Home Carboxys 2,5-Dihydro-1h-pyrrole-2-carboxylic acid

2,5-Dihydro-1h-pyrrole-2-carboxylic acid

CAS No.:
3395-35-5
Catalog Number:
AG003IFD
Molecular Formula:
C5H7NO2
Molecular Weight:
113.1146
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
100mg
98%
In Stock USA
United States
$201
- +
250mg
98%
In Stock USA
United States
$314
- +
1g
98%
In Stock USA
United States
$821
- +
Product Description
Catalog Number:
AG003IFD
Chemical Name:
2,5-Dihydro-1h-pyrrole-2-carboxylic acid
CAS Number:
3395-35-5
Molecular Formula:
C5H7NO2
Molecular Weight:
113.1146
MDL Number:
MFCD00005214
IUPAC Name:
2,5-dihydro-1H-pyrrole-2-carboxylic acid
InChI:
InChI=1S/C5H7NO2/c7-5(8)4-2-1-3-6-4/h1-2,4,6H,3H2,(H,7,8)
InChI Key:
OMGHIGVFLOPEHJ-UHFFFAOYSA-N
SMILES:
OC(=O)C1NCC=C1
EC Number:
222-243-3
NSC Number:
49883
Properties
Complexity:
130  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
113.048g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
113.116g/mol
Monoisotopic Mass:
113.048g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
49.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-2.5  
Literature
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Purification, characterization, and crystallization of human pyrroline-5-carboxylate reductase. Protein expression and purification 20060901
Alternative methods to limit extracellular bacterial activity for enumeration of intracellular bacteria. Journal of microbiological methods 20060101
Root border-like cells of Arabidopsis. Microscopical characterization and role in the interaction with rhizobacteria. Plant physiology 20050601
Synthesis of 4-aryl-2-pyrrolidones and beta-aryl-gamma-amino-butyric acid (GABA) analogues by Heck arylation of 3-pyrrolines with arenediazonium tetrafluoroborates. Synthesis of (+/-)-rolipram on a multigram scale and chromatographic resolution by semipreparative chiral simulated moving bed chromatography. The Journal of organic chemistry 20050204
Many amino acid substitutions in a hypoxia-inducible transcription factor (HIF)-1alpha-like peptide cause only minor changes in its hydroxylation by the HIF prolyl 4-hydroxylases: substitution of 3,4-dehydroproline or azetidine-2-carboxylic acid for the proline leads to a high rate of uncoupled 2-oxoglutarate decarboxylation. The Journal of biological chemistry 20041231
Oxidation of 3,4-dehydro-D-proline and other D-amino acid analogues by D-alanine dehydrogenase from Escherichia coli. FEMS microbiology letters 20040915
Overexpression of decorin by rat arterial smooth muscle cells enhances contraction of type I collagen in vitro. Arteriosclerosis, thrombosis, and vascular biology 20040101
Molecular characterization of NikD, a new flavoenzyme important in the biosynthesis of nikkomycin antibiotics. Biochemistry 20021231
Regulation of collagenase-3 and osteocalcin gene expression by collagen and osteopontin in differentiating MC3T3-E1 cells. The Journal of biological chemistry 20020705
Extracellular matrix regulates induction of alkaline phosphatase expression by ascorbic acid in human fibroblasts. Journal of cellular physiology 20011101
Properties