| Identification | Back Directory |  [Name]
  NISTC15503874 |  [CAS]
  15503-87-4 |  [Synonyms]
  Usaramin Usaramine Mucronatine NISTC15503874 (15E)-Retrorsine trans-Retrorsine (15E)-12,18-Dihydroxysenecionan-11,16-dione [1,6]Dioxacyclododecino[2,3,4-gh]pyrrolizine-2,7-dione,3-ethylidene-3,4,5,6,9,11,13,14,14a,14b-decahydro-6-hydroxy-6-(hydroxymethyl)-5-methyl-,(3E,5R,6S,14aR,14bR)- |  [Molecular Formula]
  C18H25NO6 |  [MDL Number]
  MFCD01684242 |  [MOL File]
  15503-87-4.mol |  [Molecular Weight]
  351.39 |  
 | Chemical Properties | Back Directory |  [Melting point ]
  178-180℃ |  [Boiling point ]
  583.2±50.0 °C(Predicted) |  [density ]
  1.32±0.1 g/cm3 (20 ºC 760 Torr) |  [solubility ]
  DMF: insol; DMSO: 1 mg/ml; Ethanol: insol; PBS (pH 7.2): 5 mg/ml |  [form ]
  A solid |  [pka]
  12.00±0.40(Predicted) |  [color ]
  White to off-white |  [InChI]
  InChI=1S/C18H25NO6/c1-3-12-8-11(2)18(23,10-20)17(22)24-9-13-4-6-19-7-5-14(15(13)19)25-16(12)21/h3-4,11,14-15,20,23H,5-10H2,1-2H3/b12-3+/t11-,14-,15-,18-/m1/s1 |  [InChIKey]
  BCJMNZRQJAVDLD-FXGRWVCYSA-N |  [SMILES]
  N12CC=C3COC(=O)[C@@](O)(CO)[C@H](C)C/C(=C\C)/C(=O)O[C@@]([H])([C@]13[H])CC2 |  [CAS DataBase Reference]
  15503-87-4 |  
 | Hazard Information | Back Directory |  [Hazard]
  A poison. |  [Description]
  A pyrrolizidine alkaloid first isolated from Crotalaria usararnoensis E. G. Baker, 
this base has more recently been found in C. brevifolia and C. rnucronata. The 
alkaloid has [α]20D + 6.1° (c 0.38, EtOH) or + 7.1° (c 1.83, EtOH). It yields a 
picrate, m.p. 230- 2°C (dec.); picrolonate, m.p. 148-150°C (dec.); reineckate, 
m.p. 190-2°C (dec.) and methiodide, m.p. 229-230°C (dec.). Alkaline 
hydrolysis furnishes retronecine and retronecic acid, m.p. 177-9°C. It has been 
suggested that the base may be identical with Mucronatine (q.v.). |  [Uses]
  Usaramine is a pyrrolizidine alkaloid isolated from seeds of Crolatalaria pallida. Usaramine demonstrates a highlighted antibiofilm activity against Staphylococcus epidermidis by reducing more than 50% of biofilm formation without killing the bacteria[1]. |  [Definition]
  ChEBI: LSM-2938 is a macrolide. |  [References]
  Culvenor, Smith., Austral. J. Chern., 19,2127 (1966) 
 Sawhney et al., Ind. J. Chern., 5, 655 (1967) |  
  
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