VU0029251结构式
|
常用名 | VU0029251 | 英文名 | VU0029251 |
|---|---|---|---|---|
| CAS号 | 330819-85-7 | 分子量 | 237.344 | |
| 密度 | 1.5±0.1 g/cm3 | 沸点 | 501.7±60.0 °C at 760 mmHg | |
| 分子式 | C10H11N3S2 | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | 257.2±32.9 °C |
VU0029251用途VU0029251 是一种 mGluR5 部分拮抗剂(Ki: 1.07 μM)。VU0029251 抑制表达大鼠 mGluR5 的 HEK293 细胞膜中谷氨酸诱导的钙动员 (IC50: 1.7 μM)。 |
| 英文名 | VU0029251 |
|---|---|
| 英文别名 | 更多 |
| 描述 | VU0029251 是一种 mGluR5 部分拮抗剂(Ki: 1.07 μM)。VU0029251 抑制表达大鼠 mGluR5 的 HEK293 细胞膜中谷氨酸诱导的钙动员 (IC50: 1.7 μM)。 |
|---|---|
| 相关类别 | |
| 靶点实验 |
mGluR5[1]. |
| 参考文献 |
| 密度 | 1.5±0.1 g/cm3 |
|---|---|
| 沸点 | 501.7±60.0 °C at 760 mmHg |
| 分子式 | C10H11N3S2 |
| 分子量 | 237.344 |
| 闪点 | 257.2±32.9 °C |
| 精确质量 | 237.039444 |
| LogP | 4.31 |
| InChIKey | WDDBZCKBRCTSOZ-UHFFFAOYSA-N |
| SMILES | CSc1nc(N)c2c3c(sc2n1)CCC3 |
| 蒸汽压 | 0.0±1.3 mmHg at 25°C |
| 折射率 | 1.745 |
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实验名称:qHTS screening for TAG (triacylglycerol) accumulators in algae
来源:11812
靶标:N/A
External Id:FATTTLab-Algae-Lipid
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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
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实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
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实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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实验名称:Alphascreen assay for small molecules abrogating mHTT-CaM Interaction
来源:24983
靶标:Huntingtin
External Id:KUHTS-Muma KU-CaM-Htt INH-01
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实验名称:Inhibition of LIMK1 using cofilin-2 as substrate after 60 mins by Kinase-Glo assay
来源:ChEMBL
靶标:LIM domain kinase 1
External Id:CHEMBL1839797
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实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
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实验名称:Inhibition of LIMK1 using cofilin-2 as substrate after 60 mins by TR-FRET assay
来源:ChEMBL
靶标:LIM domain kinase 1
External Id:CHEMBL1839798
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| MFCD00698485 |
| VU0029251 |
| 2-(Methylsulfanyl)-6,7-dihydro-5H-cyclopenta[4,5]thieno[2,3-d]pyrimidin-4-amine |
| 6,7-dihydro-2-(methylthio)-5h-cyclopenta[4,5]thieno[2,3-d]pyrimidin-4-amine |