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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9964 |
BOS-318
|
Others | Others |
BOS-318是一种Furin 抑制剂,具有缓慢解离,高选择性,细胞通透性等特点。 | |||
T79397 |
Neutrophil elastase inhibitor 4
|
||
Neutrophilelastase inhibitor4 (compound 4f) 是竞争性抑制HNE的化合物,具有较低的半抑制浓度(IC50: 42.30 nM)和解离常数(Ki: 8.04 nM)。此外,该化合物能够诱导T47D细胞的apoptosis,并在多种细胞系中展现出抗增殖作用,分别在T47D、RPMI 8226、A549、HSF细胞系的IC50值为21.25、34.17、29.93、99.11 nM。 | |||
T13389 |
ZD-0892
|
PI3K | PI3K/Akt/mTOR signaling |
ZD-0892 is a selective and poten neutrophil elastaset inhibitor(human neutrophil elastase and porcine pancreatic elastase with Kis of 6.7 and 200 nM, respectively). | |||
T6986 |
Sivelestat
ONO5046,EI546,西维来司他,LY544349 |
Others; SARS-CoV; Serine Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Sivelestat (ONO5046) 是一种选择性的中性粒细胞弹性蛋白酶抑制剂,其 IC50值为 44 nM,Ki 值为 200 nM。它有潜力研究 COVID-19 的急性肺损伤、急性呼吸窘迫综合征或弥散性血管内凝血。 | |||
T3107 |
Alvelestat
AZD9668,Avelestat |
Others; Serine Protease | Others; Proteases/Proteasome |
Alvelestat (AZD9668) 是一种口服活性,亲和性和选择性的中性粒细胞弹性蛋白酶 (NE) 抑制剂,pIC50=7.9 nM,Ki=为 9.4 nM,Kd=9.5 nM。 | |||
T8563 |
2-(2-bromophenyl)-5-chloro-4H-3,1-benzoxazin-4-one
|
Serine Protease | Proteases/Proteasome |
2-(2-bromophenyl)-5-chloro-4H-3,1-benzoxazin-4-one 是一种人类中性粒细胞弹性蛋白酶抑制剂。 | |||
T12613L |
BAY-85-8501
|
Serine Protease | Proteases/Proteasome |
BAY-85-8501 是选择性的人类中性脂酶抑制剂,IC50=65 pM。 | |||
T68099 |
midesteine
MR-889 |
Others | Others |
Midesteine (MR-889) 是一种可逆、慢结合、完全竞争的蛋白酶抑制剂。 | |||
T8602 |
2-CHLOROMETHYL-1,1-DIOXO-1,2-DIHYDRO-1LAMBDA*6*-BENZO[D]ISOTHIAZOL-3-ONE
|
Serine Protease | Proteases/Proteasome |
2-CHLOROMETHYL-1,1-DIOXO-1,2-DIHYDRO-1LAMBDA*6*-BENZO[D]ISOTHIAZOL-3-ONE 靶向中性粒细胞弹性蛋白酶(人)。 | |||
T10473 |
BAY-678
|
Others | Others |
BAY-678是一种人中性粒细胞弹性蛋白酶(HNE;IC50:20 nM)抑制剂,具有口服生物活性、高效性和选择性。BAY-678 是被基因结构组学联盟 (SGC) 推荐的化学探针。 | |||
T25131 |
AZD8309
AZD 8309,AZD-8309 |
Glutathione Peroxidase; CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation; Metabolism |
AZD8309 是一种强效的、可口服的趋化因子受体CXCR2的拮抗剂, 能够调节中性粒细胞的转运,可显著降低胰腺和肺部的MPO,并降低胰腺内的胰蛋白酶和弹性蛋白酶活性。AZD8309 能够用于研究炎症系列疾病。 | |||
T20762 |
Sivelestat sodium tetrahydrate
ONO-5046 sodium tetrahydrate,Elaspol,ONO 5046,ONO5046 sodium tetrahydrate,Elaspol sodium tetrahydrate,ONO-5046,Sivelestat Sodium,Sivelestat Sodium Hydrate,ONO5046 |
Serine Protease | Proteases/Proteasome |
Sivelestat sodium tetrahydrate (ONO5046 sodium tetrahydrate) 是竞争性的人类中性粒细胞弹性蛋白酶的抑制剂,其 IC50 值为 44 nM, Ki 值为 200 nM。Sivelestat (EI546) sodium tetrahydrate 有潜力用于 COVID-19的急性肺损伤/急性呼吸窘迫综合征或弥散性血管内凝血的研究。 | |||
T15285 |
FK706
|
Serine Protease | Proteases/Proteasome |
FK706 is a slow-binding and competitive human neutrophil elastase inhibitor (IC50: 83 nM; Ki: 4.2 nM). FK706 also inhibits mouse neutrophil elastase and porcine pancreatic elastase (IC50s: 22 nM and 100 nM, respectively). FK706 has an anti-inflammatory ef | |||
T10254 | AE-3763 | Serine Protease | Proteases/Proteasome |
AE-3763 is a peptide-based human neutrophil elastase inhibitor (IC50: 29 nM). | |||
