ζ-Stat

Modify Date: 2024-01-09 10:10:07

ζ-Stat Structure
ζ-Stat structure
Common Name ζ-Stat
CAS Number 3316-02-7 Molecular Weight 384.36000
Density 2.019g/cm3 Boiling Point N/A
Molecular Formula C10H8O10S3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of ζ-Stat


ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis, and has antitumor activity in vitro[1][2].

 Names

Name 8-hydroxynaphthalene-1,3,6-trisulfonic acid
Synonym More Synonyms

 ζ-Stat Biological Activity

Description ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis, and has antitumor activity in vitro[1][2].
Related Catalog
Target

aPKC-ζ:5 μM (IC50)

In Vitro ζ-Stat (0.1-20 µM) shows only 13% inhibition on PKC-ι at 20 μM, but shows a significant inhibition on PKC-ζ as 51% at 5 μM level[1]. ζ-Stat (0.1-10 µM; 3 d) significantly decreases cell proliferation of SK-MEL-2 and MeWo upon increasing the concentrations[1]. ζ-Stat (7 or 10 µM; 24-72 h) and 5-FU in combination is able to decrease the viability of LoVo CRC cells by more than 75%[2]. ζ-Stat (5 µM; 3 d) shows a significant diminution of phosphorylated, total PKC-ζ, Bcl-2 and PARP levels, and increases Caspase-3 and cleaved-PARP levels in SK-MEL-2 and MeWo cells[1]. ζ-Stat (5 µM; 1-10 h) does not show significant cytotoxicity on MEL-F-NEO, SK-MEL-2 and MeWo cells[1]. Cell Proliferation Assay[1] Cell Line: MEL-F-NEO, SK-MEL-2 and MeWo cells Concentration: 0.1, 0.5, 1, 2.5, 5, 7.5, 10 µM Incubation Time: 3 days Result: Decreased proliferation by 47.7% for 5 µM in SK-MEL-2 cells and by 50.6% for 5 µM in MeWo cells. Showed significant inhibitions on MEL-F-NEO cells 19.3% (P ≤ 0.05) at 10 μM. Western Blot Analysis[1] Cell Line: SK-MEL-2 and MeWo cells Concentration: 5 µM Incubation Time: 3 days Result: Decreased phosphorylated and total PKC-ζ levels.
References

[1]. Ratnayake WS, et, al. Oncogenic PKC-ι activates Vimentin during epithelial-mesenchymal transition in melanoma; a study based on PKC-ι and PKC-ζ specific inhibitors. Cell Adh Migr. 2018; 12(5):447-463.

[2]. Islam SMA, et, al. Atypical Protein Kinase-C inhibitors exhibit a synergistic effect in facilitating DNA damaging effect of 5-fluorouracil in colorectal cancer cells. Biomed Pharmacother. 2020 Jan; 121:109665.

 Chemical & Physical Properties

Density 2.019g/cm3
Molecular Formula C10H8O10S3
Molecular Weight 384.36000
Exact Mass 383.92800
PSA 208.48000
LogP 3.52790
Index of Refraction 1.741

 Safety Information

HS Code 2908999090

 Precursor & DownStream

Precursor  0

DownStream  1

 Customs

HS Code 2908999090
Summary 2908999090 halogenated, sulphonated, nitrated or nitrosated derivatives of phenols or phenol-alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

 Synonyms

1-Naphthol,6,8-trisulfo
1-naphthol-3,6,8-trisulfonic acid
8-Hydroxy-naphthalin-1,3,6-trisulfonsaeure
8-hydroxy-naphthalene-1,3,6-trisulfonic acid
1-Naphthol,3,6,8-trisulfo
Naphthol-(1)-trisulfonsaeure-(3.6.8)
1-naphthol-3,6,8-trisulphonic acid
1-Naphthylamin-3,6,8-trisulfonsaeure
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