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Product details
名称
LOX-IN-3
别名
液氧-IN-3
英文别名
2-Buten-1-amine, 3-fluoro-4-(8-quinolinylsulfonyl)-, (2Z)- | GLXC-25899 | (Z)-3-fluoro-4-(quinolin-8-ylsulfonyl)but-2-en-1-amine | EX-A4912 | AKOS040756172 | 2409963-83-1 | (Z)-3-fluoro-4-quinolin-8-ylsulfonylbut-2-en-1-amine | HY-138625 | PXS-5505 | UNII
英文名称
LOX-IN-3
货号
L648579-5mg
包装规格
5mg
储存温度
避光,-80℃储存
运输条件
超低温冰袋运输
产品介绍
LOX-IN-3 is an orally active lysyl oxidase (LOX) inhibitor. LOX-IN-3 can be used for fibrosis, cancer and angiogenesis research In Vitro LOX-IN-3 dihydrochloride monohydrate (Compound 33) inhibits the bovine LOX and human LOXL2 activities with IC 50 values of In Vivo LOX-IN-3 dihydrochloride monohydrate (Compound 33) (30 mg/kg; orally; once) inhibits lysyl oxidase activity in rats . LOX-IN-3 dihydrochloride monohydrate (10 mg/kg; orally; daily for 14 days) reduces kidney fibrosis in unilateral ureteric obstruction (UUO) mice model . LOX-IN-3 dihydrochloride monohydrate (15 mg/kg; orally; daily for 21 days) reduces lung fibrosis in mice . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male Wistar rats Dosage: 30 mg/kg Administration: Oral administration, single dose Result: Completely abolished lysyl oxidase activity. Plasma concentrations of tested compound are far below the IC 50 after 8 hours, the half-life of recovery is between 2-3 days (ear) and 24 hours (aorta). Animal Model: Unilateral ureteric obstruction (UUO) model of acute kidney fibrosis in mice Dosage: 10 mg/kg Administration: Oral gavage, daily for 14 days Result: Increased kidney weight and thickness and reduced the area of fibrosis. Animal Model: C57Bl/6 mice, Bleomycin-induced lung fibrosis model Dosage: 15 mg/kg Administration: Oral gavage, daily for 21 days Result: Significantly reduced the Ashcroft score and the lung weight. Form:Solid IC50& Target:IC 50 :
生化机理
LOX-IN-3 是一种口服活性赖氨酰氧化酶(LOX)抑制剂。LOX-IN-3 可用于纤维化、癌症和血管生成研究。
CAS号
2409963-83-1
分子式
C13H13FN2O2S
分子量
280.32 g/mol
PubChem编号
146317833
Isomeric SMILES
C1=CC2=C(C(=C1)S(=O)(=O)C/C(=C/CN)/F)N=CC=C2
IIUPAC Name
(Z)-3-fluoro-4-quinolin-8-ylsulfonylbut-2-en-1-amine
INCHI
1S/C13H13FN2O2S/c14-11(6-7-15)9-19(17,18)12-5-1-3-10-4-2-8-16-13(10)12/h1-6,8H,7,9,15H2/b11-6-
InChi Key
DHXXLGDTPFPYRH-WDZFZDKYSA-N
Smiles
C1=CC2=C(C(=C1)S(=O)(=O)CC(=CCN)F)N=CC=C2
PubChem CID
146317833
关联CAS
2409963-83-1
溶解性
DMSO : 125 mg/mL (445.92 mM; Need ultrasonic)
氢键供体数Hydrogen Bond Donor Count
1
氢键受体数Hydrogen Bond Acceptor Count
5
可旋转键计数Rotatable Bond Count
4
精确质量Exact Mass
280.068 Da
单同位素质量Monoisotopic Mass
280.068 Da
拓扑极表面积Topological Polar Surface Area
81.400 Ų
重原子数Heavy Atom Count
19
形式电荷Formal Charge
0
复杂度Complexity
430
同位素原子数Isotope Atom Count
0
共价键合单元计数Covalently-Bonded Unit Count
1
XLogP3
0.4
Safety
「No Dangerous Attributes」
Related
「No upstream and downstream information yet」
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LOX-IN-3 5mg

LOX-IN-3 5mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 5mg.

item number:L648579-5mg
Product model:5mg
level: 5mg
Lead Time:30days
sold 763 Items
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