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CAS 72682-79-2

:

L-Alaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-prolyl-N-(4-nitrophenyl)-

Description:
L-Alaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-prolyl-N-(4-nitrophenyl)-, identified by CAS number 72682-79-2, is a synthetic compound that features a complex structure comprising amino acids and functional groups. This substance is characterized by the presence of an alanine moiety, which contributes to its amino acid properties, and a nitrophenyl group that may impart specific reactivity and biological activity. The carboxy and oxo groups in its structure suggest potential for interactions in biochemical pathways, possibly influencing its solubility and reactivity. The presence of multiple chiral centers indicates that it may exist in different stereoisomeric forms, which can affect its biological activity and pharmacokinetics. As a compound with potential applications in pharmaceuticals or biochemistry, its characteristics, including stability, solubility, and reactivity, would be crucial for determining its utility in various chemical or biological contexts. Further studies would be necessary to elucidate its specific properties and potential applications.
Formula:C21H27N5O8
InChI:InChI=1S/C21H27N5O8/c1-12(19(30)24-14-5-7-15(8-6-14)26(33)34)23-20(31)16-4-3-11-25(16)21(32)13(2)22-17(27)9-10-18(28)29/h5-8,12-13,16H,3-4,9-11H2,1-2H3,(H,22,27)(H,23,31)(H,24,30)(H,28,29)/t12-,13-,16-/m0/s1
InChI key:InChIKey=NRPFSJAQJJYJLT-XEZPLFJOSA-N
SMILES:C([C@@H](NC(CCC(O)=O)=O)C)(=O)N1[C@H](C(N[C@H](C(NC2=CC=C(N(=O)=O)C=C2)=O)C)=O)CCC1
Synonyms:
  • L-Alaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-prolyl-N-(4-nitrophenyl)-
  • Succinyl-Ala-Pro-Ala-p-nitroanilide
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Found 1 products.
  • Suc-Ala-Pro-Ala-pNA
    Biosynth
    + Info

    Suc-Ala-Pro-Ala-pNA

    CAS:
    <p>Suc-Ala-Pro-Ala-pNA is a synthetic substrate that inhibits serine proteases. It has been shown to inhibit thrombin, trypsin, and chymotrypsin at low concentrations. Suc-Ala-Pro-Ala-pNA is used as an anticoagulant in rat neutrophils and it has also been found to have chemotactic activity for neutrophils at high concentrations. The substrate was also found to be an efficient method of detecting the presence of protease activity in plant physiology experiments. In addition to its use as a proteinase inhibitor, Suc-Ala-Pro-Ala-pNA can also be used as an antiplatelet agent.</p>
    Formula:C21H27N5O8
    Purity:Min. 95%
    Molecular weight:477.47 g/mol

    Ref: 3D-SAP-3118

    1mg
    619.00€
    100µg
    218.00€