GC43149
CAY10404
A COX-2 inhibitor
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GC18530
CAY10616
顺式3,4',5-三甲氧基-3'-羟基二苯乙烯
Pro-apoptotic analog of resveratrol -
GC48392
CAY10747
An inhibitor of the Hsp90-Cdc37 protein-protein interaction
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GC49080
CAY10786
GPR52-IN-43
A GPR52 antagonist -
GC52245
CAY10792
An anticancer agent
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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. -
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。
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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。