CAS 73207-91-7

L-Lysinamide,N-(3-carboxy-1-oxopropyl)-L-alanyl-L-phenylalanyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-

Description:

L-Lysinamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-phenylalanyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-, identified by CAS number 73207-91-7, is a complex organic compound that features a combination of amino acids and a benzopyran derivative. This substance is characterized by its multi-functional structure, which includes an amide linkage, carboxylic acid groups, and a phenylalanine residue, contributing to its potential biological activity. The presence of the benzopyran moiety suggests possible interactions with biological systems, potentially influencing pharmacological properties. Its molecular structure indicates that it may exhibit solubility in polar solvents, typical of amino acid derivatives, while the aromatic components could enhance lipophilicity. The compound's synthesis and stability may be influenced by factors such as pH and temperature, which are critical in maintaining its integrity for research or therapeutic applications. Overall, this compound's unique characteristics make it a subject of interest in medicinal chemistry and biochemistry.

Formula: C₃₂H₃₉N₅O₈

InChI: InChI=1S/C32H39N5O8/c1-19-16-29(41)45-26-18-22(11-12-23(19)26)35-31(43)24(10-6-7-15-33)36-32(44)25(17-21-8-4-3-5-9-21)37-30(42)20(2)34-27(38)13-14-28(39)40/h3-5,8-9,11-12,16,18,20,24-25H,6-7,10,13-15,17,33H2,1-2H3,(H,34,38)(H,35,43)(H,36,44)(H,37,42)(H,39,40)/t20-,24-,25-/m0/s1

InChI key: GAQKKPHZOUJFMZ-OPXMRZJTSA-N

SMILES: CC1=CC(=O)OC2=C1C=CC(=C2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC3=CC=CC=C3)NC(=O)[C@H](C)NC(=O)CCC(=O)O

Synonyms:

• 3: PN:WO0197794 SEQID: 32 claimed sequence
• Suc-AFK-AMC
• SUC-ALA-PHE-LYS-AMC
• N-(3-Carboxy-1-oxopropyl)-L-alanyl-L-phenylalanyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-L-lysinamide

Suc-Ala-Phe-Lys-AMC

CAS: 73207-91-7

A highly sensitive fluorogenic substrate for plasmin. Suc-AFK-AMC was also used for assaying gingipain K.

Formula: C₃₂H₃₉N₅O₈

Purity: > 98%

Color and Shape: White Powder

Molecular weight: 621.69

Ref: 01-4004022

Suc-Ala-Phe-Lys-AMC

CAS: 73207-91-7

Suc-AFK-AMC, a highly sensitive fluorogenic substrate for plasmin. Suc-AFK-AMC was also used for assaying gingipain K.

Formula: C₃₂H₃₉N₅O₈

Purity: 94.2%

Color and Shape: White Powder

Molecular weight: 621.69

Ref: 01-4031296

Suc-ala-phe-lys-amc

CAS: 73207-91-7

Suc-ala-phe-lys-amc

Formula: C₃₂H₃₉N₅O₈

Purity: 99%

Molecular weight: 621.68

Ref: 54-OR1126327

Suc-ala-phe-lys-amc

CAS: 73207-91-7

Formula: C₃₂H₃₉N₅O₈

Purity: 99%

Molecular weight: 621.6808

Ref: IN-DA00FG1V

Suc-Ala-Phe-Lys-amc trifluoroacetate salt

CAS: 73207-91-7

Suc-Ala-Phe-Lys-amc trifluoroacetate salt is an analog inhibitor of protein kinases that has been shown to have potential anticancer properties. It inhibits tumor cell cycle progression and induces apoptosis in cancer cells. This medicinal compound has been extensively studied for its ability to inhibit the activity of various kinases, including those involved in cancer cell proliferation and survival. Suc-Ala-Phe-Lys-amc trifluoroacetate salt has been found to be effective against various types of human cancers, including breast, prostate, and lung cancer. It is a promising candidate for the development of novel anticancer drugs due to its potent inhibitory activity against protein kinases involved in tumor growth and survival.

Formula: C₃₂H₃₉N₅O₈

Purity: Min. 95%

Molecular weight: 621.7 g/mol

Ref: 3D-YCA20791