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D4893

Sigma-Aldrich

3,4-Dehydro-L-proline

≥98% (TLC), suitable for ligand binding assays

Sinônimo(s):

(S)-3-Pyrroline-2-carboxylic acid, 3,4-Didehydro-L-proline

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About This Item

Fórmula empírica (Notação de Hill):
C5H7NO2
Número CAS:
4043-88-3
Peso molecular:
113.11
Beilstein:
5376764
Número CE:
223-738-7
Número MDL:
MFCD00065964
Código UNSPSC:
12352209
eCl@ss:
32160406
ID de substância PubChem:
24893903
NACRES:
NA.26

product name

3,4-Dehydro-L-proline,

Ensaio

≥98% (TLC)

forma

powder

técnica(s)

ligand binding assay: suitable

cor

white

pf

248-250 °C

aplicação(ões)

peptide synthesis

cadeia de caracteres SMILES

OC(=O)[C@H]1NCC=C1

InChI

1S/C5H7NO2/c7-5(8)4-2-1-3-6-4/h1-2,4,6H,3H2,(H,7,8)/t4-/m0/s1

chave InChI

OMGHIGVFLOPEHJ-BYPYZUCNSA-N

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Descrição geral

3,4-Dehydro-L-proline acts a prolyl-t-RNA synthetase.

Ações bioquímicas/fisiológicas

3,4-Dehydro-L-proline is used as a substrate and inhibitor of various enzymes. 3,4-Dehydro-L-proline may be used to inhibit extensin biosynthesis. 3,4-Dehydro-L-proline is a alternate substrate of the amino acid oxidase, NikD. 3,4-Dehydro-L-proline inhibits collagen secretion by chondorcytes.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

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Chunxiang Xu et al.
BMC plant biology, 11, 38-38 (2011-02-26)
Hydroxyproline rich glycoproteins (HRGPs) are implicated to have a role in many aspects of plant growth and development but there is limited knowledge about their localization and function during somatic embryogenesis of higher plants. In this study, the localization and
Acute respiratory failure (1985)
Annick Méjean et al.
Biochemistry, 49(1), 103-113 (2009-12-04)
Anatoxin-a and homoanatoxin-a are two potent cyanobacterial neurotoxins. We recently reported the identification of the gene cluster responsible for the biosynthesis of these toxins in cyanobacteria and proposed a biosynthetic scheme starting from L-proline and involving three polyketide synthases for
Andrew G Mark et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 12(8), 1474-1480 (2011-04-28)
The expression of chirality at surfaces, arising from the adsorption of chiral molecules, is usually discussed in terms of the molecular handedness. However, the adsorption process often leads to a new manifestation of chirality in the form of the adsorption
T Abe et al.
Journal of cellular physiology, 189(2), 144-151 (2001-10-13)
During wound healing and inflammation, fibroblasts express elevated alkaline phosphatase (ALP), but are not in contact with collagen fibrils in the fibronectin (FN)-rich granulation tissue. We hypothesized that the extracellular matrix (ECM) environment might influence the induction of ALP in
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