ChemicalBook > CAS DataBase List > SUC-ALA-GLU-PRO-PHE-PNA

SUC-ALA-GLU-PRO-PHE-PNA

Product Name: SUC-ALA-GLU-PRO-PHE-PNA
CAS No.: 128802-76-6
Chemical Name: SUC-ALA-GLU-PRO-PHE-PNA
Synonyms: Suc-AEPF-pNA;SUC-ALA-GLU-PRO-PHE-PNA;Suc-Ala-Glu-Pro-Phe-pNA≥ 98% (HPLC);Peptidyl-Prolyl Isomerase SubstratesSuc-Ala-Glu-Pr;N-(3-Carboxy-1-oxopropyl)-L-alanyl-L-α-glutamyl-L-prolyl-N-(4-nitrophenyl)-L-phenylalaninamide;L-Phenylalaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-α-glutamyl-L-prolyl-N-(4-nitrophenyl)-;(S)-4-((S)-2-(3-Carboxypropanamido)propanamido)-5-((S)-2-(((S)-1-((4-nitrophenyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)pyrrolidin-1-yl)-5-oxopentanoic acid
CBNumber: CB3775262
Molecular Formula: C32H38N6O11
Formula Weight: 682.68
MOL File: Mol file

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SUC-ALA-GLU-PRO-PHE-PNA Property

storage temp.: -15°C
form: Solid
color: White to off-white
Sequence: {Suc}-Ala-Glu-Pro-Phe-{pNA}

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC

Product number: S688138
Product name: Suc-Ala-Glu-Pro-Phe-Pna
Packaging: 1mg
Price: $65
Updated: 2021/12/16

Usbiological

Product number: 289515
Product name: Suc-Ala-Glu-Pro-Phe-pNA
Packaging: 5mg
Price: $382
Updated: 2021/12/16

Usbiological

Product number: 242089
Product name: Suc-Ala-Glu-Pro-Phe-pNA
Packaging: 25mg
Price: $516
Updated: 2021/12/16

Chem-Impex

Product number: 10021
Product name: Suc-Ala-Glu-Pro-Phe-pNA,99%(HPLC)
Purity: 99%(HPLC)
Packaging: 50MG
Price: $571.2
Updated: 2021/12/16

Chem-Impex

Product number: 10021
Product name: Suc-Ala-Glu-Pro-Phe-pNA
Purity: ≥ 99% (HPLC)
Packaging: 250MG
Price: $1995
Updated: 2021/12/16

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SUC-ALA-GLU-PRO-PHE-PNA Chemical Properties,Usage,Production

Chemical Properties

White powder

Uses

Suc-Ala-Glu-Pro-Phe-pNA (Suc-AEPF-pNA) is a chromogenic substrate for the peptidylprolyl isomerase Pin1. Suc-Ala-Glu-Pro-Phe-pNA can be used to evaluate the inhibitory effect of the target compound on Pin1, and catalytic activity of Pin1, etc[1][2].

References

[1] Subedi A, et al. Discovery of novel selenium derivatives as Pin1 inhibitors by high-throughput screening. Biochem Biophys Res Commun. 2016 Jun 3;474(3):528-533. DOI:10.1016/j.bbrc.2016.04.124
[2] Liu C, et al. Imazamethabenz inhibits human breast cancer cell proliferation, migration and invasion via combination with Pin1. Mol Med Rep. 2017 May;15(5):3210-3214. DOI:10.3892/mmr.2017.6399

SUC-ALA-GLU-PRO-PHE-PNA Preparation Products And Raw materials

Raw materials

Preparation Products

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128802-76-6, SUC-ALA-GLU-PRO-PHE-PNARelated Search:

SUC-PHE-LEU-PHE-SBZL SUC-ALA-HIS-PRO-PHE-PNA SUC-VAL-PRO-PHE-SBZL SUC-ALA-ALA-PRO-NVA-PNA SUC-ALA-ALA-VAL-AMC SUC-PHE-ALA-ALA-PHE-PNA Suc-Phe-Gly-Leu-βNA SUC-ALA-VAL-PRO-PHE-PNA SUC-PHE-PRO-PHE-PNA SUC-ALA-PHE-LYS-AMC SUC-ALA-PRO-PNA Chymotrypsin Substrate II, Fluorogenic SUC-ALA-ALA-PRO-VAL-AMC CHYMOTRYPSIN SUBSTRATE I, COLORIMETRIC SUC-GLY-PHE-GLY-PNA SUC-ALA-ILE-PRO-PHE-PNA SUC-ALA-ALA-PRO-ASP-PNA SUC-ALA-ALA-PRO-LYS-PNA

SUC-ALA-GLU-PRO-PHE-PNA

Suc-AEPF-pNA

Suc-Ala-Glu-Pro-Phe-pNA≥ 98% (HPLC)

L-Phenylalaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-α-glutamyl-L-prolyl-N-(4-nitrophenyl)-

N-(3-Carboxy-1-oxopropyl)-L-alanyl-L-α-glutamyl-L-prolyl-N-(4-nitrophenyl)-L-phenylalaninamide

Peptidyl-Prolyl Isomerase SubstratesSuc-Ala-Glu-Pr

(S)-4-((S)-2-(3-Carboxypropanamido)propanamido)-5-((S)-2-(((S)-1-((4-nitrophenyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamoyl)pyrrolidin-1-yl)-5-oxopentanoic acid

128802-76-6

C32H38N6O11

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