1-Aminocyclopropane-1-carboxylic acid

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1-Aminocyclopropane-1-carboxylic acid
1-aminocyclopropanecarboxylic acid 200.svg
Names
Other names
1-Aminocyclopropanecarboxylic acid
Identifiers
22059-21-8 N
Abbreviations ACC
ChEBI CHEBI:58360 YesY
ChEMBL ChEMBL265325 YesY
ChemSpider 520 YesY
DrugBank DB02085 YesY
Jmol 3D model [1]: Interactive image
Interactive image
KEGG C01234 YesY
PubChem 535
  • InChI=1S/C4H7NO2/c5-4(1-2-4)3(6)7/h1-2,5H2,(H,6,7) YesY
    Key: PAJPWUMXBYXFCZ-UHFFFAOYSA-N YesY
  • InChI=1/C4H7NO2/c5-4(1-2-4)3(6)7/h1-2,5H2,(H,6,7)
    Key: PAJPWUMXBYXFCZ-UHFFFAOYAF
  • [1]: C(O)(=O)C1(CC1)(N)
  • O=C(O)C1(N)CC1
Properties
C4H7NO2
Molar mass 101.1 c
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

1-Aminocyclopropane-1-carboxylic acid (ACC) is a disubstituted cyclic α-amino acid in which a three-membered cyclopropane ring is fused to the Cα atom of the amino acid.

ACC plays an important role in the biosynthesis of the plant hormone ethylene.[2][3] It is synthesized by the enzyme ACC synthase ( EC 4.4.1.14) from methionine and converted to ethylene by ACC oxidase (EC 1.14.17.4).[4]

ACC is also an exogenous partial agonist of the mammalian NMDA receptor.[5]

References

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