T17288 | ZD8321 | Serine Protease | Proteases/Proteasome |
ZD8321 is an effective inhibitor of human Neutrophil elastase (Ki: 13±1.7 nM). | |||
T31877 |
Freselestat
ONO-PO 736,ONO-6818,ONO 6818,ONO6818 |
||
Freselestat (ONO-6818) is a potent neutrophil elastase inhibitor that significantly reduces the production of interleukin 8 and C5B-9. Freselestat reduces inflammatory mediators during simulated cardiopulmonary bypass. | |||
T25520 |
ICI 200355
ICI-200,355,ICI 200,355,ICI-200355,ICI200,355,ICI200355 |
||
ICI 200355 is an inhibitor of human neutrophil elastase. | |||
T25782 |
MDL 27324
MDL-27,324,MDL-27324,MDL27,324,MDL 27,324,MDL27324 |
||
MDL 27324 is an inhibitor of human neutrophil elastase. | |||
T25781 |
MDL 101146
MDL-101146,MD 101,146,MDL101146,MDL 101,146,MDL-101,146 |
||
MDL 101146 is an orally active neutrophil elastase inhibitor. | |||
T11525L |
GW311616 hydrochloride
GW311616A |
Others | Others |
GW-311616 hydrochloride is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM). | |||
T69790 |
GW-475151
|
||
GW-475151 inhibits human neutrophil elastase (HNE). | |||
T25518 |
Ici 186756
Ici186756,Ici--186756 |
||
Ici 186756 is a novel, effective, and selective inhibitor of human neutrophil elastase. | |||
T25784 |
MDL-101146, (R)-
MDL101146, (R)- |
||
MDL-101146, (R)- is an effective orally active inhibitor of human neutrophil elastase. | |||
T3107L |
Alvelestat tosylate
|
||
Alvelestat can inhibit neutrophil elastase (NE), which acts an important role in NET formation. | |||
T25521 |
Ici 200880
Ici 200,880,Ici-200880,Ici200,880,Ic-200,880,Ici200880 |
||
Ici 200880 is a human neutrophil elastase synthetic peptide inhibitor. | |||
T25784L |
MDL-101146, (S)-
MDL101146, (S)- |
||
MDL-101146, (S)- is an effective orally active inhibitor of human neutrophil elastase. | |||
T27747 |
KRP-109
KRP 109,KRP109 |
||
KRP-109, a neutrophil elastase (NE) inhibitor, acts by decreasing expression of TGF-ß Signal Related Genes. | |||
T11525 | GW311616 | Others | Others |
GW-311616 is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM). | |||
T28244 |
Ono EI-601
OnoEI601,Ono-EI 601,Ono-EI-601 |
||
Ono EI-601 is the main metabolite of ONO-5046, the human neutrophil elastase inhibitor . | |||
T41043 |
Lonodelestat
POL6014 |
||
Lonodelestat (POL6014) is a potent, orally active and selective peptide inhibitor of human neutrophil elastase (hNE). | |||
T11865 |
Lodelaben
氯德拉苯,SC-39026,Declaben |
Others | Others |
Lodelaben is a human neutrophil elastase inhibitor with an IC50 and Ki of 0.5 and 1.5 μM, respectively. | |||
T68240 |
AZD-9819
|
||
AZD-9819 is an inhibitor of human neutrophil elastase for potential treatment of chronic obstructive pulmonary disease (COPD). | |||
T21414 |
Sivelestat sodium
ONO 5046,LY-544349,Sivelestat sodium salt,ONO-5046,ONO5046,西维来司钠,LY544349,LY 544349 |
||
Sivelestat, an inhibitor of human neutrophil elastase, is used in the treatment of acute respiratory failure. Preliminary studies show Sivelestat may improve neuropathic pain. | |||
