37
4
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2470 |
MDL-28170
Calpain Inhibitor III |
Cysteine Protease; Proteasome | Proteases/Proteasome; Ubiquitination |
MDL-28170 (Calpain Inhibitor III) 是一种选择性的、有效的、具有膜渗透性的半胱氨酸蛋白酶 (calpain)抑制剂,可在全身给药后迅速穿过血脑屏障。它还能阻断γ-secretase。 | |||
T6583 |
MG-101
ALLN,Ac-LLnL-CHO,Calpain inhibitor I,Calpain inhibitor-1,MG101,钙蛋白酶抑制剂I |
Cysteine Protease; Proteasome | Proteases/Proteasome; Ubiquitination |
MG-101 (Calpain inhibitor I) 是一种有效的半胱氨酸蛋白酶抑制剂,能够抑制钙蛋白酶I (Ki:190 pM),钙蛋白酶II (Ki:220 pM),组织蛋白酶B (Ki:150 pM)和组织蛋白酶L (Ki:500 pM)。 | |||
T38931 |
Calpain Inhibitor-1
|
Others | Others |
Calpain Inhibitor-1 (compound 36) is a highly potent and selective inhibitor of Calpain 1 (Cal1), which is a cysteine protease. It exhibits an IC50 value of 100 nM and a Ki value of 2.89 μM. | |||
T21949 |
Calpain Inhibitor XII
|
Others | Others |
(Rac)-Calpain Inhibitor XII是一种可逆的,选择性抑制钙蛋白酶I(calpain I; μ-calpain)的化合物,具有19 nM的Ki值。其对钙蛋白酶II(calpain II; m-calpain; Ki=120 nM)和组织蛋白酶B(cathepsin B; Ki=750 nM)显示出较低的抑制亲和力。(Rac)-Calpain Inhibitor XII用于研究钙蛋白酶在多种生理过程中的角色,如嗜中性粒细胞趋化性、神经元信号传导和心脏对损伤的响应。 | |||
T72439 |
Calpain Inhibitor XI
|
Others | Others |
Calpain Inhibitor XI,一种可逆的calpain-1共价抑制剂,适用于神经退行性疾病的研究。 | |||
T28786 |
SJA6017
SJA-6017,Calpain Inhibitor VI,Calpain-In-4,SJA 6017,Calpain Inhibitor 4 |
Others | Others |
SJA6017 is a inhibitor of calpain-1 (IC50 = 7.5 nM) and calpain-2 ( IC50 = 78 nM). SJA6017 also inhibits cathepsins B (IC50s = 15 nM) and cathepsins L (IC50s = 1.6 nM). SJA6017 reduces apoptotic cell death, preserves spinal cord tissue and improves functi | |||
T78632 |
Z-LLY-FMK
Calpain Inhibitor IV |
Proteasome | Proteases/Proteasome; Ubiquitination |
Z-LLY-FMK (Calpain Inhibitor IV) 为一种钙蛋白酶抑制剂,涉及调控多个细胞系统的凋亡过程。该化合物能够抑制胆总管结扎所引起的肠细胞凋亡(apoptosis)。 | |||
T14187 |
ALLM
Calpain inhibitor II |
Others | Others |
ALLM (Calpain inhibitor II), a potent calpain and cathepsin protease inhibitor, not only prevents neuronal cell death but also enhances chronic neurological function following spinal cord injury (SCI)[1][2]. | |||
T80551 |
Calpain inhibitor V
Mu-Val-HPh-FMK |
Antibiotic | Microbiology/Virology |
Calpain inhibitor V (Mu-Val-HPh-FMK) 为具抗衣原体活性的细胞渗透性不可逆钙蛋白酶抑制剂。 | |||
T63391 |
Calpain Inhibitor-2
|
Others | Others |
Calpain Inhibitor-2 是具有亲脂性的钙蛋白酶抑制剂,与黑色素瘤细胞系(A-375和B-16F1)和PC-3前列腺癌细胞相比,他们在体外具有中等到良好的抗增殖效果。Calpain Inhibitor-2 中的化合物3,在基质胶细胞侵袭测定中以2μM 浓度能够抑制了80%的DU-145细胞侵袭。 | |||
T63708 |
Calpain-2-IN-1
|
Others | Others |
Calpain-2-IN-1是选择性的钙蛋白酶-2抑制剂,能够延长 ERK 激活,进而增强学习和记忆。 | |||
T2154 |
MG-132
Z-LLL-al,Z-Leu-Leu-Leu-CHO |
Apoptosis; Proteasome; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome; Ubiquitination |
MG-132 (Z-Leu-Leu-Leu-al) 是一种 26S 蛋白酶体抑制剂 (IC50=100 nM),具有细胞渗透性、可逆性。MG-132 可作为自噬激活剂,可诱导凋亡。 | |||
T9710 |
Dazcapistat
|
Cysteine Protease | Proteases/Proteasome |
Dazcapistat 是一种有效的 calpain 抑制剂,对 calpain 1、calpain 2 和 calpain 9 的 IC50 值均 <3 μM。 | |||
T2493 |
PD 151746
|
Cysteine Protease; Proteasome | Proteases/Proteasome; Ubiquitination |
