Angustmycin A

Angustmycin A

Names
IUPAC name 2-(6-aminopurin-9-yl)-2-(hydroxymethyl)-5-methylideneoxolane-3,4-diol[1]
Other names Decoyinine 4′,5′-Didehydro-1′-C-(hydroxymethyl)adenosine
Identifiers
CAS Number	2004-04-8 N
3D model ( JSmol )	Interactive image
ChEMBL	ChEMBL1444741
ChemSpider	108484
ECHA InfoCard	100.213.257
EC Number	687-357-1
PubChem CID	121578
CompTox Dashboard (EPA)	DTXSID50173859
InChI InChI=1S/C11H13N5O4/c1-5-7(18)8(19)11(2-17,20-5)16-4-15-6-9(12)13-3-14-10(6)16/h3-4,7-8,17-19H,1-2H2,(H2,12,13,14) Key: UZSSGAOAYPICBZ-UHFFFAOYSA-N
SMILES C=C1[C@H]([C@H]([C@](O1)(CO)N2C=NC3=C(N=CN=C32)N)O)O
Properties
Chemical formula	C11H13N5O4
Molar mass	279.256 g·mol−1
Hazards
GHS labelling:[2]
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Angustmycin A is a purine antibiotic and metabolite from Streptomyces bacteria with the molecular formula C₁₁H₁₃N₅O₄.^[3][1] Angustmycin A is also a cytokinin.^[4][5][6]

References

Further reading

• Hoeksema, H.; Slomp, G.; van Tamelen, E. E. (1 January 1964). "Angustmycin A and decoyinine". Tetrahedron Letters. 5 (27): 1787–1795.
  ISSN 0040-4039
  .
• McCarthy, James R.; Robins, Roland K.; Robins, Morris J. (August 1968). "Purine nucleosides. XXII. Synthesis of angustmycin A (decoyinine) and related unsaturated nucleosides". Journal of the American Chemical Society. 90 (18): 4993–4999.
  PMID 5665542
  .

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