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Aminoshikimic acid information


Aminoshikimic acid
Names
Preferred IUPAC name
(3R,4S,5R)-5-Amino-3,4-dihydroxycyclohex-1-ene-1-carboxylic acid
Other names
Aminoshikimate
Identifiers
CAS Number
  • 178948-66-8 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 391778 checkY
PubChem CID
  • 443636
UNII
  • 74Z3GVA58B checkY
CompTox Dashboard (EPA)
  • DTXSID70332123 Edit this at Wikidata
InChI
  • InChI=1S/C7H11NO4/c8-4-1-3(7(11)12)2-5(9)6(4)10/h2,4-6,9-10H,1,8H2,(H,11,12)/t4-,5-,6+/m1/s1 checkY
    Key: GSAKPGCLECHWSP-PBXRRBTRSA-N checkY
  • InChI=1/C7H11NO4/c8-4-1-3(7(11)12)2-5(9)6(4)10/h2,4-6,9-10H,1,8H2,(H,11,12)/t4-,5-,6+/m1/s1
    Key: GSAKPGCLECHWSP-PBXRRBTRBE
SMILES
  • O=C(O)/C1=C/[C@@H](O)[C@@H](O)[C@H](N)C1
Properties
Chemical formula
C7H11NO4
Molar mass 173.168 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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Infobox references

Aminoshikimic acid is a synthetic crystalline carboxylic acid. It is characterized by multiple stereogenic centers and functional groups arrayed around a six-membered carbocyclic ring. Aminoshikimic acid is also an alternative to shikimic acid as a starting material for the synthesis of neuraminidase inhibitors such as the antiinfluenza agent oseltamivir (Tamiflu).

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Aminoshikimic acid

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Aminoshikimic acid is a synthetic crystalline carboxylic acid. It is characterized by multiple stereogenic centers and functional groups arrayed around...

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Shikimic acid

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additional costs, for example, shikimic acid for oseltamivir. Aminoshikimic acid is also an alternative to shikimic acid as a starting material for the synthesis...

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Aminoshikimate pathway

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Aminoshikimate pathway has been assembled in E. coli to synthesize aminoshikimic acid, which is a promising starting material for the synthesis of anti-influenza...

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C7H11NO4

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0688 u) may refer to: ACPD, or 1-Amino-1,3-dicarboxycyclopentane Aminoshikimic acid Oxaceprol This set index page lists chemical structure articles associated...

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