PD151746 is a calpain inhibitor with a 20-fold selectivity for u-calpain (Ki = 0.26 ± 0.03 μM) over m-calpain (Ki = 5.33 ± 0.77 μM). Its IC50 values are 0.26 ± 0.03 μM (Ki for μ-calpain) and 5.33 ± 0.77 μM (Ki for m-calpain) [1]. In vitro, PD151746 targets calpain and reduces oxLDL-induced cytotoxicity [2]. | |||
T6432 |
Calpeptin
|
Apoptosis; Cysteine Protease; Proteasome | Apoptosis; Proteases/Proteasome; Ubiquitination |
Calpeptin 是一种具有细胞穿透性的calpain 抑制剂,也是cathepsin K 抑制剂,其对人血小板 Calpain I 的ID50值为40 nM。 | |||
T3525 |
PD150606
|
Cysteine Protease | Proteases/Proteasome |
PD150606 是一种具有选择性的非肽 calpain 抑制剂,具有神经保护活性,抑制 μ-calpains 和 m-calpains ,抑制红藻氨酸诱导的 Ca2+ 内流,干扰兴奋性毒性依赖性运动神经元死亡。 | |||
TP2056L |
Acetyl-Calpastatin (184-210)(human) acetate
Acetyl-Calpastatin (184-210) (human) acetate(123714-50-1 Free base ) |
Cysteine Protease | Proteases/Proteasome |
Acetyl-Calpastatin (184-210)(human) acetate 是一种有效,选择性和可逆的钙蛋白酶 (calpain) 抑制剂,对 μ-钙蛋白酶和组织蛋白酶 L 的 Ki 值分别为 0.2 nM 和 6 μM。 | |||
T60150 |
(1S,2R)-Alicapistat
|
Cysteine Protease | Proteases/Proteasome |
(1S,2R)-Alicapistat ((1S,2R)-ABT-957) is a highly efficient, orally active compound that selectively inhibits human calpains 1 and 2, with promising implications for Alzheimer's disease (AD) therapy [1]. This compound effectively addresses the metabolic liability associated with carbonyl reduction, while demonstrating potent inhibition of calpain 1 with an IC50 value of 395 nM [2]. | |||
T36352 |
Suc-Leu-Tyr-AMC
|
||
Suc-Leu-Tyr-AMC 是钙蛋白酶 I 和 II 以及木瓜蛋白酶(另一种半胱氨酸蛋白酶)的荧光底物,用于测量 20S 蛋白酶体的糜蛋白酶样肽酶活性(Ex-max:360 nm;Em-max:460 nm)。Suc-Leu-Tyr-AMC 也能被大肠杆菌的 Ti 蛋白酶裂解。 | |||
T6040 |
Aloxistatin
E64d,Loxistatin,阿洛司他丁,E64c ethyl ester |
SARS-CoV; Cysteine Protease | Microbiology/Virology; Proteases/Proteasome |
Aloxistatin (E64d) 是一种不可逆的、可透过膜的溶酶体和细胞溶质半胱氨酸蛋白酶抑制剂,能够抑制完整血小板中的钙蛋白酶活性。它是一种半胱氨酸蛋白酶抑制剂,具有血小板聚集抑制活性。 | |||
T23598 |
A-953227
A 953227,A953227 |
Others | Others |
A-953227 is a highly effective and selective inhibitor of calpain. A-953227 features enhanced selectivity versus related cysteine protease cathepsins, favorable microsomal stability, and efficacy in cellular assays. | |||
T68728 |
EP 459
|
Others | Others |
EP 459 is a thiol and calpain protease inhibitor. | |||
T13486 |
Neurodegenerative Disorder-Targeting Compound 1
|
Others | Others |
Neurodegenerative Disorder-Targeting Compound 1 是一种靶向 calpain 的抑制剂。 | |||
T84437 |
Ac-Calpastatin (184-210)
Calpastatin Peptide B27-WT |
Others | Others |
Calpastatin (184-210), an acetylated synthetic peptide derived from human calpastatin, effectively inhibits the calcium-dependent cysteine proteases, calpain I (µ-calpain) and calpain II (m-calpain), which require micromolar and millimolar calcium concentrations, respectively. Unlike its action on calpains, this 27 amino acid peptide does not inhibit papain (a cysteine protease) or trypsin (a serine protease). Encoded by exon 1B of Ac-calpastatin (184-210), it aligns with a section of inhibitory... | |||
T80103 |
Z-Leu-Tyr-Chloromethylketone
|
||
