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Vinamidine-d3-N-formyl-1-hydroxide Sulfate
For research use only. Not for therapeutic Use.
Vinamidine-d3-N-formyl-1-hydroxide Sulfate(Cat No.:R062240)is a high-purity, deuterated chemical compound essential for advanced pharmaceutical research. This isotopically labeled version of Vinamidine, featuring three deuterium atoms, is critical for studies involving drug metabolism, pharmacokinetics, and biochemical pathways. The incorporation of stable isotopes ensures precise and reliable analytical results, enhancing the accuracy of experimental outcomes. Ideal for research applications, Vinamidine-d3-N-formyl-1-hydroxide Sulfate seamlessly integrates into existing protocols, offering a robust and cost-effective solution for high-precision scientific investigations and drug development.
Catalog Number | R062240 |
CAS Number | NA |
Synonyms | (3aR,3a1R,4R,5S,10bR)-Methyl 4-acetoxy-3a-ethyl-6-formyl-9-((5S,7S)-3-formyl-5-((R)-1-hydroxy-2-oxobutyl)-7-(methoxycarbonyl)-1,2,3,4,5,6,7,8-octahydroazonino[5,4-b]indol-7-yl)-5-hydroxy-8-methoxy-3a,3a1,4,5,5a,6,11,12-octahydro-1H-indolizino[8,1-cd] |
Molecular Formula | C₄₆H₅₁D₃N₄O₁₂ . x( H₂O₄S) |
Purity | ≥95% |
Storage | Store at -20°C |
IUPAC Name | methyl (1R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-8-formyl-4-[(5S,7S)-3-formyl-5-[(1R)-1-hydroxy-2-oxobutyl]-7-(trideuteriomethoxycarbonyl)-1,2,4,5,6,8-hexahydroazonino[5,4-b]indol-7-yl]-10-hydroxy-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate;sulfuric acid |
InChI | InChI=1S/C46H54N4O12.H2O4S/c1-7-34(54)36(55)27-22-45(41(56)60-5,37-29(14-18-48(23-27)24-51)28-12-9-10-13-32(28)47-37)31-20-30-33(21-35(31)59-4)50(25-52)39-44(30)16-19-49-17-11-15-43(8-2,38(44)49)40(62-26(3)53)46(39,58)42(57)61-6;1-5(2,3)4/h9-13,15,20-21,24-25,27,36,38-40,47,55,58H,7-8,14,16-19,22-23H2,1-6H3;(H2,1,2,3,4)/t27-,36+,38-,39?,40+,43+,44+,45-,46-;/m0./s1/i5D3; |
InChIKey | JNUKVPXJAAGRRJ-CYQSBIHXSA-N |
SMILES | [2H]C([2H])([2H])OC(=O)[C@@]1(C[C@@H](CN(CCC2=C1NC3=CC=CC=C23)C=O)[C@H](C(=O)CC)O)C4=C(C=C5C(=C4)[C@]67CCN8[C@H]6[C@@](C=CC8)([C@H]([C@@](C7N5C=O)(C(=O)OC)O)OC(=O)C)CC)OC.OS(=O)(=O)O |