1-Pyrroline-5-carboxylic acid

1-Pyrroline-5-carboxylic acid: 1-Pyrroline-5-carboxylic acid

IUPAC name

3,4-dihydro-2H-pyrrole-2-carboxylic acid

Identifiers

CAS number 2906-39-0

PubChem 1196

ChemSpider 1159^Y

KEGG C04322^Y

MeSH Delta-1-pyrroline-5-carboxylate

ChEBI CHEBI:1372^Y

ChEMBL CHEMBL1161508^Y

Jmol-3D images Image 1
Image 2

SMILES

C1CC(N=C1)C(=O)O
O=C(O)C1/N=C\CC1

InChI

InChI=1S/C5H7NO2/c7-5(8)4-2-1-3-6-4/h3-4H,1-2H2,(H,7,8)^Y
Key: DWAKNKKXGALPNW-UHFFFAOYSA-N^Y
InChI=1/C5H7NO2/c7-5(8)4-2-1-3-6-4/h3-4H,1-2H2,(H,7,8)
Key: DWAKNKKXGALPNW-UHFFFAOYAB

Properties

Molecular formula C₅H₇NO₂

Molar mass 113.115 g/mol

Y acid (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)

Infobox references

1-Pyrroline-5-carboxylic acid, also known as 1-pyrroline-5-carboxylate, delta-1-pyrroline-5-carboxylic acid, and P5C, is an imino acid. The stereoisomer (S)-1-pyrroline-5-carboxylate is a biosynthetic metabolite that is synthesized from proline by the enzyme pyrroline-5-carboxylate reductase and converted into the amino acid glutamate by the enzyme 1-pyrroline-5-carboxylate dehydrogenase.

v · Amino acid metabolism metabolic intermediates

K→acetyl-CoA

lysine→

Saccharopine · Allysine · α-Aminoadipic acid · α-Aminoadipate · Glutaryl-CoA · Glutaconyl-CoA · Crotonyl-CoA · β-Hydroxybutyryl-CoA

leucine→

α-Ketoisocaproic acid · Isovaleryl-CoA · 3-Methylcrotonyl-CoA · 3-Methylglutaconyl-CoA · HMG-CoA

tryptophan→alanine→

N'-Formylkynurenine · Kynurenine · Anthranilic acid · 3-Hydroxykynurenine · 3-Hydroxyanthranilic acid · 2-Amino-3-carboxymuconic semialdehyde · 2-Aminomuconic semialdehyde · 2-Aminomuconic acid · Glutaryl-CoA

G

G→pyruvate→citrate

glycine→serine→

3-Phosphoglyceric acid
glycine→creatine: Glycocyamine · Phosphocreatine · Creatinine

G→glutamate→
α-ketoglutarate

histidine→

Urocanic acid · Imidazol-4-one-5-propionic acid · Formiminoglutamic acid · Glutamate-1-semialdehyde

proline→

1-Pyrroline-5-carboxylic acid

arginine→

Ornithine · Putrescine · Agmatine

other

cysteine+glutamate→glutathione: γ-Glutamylcysteine

G→propionyl-CoA→
succinyl-CoA

valine→

α-Ketoisovaleric acid · Isobutyryl-CoA · Methacrylyl-CoA · 3-Hydroxyisobutyryl-CoA · 3-Hydroxyisobutyric acid · 2-Methyl-3-oxopropanoic acid

isoleucine→

2,3-Dihydroxy-3-methylpentanoic acid · 2-Methylbutyryl-CoA · Tiglyl-CoA · 2-Methylacetoacetyl-CoA

methionine→

generation of homocysteine: S-Adenosyl methionine · S-Adenosyl-L-homocysteine · Homocysteine
conversion to cysteine: Cystathionine · alpha-Ketobutyric acid+Cysteine

threonine→

α-Ketobutyric acid

propionyl-CoA→

Methylmalonyl-CoA

G→fumarate

phenylalanine→tyrosine→

4-Hydroxyphenylpyruvic acid · Homogentisic acid · 4-Maleylacetoacetate

G→oxaloacetate

see urea cycle

Other

Cysteine metabolism

Cysteine sulfinic acid

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m(A16/C10),i(k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)

biochemical families: prot · nucl · carb (glpr, alco, glys) · lipd (fata/i, phld, strd, gllp, eico) · amac/i · ncbs/i · ttpy/i

Categories:
Pyrrolines
Carboxylic acids
Biochemistry stubs

1-Pyrroline-5-carboxylic acid

IUPAC name 3,4-dihydro-2H-pyrrole-2-carboxylic acid
Identifiers
CAS number	2906-39-0
PubChem	1196
ChemSpider	1159^Y
KEGG	C04322^Y
MeSH	Delta-1-pyrroline-5-carboxylate
ChEBI	CHEBI:1372^Y
ChEMBL	CHEMBL1161508^Y
Jmol-3D images	Image 1 Image 2
SMILES C1CC(N=C1)C(=O)O O=C(O)C1/N=C\CC1
InChI InChI=1S/C5H7NO2/c7-5(8)4-2-1-3-6-4/h3-4H,1-2H2,(H,7,8)^Y Key: DWAKNKKXGALPNW-UHFFFAOYSA-N^Y InChI=1/C5H7NO2/c7-5(8)4-2-1-3-6-4/h3-4H,1-2H2,(H,7,8) Key: DWAKNKKXGALPNW-UHFFFAOYAB
Properties
Molecular formula	C₅H₇NO₂
Molar mass	113.115 g/mol
Y acid (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Игры ⚽ Нужна курсовая?

Look at other dictionaries:

Pyrroline — Pyrrolines, also known under the name dihydropyrroles, are three different heterocyclic organic chemical compounds which differ in the position of the double bond. Pyrrolines are formally derived from the aromate pyrrole by hydrogenation. 1… … Wikipedia
Pyrroline-5-carboxylate reductase — In enzymology, a pyrroline 5 carboxylate reductase (EC number|1.5.1.2) is an enzyme that catalyzes the chemical reaction:L proline + NAD(P)+ ightleftharpoons 1 pyrroline 5 carboxylate + NAD(P)H + H+The 3 substrates of this enzyme are L proline,… … Wikipedia
Acide 1-pyrroline-5-carboxylique — Structure de l acide 1 pyrroline 5 carboxylique Général No CAS … Wikipédia en Français
Glutamic acid — Glutamic acid … Wikipedia
Homogentisic acid — IUPAC name (2,5 Dihydroxyphenyl)acetic acid … Wikipedia
1-Pyrroline-5-carboxylate dehydrogenase — In enzymology, a 1 pyrroline 5 carboxylate dehydrogenase (EC number|1.5.1.12) is an enzyme that catalyzes the chemical reaction: (S) 1 pyrroline 5 carboxylate + NAD+ + 2 H2O ightleftharpoons L glutamate + NADH + H+The three substrates of this… … Wikipedia
2-Methyl-3-oxopropanoic acid — IUPAC name 2 Methyl 3 oxopropanoic acid … Wikipedia
Oxaloacetic acid — Oxaloacetic acid … Wikipedia
3-Phosphoglyceric acid — 3 Phosphoglyceric acid … Wikipedia
Formiminoglutamic acid — IUPAC name N (aminomethylidene) L glutamic acid … Wikipedia

Academic Dictionaries and Encyclopedias

1-Pyrroline-5-carboxylic acid

Look at other dictionaries:

Share the article and excerpts

Academic Dictionaries and Encyclopedias

Wikipedia

1-Pyrroline-5-carboxylic acid

Look at other dictionaries:

Share the article and excerpts

Direct link