
JNJ-42165279FAAH inhibitor |
Sample solution is provided at 25 µL, 10mM.
































Quality Control & MSDS
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- Purity = 98.00%
- COA (Certificate Of Analysis)
- MSDS (Material Safety Data Sheet)
- Datasheet
Chemical structure


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Cas No. | 1346528-50-4 | SDF | Download SDF |
Chemical Name | N-(4-chloro-3-pyridinyl)-4-[(2,2-difluoro-1,3-benzodioxol-5-yl)methyl]-1-piperazinecarboxamide | ||
Canonical SMILES | ClC1=CC=NC=C1NC(N2CCN(CC3=CC=C(OC(F)(F)O4)C4=C3)CC2)=O | ||
Formula | C18H17ClF2N4O3 | M.Wt | 410.8 |
Solubility | ≤30mg/ml in ethanol;30mg/ml in DMSO;30mg/ml in dimethyl formamide | Storage | Store at -20°C |
Physical Appearance | A crystalline solid | Shipping Condition | Evaluation sample solution : ship with blue ice.All other available size:ship with RT , or blue ice upon request |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. |
JNJ-42165279 is a potent and irreversible inhibitor of fatty acid amide hydrolase (FAAH) [1]. JNJ-42165279 covalently inactivates the FAAH enzyme [1]. JNJ-42165279 is highly selective with regard to other enzymes, ion channels, transporters, and receptors. The fatty acid amide hydrolase interrupt the actions through degrading various endogenous lipid signaling molecules. FAAH degrades several fatty acid ethanolamides rapidly, such as FAAH’s primary substrate, AEA (N-arachidonyl ethanolamide or anandamide), PEA (N-palmitoyl ethanolamide), and OEA (N-oleoyl ethanolamide) [1].
In vitro: JNJ-42165279 inhibited recombinant human and rat FAAH with the IC50s of 70 ± 8 nM and 313 ± 28 nM, respectively [1]. JNJ-42165279 (10 μM) exhibited high selectivity against a panel of receptors, enzymes, transporters, and ion-channels. JNJ-42165279 (10 μM) showed no inhibitory effects against CYPS (1A2, 2C8, 2C9, 2C19, 2D6, 3A4) or hERG [1].
In vivo: In the rat spinal nerve ligation (SNL or Chung) model of neuropathic pain, JNJ-42165279 exhibited analgesic properties. JNJ-42165279 dose-dependently reversed the robust tactile allodynia. The ED90 was 22 mg/kg, which corresponds to a plasma concentration of 2.5 μM at 30 min [1].
References:[1] Keith J M, Jones W M, Tichenor M, et al. Preclinical characterization of the FAAH inhibitor JNJ-42165279[J]. ACS medicinal chemistry letters, 2015, 6(12): 1204-1208.
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希望有大神赐教!谢谢!
指导意见:
毕竟阴道上皮是鳞状上皮,而输尿管,膀胱,尿道的上皮是柱状上皮,形态上是不一样的.所以您要是对您的结果出怀疑态度,首先:重新留尿,做一个复检(留尿时注意防止阴道分泌物污染);或者让值班医生分析一下是那种类型的上皮(鳞状还是柱状).所以不要担心这个结果.一般情况下污染的比较多.
病情描述(发病时间、主要症状等):
体检血常规中血小板计数343.血小板比积0.39.
尿检中白细胞计数26.2.上皮细胞计数10.30
心电图下写窦性心律,p-r间期偏短
想得到怎样的帮助:
有没有什么大问题
如题,求助。做肝癌细胞侵袭、迁移实验,用哪种细胞株比较好?
2:红细胞计数(RBC)(参考值:3.5~5.5),(单位:10^12/L)
3:血红蛋白浓度(HB)(参考值:120~160),(单位:g/L)
4:红细胞压积(HCT)(参考值:40~48),(单位:%)
5:平均红细胞体积(MCV)(参考值:80~97),(单位:fL)
6:平均红细胞血红蛋白含量(MCH)(参考值:26.5~33.5),(单位:pg)
7:平均红细胞血红蛋白浓度(MCHC)(参考值:300~360),(单位:g/L)
8:血小板计数(PLT)(参考值:100~300),(单位:10^9/L)
9:淋巴细胞比值(LY%)(参考值:17~48),(单位:%)
10:单核细胞比例(MONO%)(参考值:4-10),(单位:%)
11:中性粒细胞比例(NEUT%)(参考值:43~76),(单位:%)
12:淋巴细胞计数(LY)(参考值:0.8~4.0),(单位: 10^9/L)
13:单核细胞计数(MONO)(参考值:0.3~0.8),(单位:10^9/L)
14:中性粒细胞计数(NEUT)(参考值:1.2~6.8),(单位:10^9/L)
15:红细胞分布宽度(参考值:11~14.5),(单位:%)
16:血小板体积分布宽度(PDW)(参考值:9~18),(单位:%)
17:平均血小板体积(MPV)(参考值:7.4~12.5),(单位:fL)
18:大血小板比例(P-LCR)(参考值:10~50),(单位:%)

