succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide
succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide Basic information
- Product Name:
- succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide
- Synonyms:
-
- succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide
- Suc-AFPF-pNA
- N-(3-Carboxy-1-oxopropyl)-L-alanyl-L-phenylalanyl-L-prolyl-N-(4-nitrophenyl)-L-phenylalaninamide
- 4-[[(2S)-1-[[(2S)-1-(4-nitro-N-[(2S)-1-oxo-3-phenyl-1-[[(2S)-pyrrolidine-2-carbonyl]amino]propan-2-yl]anilino)-1-oxo-3-phenylpropan-2-yl]amino]-1-oxopropan-2-yl]amino]-4-oxobutanoic acid
- L-Phenylalaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-phenylalanyl-L-prolyl-N-(4-nitrophenyl)-
- CAS:
- 128802-73-3
- MF:
- C36H40N6O9
- MW:
- 700.74
- Mol File:
- 128802-73-3.mol
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succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide Chemical Properties
- Boiling point:
- 1126.9±65.0 °C(Predicted)
- Density
- 1.352±0.06 g/cm3(Predicted)
- pka
- 4.69±0.10(Predicted)
- Sequence
- {Suc}-Ala-Phe-Pro-Phe-{pNA}
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succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide Usage And Synthesis
Uses
Suc-Ala-Phe-Pro-Phe-pNA is a peptide substrate[1].
References
[1] Hübner D, et al. Peptidyl-prolyl cis-trans isomerase activity as studied by dynamic proton NMR spectroscopy. FEBS Lett. 1991 Jun 17;284(1):79-81. DOI:10.1016/0014-5793(91)80766-v
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succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide(128802-73-3)Related Product Information
- SUC-PHE-LEU-PHE-SBZL
- SUC-ALA-HIS-PRO-PHE-PNA
- SUC-VAL-PRO-PHE-SBZL
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- SUC-ALA-ALA-VAL-AMC
- SUC-PHE-ALA-ALA-PHE-PNA
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- SUC-ALA-GLU-PRO-PHE-PNA
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- SUC-ALA-PHE-LYS-AMC
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- Chymotrypsin Substrate II, Fluorogenic
- SUC-ALA-ALA-PRO-VAL-AMC
- CHYMOTRYPSIN SUBSTRATE I, COLORIMETRIC
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- SUC-ALA-ALA-PRO-ASP-PNA