Z-Leu-Tyr-Chloromethylketone是一种抑制剂,专门针对钙蛋白酶(calpain)活性。 | |||
T25011 |
AK-295
CX295,CX 295,AK295,CX-295 |
Others | Others |
AK 295, also known as CX 295, is a dipeptide inhibitor of alpha-ketoamide calpain. | |||
T25009 |
AK 275
AK275,AK-275 |
Others | Others |
AK 275 is a calpain inhibitor that prevents degradation of cytoskeletal and myelin proteins in spinal cord in vitro. | |||
T83527 |
(Rac)-Neurodegenerative Disorder-Targeting Compound 1
|
Others | Others |
(Rac)-Neurodegenerative Disorder-Targeting Compound 1为一种针对神经退行性疾病的化合物,具有calpain抑制活性。 | |||
TP2056 |
Acetyl-Calpastatin(184-210)(human)
Acetyl-Calpastatin (184-210) (human) |
||
Selective calpain inhibitor. Strongly inhibits calpain I (Ki = 0.2 nM) and II but does not inhibit papain, trypsin and cathepsin L (Ki = 6 μM). Increases secretion of amyoid β-protein (Aβ) 42, Aβ40 and Aβ42 ratio. | |||
T23596 |
A-933548
A933548,A 933548 |
Others | Others |
A-933548 is a potent Calpain inhibitor. A-933548 features enhanced selectivity versus related cysteine protease cathepsins, favorable microsomal stability, and efficacy in cellular assays. | |||
T75794 |
Acetyl-Calpastatin(184-210)(human) TFA
|
||
Acetyl-Calpastatin(184-210)(human) TFA 是一种有效,选择性和可逆的钙蛋白酶 (calpain) 抑制剂,对 μ-钙蛋白酶和组织蛋白酶 L 的Ki 值分别为 0.2 nM 和 6 μM。 | |||
T76364 |
Ac-Leu-Leu-Norleucinol
|
||
Ac-Leu-Leu-Norleucinol 是钙蛋白酶抑制剂,可用于研究对 Acetaminophen 引起的急性肝损伤,并能够降低诱导引发的谷草转氨酶 (ALT) 和谷丙转氨酶 (AST) 水平。 | |||
T80241 |
Calpastatin subdomain B
|
Proteasome | Proteases/Proteasome; Ubiquitination |
Calpastatin subdomain B为具有生物活性的肽,其作用为抑制钙蛋白酶活性。 | |||
T36854 |
Pheleuin
|
Others | Others |
Pheleuin is a pyrazinone derivative synthesized from a dipeptide aldehyde. Although the biological activity of this compound has not been reported, similar diketopiperazines are known to inhibit calpain and/or regulate S. aureus virulence factor expression. | |||
T14187L |
ALLM acetate(110115-07-6 Free base)
|
||
ALLM acetate(110115-07-6 Free base) 是一种有效的钙蛋白酶和组织蛋白酶抑制剂,不仅可以防止神经元细胞死亡,还可以增强脊髓损伤(SCI)后的慢性神经功能。 | |||
T68547 |
SNJ-1945
|
Others | Others |
SNJ-1945 is a calpain inhibitor with more favorable retinal penetration, high oral bioavailability, and long half-life. SNJ1945 rescued defective function in lissencephaly. SNJ-1945 protects SH-SY5Y cells against MPP(+) and rotenone. SNJ-1945 reduces murine retinal cell death in vitro and in vivo. SNJ-1945 has good aqueous solubility, can prevents the heart from KCl arrest-reperfusion injury associated with the impairment of total Ca(2+) handling by inhibiting the proteolysis of alpha-fodrin a... | |||
T83406 |
2,3-Diphospho-D-glyceric acid pentasodium salt
2,3-DPG pentasodium salt |
Others | Others |
2,3-Diphospho-D-glyceric acid pentasodium salt 是一种聚磷化合物,具有明显的阴离子性质。它在红细胞的凹中心起作用,通过结合血红蛋白降低氧亲和力。作为血管钙化 (VC) 的内源性选择性抑制剂,2,3-Diphospho-D-glyceric acid 能显著推迟结晶钙蛋白颗粒 (CPP) 的生成,并在小鼠血管平滑肌细胞系 (MOVAS) 中抑制钙化作用,同时不引起细胞毒性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37753 |
Aureusimine B
|
Cysteine Protease; Antibacterial | Microbiology/Virology; Proteases/Proteasome |
