Fluorizoline
CAS No. 1362243-70-6
Fluorizoline( —— )
Catalog No. M34601 CAS No. 1362243-70-6
Fluorizoline is a PHB-binding compound with anticancer and antiproliferative activity that induces apoptosis by inducing selective targeting of the BH3 protein NOXA to PHB.Fluorizoline inhibits protein synthesis and has been used in studies of leukemia.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
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Biological Information
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Product NameFluorizoline
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NoteResearch use only, not for human use.
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Brief DescriptionFluorizoline is a PHB-binding compound with anticancer and antiproliferative activity that induces apoptosis by inducing selective targeting of the BH3 protein NOXA to PHB.Fluorizoline inhibits protein synthesis and has been used in studies of leukemia.
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DescriptionFluorizoline 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.
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In VitroApoptosis Analysis Cell Line:Primary CLL cells Concentration:1.25 to 20 μM Incubation Time:24 hours Result:Strongly reduced cell viability and induced apoptosis in a dose-dependent manner.Western Blot Analysis Cell Line:Primary CLL cells Concentration:5, 10 μM Incubation Time:48 hours Result:Caused an increase of NOXA protein levels.
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In Vivo——
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Synonyms——
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PathwayApoptosis
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TargetApoptosis
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RecptorApoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number1362243-70-6
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Formula Weight362.2
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Molecular FormulaC15H8Cl2F3NS
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (138.05 mM; Ultrasonic )
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SMILESFC1(F)N=C(SC1(F)c1ccc(Cl)cc1)c1ccc(Cl)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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HYPOCRELLIN B
HYPOCRELLIN B are photosensitive pigments isolated from Hypocrella bambusae Sacc. Hypocrellin B causes DNA strand breakage induces apoptosis in ovarian cancer cells and inhibits proliferation of Staphylococcus by increasing ROS levels and damaging cell walls.
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VPC-70063
VPC-70063 is an inhibitor of c-Myc-MAX. VPC-70063 exhibits Myc-Max transcriptional activity inhibition of 106% with an IC50 of 8.9 μM and Myc-Max/UBE2C downstream pathway inhibition of 94%. VPC-70063 can be used for studies about anticancer.
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Ecteinascidin 770
A tetrahydroisoquinoline alkaloid with potent anticaner activities; shows cytotoxicity against human cell lines HCT116, QG56, and DU145 with IC50 of 0.60, 2.4, and 0.81 nM, respectively.
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