ChemicalBook > CAS DataBase List > 3,9-bis((ethylthio)methyl)-K-252a

3,9-bis((ethylthio)methyl)-K-252a

Product Name
3,9-bis((ethylthio)methyl)-K-252a
CAS No.
156177-65-0
Chemical Name
3,9-bis((ethylthio)methyl)-K-252a
Synonyms
Kt7515;C106592;Cep1347;Kt-7515;Kt 7515;Cep-1347;Cep 1347;9-Bis(etsm)-K-252a;CEP-1347 (KT-7515;3,9-Bis(etsm)-K-252a
CBNumber
CB21381603
Molecular Formula
C33H33N3O5S2
Formula Weight
615.76
MOL File
156177-65-0.mol
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3,9-bis((ethylthio)methyl)-K-252a Property

Boiling point:
786.8±60.0 °C(Predicted)
Density 
1.53±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
<6.16mg/ml in DMSO
form 
solid
pka
11.94±0.40(Predicted)
color 
Pale yellow
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Safety

HS Code 
2922500090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Tocris
Product number
4924
Product name
CEP1347
Purity
≥97%(HPLC)
Packaging
1
Price
$288
Updated
2021/12/16
TRC
Product number
C256695
Product name
CEP1347
Packaging
0.5mg
Price
$450
Updated
2021/12/16
Usbiological
Product number
254917
Product name
CEP 1347
Packaging
1mg
Price
$603
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
KIN0000067
Product name
CEP-1347
Purity
95.00%
Packaging
5MG
Price
$495.73
Updated
2021/12/16
ApexBio Technology
Product number
B7720
Product name
CEP1347
Packaging
1mg
Price
$417
Updated
2021/12/16
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3,9-bis((ethylthio)methyl)-K-252a Chemical Properties,Usage,Production

Uses

CEP 1347 (cas# 156177-65-0) is a useful research chemical.CEP 1347 promotes neuronal survival in culture and in vivo.

Biological Activity

cep-1347, also called kt 7515, is an inhibitor of the c-jun n-terminal kinase (jnk) signaling pathway, with an ic50 value for jnk1 activation of 20 ± 2 nm in rat embryonic motoneurons [1].the jnk pathway, also known as the stress-activated protein kinase (sapk) pathway, is one of the signaling cascades that mediate the apoptotic death in response to a variety of stressful stimuli. jnk activation by phosphorylation is important for neuronal cell death after injury in vivo and after trophic factor withdrawal in vitro [2].cep-1347 induced neuronal survival. jnk1 activity in untreated cell cultures increased approximately fourfold within 24 hr after plating. as early as 15 min after the application of cep-1347 at 500 nm, the activity of jnk1 sharply decreased to ~50% of control levels. for the next 24 hr, the activity of jnk1 continued to decrease. cultures rich in motoneurons were grown in the presence of cep-1347 at increasing concentrations, and the ic50 for jnk1 activity at 22 hr was 21 ± 2 nm, whereas the ec50 for cell survival at 5 d was 20 ± 2 nm [1].cep-1347 can affect noise-induced hearing loss. data showed that hearing thresholds 2 d before noise exposure showed no significant difference between the noise-exposed control and treated group. hearing threshold shifts in all guinea pigs 2 d after the noise exposure. by day 6 after exposure, threshold shifts were significantly less in the cep-1347 group than in the noise-exposed control group. by 2 weeks after exposure, the difference between the two groups became more pronounced [2].

in vivo

CEP-1347 (0-60 mg/kg; Subcutaneous injection (s.c.)) in rats treated with Caerulein (HY-A0190) (10 μg/kg; Intravenous injection (i.v.)) can dose-dependent inhibit Caerulein Induced JNK activation and improve pancreatitis induced by pancreatin[6].

Animal Model:male white Sprague-Dawley rats[6]
Dosage:Caerulein (HY-A0190): 10 μg/kg; CEP-1347: 0-60 mg/kg
Administration:Caerulein: Intravenous injection (i.v.); CEP-1347: Subcutaneous injection (s.c.)
Result:Caerulein-induced JNK activation was dose-dependent inhibited.

IC 50

JNK1

storage

Store at -20°C

References

[1]. maroney ac, glicksman ma, basma an, et al. motoneuron apoptosis is blocked by cep-1347 (kt 7515), a novel inhibitor of the jnk signaling pathway[j]. the journal of neuroscience, 1998, 18(1): 104-111.
[2]. pirvola u, liang xq, virkkala j, et al. rescue of hearing, auditory hair cells, and neurons by cep-1347/kt7515, an inhibitor of c-jun n-terminal kinase activation[j]. the journal of neuroscience, 2000, 20(1): 43-50.

3,9-bis((ethylthio)methyl)-K-252a Preparation Products And Raw materials

Raw materials

Preparation Products

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3,9-bis((ethylthio)methyl)-K-252a Suppliers

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156177-65-0, 3,9-bis((ethylthio)methyl)-K-252aRelated Search:


  • 3,9-bis((ethylthio)methyl)-K-252a
  • 3,9-Bis(etsm)-K-252a
  • C106592
  • Cep 1347
  • Cep1347
  • Cep-1347
  • Kt 7515
  • Kt7515
  • Kt-7515
  • SCMLRESZJCKCTC-KMYQRJGFSA-N
  • 3;9-BIS(ETSM)-K-252A; CEP 1347; CEP-1347; CEP1347; KT 7515
  • 9-Bis(etsm)-K-252a
  • (9S,10R,12R)-5-16-Bis[(ethylthio)methyl]-2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid methyl ester
  • CEP-1347 (KT-7515
  • 9,12-Epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid, 5,16-bis[(ethylthio)methyl]-2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-, methyl ester, (9S,10R,12R)-
  • 9,12-Epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylicacid,5,16-bis[(ethylthio)methyl]-2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-,methyl ester, (9S,10R,12
  • 156177-65-0
  • C33H33N3O5S2