CAS 95462-14-9
:Formula:C15H25NO6
InChI:InChI=1S/C15H25NO6/c1-9(2)15(20,10(3)17)14(19)22-8-11-4-6-16(21)7-5-12(18)13(11)16/h4,9-10,12-13,17-18,20H,5-8H2,1-3H3/t10-,12-,13-,15+,16?/m1/s1
InChI key:DNAWGBOKUFFVMB-JXSDSIQZSA-N
SMILES:C[C@H]([C@@](C(C)C)(C(=O)OCC1=CC[N+]2([C@H]1[C@@H](CC2)O)[O-])O)O
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Intermedine N-oxide
CAS:Intermedine N-oxide is a useful organic compound for research related to life sciences and the catalog number is T123865.Formula:C15H25NO6Color and Shape:SolidMolecular weight:315.36Intermedine-N-oxide 100 µg/mL in Water
CAS:Controlled ProductFormula:C15H25NO6Color and Shape:Single SolutionMolecular weight:315.36Intermedine N-oxide
CAS:Natural alkaloidFormula:C15H25NO6Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:315.36Intermedine N-Oxide
CAS:Controlled ProductFormula:C15H25NO6Color and Shape:NeatMolecular weight:315.36(1R,7aR)-1-hydroxy-7-((((S)-2-hydroxy-2-((R)-1-hydroxyethyl)-3-(methyl-d3)butanoyl-3,4,4,4-d4)oxy)methyl)-2,3,5,7a-tetrahydropyrrolizine 4(1H)-oxide
CAS:Controlled ProductFormula:C15D7H18NO6Color and Shape:NeatMolecular weight:322.405Intermedine N-oxide
CAS:Intermedine N-oxide is a naturally occurring pyrrolizidine alkaloid derivative, commonly found in certain plant species such as those belonging to the Boraginaceae family. These alkaloids are synthesized by plants as secondary metabolites, serving as chemical defense mechanisms against herbivores and pathogens. The mode of action involves interfering with cellular processes, often through the inhibition of protein and nucleic acid synthesis. This can result in various biological effects, depending on the concentration and specific cellular context.
Formula:C15H25NO6Purity:Min. 95%Color and Shape:PowderMolecular weight:315.36 g/mol
