Neprilysin
Neprilysin(脑啡肽酶)
Neprilysin (NEP) is a type II membrane metalloendopeptidase composed of ∼750 residues with an active site containing a zinc-binding motif (HEXXH) at the extracellular carboxyl terminal domain. Neprilysin is capable of degrading the monomeric and the oligomeric forms of Aβ peptide. Neprilysin is the dominant Aβ peptide-degrading enzyme in the brain; Neprilysin becomes inactivated and down-regulated during both the early stages of Alzheimer’s disease (AD) and aging.
Neprilysin is a neutral endopeptidase and its inhibition increases bioavailability of natriuretic peptides, bradykinin, and substance P, resulting in natriuretic, vasodilatatory, and anti-proliferative effects.
Neprilysin 相关产品(12)
- GC31583SQ28603 (SQ28,603)CAS: 100845-83-8
SQ28603 (SQ28,603) 是中性肽链内切酶 3.4.24.11 (NEP) 的有效选择性抑制剂,NEP 是一种降解心房利钠肽 (ANP) 的酶。
- GC38856TD-0212 TFACAS: 1073549-11-7纯度: >98.00%
TD-0212 TFA 是一种具有口服活性的、血管紧张素II型1受体AT1 和脑啡肽酶 (NEP)的双抑制剂,其对AT1的pKi值为 8.9, 对NEP 的pIC50值为9.2。
- GC63732Sacubitril-13C4 hemicalcium salt
Sacubitril-13C4 (AHU-377-13C4) hemicalcium salt 是 13C 和氘代标记的 Sacubitril hemicalcium salt。Sacubitril (AHU-377) hemicalcium salt 是有效的NEP抑制剂,IC50值为5 nM。Sacubitril hemicalcium salt 是研究心力衰竭药物 LCZ696 的一个组分。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC10146 | AHU-377(Sacubitril) | 149709-62-6 | >99.00% | |
A prodrug form of LBQ657 | ||||
| GC11784 | LCZ696 | 936623-90-4 | >99.50% | |
A dual angiotensin II receptor antagonist and neprilysin inhibitor | ||||
| GC16138 | AHU-377 hemicalcium salt | 1369773-39-6 | >99.50% | |
A prodrug form of LBQ657 | ||||
| GC16768 | Phosphoramidon Disodium Salt | 164204-38-0 | - | |
An inhibitor of NEP and NEP2 | ||||
| GC17017 | Racecadotril | 81110-73-8 | >98.50% | |
An enkephalinase inhibitor | ||||
| GC30786 | Sacubitrilat (LBQ-657) | 149709-44-4 | >98.00% | |
A neprilysin inhibitor | ||||
| GC31267 | NEP-In-1 | 465527-94-0 | - | |
NEP-IN-1是一种中性肽链内切酶(NEP)抑制剂,抑制dNEP,IC50为2nM。 | ||||
| GC31583 | SQ28603 (SQ28,603) | 100845-83-8 | - | |
SQ28603 (SQ28,603) 是中性肽链内切酶 3.4.24.11 (NEP) 的有效选择性抑制剂,NEP 是一种降解心房利钠肽 (ANP) 的酶。 | ||||
| GC31608 | Candoxatril (UK 79300) | 123122-55-4 | - | |
Candoxatril (UK 79300) 是一种中性肽链内切酶 (NEP) 抑制剂。 | ||||
| GC32671 | NEP-IN-2 | 145775-14-0 | - | |
NEP-IN-2是一种neutralendopeptidase抑制剂,主要用于研究动脉粥样硬化、再狭窄症的扩散等症状。 | ||||
| GC38856 | TD-0212 TFA | 1073549-11-7 | >98.00% | |
TD-0212 TFA 是一种具有口服活性的、血管紧张素II型1受体AT1 和脑啡肽酶 (NEP)的双抑制剂,其对AT1的pKi值为 8.9, 对NEP 的pIC50值为9.2。 | ||||
| GC63732 | Sacubitril-13C4 hemicalcium salt | - | - | |
Sacubitril-13C4 (AHU-377-13C4) hemicalcium salt 是 13C 和氘代标记的 Sacubitril hemicalcium salt。Sacubitril (AHU-377) hemicalcium salt 是有效的NEP抑制剂,IC50值为5 nM。Sacubitril hemicalcium salt 是研究心力衰竭药物 LCZ696 的一个组分。 | ||||
