ChemicalBook--->CAS DataBase List--->195514-63-7

195514-63-7

195514-63-7 Structure

195514-63-7 Structure
IdentificationBack Directory
[Name]

AP1903
[CAS]

195514-63-7
[Synonyms]

AP1903
CS-1237
Rimiducid(AP1903)
AP1903 (Rimiducid
AP1903;RIMIDUCID;AP-1903
RIMIDUCID;AP-1903;AP 1903
2-Piperidinecarboxylic acid, 1-[(2S)-1-oxo-2-(3,4,5-trimethoxyphenyl)butyl]-, 2,2'-[1,2-ethanediylbis[imino(2-oxo-2,1-ethanediyl)oxy-3,1-phenylene[(1R)-3-(3,4-dimethoxyphenyl)propylidene]]] ester, (2S,2'S)-
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C78H98N4O20
[MDL Number]

MFCD25976784
[MOL File]

195514-63-7.mol
[Molecular Weight]

1411.63
Chemical PropertiesBack Directory
[Boiling point ]

1307.5±65.0 °C(Predicted)
[density ]

1?+-.0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMSO:97.05(Max Conc. mg/mL);68.75(Max Conc. mM)
Ethanol:120.58(Max Conc. mg/mL);85.42(Max Conc. mM)
[form ]

A solid
[pka]

13.70±0.46(Predicted)
Spectrum DetailBack Directory
[Spectrum Detail]

AP1903(195514-63-7)MS
AP1903(195514-63-7)1HNMR
Hazard InformationBack Directory
[Biological Activity]

AP1903 (Rimiducid) is a dimerizing agent that acts by cross-linking the FKBP domain, initiating Fas signaling and causing apoptosis.It dimerizes the Caspase 9 suicide switch and rapidly induces apoptosis.
[in vitro]

The human fibrosarcoma line HT1080 is engineered to express stably a fusion protein comprising a myristoylation sequence, two copies of F36V-FKBP, and the human first apoptosis signal (Fas) intracellular domain. Rimiducid (AP1903) elicits potent and dose-dependent apoptotic death of these engineered cells in culture, with an EC 50 of ≈0.1 nM. Maximal killing occurred in the presence of 3 to 10 nM Rimiducid (AP1903), and the IC 50 is approximately 0.2 nM. LV′VFas-transduced T lymphocytes expressing high levels of CD25 (top panel) are eliminated by with 66%±7.5% (n=10) efficiency. When cells are examined after CD25 expression returned to basal levels, 63%±4.7% (n=9) killing is observed after Rimiducid treatment.

[in vivo]

AP1903 elicits a dose-dependent decrease in serum human GH levels, with a half-maximal effective dose of 0.4±0.1 mg /kg.

[target]

EC50: 0.1 nM (FKBP, in HT1080 cells)
Fas receptor

[storage]

Store at -20°C
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