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450839-40-4

450839-40-4 Structure

450839-40-4 Structure
IdentificationBack Directory
[Name]

ABT-100
[CAS]

450839-40-4
[Synonyms]

ABT-100
ABT-100 (ABT100)
[Molecular Formula]

C27H19F3N4O3
[MDL Number]

MFCD32857139
[MOL File]

450839-40-4.mol
[Molecular Weight]

504.46
Chemical PropertiesBack Directory
[Boiling point ]

722.0±60.0 °C(Predicted)
[density ]

1.29±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C, protect from light
[solubility ]

Acetonitrile: Slightly soluble: 0.1-1 mg/ml
DMSO: Sparingly soluble: 1-10 mg/ml
[form ]

Solid
[pka]

12.15±0.29(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

ABT-100 is a potent, highly selective and orally active farnesyltransferase inhibitor. ABT-100 inhibits cell proliferation (IC50s of 2.2 nM, 3.8 nM, 5.9 nM, 6.9 nM, 9.2 nM, 70 nM and 818 nM for EJ-1, DLD-1, MDA-MB-231, HCT-116, MiaPaCa-2, PC-3, and DU-145 cells, respectively), increases apoptosis and decreases angiogenesis. ABT-100 possesses broad-spectrum antitumor activity[1].
[in vivo]

ABT-100 (6.25-12.5 mg/kg/day; subcutaneous injection; daily; for 21 days; C.B-17 scid male mice) treatment regresses EJ-1 tumors in mice[1].

Animal Model:C.B-17 scid male mice with EJ-1 cells[1]
Dosage:6.25 mg/kg/day, 12.5 mg/kg/day
Administration:Subcutaneous injection; daily; for 21 days
Result:Regressed EJ-1 tumors in C.B-17 scid male mice.
[References]

[1] Ferguson D, et al. Antitumor activity of orally bioavailable farnesyltransferase inhibitor, ABT-100, is mediated by antiproliferative, proapoptotic, and antiangiogenic effects in xenograft models. Clin Cancer Res. 2005 Apr 15;11(8):3045-54. DOI:10.1158/1078-0432.CCR-04-2041
Spectrum DetailBack Directory
[Spectrum Detail]

ABT-100(450839-40-4)1HNMR
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