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

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
Molecular Weight:
615.77
MDL Number:
MFCD27991285
MOL File:
156177-65-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:22

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

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
FDA UNII 200HA2LIMK

SAFETY

Risk and Safety Statements

HS Code  2922500090

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

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Usbiological 254917 CEP 1347 ≥97%(HPLC) 156177-65-0 1mg $718 2026-06-03 Buy
Biosynth FE29092 CEP 1347 156177-65-0 1mg $629.66 2026-06-04 Buy
Biosynth FE29092 CEP 1347 156177-65-0 5mg $2676.05 2026-06-04 Buy
Biosynth FE29092 CEP 1347 156177-65-0 10mg $4281.7 2026-06-04 Buy
ChemScene CS-0002594 CEP-1347 98.5% 156177-65-0 1mg $1246 2026-06-04 Buy
Product number Packaging Price Buy
254917 1mg $718 Buy
FE29092 1mg $629.66 Buy
FE29092 5mg $2676.05 Buy
FE29092 10mg $4281.7 Buy
CS-0002594 1mg $1246 Buy

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

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

Global Suppliers ( 32)
Supplier Tel Email Country ProdList Advantage
AdooQ BioScience, LLC +1 (866) 930-6790 info@adooq.com United States 2774 58
SPIRO PHARMA eric_feng1954@126.com China 9239 55
BOC Sciences 16314854226; +8616314854226 inquiry@bocsci.com United States 19852 58
InvivoChem +1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6378 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD 86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6288 58
ShangHai ChuanQian Chemcial Technique Centre 15869524721 3525679403@qq.com China 4565 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8137 58
Wuhan Topule +86-02787215551 19945035818 2936752263@qq.com China 7983 58
InvivoChem 13549236410 sales@invivochem.cn China 6745 58
Wuhan Yingnuo Pharmaceutical Technology Co., Ltd. +86-027-59232304 15387063101 1276242629@qq.com China 9977 58

156177-65-0 (3,9-bis((ethylthio)methyl)-K-252a) Related 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