Names | |
---|---|
IUPAC name
(3R,10aR)-3-(hydroxymethyl)-2-methyl-7-nitro-2,3-dihydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
| |
| |
Properties | |
C13H11N3O5S2 | |
Molar mass | 353.37 g·mol−1 |
Appearance | Yellow powder |
Melting point | 181-182 °C |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Glionitrin A is an antibiotic-anticancer compound made by microbes found in an abandoned mine. [1] The total synthesis of (−)-glionitrin A was reported by Daniel Strand and co-workers in 2021. [2]
Names | |
---|---|
IUPAC name
(3R,10aR)-3-(hydroxymethyl)-2-methyl-7-nitro-2,3-dihydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
| |
| |
Properties | |
C13H11N3O5S2 | |
Molar mass | 353.37 g·mol−1 |
Appearance | Yellow powder |
Melting point | 181-182 °C |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Glionitrin A is an antibiotic-anticancer compound made by microbes found in an abandoned mine. [1] The total synthesis of (−)-glionitrin A was reported by Daniel Strand and co-workers in 2021. [2]