Aureusimine B 是一种钙蛋白酶抑制剂,由金黄色葡萄球菌生物膜产生,可能是金黄色葡萄球菌生物膜感染的潜在生物标志物。 | |||
T19384 |
Isovalerylcarnitine
|
Apoptosis; Cysteine Protease | Apoptosis; Proteases/Proteasome |
Isovalerylcarnitine (3-methylbutyrylcarnitine) 是 L-亮氨酸分解代谢和异戊酸的积累产生的小分子化合物,也是一种具有选择性和有效性的钙蛋白酶 (calpain) 激活剂,可促使细胞凋亡,与异戊酸血症有关,可作为异戊酸血症的标志。 | |||
T36931 |
Penicillide
|
Others | Others |
Penicillide is a fungal metabolite originally isolated from Penicillium that has diverse biological activities. It is an inhibitor of calpain 2/m-calpain (IC50 = 7.1 μM) and acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 22.9 μM). It is also an antagonist of oxytocin receptors (IC50 = 67 μM). Penicillide inhibits RNA synthesis in P388 murine leukemia cells. | |||
TN1086 |
Dehydrotrametenolic acid
Dehydroeburicoic acid,去氢齿孔酸,松苓新酸 |
Apoptosis; TNF; NOS; Caspase; NO Synthase | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Dehydrotrametenolic acid (Dehydroeburicoic acid) 是从茯苓的菌核中分离的一种甾醇,具有抗肿瘤活性、抗炎和抗糖尿病作用。它通过 caspase-3途径诱导细胞凋亡。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01031 |
CAPN2 Protein, Human, Recombinant (His)
Calpain-2 catalytic subunit,Millimolar-calpain<... |
Human | E. coli |
Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. Proteolytically cleaves MYOC at 'Arg-226'. Proteolytically cleaves CPEB3 following neuronal stimulation which abolishes CPEB3 translational repressor activity, leading to translation of CPEB3 target mRNAs. CAPN2 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 82... | |||
TMPH-01029 |
CAPN1 Protein, Human, Recombinant (His)
CANPL1,CAPN1,Calpain-1 catalytic subunit,Micromolar... |
Human | E. coli |
Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. Proteolytically cleaves CTBP1 at 'Asn-375', 'Gly-387' and 'His-409'. CAPN1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 85.9 kDa and the accession number is P07384. | |||
TMPH-02557 |
CAPN1 Protein, Mouse, Recombinant (His)
CANP 1,Calpain-1 catalytic subunit,muCANP,CANPL1,Ca... |
Mouse | E. coli |
Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. Proteolytically cleaves CTBP1 at 'Asn-375', 'Gly-388' and 'His-410'. | |||
TMPH-01030 |
CAPN14 Protein, Human, Recombinant (His & Myc)
Calpain-14,Calcium-activated neutral proteinase 14,... |
Human | Baculovirus Insect Cells |
Calcium-regulated non-lysosomal thiol-protease. CAPN14 Protein, Human, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 78.6 kDa and the accession number is A8MX76. | |||
TMPJ-00926 |
GCA Protein, Human, Recombinant (GST)
GCA,Grancalcin,GCL |
Human | E. coli |
Grancalcin (GCA) is a member of the penta EF hand subfamily which includes sorcin, calpain and ALG2. Grancalcin is highly expressed bone marrow and also can detected in neutrophils and macrophages. Grancalcin interacts with L-plastin which known to have actin bundling activity. It indicates that Grancalcin may play an important role in the adhesion of neutrophils to fibronectin. Furthermore, Grancalcin localization is dependent upon calcium and magnesium. It associates with both the granule and ... |