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D4893

Sigma-Aldrich

3,4-Dehydro-L-proline

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

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C5H7NO2
Numero CAS:
4043-88-3
Peso molecolare:
113.11
Beilstein:
5376764
Numero CE:
223-738-7
Numero MDL:
MFCD00065964
Codice UNSPSC:
12352209
eCl@ss:
32160406
ID PubChem:
24893903
NACRES:
NA.26

product name

3,4-Dehydro-L-proline,

Saggio

≥98% (TLC)

Forma fisica

powder

tecniche

ligand binding assay: suitable

Colore

white

Punto di fusione

248-250 °C

applicazioni

peptide synthesis

Stringa SMILE

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
OMGHIGVFLOPEHJ-BYPYZUCNSA-N

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Descrizione generale

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

Azioni biochim/fisiol

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.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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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
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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
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
M Bucher et al.
Plant molecular biology, 35(4), 497-508 (1998-02-12)
A differential screen of a tomato root hair cDNA library resulted in the cloning of two cDNAs, Dif10 and Dif54, whose corresponding genes are preferentially expressed in root hair cells as determined by analysis of mRNA levels in various tomato
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