P4359
Pifithrin-α
≥95% (HPLC), powder
동의어(들):
2-(2-Imino-4,5,6,7-tetrahydrobenzothiazol-3-yl)-1-p-tolylethanone hydrobromide, PFT-α
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About This Item
Linear Formula:
C16H18N2OS·HBr
CAS Number:
Molecular Weight:
367.30
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.77
분석
≥95% (HPLC)
양식
powder
저장 조건
protect from light
색상
off-white
mp
192.1-192.5 °C (lit.)
solubility
DMSO: 20 mg/mL
배송 상태
wet ice
저장 온도
−20°C
SMILES string
Br[H].Cc1ccc(cc1)C(=O)CN2C(=N)SC3=C2CCCC3
InChI
1S/C16H18N2OS.BrH/c1-11-6-8-12(9-7-11)14(19)10-18-13-4-2-3-5-15(13)20-16(18)17;/h6-9,17H,2-5,10H2,1H3;1H
InChI key
HAGVCKULCLQGRF-UHFFFAOYSA-N
애플리케이션
Pifithrin-α has been used:
- to study the effect of specific p53 inhibitor on p53-upregulated modulator of apoptosis (PUMA) expression after transient global cerebral ischemia (tGCI)
- as p53 inhibitor to treat PA1 cells
- as a tumor protein p53 (TRP53) inhibitor, to treat mouse lung epithelial-12 (MLE-12) cells
생화학적/생리학적 작용
Pifithrin-α is a reversible inhibitor of p53-mediated apoptosis and p53-dependent gene transcription such as cyclin G, p21/waf1, and mdm2 expression. Pifithrin-α enhances cell survival after genotoxic stress such as UV irradiation and treatment with cytotoxic compounds including doxorubicin, etopoxide, paclitaxel, and cytosine-β-D-arabinofuranoside. Pifithrin-α protects mice from lethal whole body γ-irradiation without an increase in cancer incidence. The protective effect is not seen in p53-null mice or cells expressing a dominant negative mutant of the p53 gene. Protection is conferred by the transient expression of p53 in p53-deficient cell lines.
특징 및 장점
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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