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User:Ksklwsk2

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Ksklwsk2[1]
Names
Other names
Alaninamide, Bryamycin, Thiactin
Identifiers
3D model (JSmol)
ChEMBL
UNII
  • C[C@@H](O)[C@@](C)(O)[C@@H](C2=NC6=CS2)NC(C1CSC(/C(NC([C@@H](NC(C3=CS[C@]([C@]4(NC([C@@H](NC(C(NC([C@H](C)NC%10=O)=O)=C)=O)C)=O)C(C5=CSC([C@H]([C@@H](C)OC(C8=CC([C@H](C)O)=C(C=CC(N[C@]([H])%10[C@H](CC)C)[C@@H]9O)C9=N8)=O)NC6=O)=N5)N=C(C7=NC(C(NC(C(NC(C(N)=O)=C)=O)=C)=O)=CS7)CC4)=N3)=O)[C@@H](C)O)=O)=C/C)=N1)=O
Properties
C72H85N19O18S5
Molar mass 1664.83 g/mol
Appearance White to off-white powder
Melting point 246−256 °C
Insoluble
Solubility in other solvents Soluble in CHCl3, CH2Cl2, dioxane, pyridine, glacial acetic acid, DMF. Practically insoluble in the lower alcohols, nonpolar organic solvents, diluted aqueous acids or bases. May be dissolved by methanolic acid or base, but with decomposition.[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Background

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History

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Applications

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Biosynthesis

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Total Synthesis

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Synthetic scheme

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References

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