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733805-92-0

733805-92-0 Structure

733805-92-0 Structure
IdentificationBack Directory
[Name]

Pyrano[2,3-e]isoindole-8(2H)-pentanoic acid, 2-[(3E)-4,8-dimethyl-3,7-nonadien-1-yl]-α-[(2S,3S)-2-[(3E)-4,8-dimethyl-3,7-nonadien-1-yl]-3,4,7,9-tetrahydro-3,5-dihydroxy-2-methyl-7-oxopyrano[2,3-e]isoindol-8(2H)-yl]-3,4,7,9-tetrahydro-3,5-dihydroxy-2-methyl-7-oxo-, (αS,2S,3S)-
[CAS]

733805-92-0
[Synonyms]

Pyrano[2,3-e]isoindole-8(2H)-pentanoic acid, 2-[(3E)-4,8-dimethyl-3,7-nonadien-1-yl]-α-[(2S,3S)-2-[(3E)-4,8-dimethyl-3,7-nonadien-1-yl]-3,4,7,9-tetrahydro-3,5-dihydroxy-2-methyl-7-oxopyrano[2,3-e]isoindol-8(2H)-yl]-3,4,7,9-tetrahydro-3,5-dihydroxy-2-methyl-7-oxo-, (αS,2S,3S)-
[Molecular Formula]

C51H68N2O10
[MOL File]

733805-92-0.mol
[Molecular Weight]

869.09
Chemical PropertiesBack Directory
[Boiling point ]

1017.5±65.0 °C(Predicted)
[density ]

1.211±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

3.46±0.21(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Description]

Orniplabin, also known as SMTP-7 is a dual inhibitor of thrombolysis and soluble epoxide hydrolase. SMTP-7 promotes thrombolysis and inhibits soluble epoxide hydrolase.
[Uses]

Orniplabin (SMTP-7) is a low-molecular-weight compound that enhances plasminogen–fibrin binding, urokinase-catalyzed activation of plasminogen, and urokinase and plasminogen-mediated fibrin degradation. Orniplabin shows potential thrombolytic and anti-inflammatory effects. Orniplabin inhibits ROS[1][2].
[References]

[1] Shibata K, et al. A novel finding of a low-molecular-weight compound, SMTP-7, having thrombolytic and anti-inflammatory effects in cerebral infarction of mice. Naunyn Schmiedebergs Arch Pharmacol. 2010 Sep;382(3):245-53. DOI:10.1007/s00210-010-0542-5
[2] Shibata K, et al. Neuroprotective mechanisms of SMTP-7 in cerebral infarction model in mice. Naunyn Schmiedebergs Arch Pharmacol. 2011 Jul;384(1):103-8. DOI:10.1007/s00210-011-0642-x
733805-92-0 suppliers list
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