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Caspase

Caspase

Caspases (cysteine-aspartic proteases, cysteine aspartases or cysteine-dependent aspartate-directed proteases) are a family of protease enzymes playing essential roles in programmed cell death (including apoptosis, pyroptosis and necroptosis) and inflammation. They are named caspases due to their specific cysteine protease activity – a cysteine in its active site nucleophilically attacks and cleaves a target protein only after an aspartic acid residue.
TargetMol
1 2 3 4 5 6 7 8 9 10
Cat. No. Product Name CAS No. Purity Chemical Structure
T82388 Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone
化合物 Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone
1926163-65-6 98%
Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone 是一种细胞渗透性且无毒的抑制剂,它能与活化的caspase-3在凋亡细胞内不可逆结合。该抑制剂的荧光强度可通过流式细胞仪、微孔板读数器或荧光显微镜检测。
T82774 Caspase-3 activator 3
化合物 Caspase-3 activator 3
98%
Caspase-3 activator 3 (compound 2h) 通过激活caspase 3诱导HL-60和K562细胞apoptosis,表现出抗白血病活性。其对HL-60细胞的IC50值为42.89 μM,对K562细胞的IC50值为33.61 μM。
T82775 Caspase-3 activator 2
化合物 Caspase-3 activator 2
98%
Caspase-3 activator 2 (Compound 2f) 是诱导细胞凋亡的caspase 3激活剂,适用于癌症研究。该化合物对 HL-60 细胞和 K562 细胞展示出细胞毒性,IC50 值分别为 33.52 μM 和 76.90 μM。
T83205 Ac-DNLD-CHO
化合物 Ac-DNLD-CHO
775289-20-8 98%
Ac-DNLD-CHO(Ac-Asp-Asn-Leu-Asp-CHO)是一种有效的Caspase-3/7抑制剂,具有较低的IC50(分别为9.89, 245 nM)和Kiapp(分别为0.68、55.7 nM)。该化合物在研究caspase介导的细胞凋亡过程中具有重要应用价值,适用于神经退行性疾病和病毒感染疾病的相关研究...
T78586L Ac-IETD-CHO TFA
Ac-IETD-CHO 三氟乙酸盐
98%
Ac-IETD-CHO TFA 是一种 granzyme B 和 caspase-8 抑制剂,通过阻断 caspase3 前体裂解抑制 caspase8 活性。Ac-IETD-CHO TFA 抑制 Fas 介导的细胞凋亡(Apoptosis)。
T21523 β-Tocotrienol
化合物 T21523
490-23-3 98%
Beta-Tocotrienol to serve as a new anticancer agent for treating human lung and brain cancers. It inhibits the growth of both A549 (GI50=1.38±0.334μM) and U87MG ...
TN1642 Ferruginol
化合物Ferruginol
514-62-5 98%
Ferruginol has anti-plasmodial, leishmanicidal, anti-ulcerogenic, cardioprotective, anticancer, anti-oxidative and anti-inflammatory activities, it can induce ap...
TN4496 Marginatoxin
化合物 TN4496
1422536-56-8 98%
Marginatoxin may be a promising chemopreventive agent for treating hepatocellular carcinoma, it induces human hepatoma BEL-7402 cells apoptosis in vitro and in v...
TN4877 Quercetin 3,4'-dimethyl ether
化合物 TN4877
33429-83-3 98%
Quercetin 3,4'-dimethyl ether shows anti-lipid peroxidation activity (IC 50 values of 0.3 uM), it also shows anti-inflammatory activity. Quercetin 3,4'-dimethyl ...
TN5033 Skullcapflavone I
化合物 TN5033
41060-16-6 98%
Skullcapflavone I has anti-inflammatory and anti-allergic potential, it can significantly inhibit LPS stimulated NO and PGE(2) release in J774A.1 macrophages and...
TN2835 28-Deoxonimbolide
化合物 TN2835
126005-94-5 98%
28-Deoxonimbolide exhibits potent cytotoxic activity against HL60 leukemia cells.
TN2977 3-O-trans-p-Coumaroyltormentic acid
化合物 TN2977
121064-78-6 98%
3-O-(E)-p-coumaroyl tormentic acid may be promising lead compound for developing an effective drug for treatment of leukemia, it induces apoptotic cell death in ...
T10548 Biotin-VAD-FMK
化合物 T10548
1135688-15-1 98%
Biotin-VAD-FMK is a cell-permeable, irreversible biotin-labeled inhibitor of caspase. It is used to identify active caspases in cell lysates.
T4366 Quinovic acid
化合物 T4366
465-74-7 98%
Quinovic acid shows some anti-tumour activities, quinovic acid glycosides have a potent inhibitory effect on the growth of human bladder cancer cell lines by ind...
T13797 Nivalenol
雪腐镰刀菌烯醇
23282-20-4 98%
Nivalenol 是一种由禾谷镰刀菌产生的真菌代谢物。 Nivalenol 通过 caspase 和内在凋亡途径诱导细胞死亡,从而影响免疫系统并引起呕吐、生长迟缓和生殖障碍。
TN3525 Boehmenan
化合物 TN3525
57296-22-7 98%
(±)-Boehmenan shows potent protein-tyrosine phosphatase 1B (PTP1B) inhibitory activity in vitro with the IC(50) values of 43.5 uM, it inhibits PTP1B activity in ...
TN2511 Britannilactone diacetate
化合物 TN2511
1286694-67-4 98%
1,6-O,O-Diacetylbritannilactone(OODBL) has anti-inflammatory activity, it has a potential therapeutic efficacy on inflammatory diseases especially allergic airwa...
