MK-8719 - ≥98% , CAS No.1382799-40-7

CAS: 1382799-40-7 Cat. No.: M414247 Summenformel: C₉H₁₄F₂N₂O₃S Molekulargewicht: 268.28

QUALITÄT & REINHEIT ≥98%

Synonyms

5H-​Pyrano[3,​2-​d]​thiazole-​6,​7-​diol,5-​(difluoromethyl)​-​2-​(ethylamino)​-​3a,​6,​7,​7a-​tetrahydro-​,(3aR,​5S,​6S,​7R,​7aR)​-

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Information

MK-8719 MK-8719 is a selective and potent small molecule inhibitor of the O-GlcNAcase (OGA) enzyme with ki of 7.9nM for hOGA.

Targets

hOGA (Cell-free assay) 7.9nM(Ki)

In vitro

MK-8719 is a potent inhibitor of the human OGA enzyme with comparable activity against the corresponding enzymes from mouse, rat, and dog.

In vivo

oral administration of MK-8719 elevates brain and peripheral blood mononuclear cell O-GlcNAc levels in a dose-dependent manner. In addition, positron emission tomography imaging studies demonstrate robust target engagement of MK-8719 in the brains of rats and rTg4510 mice. In the rTg4510 mouse model of human tauopathy, MK-8719 significantly increases brain O-GlcNAc levels and reduces pathologic tau. The reduction in tau pathology in rTg4510 mice is accompanied by attenuation of brain atrophy, including reduction of forebrain volume loss as revealed by volumetric magnetic resonance imaging analysis.

Cell Research(from reference)

Cell lines：PC-12 cells 

Concentrations：up to 1 mM 

Incubation Time：24 h 

Spezifikationen

Synonyme

5H-​Pyrano[3,​2-​d]​thiazole-​6,​7-​diol,5-​(difluoromethyl)​-​2-​(ethylamino)​-​3a,​6,​7,​7a-​tetrahydro-​,(3aR,​5S,​6S,​7R,​7aR)​-

Spezifikationen & Reinheit

≥98%

Biochemische und physiologische Mechanismen

MK-8719 is a selective and potent small molecule inhibitor of the O-GlcNAcase (OGA) enzyme with ki of 7.9nM for hOGA.

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

528765478

Kanonisches Lächeln

CCNC1=NC2C(C(C(OC2S1)C(F)F)O)O

IUPAC Name

(3aR,5S,6S,7R,7aR)-5-(difluoromethyl)-2-(ethylamino)-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d][1,3]thiazole-6,7-diol

InChIKey

UDQTXCHQKHIQMH-KYGLGHNPSA-N

INCHI

1S/C9H14F2N2O3S/c1-2-12-9-13-3-4(14)5(15)6(7(10)11)16-8(3)17-9/h3-8,14-15H,2H2,1H3,(H,12,13)/t3-,4-,5+,6+,8-/m1/s1

Isomere SMILES

CCNC1=N[C@@H]2[C@H]([C@@H]([C@H](O[C@@H]2S1)C(F)F)O)O

Molekulargewicht

268.28

Reaxy-Rn

58819117

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=58819117&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Monosaccharides
• Alternative Parents: Oxanes Thiazolines Monothioacetals Secondary alcohols Isothioureas 1,2-diols Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Carboximidamides Azacyclic compounds Organofluorides Hydrocarbon derivatives Amines Alkyl fluorides
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Oxane - Monosaccharide - Meta-thiazoline - Monothioacetal - 1,2-diol - Isothiourea - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Hydrocarbon derivative - Amine - Alkyl halide - Alkyl fluoride - Alcohol - Aliphatic heteropolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as monosaccharides. These are compounds containing one carbohydrate unit not glycosidically linked to another such unit, and no set of two or more glycosidically linked carbohydrate units. Monosaccharides have the general formula CnH2nOn.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

OGA Tchem Protein O-GlcNAcase (4 Activities)

Discover Target: OGA

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Chemische und physikalische Eigenschaften

• Löslichkeit: Solubility (25°C) In vitro DMSO: 54 mg/mL (201.28 mM); Water: 54 mg/mL (201.28 mM); Ethanol: 54 mg/mL (201.28 mM)