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名称
Larazotide acetate, 神经元乙酰胆碱受体;α3/β4 部分激动剂
分子类型
蛋白质
别名
醋酸拉唑肽
英文别名
F77451 | Larazotide acetate | Glycine, glycylglycyl-L-valyl-L-leucyl-L-valyl-L-glutaminyl-L-prolyl-, monoacetate | UNII-FO8S2IW40N | Larazotide acetate [USAN] | DTXSID401007986 | FO8S2IW40N | D09352 | Q25327025 | Glycylglycyl-L-valyl-L-leucyl-L-valyl-L-gl
英文名称
Larazotide acetate
货号
L646246-5mg
包装规格
5mg
浓度
≥98%
储存温度
干燥,-80℃储存
运输条件
超低温冰袋运输
产品介绍
Larazotide acetate is a peptide which is an orally active zonulin antagonist. Larazotide acetate shows antiviral activity to varicella-zoster virus (VZV) with EC 50 s of 44.14 and 59.06 μM for strain OKA and 07-1, respectively. Larazotide acetate can be used for the research of celiac disease and infection . In Vitro Larazotide acetate (1-100 μM; 5 d) affects Vero cell growth. Larazotide acetate (1-100 μM; 3 d) shows antiviral activity to varicella-zoster virus (VZV) with EC 50 s of 44.14 and 59.06 μM for strain OKA and 07-1, respectively. Larazotide acetate (1 and 3 mM; 72 h) inhibits cytokine-induced tight junction permeability in Caco-2 cells. Larazotide acetate (12.5 mM; 1 h) inhibits PTG-induced ZO-1 redistribution and actin cytoskeletal rearrangement in IEC6 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Cytotoxicity AssayCell Line: Vero cell line Concentration: 1-100 μM Incubation Time: 5 days Result: Inhibited Vero cell growth with an CC 50 value of 82.5 μM. In Vivo Larazotide acetate (250 μg; i.p. twice a week for 7 weeks) inhibits intestinal permeability in gluten-sensitive transgenic mice . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: HLA-HCD4/DQ8 double transgenic miceDosage: 250 μg Administration: Intraperitoneal injection; 250 μg twice a week for 7 weeks Result: Improved barrier function parameters and reduced macrophage counts in the lamina propria to control levels. Form:Solid IC50& Target:Paracellular permeability
生化机理
醋酸拉拉唑肽是一种多肽,是一种口服活性佐宁拮抗剂。醋酸拉拉唑肽对水痘-带状疱疹病毒(VZV)具有抗病毒活性,对 OKA 株和 07-1 株的 EC 50 s 分别为 44.14 和 59.06 μM。醋酸拉拉唑肽可
CAS号
881851-50-9
分子式
C34H59N9O12
分子量
785.89 g/mol
PubChem编号
44146842
Isomeric SMILES
CC(C)C[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(=O)N)C(=O)N1CCC[C@H]1C(=O)NCC(=O)O)NC(=O)[C@H](C(C)C)NC(=O)CNC(=O)CN.CC(=O)O
IIUPAC Name
acetic acid;2-[[(2S)-1-[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[2-[(2-aminoacetyl)amino]acetyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]-3-methylbutanoyl]amino]-5-oxopentanoyl]pyrrolidine-2-carbonyl]amino]acetic acid
INCHI
1S/C32H55N9O10.C2H4O2/c1-16(2)12-20(38-30(49)26(17(3)4)39-24(44)14-35-23(43)13-33)28(47)40-27(18(5)6)31(50)37-19(9-10-22(34)42)32(51)41-11-7-8-21(41)29(48)36-15-25(45)46;1-2(3)4/h16-21,26-27H,7-15,33H2,1-6H3,(H2,34,42)(H,35,43)(H,36,48)(H,37,50)(H,38,49)(H,39,44)(H,40,47)(H,45,46);1H3,(H,3,4)/t19-,20-,21-,26-,27-;/m0./s1
InChi Key
NYGCNONRVCGHAT-UFIKZEAMSA-N
Smiles
CC(C)CC(C(=O)NC(C(C)C)C(=O)NC(CCC(=O)N)C(=O)N1CCCC1C(=O)NCC(=O)O)NC(=O)C(C(C)C)NC(=O)CNC(=O)CN.CC(=O)O
PubChem CID
44146842
溶解性
H2O : 16.67 mg/mL (21.21 mM; Need ultrasonic) DMSO : 3.2 mg/mL (4.07 mM; Need ultrasonic and warming)
氢键供体数Hydrogen Bond Donor Count
10
氢键受体数Hydrogen Bond Acceptor Count
13
可旋转键计数Rotatable Bond Count
21
精确质量Exact Mass
785.428 Da
单同位素质量Monoisotopic Mass
785.428 Da
拓扑极表面积Topological Polar Surface Area
339.000 Ų
重原子数Heavy Atom Count
55
形式电荷Formal Charge
0
复杂度Complexity
1320.000
同位素原子数Isotope Atom Count
0
共价键合单元计数Covalently-Bonded Unit Count
2
作用类型
部分激动剂
作用机制
神经元乙酰胆碱受体;α3/β4 部分激动剂
Safety
「No Dangerous Attributes」
Related
「No upstream and downstream information yet」
Technical Documents
「No technical documents」
Articles
「No related articles yet」
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Research chemical 5mg; ≥98%

Research chemical 5mg; ≥98%; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 5mg; ≥98%.

item number:L646246-5mg
Product model:5mg
level: 5mg; ≥98%
Lead Time:30days
sold 811 Items
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