T19202 |
BAY-678 racemate
|
Others | Others |
BAY-678 racemate is a racemate of BAY-678. BAY-678 is an orally bioavailable, selective and cell-permeable inhibitor of human neutrophil elastase (HNE; IC50: 20 nM). | |||
T80553 |
MeOSuc-AAPA-CMK
|
||
MeOSuc-AAPA-CMK为一种针对人中性粒细胞弹性蛋白酶 (elastase) 的高效抑制剂。 | |||
T62846 | Freselestat quarterhydrate | ||
Freselestat quarterhydrate (ONO-6818 quarterhydrate) 是一种有效的、口服具有活力的嗜中性粒细胞弹性蛋白酶 (neutrophil elastase) 抑制剂 (Ki: 12.2 nM)。Freselestat quarterhydrate 对其他蛋白酶(例如胰蛋白酶,蛋白酶3,胰弹性蛋白酶,凝血酶,纤溶酶,胶原酶,组织蛋白酶G 和鼠巨噬细胞弹性蛋白酶)的活性低 100 倍以上,表现出有效的抗炎作用。 | |||
T38363 |
MeOSuc-AAPV-pNA
|
||
Proteinase 3 (PR3, myeloblastin) is a polymorphonuclear leukocyte serine proteinase that degrades matrix proteins including fibronectin, laminin, vitronectin, and collagen type IV to generate antimicrobial peptides. Neutrophil elastase is a serine proteinase that is secreted by neutrophils during inflammation to destroy pathogens. Evaluating these enzymes is helpful to understanding inflammatory autoimmune processes. MeOSuc-AAPV-pNA is a highly sensitive peptide substrate that is hydrolyzed by b... | |||
T72111 |
Ala-Ala-Pro-Val-chloromethylketone
AAPV-CMK |
||
Ala-Ala-Pro-Val-chloromethylketone 是不可逆的 NE 抑制剂,适用于慢性炎症性气道疾病研究。 | |||
T12613 |
(R)-BAY-85-8501
|
Others | Others |
(R)-BAY-85-8501 is the less active enantiomer of BAY-85-8501. BAY-85-8501 is a selective and potent Human Neutrophil Elastase (HNE)inhibitor(IC50 of 65 pM). | |||
T73657 |
Tiprelestat
|
||
Tiprelestat为有效的人类中性粒细胞弹性蛋白酶(elastase)抑制剂,展现抗菌及抗炎活性,适用于炎症/免疫疾病研究。 | |||
T36339 |
Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp
|
||
Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp is a fluorescence-quenched peptide substrate for human neutrophil elastase (kcat/Km = 531 mM-1s-1). Enzymatic peptide hydrolysis disrupts the Abz:EDDnp donor-acceptor pair allowing fluorescence measurement of Abz (ex = 320 nm; em = 420 nm). | |||
T76248 |
Tutuilamide A
|
||
Tutuilamide A为一有效抑制剂,针对猪胰弹性蛋白酶(PPE)展现出1.2 nM的IC50值。此外,该化合物亦对人中性粒细胞弹性蛋白酶(HNE; IC50=0.73 nM)及激肽释放酶7(KLK7; IC50=5.0 nM)有抑制作用。 | |||
T76216 |
Lonodelestat TFA
|
||
Lonodelestat TFA (POL6014 TFA) 是一种有效的、口服活性的、选择性的肽类hNE抑制剂,展现了治疗囊性纤维化(CF)的潜力。 | |||
T10473L |
BAY-677
|
Others | Others |
BAY-677, serving as an inactive control for BAY-678, is distinguished by BAY-678's capabilities as an orally bioavailable, selective, and cell-permeable inhibitor of human neutrophil elastase (HNE), showcasing a high potency with an IC50 of 20 nM[1]. Furthermore, BAY-678 has been publicly nominated as a chemical probe by the Structural Genomics Consortium (SGC)[2]. | |||
T79496 |
Cathepsin C-IN-6
|
||
CathepsinC-IN-6 (compound 2) 是基于E-64c-肼的cathepsin C抑制剂,展现抗炎活性。能有效抑制中性粒细胞弹性蛋白酶的激活,对于中性粒细胞浓度高的炎症性疾病(例如慢性阻塞性肺疾病)有潜在治疗作用。 | |||
T73532 | JO146 | ||
JO146为针对沙眼衣原体高温需要蛋白A(CtHtrA)的蛋白酶抑制剂,其对CtHtrA和人中性粒细胞弹性蛋白酶(HNE)的IC50值分别为21.86 μM和1.15 μM,可应用于细菌感染的抑制。 | |||
T21989 |
SSR 69071
|
