MCTR2

MCTR2 Suppliers list
Company Name: Shanghai Hongye Biotechnology Co. Ltd  
Tel: 400-9205774
Email: sales@glpbio.cn
Products Intro: Product Name:MCTR2
CAS:1784701-62-7
Purity:>98% Package:1mg;10mg;50mg;100mg;
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:MCTR2
CAS:1784701-62-7
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: Shanghai Yiyan Biotechnology Co. , Ltd.  
Tel: 021-69985186 13611928337
Email: 3427709316@qq.com
Products Intro: Product Name:MCTR2
CAS:1784701-62-7
Company Name: Shanghai Yifei Biotechnology Co. , Ltd.  
Tel: 021-65675885 18964387627
Email: customer_service@efebio.com
Products Intro: Product Name:MCTR2
CAS:1784701-62-7
Purity:97% Package:10μg;25μg;50μg
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:MCTR2
CAS:1784701-62-7
Purity:0 Package:25μg/RMB 6330
MCTR2 Basic information
Product Name:MCTR2
Synonyms:MCTR2;Glycine, S-[(1R,2E,4E,6Z,9Z)-12-carboxy-1-[(1S,3Z,6Z)-1-hydroxy-3,6-nonadien-1-yl]-2,4,6,9-dodecatetraen-1-yl]-L-cysteinyl-;S-?[(1R,?2E,?4E,?6Z,?9Z)?-?12-Carboxy-?1-?[(1S,?3Z,?6Z)?-?1-?hydroxy-?3,?6-?nonadien-?1-?yl]?-?2,?4,?6,?9-?dodecatetraen-?1-?yl]?-?L-?cysteinyl-glycine
CAS:1784701-62-7
MF:C27H40N2O6S
MW:520.68
EINECS:
Product Categories:
Mol File:1784701-62-7.mol
MCTR2 Structure
MCTR2 Chemical Properties
Boiling point 801.3±65.0 °C(Predicted)
density 1.163±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 1 mg/ml; Ethanol:Water (95:5): 2 mg/ml; PBS (pH 7.2): 100 μg/ml
pka3.03±0.10(Predicted)
Safety Information
MSDS Information
MCTR2 Usage And Synthesis
DescriptionMaresin conjugates in tissue regeneration 2 (MCTR2) is a specialized pro-resolving mediator (SPM) synthesized from docosahexaenoic acid (DHA; ) in macrophages at the site of inflammation. DHA is oxidized to maresin 1 (MaR1; ), which is converted to MCTR1 by glutathione S-transferase Mu 4 or leukotriene C4 synthase then to MCTR2 by γ-glutamyl transferase. MCTR2 accelerates tissue regeneration in planaria (1 and 100 nM). Pretreatment with MCTR2 prior to E. coli administration reduces neutrophil infiltration, shortens the inflammatory resolution period, and increases phagocytosis of E. coli by macrophages. When administered at a dose of 100 ng 12h post E. coli infection in a mouse model of peritonitis, MCTR2 selectively reduced the amount of the eicosanoids PGD2 and PGF in the exudate.
UsesS-?[(1R,?2E,?4E,?6Z,?9Z)?-?12-Carboxy-?1-?[(1S,?3Z,?6Z)?-?1-?hydroxy-?3,?6-?nonadien-?1-?yl]?-?2,?4,?6,?9-?dodecatetraen-?1-?yl]?-?L-?cysteinyl-glycine is synthesized from omega-3 essential fatty acids and utilized by macrophages in molecular pathways related to tissue regeneration and inflammation.
DefinitionChEBI: (13R)-S-cysteinylglycinyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid is a docosanoid that is (14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid in which a cysteinylglycinyl group is attached at position 13R via a sulfide linkage. It has a role as a human metabolite. It is a docosanoid, an organic sulfide, a secondary alcohol, a dicarboxylic acid and a dipeptide. It is a conjugate acid of a (13R)-glycinylcystein-S-yl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoate(1-).
MCTR2 Preparation Products And Raw materials
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