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CAS: 1233332-14-3
分子式: C27H29ClN2O3
分子量: 464.98
中文名称: 
n-[[3′-[[(1R)-1-(4-chloro-3-methylphenyl)ethyl]amino]-3,5-dimethyl[1,1′-biphenyl]-4-yl]carbonyl]-l-alanine
(S)-2-({3′-[(R)-1-(4-chloro-3-methyl-phenyl)-ethylamino]-3,5-dimethyl-biphenyl-4-carbonyl}-amino)-propionic acid
英文名称: 
nibr-0213
nibr0213
nibr 0213
推荐供应商
货号品牌产品名称规格包装、参考价格详情
R727699MACKLIN(3'-(((R)-1-(4-氯-3-甲基苯基)乙基)氨基)-3,5-二甲基-[1,1'-联苯]-4-羰基)-L-丙氨酸99%407元/1mg;   1420元/5mg;   2130元/10mg;   展开
储存:-20°C, 干燥
SML2099Sigma-AldrichNIBR-0213≥98% (HPLC)1649.92元/5 MG;   5909.96元/25 MG;   展开

产品说明

应用

NIBR-0213 may be used as a selective sphingosine-1-phosphate receptor 1 (S1P1) antagonist to assess S1P-mediated nuclear factor kappa B (NF-κB)-p65 nuclear translocation in human induced astrocytes.

生化/生理作用

NIBR-0213 is an orally active, potent and S1P1-selective sphingosine 1-phosphate (S1P) receptor antagonist that blocks S1P1-selective ligand AUY954-induced Ca2+ mobilization (IC50 = 2.5 nM using human S1P1-transfected HeLa cells; IC50 >10 μM with human S1P2, S1P3, or S1P4 transfectants) and S1P-induced GTPγS recruitment (IC50 = 2.0/2.3/8.5 nM using membrane from human/murine/rat S1P1-transfected CHO cells; IC50 >10 μM with membrane from human S1P5 transfectant). NIBR-0213 induces long-lasting peripheral blood lymphocyte reduction in rats (EDmax = 1 mg/kg, ED50 = 0.2 mg/kg; p.o.) and exhibits therapeutic efficacy (30 mg/kg p.o; BID) in experimental autoimmune encephalomyelitis (EAE), a murine model of multiple sclerosis (MS), with no adverse effects to the animals.

基本信息

经验(实验)分子式C27H29ClN2O3
分子量464.98
MDL编号MFCD25977008

产品性质

测定≥98% (HPLC)
形式powder
颜色 white to beige
溶解性DMSO: 2 mg/mL, clear
储存温度−20℃
SMILES stringC[C@@H](C(O)=O)NC(C1=C(C)C=C(C2=CC=CC(N[C@@H](C3=CC=C(Cl)C(C)=C3)C)=C2)C=C1C)=O

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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