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Haematopodin B

From Wikipedia, the free encyclopedia
Haematopodin B
Names
Preferred IUPAC name
(6aR)-2-Imino-2,4,6,6a,9,10-hexahydro-3H,8H-[1,3]oxazino[3,2-a]pyrrolo[4,3,2-de]quinolin-3-one
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C13H13N3O2/c14-8-5-9-11-7(6-15-12(11)13(8)17)4-10-16(9)2-1-3-18-10/h5-6,10,14-15H,1-4H2/t10-/m1/s1
    Key: CLAPNKMEQIYQLC-SNVBAGLBSA-N
  • C1CN2[C@@H](CC3=CNC4=C3C2=CC(=N)C4=O)OC1
Properties
C13H13N3O2
Molar mass 243.266 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Haematopodin B is a chemical compound that is found in the mushroom Mycena haematopus.[2] It decomposes to haematopodin under the influence of air and light.[2]

References

[edit]
  1. ^ "KNApSAcK Metabolite Information - C00056367". www.knapsackfamily.com.
  2. ^ a b Baumann, C.; Bröckelmann, M.; Fugmann, B.; Steffan, B.; Steglich, W.; Sheldrick, W.S. (1993). "Pigments of fungi. 62. Haematopodin, an unusual pyrrologuinone derivative isolated from the fungus Mycena haematopus, Agaricales". Angewandte Chemie International Edition in English. 32 (7): 1087–89. doi:10.1002/anie.199310871.