(Q27125430)

L-phenylalanine biosynthetic process from chorismate via L-arogenate

subject has role

reaction intermediate

1 reference

arogenate dehydrogenase (NADP+) activity

1 reference

aspartate-prephenate aminotransferase activity

1 reference

glutamate-prephenate aminotransferase activity

1 reference

arogenate dehydratase activity

1 reference

cyclohexadienyl dehydrogenase activity

1 reference

mass

226.072 dalton

1 reference

L-Arogenate (English)

6 October 2016

chemical formula

C₁₀H₁₂NO₅⁻

1 reference

based on heuristic

inferred from SMILES

canonical SMILES

C1=CC(C=CC1O)(CC(C(=O)[O-])[NH3+])C(=O)[O-]

1 reference

L-Arogenate (English)

6 October 2016

isomeric SMILES

C1=CC(C=CC1O)(C[C@@H](C(=O)[O-])[NH3+])C(=O)[O-]

1 reference

L-Arogenate (English)

InChI=1S/C10H13NO5/c11-7(8(13)14)5-10(9(15)16)3-1-6(12)2-4-10/h1-4,6-7,12H,5,11H2,(H,13,14)(H,15,16)/p-1/t6?,7-,10?/m0/s1

6 October 2016

Identifiers

InChI

1 reference

L-Arogenate (English)

MIEILDYWGANZNH-DSQUFTABSA-M

6 October 2016

InChIKey

2 references

L-Arogenate (English)

6 October 2016

ChEBI release 2020-09-01

1 reference

1-[(2S)-2-Ammonio-2-carboxylatoethyl]-4-hydroxy-2,5-cyclohexadiene-1-carboxylate (English)

6 October 2016

2 references

L-Arogenate (English)

matched by identifier from

6 October 2016

InChIKey

MIEILDYWGANZNH-DSQUFTABSA-M

ChEBI ID

58180

mapping relation type

2 references

L-arogenate(1-) (English)