OM99-2

OM99-2 Suppliers list
Company Name: GL Biochem (Shanghai) Ltd  
Tel: 21-61263452 13641803416
Email: ymbetter@glbiochem.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: Chemsky (shanghai) International Co.,Ltd  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: Creative Peptides   
Tel:
Email: info@creative-peptides.com
Company Name: Nanjing Peptide Biotech Ltd.  
Tel: 025-58361106-805 15951641583
Email: zhao.xu@njpeptide.com
OM99-2 Basic information
Product Name:OM99-2
Synonyms:OM99-2;H-GLU-VAL-ASN-[(2R,4S,5S)-5-AMINO-4-HYDROXY-2,7-DIMETHYL-OCTANOYL]-ALA-GLU-PHE-OH;EVNL-PSI-AAEF;GLU-VAL-ASN-(2R,4S,5S)-5-AMINO-*4-HYDROXY-2,7-DIMET;[2-AMINOBENZOYL-GLY1]-GALANIN FRAGMENT (1-10)-LYS(RETRO-M-NITRO-TYR) AMIDE HUMAN;[2-aminobenzoyl-gly1]-galanin fragment (1-10)-lys(retro-m-nitro-tyr) amide, human trifluoroacetate salt;glu-val-asn-[(2r,4s,5s)-5-amino-4-hydroxy-2,7-dimethyloctanoyl]-ala-glu-phe;OM99-2;[2-AMINOBENZOYL-GLY1]-GALANIN FRAGMENT (1-10)-LYS(RETRO-M-NITRO-TYR) AMIDE, HUMAN TRIFLUOROACETATE SALT
CAS:314266-76-7
MF:C41H64N8O14
MW:892.99
EINECS:
Product Categories:Galanin Degrading Zinc-MetallopeptidaseEnzyme Substrates;Galanin degrading zinc-metallopeptidasePeptides for Cell Biology;Enzyme Substrates;Galanins;Neuropeptides;Protease Substrates;Substrates by Enzyme
Mol File:314266-76-7.mol
OM99-2 Structure
OM99-2 Chemical Properties
Boiling point 1346.5±65.0 °C(Predicted)
density 1.289±0.06 g/cm3(Predicted)
storage temp. −20°C
form solid
pka3.48±0.10(Predicted)
InChIKeyJCNFYXCBSRPSLY-QYTLZHMISA-N
Safety Information
Safety Statements 22-24/25
WGK Germany 3
Storage Class10 - Combustible liquids
MSDS Information
OM99-2 Usage And Synthesis
UsesOM99-2, an eight residue peptidomimetic, tight-binding inhibitor of human brain memapsin 2 with a Ki value of 9.58 nM[1]. OM99-2 is significantly advanced the development of BACE1 inhibitor[2]. OM99-2 has the potential for the research of the Alzheimer's disease[3].
Biological ActivityCell permeable: no', 'Primary Target
human brain memapsin 2', 'Product does not compete with ATP.', 'Reversible: no', 'Target Ki: 1.6 nM against recombinant memapsin 2; 9.58 nM against recombinant pro-memapsin 2; 48 nM against cathepsin D
IC 50BACE1
References[1] Ghosh AK, et al. Design of Potent Inhibitors for Human Brain Memapsin 2 (β-Secretase). J Am Chem Soc. 2000;122(14):3522-3523. DOI:10.1021/ja000300g
[2] Zhao J, et al. Targeting Amyloidogenic Processing of APP in Alzheimer's Disease. Front Mol Neurosci. 2020;13:137. Published 2020 Aug 4. DOI:10.3389/fnmol.2020.00137
[3] Dash C, et al. Aspartic peptidase inhibitors: implications in drug development. Crit Rev Biochem Mol Biol. 2003;38(2):89-119. DOI:10.1080/713609213
[4] Park H, et al. Determination of the active site protonation state of beta-secretase from molecular dynamics simulation and docking experiment: implications for structure-based inhibitor design. J Am Chem Soc. 2003;125(52):16416-16422. DOI:10.1021/ja0304493
OM99-2 Preparation Products And Raw materials
Tag:OM99-2(314266-76-7) Related Product Information
[2-Aminobenzoyl-Gly1]-galanin fragment (1-10)-Lys(retro-m-nitro-Tyr) amide, human trifluoroacetate salt Glu-Val-Asn-[(2R,4S,5S)-5-amino-4-hydroxy-2,7-dimethyloctanoyl]-Ala-Glu-Phe trifluoroacetate salt OM99-2 Elenbecestat(E2609) LY2811376 Aloeresin D