CB2 receptor agonist 3结构式
|
常用名 | CB2 receptor agonist 3 | 英文名 | CB2 receptor agonist 3 |
|---|---|---|---|---|
| CAS号 | 919077-81-9 | 分子量 | 440.365 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | 632.9±55.0 °C at 760 mmHg | |
| 分子式 | C24H23Cl2N3O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 336.6±31.5 °C |
CB2 receptor agonist 3用途CB2受体激动剂3是一种稳健和选择性的CB2大麻素激动剂,CB2和CB1的Kis分别为7.6和900 nM。CB2受体激动剂3显著增加HL-60细胞中P-ERK 1/2的表达[1]。 |
| 英文名 | N-cyclohexyl-1-(2,4-dichlorophenyl)-6-methyl-4H-indeno[1,2-c]pyrazole-3-carboxamide |
|---|---|
| 英文别名 | 更多 |
| 描述 | CB2受体激动剂3是一种稳健和选择性的CB2大麻素激动剂,CB2和CB1的Kis分别为7.6和900 nM。CB2受体激动剂3显著增加HL-60细胞中P-ERK 1/2的表达[1]。 |
|---|---|
| 相关类别 | |
| 体外研究 | CB2受体激动剂3(化合物2a)在基于人类早幼粒细胞白血病HL-60细胞的体外模型中也显示为激动剂[1]。 |
| 参考文献 |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 沸点 | 632.9±55.0 °C at 760 mmHg |
| 分子式 | C24H23Cl2N3O |
| 分子量 | 440.365 |
| 闪点 | 336.6±31.5 °C |
| 精确质量 | 439.121826 |
| PSA | 46.92000 |
| LogP | 6.58 |
| InChIKey | SPEFJYZGXZENAF-UHFFFAOYSA-N |
| SMILES | Cc1ccc2c(c1)Cc1c(C(=O)NC3CCCCC3)nn(-c3ccc(Cl)cc3Cl)c1-2 |
| 蒸汽压 | 0.0±1.9 mmHg at 25°C |
| 折射率 | 1.700 |
|
实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
|
|
实验名称:Intrinsic activity at CB2 receptor assessed as induction of ERK1/2 phosphorylation in...
来源:ChEMBL
靶标:Cannabinoid receptor 2
External Id:CHEMBL910421
|
|
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
|
|
实验名称:Selectivity for CD1 mouse CB2 receptor over CB1 receptor
来源:ChEMBL
靶标:Cannabinoid receptor 2
External Id:CHEMBL911050
|
|
实验名称:Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VER...
来源:ChEMBL
靶标:Severe acute respiratory syndrome coronavirus 2
External Id:CHEMBL4513082
|
|
实验名称:Displacement of [3H]CP 55940 from human CB2 receptor in cell free system
来源:ChEMBL
靶标:Cannabinoid receptor 2
External Id:CHEMBL1670561
|
|
实验名称:Rescue cell viability in cybrid cells with a genetic mutation in complex 1 of the mit...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1315
|
|
实验名称:qHTS for Inhibitors of Polymerase Kappa
来源:NCGC
靶标:DNA polymerase kappa [Homo sapiens]
External Id:PolK100
|
|
实验名称:Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Cac...
来源:ChEMBL
靶标:Severe acute respiratory syndrome coronavirus 2
External Id:CHEMBL4303805
|
|
实验名称:SARS-CoV-2 3CL-Pro protease inhibition percentage at 20µM by FRET kind of response f...
来源:ChEMBL
靶标:Replicase polyprotein 1ab
External Id:CHEMBL4495582
|
| nor-Binaltorphimine dihydrochloride |
| HMS3269N05 |
| N-Cyclohexyl-1-(2,4-dichlorophenyl)-6-methyl-1,4-dihydroindeno[1,2-c]pyrazole-3-carboxamide |
| GP 2A |