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商品详情
名称
Ziresovir, 融合糖蛋白 F0 抑制剂
分子类型
小分子
别名
齐瑞索韦
英文别名
4-(4-(((3-Aminooxetan-3-yl)methyl)amino)-6-methylquinazolin-2-yl)-2,3,4,5-tetrahydro-1H-1lambda6,4-benzothiazepine-1,1-dione | AK0529 | AK-0529 | SCHEMBL14704847 | N-((3-aminooxetan-3-yl)methyl)-2-(1,1-dioxo-3,5-dihydro-2H-1lambda6,4-benzothiazepin-4-yl)-
英文名称
Ziresovir
货号
Z649795-5mg
包装规格
5mg
浓度
≥95%
储存温度
-20°C储存
运输条件
超低温冰袋运输
产品介绍
Ziresovir (AK0529;RO-0529) is a potent, selective, and orally bioavailable respiratory syncytial virus (RSV) fusion (F) protein ( RSV F ) protein inhibitor. Ziresovir shows anti-RSV activity ( EC 50 =3 nM) and highlights pharmacokinetics in animal species In Vitro Ziresovir shows different efficacy in Wild Type (WT) and Mutant Strains RSV with EC 50 /EC 90 values (μM) of 0.003/0.005 (WT), 2.1/10.0 (D486N), and >10/>10 (D489A), respectively. RO-0529 (100 nM; 4 d) inhibits RSV F protein-induced cell–cell fusion process, and suppresses the syncytia formation induced by the RSV F protein. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo Ziresovir (12.5 mg/kg, 50 mg/kg; p.o.; twice daily; 4 d) results reduction of RSV titer in mouse lung . Ziresovir (10 mg/kg; p.o.; single dose) exhibits good oral exposure and bioavailability with F(%) of 32% in male Wistar-Han rats . Ziresovir (150 mg/kg; p.o.; single dose) demonstrates a high tissue distribution to lung than plasma in CD-1 Mice . Pharmacokinetics of Ziresovir in male Wistar-Han rats Dose (mg/kg) AUC 0-24h (p.o.) (ng·h/mL) CL (mL/min/kg) T 1/2 (i.v.) (h) V ss (L/kg) F (%) 2 mg/kg (iv) or 10 mg/kg (po) 906 58 1.2 3.9 32 Pharmacokinetics of Ziresovir in CD-1 Mice Dose (mg/kg) AUC 0-24h (p.o.) (μg·h/L) tissue/lasma AUC 0-24h ratio (μg·h/L) T 1/2 (h) T max (h) C max (μg/L) plasma 8,380 1 1.02 0.25 5090 lung 72,400 8.6 3.31 1 22700 MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Female BALB/c mice infected by RSV Dosage: 12.5 mg/kg, 50 mg/kg Administration: Oral gavage; twice daily; 4 days Result: Resulted >1 log unit of viral titer reduction in the lung of infected mice at the dose level as low as 12.5 mg/kg. Reduced viral titer to 1.9 log units compared to vehicle at 50 mg/kg dose. Form:Solid IC50& Target:RSV F protein (respiratory syncytial virus fusion protein), EC50: 3 nM (RSV F)
生化机理
Ziresovir(AK0529;RO-0529)是一种强效、选择性和口服生物可用的呼吸道合胞病毒(RSV)融合(F)蛋白(RSV F)抑制剂。Ziresovir 具有抗 RSV 活性(EC 50 =3 nM),在动物体内的药代动力学表现突出
CAS号
1422500-60-4
分子式
C22H25N5O3S
分子量
439.53 g/mol
PubChem编号
71262247
Isomeric SMILES
CC1=CC2=C(C=C1)N=C(N=C2NCC3(COC3)N)N4CCS(=O)(=O)C5=CC=CC=C5C4
IIUPAC Name
N-[(3-aminooxetan-3-yl)methyl]-2-(1,1-dioxo-3,5-dihydro-2H-1\u03bb6,4-benzothiazepin-4-yl)-6-methylquinazolin-4-amine
INCHI
1S/C22H25N5O3S/c1-15-6-7-18-17(10-15)20(24-12-22(23)13-30-14-22)26-21(25-18)27-8-9-31(28,29)19-5-3-2-4-16(19)11-27/h2-7,10H,8-9,11-14,23H2,1H3,(H,24,25,26)
InChi Key
GAAICKUTDBZCMT-UHFFFAOYSA-N
Smiles
CC1=CC2=C(C=C1)N=C(N=C2NCC3(COC3)N)N4CCS(=O)(=O)C5=CC=CC=C5C4
PubChem CID
71262247
关联CAS
1422500-60-4
MeSH Entry Terms
AK-0529;AK0529;N-((3-aminooxetan-3-yl)methyl)-2-(1,1-dioxo-3,5-dihydro-2H-1lambda6,4-benzothiazepin-4-yl)-6-methylquinazolin-4-amine;RO-0529;RO0529;ziresovir
溶解性
DMSO : 125 mg/mL (284.39 mM; Need ultrasonic)
氢键供体数Hydrogen Bond Donor Count
2
氢键受体数Hydrogen Bond Acceptor Count
8
可旋转键计数Rotatable Bond Count
4
精确质量Exact Mass
439.168 Da
单同位素质量Monoisotopic Mass
439.168 Da
拓扑极表面积Topological Polar Surface Area
119.000 Ų
重原子数Heavy Atom Count
31
形式电荷Formal Charge
0
复杂度Complexity
740.000
同位素原子数Isotope Atom Count
0
共价键合单元计数Covalently-Bonded Unit Count
1
XLogP3
1.800
ALogP
1.8
作用类型
抑制剂
作用机制
融合糖蛋白 F0 抑制剂
危险属性
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上下游信息
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Ziresovir, 融合糖蛋白 F0 抑制剂 5mg

品牌:阿拉丁
货号:Z649795-5mg
级别: ≥95%
货期:30天
已售 720 件
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