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About This Item
经验公式（希尔记法）:
C7H7FO2S
CAS号:
分子量:
174.19
Beilstein:
2088311
EC 号:
MDL编号:
UNSPSC代码:
12352202
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SMILES字符串
FS(=O)(=O)Cc1ccccc1
InChI
1S/C7H7FO2S/c8-11(9,10)6-7-4-2-1-3-5-7/h1-5H,6H2
InChI key
YBYRMVIVWMBXKQ-UHFFFAOYSA-N
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生化/生理作用
PMSF was shown to inhibit activity of cathepsin-G thereby preventing the neutrophil-induced lysis of neuroblastoma tumor cells in in vitro studies.
法规信息
新产品
E Barker et al.
Cancer research, 53(2), 362-367 (1993-01-15)
Neutrophils mediate the lysis of human neuroblastoma cells coated with human/mouse chimeric anti-GD2 ganglioside antibody ch14.18. This study examined the mechanism(s) by which this occurs. Neutrophil degranulation was found to be a required step for lysis, since release of granular
Lise Boussemart et al.
Nature, 513(7516), 105-109 (2014-08-01)
In BRAF(V600)-mutant tumours, most mechanisms of resistance to drugs that target the BRAF and/or MEK kinases rely on reactivation of the RAS-RAF-MEK-ERK mitogen-activated protein kinase (MAPK) signal transduction pathway, on activation of the alternative, PI(3)K-AKT-mTOR, pathway (which is ERK independent)
Selective neuronal differentiation of neural stem cells induced by nanosecond microplasma agitation.
Z Xiong et al.
Stem cell research, 12(2), 387-399 (2014-01-01)
An essential step for therapeutic and research applications of stem cells is their ability to differentiate into specific cell types. Neuronal cells are of great interest for medical treatment of neurodegenerative diseases and traumatic injuries of central nervous system (CNS)
Con Dogovski et al.
PLoS biology, 13(4), e1002132-e1002132 (2015-04-23)
Successful control of falciparum malaria depends greatly on treatment with artemisinin combination therapies. Thus, reports that resistance to artemisinins (ARTs) has emerged, and that the prevalence of this resistance is increasing, are alarming. ART resistance has recently been linked to
Sylvie Bannwarth et al.
Brain : a journal of neurology, 137(Pt 8), 2329-2345 (2014-06-18)
Mitochondrial DNA instability disorders are responsible for a large clinical spectrum, among which amyotrophic lateral sclerosis-like symptoms and frontotemporal dementia are extremely rare. We report a large family with a late-onset phenotype including motor neuron disease, cognitive decline resembling frontotemporal
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