3395-35-5 | 2,5-Dihydro-1h-pyrrole-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
25mg	98%	in stock	$74.00	$52.00
100mg	98%	in stock	$208.00	$146.00
250mg	98%	in stock	$337.00	$236.00
500mg	97%	in stock	$412.00	$289.00
1g	97%	in stock	$600.00	$420.00

Description

• Catalog Number: AB63649
• 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
• SMILES: OC(=O)C1NCC=C1
• NSC Number: 49883

Computed Properties

• Complexity: 130
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: -2.5

Literature

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  Journal of the American Chemical Society 20111012

• Recognition and ordering at surfaces: the importance of handedness and footedness.

  Chemphyschem : a European journal of chemical physics and physical chemistry 20110606

• Conformational preferences and cis-trans isomerization of L-3,4-dehydroproline residue.

  Biopolymers 20090101

• Roles of extensins in cotyledon primordium formation and shoot apical meristem activity in Nicotiana tabacum.

  Journal of experimental botany 20081001

• 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