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1627710-50-2

CAS No.
1627710-50-2
Chemical Name:
1627710-50-2
Synonyms
LJH685;CS-2182;LJH685(LJH-685);LJH-685;LJH 685;LJH685;2,6-Difluoro-4-[4-[4-(4-methyl-1-piperazinyl)phenyl]-3-pyridinyl]phenol;Phenol, 2,6-difluoro-4-[4-[4-(4-methyl-1-piperazinyl)phenyl]-3-pyridinyl]-;LJH685,S6K,LJH-685,Apoptosis,inhibit,Ribosomal S6 Kinase (RSK),LJH 685,Inhibitor
CBNumber:
CB03060937
Molecular Formula:
C22H21F2N3O
Molecular Weight:
381.42
MDL Number:
MOL File:
1627710-50-2.mol
Last updated:2023-06-08 09:02:45

1627710-50-2 Properties

Boiling point 481.1±45.0 °C(Predicted)
Density 1.257±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form crystalline solid
pka 5.86±0.25(Predicted)
FDA UNII 27CZQ807C1

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
HS Code  2933998090
NFPA 704
0
2 0

1627710-50-2 price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 19913 LJH685 ≥98% 1627710-50-2 1mg $32 2024-03-01 Buy
Cayman Chemical 19913 LJH685 ≥98% 1627710-50-2 5mg $116 2024-03-01 Buy
Cayman Chemical 19913 LJH685 ≥98% 1627710-50-2 10mg $214 2024-03-01 Buy
Cayman Chemical 19913 LJH685 ≥98% 1627710-50-2 25mg $456 2024-03-01 Buy
TRC L468875 LJH685 1627710-50-2 10mg $625 2021-12-16 Buy
Product number Packaging Price Buy
19913 1mg $32 Buy
19913 5mg $116 Buy
19913 10mg $214 Buy
19913 25mg $456 Buy
L468875 10mg $625 Buy

1627710-50-2 Chemical Properties,Uses,Production

Uses

LJH685 is a selective and potent RSK inhibitor (1). The p90 ribosomal S6 kinase (RSK) family of serine/threonine kinases is linked to various cancers and its substrate phosphorylation is also related to the regulation of cell survival, proliferation, and cell polarity (2).

Biological Activity

ljh685 is a rsk (p90 ribosomal s6 kinase) inhibitor.the p90 ribosomal s6 kinase (rsk) family of serine/threonine kinases is found to be expressed in a variety of cancers and its substrate phosphorylation has been implicated in direct regulation of cell proliferation, cell survival, as well as cell polarity.

in vitro

in a previous study, the structural analysis results confirmed the binding of ljh685 to the rsk2 n-terminal kinase atp-binding site, which suggested that the inhibitor ljh685 adopted an unusual nonplanar conformation that explained its excellent selectivity for rsk family kinases. in addition, ljh685 and it analog lji308 could efficiently inhibit rsk activity in vitro and in cells. moreover, in a subset of examined cell lines, the cellular inhibition of rsk and its phosphorylation of yb1 on ser102 were found to be closely associate with the inhibition of cell growth in an anchorage-independent growth setting [1].

IC 50

6 nm, 5 nm and 4 nm for the biochemical activities of rsk1, rsk2, and rsk3, respectively

References

[1] aronchik i, appleton ba,basham se,crawford k,del rosario m,doyle lv,estacio wf,lan j,lindvall mk,luu ca,ornelas e,venetsanakos e,shafer cm,jefferson ab. novel potent and selective inhibitors of p90 ribosomal s6 kinase reveal the heterogeneity of rsk function in mapk-driven cancers. mol cancer res.2014 may;12(5):803-12.

1627710-50-2 Preparation Products And Raw materials

Raw materials

Preparation Products

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LJH685 Phenol, 2,6-difluoro-4-[4-[4-(4-methyl-1-piperazinyl)phenyl]-3-pyridinyl]- CS-2182 LJH-685;LJH 685;LJH685 LJH685(LJH-685) 2,6-Difluoro-4-[4-[4-(4-methyl-1-piperazinyl)phenyl]-3-pyridinyl]phenol LJH685,S6K,LJH-685,Apoptosis,inhibit,Ribosomal S6 Kinase (RSK),LJH 685,Inhibitor 1627710-50-2 C22H21F2N3O