Pifithrin-μ
- Product Name
- Pifithrin-μ
- CAS No.
- 64984-31-2
- Chemical Name
- Pifithrin-μ
- Synonyms
- 2-Phenylethynesulfonamide;PFT;PIFITHRIN-MU;PHENYLETHYNESULFONAMIDE;2-PHENYLACETYLENESULFONAMIDE;2-(3-chlorophenyl)-ethynesulfonamide;Pftmu;CS-1119;NSC 303580;Pifithrin--
- CBNumber
- CB3501588
- Molecular Formula
- C8H7NO2S
- Formula Weight
- 181.21
- MOL File
- 64984-31-2.mol
Pifithrin-μ Property
- Melting point:
- 135.0 to 139.0 °C
- Boiling point:
- 351.7±25.0 °C(Predicted)
- Density
- 1.39±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMSO: soluble >10mg/mL, clear
- form
- solid
- pka
- 7.96±0.60(Predicted)
- color
- White or off-white
- Stability:
- Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
- InChIKey
- ZZUZYEMRHCMVTB-UHFFFAOYSA-N
Safety
- Hazard Codes
- Xn
- Risk Statements
- 22-36/37/38
- Safety Statements
- 26
- WGK Germany
- 3
- HS Code
- 2935.90.9500
- HazardClass
- IRRITANT
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- P0122
- Product name
- Pifithrin-μ
- Purity
- ≥97% (HPLC), solid
- Packaging
- 5mg
- Price
- $107
- Updated
- 2024/03/01
- Product number
- 506155
- Product name
- Pifithrin-μ
- Packaging
- 10mg
- Price
- $144
- Updated
- 2024/03/01
- Product number
- P2048
- Product name
- Pifithrin-μ
- Purity
- >98.0%(HPLC)(N)
- Packaging
- 10mg
- Price
- $29
- Updated
- 2024/03/01
- Product number
- P2048
- Product name
- Pifithrin-μ
- Purity
- >98.0%(HPLC)(N)
- Packaging
- 100mg
- Price
- $164
- Updated
- 2024/03/01
- Product number
- 10748
- Product name
- Pifithrin-μ
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $54
- Updated
- 2024/03/01
Pifithrin-μ Chemical Properties,Usage,Production
Description
In addition to its transactivational functions, p53 mediates apoptosis by binding with the anti-
Uses
A small molecule inhibitor of p53 binding to mitochondria protects mice from gamma radiation
Uses
Pifithrin-μ has been used:
- to treat microglial cell line to analyse its neuroprotective effect on M1-like and M2-like phenotype
- as heat shock protein (HSP)-70 inhibitor, to treat transfected Marc-145 cells
- to inhibit heat shock cognate 70 (Hsc70) to elucidate heat shock chaperones mouse embryonic stem cells
Definition
ChEBI: 2-phenylethynesulfonamide is a member of benzenes.
General Description
A cell-permeable sulfonamide that blocks p53 interaction with Bcl-xL and Bcl-2 proteins and selectively inhibits p53 translocation to mitochondria without affecting the transactivation function of p53. Effectively protects against γ radiation-induced cell death in vitro and animal lethality in vivo. Because Pifithrin-μ targets only the mitochondrial branch of the p53 pathway without affecting the important transcriptional functions of p53, it is superior to Pifithrin-α (Cat. No. 506132) in in vivo studies. Shown to selectively interact with inducible HSP70 and disrupt its functions.
Biological Activity
Inhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and Bcl-XL. Displays no effect on the transactivational or cell cycle checkpoint control function of p53. Potentially increases reprogramming efficiency of human somatic cells to induced pluripotent stem cells (iPSCs) by silencing p53. Reduces cell death induced by γ -radiation in vitro and protects mice from doses of radiation that cause lethal hematopoietic syndrome. Selectively inhibits heat shock protein 70 (HSP70) activity.
Biochem/physiol Actions
Pifithrin-μ is an inhibitor of p53 binding and anti-apoptotic, which directly inhibits p53 binding to mitochondria as well as to Bcl-xL and Bcl-2 proteins. PFTμ rescues cells from lethal γ-irradiation-induced cell death. Because pifithrin-μ shuts down only the p53-mitochondrial pathway without affecting the transcriptional functions of p53, it is superior to pifithrin-α.
Enzyme inhibitor
This cell-permeable sulfonamide-based inhibitor and anti-apoptotic factor (FW = 181.20 g/mol; CAS 64984-31-2; Solubility: >10 mg/mL DMSO, <2 mg/mL H2O; pKa = 8; Symbol = PFTμ and PAS), also known as 2- phenylethynesulfonamide, targets p53 and Heat Shock Protein-70, or HSP 70. Because it only targets the mitochondrial branch of the p53 pathway without affecting the important transcriptional functions of p53, Pifithrin-μ is recommended over Pifithrin-α for in vivo studies. PFTμ exhibits high specificity for p53 and does not protect cells from apoptosis induced by overexpression of the proapoptotic protein Bax or by treatment with dexamethasone. With B-chronic lymphocytic leukemia (CLL) cells, Pifithrin-μ (5–20 μM) initiated apoptosis within 24 hours, with maximal death at 48 hours, as assessed by cell morphology, cleavage of poly(ADPribose) polymerase (PARP), caspase-3 activation, and annexin V staining.
storage
+4°C
References
1) Leu et al. (2009), The therapeutic potential of p53 reactivation by nutlin-3a in ALK+ anaplastic large cell lymphoma with wild-type or mutated p53; Mol. Cell, 36 15 2) Strom et al. (2006), Small-molecule inhibitor of p53 binding to mitochondria protects mice from gamma radiation.; Nat. Chem. Biol., 2 474
Pifithrin-μ Preparation Products And Raw materials
Raw materials
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View Lastest Price from Pifithrin-μ manufacturers
- Product
- Pifithrin-μ 64984-31-2
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 50000KG/month
- Release date
- 2023-09-28
- Product
- Pifithrin-μ 64984-31-2
- Price
- US $7.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- JD 789
- Release date
- 2019-09-02