SUN B8155结构式
|
常用名 | SUN B8155 | 英文名 | SUN B8155 |
|---|---|---|---|---|
| CAS号 | 345893-91-6 | 分子量 | 273.28700 | |
| 密度 | 1.34g/cm3 | 沸点 | 419ºC at 760 mmHg | |
| 分子式 | C14H15N3O3 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 207.2ºC | |
| 符号 |
GHS06 |
信号词 | Danger |
SUN B8155用途SUN B8155是降钙素(CT)受体的非肽激动剂,选择性地模拟降钙素的生物作用。降钙素是一种主要由甲状腺分泌的32个氨基酸的肽激素,在维持骨内稳态方面起着重要作用[1]。 |
| 英文名 | SUN-B 8155,5-[1-[(2-Aminophenyl)imino]ethyl]-1,6-dihydroxy-4-methyl-2(1H)-pyridone |
|---|---|
| 英文别名 | 更多 |
| 描述 | SUN B8155是降钙素(CT)受体的非肽激动剂,选择性地模拟降钙素的生物作用。降钙素是一种主要由甲状腺分泌的32个氨基酸的肽激素,在维持骨内稳态方面起着重要作用[1]。 |
|---|---|
| 相关类别 | |
| 体外研究 | SUN B8155(1-1000μM;1小时)以浓度依赖性方式刺激T47D细胞内cAMP的形成;在最高浓度下,合成的cAMP浓度增加了约42倍。SUN B8155还刺激大鼠骨肉瘤衍生细胞系UMR106-06中的cAMP形成[1]。SUN B8155不刺激CHO/hPTHR或亲代CHO细胞中的cAMP形成,但以浓度依赖性方式充分刺激CHO/hCTR细胞中的cAMP形成,EC50为21μM[1]。 |
| 体内研究 | SUN B8155(100 mg/kg;i.p.)可使给药后30分钟的血清钙浓度显著降低约9%。人CT在给药后30分钟(0.1和0.3μg/kg)和60分钟(0.3μg/kg)时也以剂量依赖性方式降低血钙[1]。 |
| 参考文献 |
| 密度 | 1.34g/cm3 |
|---|---|
| 沸点 | 419ºC at 760 mmHg |
| 分子式 | C14H15N3O3 |
| 分子量 | 273.28700 |
| 闪点 | 207.2ºC |
| 精确质量 | 273.11100 |
| PSA | 100.84000 |
| LogP | 2.40370 |
| InChIKey | SGJLINMLDNLWOS-UHFFFAOYSA-N |
| SMILES | CC(=Nc1ccccc1N)c1c(C)cc(=O)n(O)c1O |
| 折射率 | 1.637 |
| 符号 |
GHS06 |
|---|---|
| 信号词 | Danger |
| 危害声明 | H301 |
| 警示性声明 | P301 + P310 |
| 个人防护装备 | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
| 危险品运输编码 | UN 2811 6.1 / PGIII |
|
Discovery of a non-peptide small molecule that selectively mimics the biological actions of calcitonin.
Biochim. Biophys. Acta 1526 , 183-190, (2001) Calcitonin (CT), a 32-amino acid peptide hormone secreted mainly from the thyroid gland, plays an important role in maintaining bone homeostasis. To discover non-peptide small molecules with biologica... |
|
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: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: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: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
|
|
实验名称:Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
来源:23265
External Id:IucA Pilot Assay Tocris Library
|
|
实验名称:Antiviral activity against HBV infected in human HepDES19 cells assessed as inhibitio...
来源:ChEMBL
靶标:Hepatitis B virus
External Id:CHEMBL5620890
|
|
实验名称:Enzymatic assay of human HDAC6 with commercial peptide substrate
来源:ChEMBL
靶标:Histone deacetylase 6
External Id:CHEMBL4808149
|
| 5-[1-[(2-Aminophenyl)imino]ethyl]-1,6-dihydroxy-4-methyl-2(1H)-pyridinone |