||
SSR69071 是一种有效的,具有口服活性的选择性中性粒细胞弹性蛋白酶 (neutrophil elastase) 抑制剂。SSR69071 对人弹性蛋白酶 (Ki=0.0168 nM) 的亲和力高于对大鼠 (Ki=3 nM)、小鼠 (Ki=1.8 nM) 和兔 (Ki=58 nM) 弹性蛋白酶。SSR69071 减少缺血再灌注损伤后的心肌梗死面积。SSR69071 还具有治疗慢性阻塞性肺病、哮喘、肺气肿、囊性纤维化和多种炎症性疾病的潜力。 | |||
T80254 |
Elafin(human)
|
||
Elafin,亦称为ESI(elafin-specific inhibitor)或SKALP(skin anti-leucoprotease),为一种低分子量抑制剂,专一性地抑制肺部中性粒细胞中的HNE(人中性粒细胞弹性蛋白酶)和proteinase 3。同时,Elafin对Pseudomonas aeruginosa和Staphylococcus aureus亦具有抗生素效果。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TJS0314 |
5,7-Dihydroxy-4-methylcoumarin
Methyl-2H-Chromen-2-One,5,7-二羟基-4-甲基香豆素,4-Methyllimetol,4-Methyl-5,7-Dihydroxycoumarin |
Others; Antibacterial; Antifungal | Microbiology/Virology; Others |
5,7-Dihydroxy-4-methylcoumarin (Methyl-2H-Chromen-2-One) 是墨西哥龙蒿中的一种香豆素衍生物。它抑制人类中性粒细胞氧化代谢和弹性蛋白酶活性,有抗真菌和抗细菌活性。 | |||
TN4584 |
Morolic acid
|
IL Receptor; COX; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Morolic acid and moronic acid have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an insulin sensitization with consequent changes of glucose, cholesterol and triglycerides, in part mediated by inhibition of 11β-HSD 1. Moro |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01773 |
ELANE Protein, Human, Recombinant (GST)
Neutrophil elastase,ELA2,Medullasin,El... |
Human | E. coli |
Modifies the functions of natural killer cells, monocytes and granulocytes. Inhibits C5a-dependent neutrophil enzyme release and chemotaxis. Capable of killing E.coli but not S.aureus in vitro; digests outer membrane protein A (ompA) in E.coli and K.pneumoniae. ELANE Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 52.6 kDa and the accession number is P08246. | |||
TMPY-00672 |
Azurocidin/CAP37 Protein, Human, Recombinant (His)
AZU,NAZC,azurocidin 1,hHBP,AZAMP,HUMAZUR,CAP37,HBP,AZU1 |
Human | HEK293 Cells |
Azurocidin (AZU1), also known as heparin-binding protein (HBP) or cationic antimicrobial protein 37 (CAP37), is an azurophil granule antibiotic protein, with monocyte chemotactic and antibacterial activity. The Azurophil granules, specialized lysosomes of the neutrophil, contain at least 10 proteins implicated in the killing of microorganisms. Azurocidin is a member of the serine protease family that includes Cathepsin G, neutrophil elastase (NE), and proteinase 3 (PR3), however, Azurocidin is n... | |||
TMPY-01909 |
Elafin Protein, Human, Recombinant (His)
WAP3,ESI,peptidase inhibitor 3,SKALP,cementoin,MGC13613,WFDC... |
Human | HEK293 Cells |
Elafin, also known as Elastase-specific inhibitor, Peptidase inhibitor 3, Protease inhibitor WAP3, Skin-derived antileukoproteinase, WAP four-disulfide core domain protein 14, PI3, WAP3 and WFDC14, is a secreted protein that contains one WAP domain. Elafin / PI3 consists of two domains: the transglutaminase substrate domain (cementoin moiety) and the elastase inhibitor domain. The transglutaminase substrate domain at the N-terminus serves as an anchor to localize elafin covalently to specific si... |