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Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro-

CAS No.
1362243-70-6
Chemical Name:
Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro-
Synonyms
Fluorizoline;Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro-
CBNumber:
CB98192144
Molecular Formula:
C15H8Cl2F3NS
Molecular Weight:
362.2
MDL Number:
MFCD32174345
MOL File:
1362243-70-6.mol
Last updated:2024-10-23 13:36:13

Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro- Properties

Boiling point 404.6±55.0 °C(Predicted)
Density 1.47±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 50 mg/mL (138.05 mM; Need ultrasonic)
pka -6.37±0.60(Predicted)
form Solid
color White to off-white

Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro- Chemical Properties,Uses,Production

Biological Activity

Fluorizoline selectively and directly binds to prohibitin 1 (PHB1) and 2 (PHB2), and induces apoptosis. Fluorizoline reduces chronic lymphocytic leukemia (CLL) cell viability through the upregulation of NOXA and BIM. Fluorizoline exerts antitumor action in a p53-independent manner[1]. Fluorizoline (1.25-20 μM; 24 hours) induces apoptosis in primary CLL cells ex vivo[1]. Fluorizoline (5-10 μM; 48 hours) causes an increase of NOXA protein levels[1]. Fluorizoline reduces the percentage of viable normal B and T cells (48.6% and 82.8% of viable cells at 24 hours of treatment with 10 μM Fluorizoline in normal CD19+ and CD3+ populations, respectively) with mean EC50 values of 10.9 μM and 19.1 μM at 24 hours for normal B and T cells, respectively[1]. Fluorizoline (15 mg/kg; ip; three times a week for five weeks) becomes very rapidly (3 weeks) leukemic, as reflected by the increase in the percentage and the number of CD5+CD19+ CLL cells in the blood in 6-week-old recipient C57BL/6 Eμ-TCL1 mouse model of CLL. Fluorizoline does not induce apoptosis in vivo. Fluorizoline does not control disease development in the spleen as indicated by enlarged spleens[2].

References

[1]. Ana M Cosialls, et al. The prohibitin-binding compound fluorizoline induces apoptosis in chronic lymphocytic leukemia cells through the upregulation of NOXA and synergizes with ibrutinib, 5-aminoimidazole-4-carboxamide riboside or venetoclax. Haematologica. 2017 Sep;102(9):1587-1593. [2]. Marina Wierz, et al. The prohibitin-binding compound fluorizoline induces apoptosis in chronic lymphocytic leukemia cells ex vivo but fails to prevent leukemia development in a murine model. Haematologica. 2018 Apr;103(4):e154-e157.

Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro- Preparation Products And Raw materials

Raw materials

Preparation Products

Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro- Suppliers

Global( 3)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
support@targetmol.com United States 38631 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11974 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 19704 58

View Lastest Price from Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro- manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fluorizoline pictures 2024-10-24 Fluorizoline
1362243-70-6
US $58.00 / mg 99.52% 10g TargetMol Chemicals Inc.
  • Fluorizoline pictures
  • Fluorizoline
    1362243-70-6
  • US $58.00 / mg
  • 99.52%
  • TargetMol Chemicals Inc.
Thiazole, 2,5-bis(4-chlorophenyl)-4,4,5-trifluoro-4,5-dihydro- Fluorizoline 1362243-70-6 C15H8Cl2F3NS