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ChemicalBook--->CAS DataBase List--->1810710-59-8

1810710-59-8

1810710-59-8 Structure

1810710-59-8 Structure
IdentificationBack Directory
[Name]

PCTR1
[CAS]

1810710-59-8
[Synonyms]

PCTR1
[Molecular Formula]

C32H47N3O9S
[MOL File]

1810710-59-8.mol
[Molecular Weight]

649.8
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 1 mg/ml; Ethanol/H20 (95:5): 2 mg/ml; PBS (pH 7.2): 0.1 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
Hazard InformationBack Directory
[Description]

Protectin conjugates in tissue regeneration 1 (PCTR1) is a specialized pro-resolving mediator (SPM) synthesized from docosahexaenoic acid (DHA; ).1 DHA is oxidized to 16S,17S-epoxy-protectin, which is then converted to PCTR1 by glutathione S-transferase.1,2 PCTR1 levels increase during resolution of acute microbial-induced peritonitis in mice.3 PCTR1 (30 ng, i.p.) administration 12 hours post-infection increases macrophage numbers and activity and shortens the resolution phase of inflammation by 57%. It also reduces the levels of PGE2 , PGD2 , and TXB2 in peritoneal exudates.
[storage]

Store at -20°C
[References]

1. Rodriguez, A.R., and Spur, B.W. Total synthesis of pro-resolving and tissue-regenerative protectin sulfido-conjugates Tetrahedron Lett. 56(42),5811-5815(2015).
2. Aursnes, M., Tungen, J.E., Colas, R.A., et al. Synthesis of the 16S,17S-epoxyprotectin intermediate in the biosynthesis of protectins by human macrophages J. Nat. Prod. 8(12),2924-2931(2015).
3. Ramon, S., Dalli, J., Sanger, J.M., et al. The protectin PCTR1 is produced by human M2 macrophages and enhances resolution of infectious inflammation Am. J. Pathol. 186(4),962-973(2016).
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