ChemicalBook--->CAS DataBase List--->312946-37-5

312946-37-5

312946-37-5 Structure

312946-37-5 Structure
IdentificationBack Directory
[Name]

LDN-27219
[CAS]

312946-37-5
[Synonyms]

184663
CS-1194
LDN-27219
LDN-27219 (LDN 27219
LDN-27219 >=98% (HPLC)
2-({4-oxo-3,5-diphenyl-3H,4H-thieno[2,3-d]pyrimid in-2-yl}sulfanyl)acetohydrazide
2-((4-oxo-3,5-diphenyl-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl)thio)acetohydrazide
2-[(3,4-Dihydro-4-oxo-3,5-diphenylthieno[2,3-d]pyrimidin-2-yl)thio]-acetic acid hydrazide
Acetic acid, 2-[(3,4-dihydro-4-oxo-3,5-diphenylthieno[2,3-d]pyrimidin-2-yl)thio]-, hydrazide
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C20H16N4O2S2
[MOL File]

312946-37-5.mol
[Molecular Weight]

408.5
Chemical PropertiesBack Directory
[density ]

1.45±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

DMSO: soluble15mg/mL, clear
[form ]

powder
[pka]

11.87±0.37(Predicted)
[color ]

white to beige
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

LDN 27219 is a transglutaminase inhibitor.
[Biological Activity]

LDN-27219 is a revesible inhibitor of transglutaminase 2 (TG2) th at binds to the GTP binidng site of the enzyme and inhbits activity with and IC50 of 600 nM.''LDN-27219 is a thieno[2,3-d]pyrimidine-4-one-acylhydrazide derivative. Closed conformation of TG2 induced by LDN-27219 can be a potential therapeutic strategy for age-related vascular dysfunction and lowering blood pressure.
[in vivo]

LDN-27219 (0.1-2 mg/kg; i.v. once) affects vivo arterial pressure and shows larger effects on older rats[2].

Animal Model:12 to 14-week-old male Wistar rats[2]
Dosage:0.1, 1 and 2 mg/kg
Administration:Intravenous injection; 0.1, 1 and 2 mg/kg once
Result:Dose-dependently decreased mean arterial pressure of mice.
Animal Model:12 to 14- and 35 to 40-week-old male Wistar rats
Dosage:0.1, 1 and 2 mg/kg
Administration:Intravenous injection; 0.1, 1 and 2 mg/kg once
Result:Decreased mean arterial pressure in old group more significant than young group.
[storage]

Store at +4°C
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