阿利克仑

阿利克仑

货号:
IA3120

品牌:
Jinpan

阿利克仑

暂无详情
产品简介
EC EINECS 605-672-4
MDL MFCD09839018
描述 是肾素抑制剂。
别名 阿里斯基伦;CGP-60536
英文名称 Aliskiren
CAS 173334-57-1
分子式 C30H53N3O6
分子量 551.76
纯度 ≥98%
单位
生物活性 Aliskiren is the fourth class of pharmacological agents that modify the function of RAAS. It is an octanamide, is the first known representative of a new class of completely nonpeptide, low-molecular-weight, orally active transition-state renin inhibitors. [1]
In Vitro Aliskiren has good water solubility and low lipophilicity, and is resistant to biodegradation by peptidases in the intestine, blood circulation, and the liver. Aliskiren has 10,000-fold higher affinity for renin than for other aspartic peptidases[1].
In Vivo In short-term studies, Aliskiren is effective in lowering blood pressure either alone or in combination with valsartan and hydrochlorothiazide, and had a low incidence of serious adverse effects. Aliskiren has a half-life of approximately 40 h, making it suitable for once-daily dosing, with less potential for loss of efficacy between doses than shorter acting agents. Aliskiren exhibits oral bioavailability due to its low molecular weight (609.8 Da) and nonpeptide structure, making it more resistant to gastrointestinal enzyme disintegration. However, it is still poorly absorbed (oral bioavailability, ~2.5%). Aliskiren is 50% protein bound, and the apparent volume of distribution is 135 L. Aliskiren is slightly metabolized in humans (about 20%) and is approximately 50% metabolized in rodents. Aliskiren effectively reduces functional plasma renin activity by binding to renin with high affinity, preventing it from converting angiotensinogen to angiotensin I. The inhibition of renin by aliskiren is associated with a reduction in circulating levels of angiotensin I and II, with a resultant increase in plasma renin concentration and inhibit activation of mitogen-activated protein kinases ERK1 (p44) and ERK2 (p42). It prevents hypertrophy and proliferation. Aliskiren is well tolerated, with the most common adverse events reported as headache, dizziness, and fatigue[1].
SMILES COCCCOC1=CC(C[C@@H](C[C@@H]([C@H](C[C@H](C(NCC(C)(C(N)=O)C)=O)C(C)C)O)N)C(C)C)=CC=C1OC
靶点 Renin
数据来源文献 [1] Pranay Wal, et al. J Pharm Bioallied Sci. 2011, 3(2): 189–193.
规格 50mg 100mg

是一种肾素抑制剂,具有降压活性。

Aliskiren Hemifumarate;阿利克仑半富马酸盐

Aliskiren Hemifumarate;阿利克仑半富马酸盐

货号:
IA3960

品牌:
Jinpan

Aliskiren Hemifumarate;阿利克仑半富马酸盐

暂无详情
产品简介
MDL MFCD10566724
EC EINECS 630-415-8
别名 半延胡索酸阿利吉仑; 富马酸阿利吉仑
CAS 173334-58-2
分子式 C30H53N3O6·1/2C4H4O4
分子量 609.79
储存条件 -20℃
纯度 ≥98%
单位
生物活性 Aliskiren Hemifumarate是一种直接肾素抑制剂,IC50为1.5 nM。[1]
In Vitro Aliskiren hemifumarate似乎会结合到疏水性S1/S3-结合口袋和从S3-结合位点延伸到肾素疏水核的大的,明显的亚口袋。Aliskiren hemifumarate的口服利用度在大鼠,狨猴和人类中分别为2.4%,16%和2.5%。[2]
In Vivo 在钠耗竭的狨猴体内,Aliskiren hemifumarate (< 10 mg/kg,口服)抑制血浆肾素活性,并降低血压。[3]在轻度至中度高血压患者中,Aliskiren hemifumarate每天一次口服治疗有效降低血压,并且具有安全性和耐受性。[4]
SMILES O=C(O)/C=C/C(O)=O.O=C(NCC(C)(C(N)=O)C)[C@@H](C[C@@H]([C@H](C[C@@H](C(C)C)CC1=CC=C(OC)C(OCCCOC)=C1)N)O)C(C)C.O=C(NCC(C)(C(N)=O)C)[C@H](C(C)C)C[C@H](O)[C@@H](N)C[C@@H](C(C)C)CC2=CC=C(OC)C(OCCCOC)=C2
靶点 Renin
数据来源文献 [1] Nakamura Y, et al. ACS Med Chem Lett, 2012, 3(9), 754–758.
[2] Buczko W, et al. Pharmacol Rep, 2008, 60(5), 623-631.
[3] Wood JM, et al. Biochem Biophys Res Commun, 2003, 308(4), 698-705.
[4] Gradman AH, et al. Circulation, 2005, 111(8), 1012-1018.
规格 25mg 50mg

是肾素的直接抑制剂。