L-(+)-2-Amino-6-phosphonohexanoic acid结构式
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常用名 | L-(+)-2-Amino-6-phosphonohexanoic acid | 英文名 | L-(+)-2-Amino-6-phosphonohexanoic acid |
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| CAS号 | 98575-76-9 | 分子量 | 211.15 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C6H14NO5P | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | L-(+)-2-Amino-6-phosphonohexanoic acid |
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| 分子式 | C6H14NO5P |
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| 分子量 | 211.15 |
| InChIKey | QIOXWRQXHFVNLV-YFKPBYRVSA-N |
| SMILES | C(CCP(=O)(O)O)C[C@@H](C(=O)O)N |
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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
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实验名称:Validation qHTS for agonist of cAMP-regulated guanine nucleotide exchange factor 3 (E...
来源:NCGC
External Id:epac1-activator-v
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实验名称:Validation qHTS for antagonist of cAMP-regulated guanine nucleotide exchange factor 3...
来源:NCGC
External Id:epac1-inhibitor-v
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实验名称:Validation qHTS for agonist of cAMP-regulated guanine nucleotide exchange factor 4 (E...
来源:NCGC
External Id:epac2-activator-v2
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实验名称:Validation qHTS for antagonist of cAMP-regulated guanine nucleotide exchange factor 4...
来源:NCGC
External Id:epac2-inhibitor-v2
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
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实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
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实验名称:Inhibition of Mycobacterium tuberculosis glutamine synthetase at 1 mM in water
来源:ChEMBL
靶标:N/A
External Id:CHEMBL959110
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实验名称:qHTS for Inhibitors of Polymerase Kappa
来源:NCGC
靶标:DNA polymerase kappa [Homo sapiens]
External Id:PolK100
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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