TN3708 Coronarin D
化合物 TN3708
119188-37-3 98%
Coronarin D shows promising antifungal activity against C. albicans in vitro, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration...
T14003 15-Acetoxyscirpenol
15-乙酰蛇形菌素
2623-22-5 98%
15-Acetoxyscirpenol, a member of the acetoxyscirpenol moiety mycotoxins (ASMs), potently induces apoptosis and inhibits the growth of Jurkat T cells in a dose-de...
T2S0606 Bakkenolide A
蜂斗菜内酯A
19906-72-0 98%
Bakkenolide A has antifeedant and growth inhibitory effects on neonate variegated cutworms, it inhibits leukemia by regulation of HDAC3 and PI3K/Akt-related sign...
Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone
T82388
Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone 是一种细胞渗透性且无毒的抑制剂,它能与活化的caspase-3在凋亡细胞内不可逆结合。该抑制剂的荧光强度可通过流式细胞仪、微孔板读数器或荧光显微镜检测。
Caspase-3 activator 3
T82774
Caspase-3 activator 3 (compound 2h) 通过激活caspase 3诱导HL-60和K562细胞apoptosis,表现出抗白血病活性。其对HL-60细胞的IC50值为42.89 μM,对K562细胞的IC50值为33.61 μM。
Caspase-3 activator 2
T82775
Caspase-3 activator 2 (Compound 2f) 是诱导细胞凋亡的caspase 3激活剂,适用于癌症研究。该化合物对 HL-60 细胞和 K562 细胞展示出细胞毒性,IC50 值分别为 33.52 μM 和 76.90 μM。
Ac-DNLD-CHO
T83205
Ac-DNLD-CHO(Ac-Asp-Asn-Leu-Asp-CHO)是一种有效的Caspase-3/7抑制剂,具有较低的IC50(分别为9.89, 245 nM)和Kiapp(分别为0.68、55.7 nM)。该化合物在研究caspase介导的细胞凋亡过程中具有重要应用价值,适用于神经退行性疾病和病毒感染疾病的相关研究...
Ac-IETD-CHO TFA
T78586L
Ac-IETD-CHO TFA 是一种 granzyme B 和 caspase-8 抑制剂,通过阻断 caspase3 前体裂解抑制 caspase8 活性。Ac-IETD-CHO TFA 抑制 Fas 介导的细胞凋亡(Apoptosis)。
β-Tocotrienol
T21523
Beta-Tocotrienol to serve as a new anticancer agent for treating human lung and brain cancers. It inhibits the growth of both A549 (GI50=1.38±0.334μM) and U87MG ...
Ferruginol
TN1642
Ferruginol has anti-plasmodial, leishmanicidal, anti-ulcerogenic, cardioprotective, anticancer, anti-oxidative and anti-inflammatory activities, it can induce ap...
Marginatoxin
TN4496
Marginatoxin may be a promising chemopreventive agent for treating hepatocellular carcinoma, it induces human hepatoma BEL-7402 cells apoptosis in vitro and in v...
Quercetin 3,4'-dimethyl ether
TN4877
Quercetin 3,4'-dimethyl ether shows anti-lipid peroxidation activity (IC 50 values of 0.3 uM), it also shows anti-inflammatory activity. Quercetin 3,4'-dimethyl ...
Skullcapflavone I
TN5033
Skullcapflavone I has anti-inflammatory and anti-allergic potential, it can significantly inhibit LPS stimulated NO and PGE(2) release in J774A.1 macrophages and...
28-Deoxonimbolide
TN2835
28-Deoxonimbolide exhibits potent cytotoxic activity against HL60 leukemia cells.
3-O-trans-p-Coumaroyltormentic acid
TN2977
3-O-(E)-p-coumaroyl tormentic acid may be promising lead compound for developing an effective drug for treatment of leukemia, it induces apoptotic cell death in ...
Biotin-VAD-FMK
T10548
Biotin-VAD-FMK is a cell-permeable, irreversible biotin-labeled inhibitor of caspase. It is used to identify active caspases in cell lysates.
Quinovic acid
T4366
Quinovic acid shows some anti-tumour activities, quinovic acid glycosides have a potent inhibitory effect on the growth of human bladder cancer cell lines by ind...
Nivalenol
T13797
Nivalenol 是一种由禾谷镰刀菌产生的真菌代谢物。 Nivalenol 通过 caspase 和内在凋亡途径诱导细胞死亡,从而影响免疫系统并引起呕吐、生长迟缓和生殖障碍。
Boehmenan
TN3525
(±)-Boehmenan shows potent protein-tyrosine phosphatase 1B (PTP1B) inhibitory activity in vitro with the IC(50) values of 43.5 uM, it inhibits PTP1B activity in ...
Britannilactone diacetate
TN2511
1,6-O,O-Diacetylbritannilactone(OODBL) has anti-inflammatory activity, it has a potential therapeutic efficacy on inflammatory diseases especially allergic airwa...
Coronarin D
TN3708
Coronarin D shows promising antifungal activity against C. albicans in vitro, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration...
15-Acetoxyscirpenol
T14003
15-Acetoxyscirpenol, a member of the acetoxyscirpenol moiety mycotoxins (ASMs), potently induces apoptosis and inhibits the growth of Jurkat T cells in a dose-de...
Bakkenolide A
T2S0606
Bakkenolide A has antifeedant and growth inhibitory effects on neonate variegated cutworms, it inhibits leukemia by regulation of HDAC3 and PI3K/Akt-related sign...
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