(R)-Mirtazapine结构式
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常用名 | (R)-Mirtazapine | 英文名 | (R)-Mirtazapine-13C-d3 |
|---|---|---|---|---|
| CAS号 | 61364-37-2 | 分子量 | 265.353 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 432.4±45.0 °C at 760 mmHg | |
| 分子式 | C17H19N3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 215.3±28.7 °C |
(R)-Mirtazapine用途(R)-Mirtazapine ((R)-Org3770) 是 Mirtazapine 的 R(−)-对映异构体,在急性热伤害感受动物模型中具有抗伤害感受的作用。(R)-Mirtazapine 是 5-HT3 受体拮抗剂,在体内主要经 CYP3A4 代谢。 |
| 中文名 | 米氮平 |
|---|---|
| 英文名 | (R)-1,2,3,4,10,14b-Hexahydro-2-methylpyrazino(2,1-a)pyrido(2,3-c)(2)benzazepine |
| 英文别名 | 更多 |
| 描述 | (R)-Mirtazapine ((R)-Org3770) 是 Mirtazapine 的 R(−)-对映异构体,在急性热伤害感受动物模型中具有抗伤害感受的作用。(R)-Mirtazapine 是 5-HT3 受体拮抗剂,在体内主要经 CYP3A4 代谢。 |
|---|---|
| 相关类别 | |
| 靶点实验 |
5-HT3 receptor[1] |
| 参考文献 |
| 密度 | 1.2±0.1 g/cm3 |
|---|---|
| 沸点 | 432.4±45.0 °C at 760 mmHg |
| 分子式 | C17H19N3 |
| 分子量 | 265.353 |
| 闪点 | 215.3±28.7 °C |
| 精确质量 | 265.157898 |
| PSA | 19.37000 |
| LogP | 2.75 |
| InChIKey | RONZAEMNMFQXRA-INIZCTEOSA-N |
| SMILES | CN1CCN2c3ncccc3Cc3ccccc3C2C1 |
| 蒸汽压 | 0.0±1.0 mmHg at 25°C |
| 折射率 | 1.668 |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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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
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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
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| (R)-1,2,3,4,10,14b-Hexahydro-2-methylpyrazino(2,1-a)pyrido(2,3-c)(2)benzazepine |
| (14bR)-2-Methyl-1,2,3,4,10,14b-hexahydropyrazino[2,1-a]pyrido[2,3-c][2]benzazepine |
| (R)-1,2,3,4,10,14b-hexahydro-2-methylpyrazino[2,1-a]pyrido[2,3-c][2]benzazepine |
| BIDD:GT0798 |