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pf-5274857

Product Name
pf-5274857
CAS No.
1373615-35-0
Chemical Name
pf-5274857
Synonyms
CS-601;pf-5274857;PF-5274857 freebase;pf-5274857 USP/EP/BP;PF5274857;PF 5274857;PF-5274857 hydrochloride;PF-5274857;PF 5274857;PF5274857;1-(4-(5-Chloro-4-(3,5-dimethylpyridin-2-yl)pyridin-2-yl)piperazin-1-yl)-3-(methylsulfonyl)prop;1-[4-(5'-Chloro-3,5-dimethyl[2,4'-bipyridin]-2'-yl)-1-piperazinyl]-3-(methylsulfonyl)-1-propanone;1-(4-(5'-Chloro-3,5-dimethyl-[2,4'-bipyridin]-2'-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one
CBNumber
CB62640301
Molecular Formula
C20H25ClN4O3S
Formula Weight
436.96
MOL File
1373615-35-0.mol
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pf-5274857 Property

storage temp. 
Sealed in dry,Store in freezer, under -20°C
solubility 
H2O: soluble3mg/mL, clear (warmed)
form 
powder
color 
white to beige
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Safety

WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H317May cause an allergic skin reaction

H319Causes serious eye irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
PZ0217
Product name
PF-5274857 hydrochloride
Purity
≥98% (HPLC)
Packaging
5mg
Price
$105
Updated
2022/05/15
Tocris
Product number
5262
Product name
PF-5274857 hydrochloride
Purity
≥98%(HPLC)
Packaging
10
Price
$185
Updated
2021/12/16
TRC
Product number
P293910
Product name
PF-5274857
Packaging
25mg
Price
$310
Updated
2021/12/16
ApexBio Technology
Product number
A8500
Product name
PF-5274857
Packaging
10mM(in 1mL DMSO)
Price
$329
Updated
2021/12/16
ChemScene
Product number
CS-1206
Product name
PF-5274857
Purity
98.12%
Packaging
50mg
Price
$450
Updated
2021/12/16
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pf-5274857 Chemical Properties,Usage,Production

Uses

PF-5274857 is a potent and selective Smoothened (Smo) antagonist, inhibits Hedgehog (Hh) signaling, respectively, and can penetrate the blood–brain barrier.

Biological Activity

pf-5274857 is an inhibitor of hedgehog (hh) signaling pathway and is identified as a potent and selective antagonist of smoothened (smo) with an ic50 of 5.8 nm.smoothened, a g protein-coupled receptor, is a component of the hedgehog signaling pathway and is conserved from flies to humans. this protein is the molecular target of the teratogen cyclopamine. smo can act as an oncogene and the activation of smo mutations leads to unregulated activation of the hedgehog pathway and cancer.in mef cells, treatment of pf-5274857 completely blocked shh-induced hh pathway activity, which was measured by the transcriptional activity of smo downstream gene gli1.

Enzyme inhibitor

This brain-penetrating Smoothened (Smo) antagonist (FW = 436.96 g/mol; CAS 1373615-35-0), also known as 1-(4-(5-chloro-4-(3,5-dimethylpyridin- 2-yl)pyridin-2-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one, potentlyand selectively inhibits Hedgehog (Hh) signaling (IC50 = 5.8 nM; Ki = 4.6 nM). PF-5274857 elicits robust antitumor activity in a mouse model of medulloblastoma (IC50 = 8.9 nmol/L), with down-regulation of Gli1, a marker closely linked to the tumor growth inhibition in patched (+/-) medulloblastoma mice. PF-5274857 also inhibits Smo activity within the brain of primary medulloblastoma mice, improving survival. PF-5274857 is orally available and metabolically stable in vivo. Other Hedgehog inhibitors include: GANT61, BMS-833923, Purmorphamine, SANT-1, LY2940680, Cyclopamine, LDE225 (or NVP-LDE225, Erismodegib), Vismodegib (GDC-0449)

in vivo

pf-5274857 showed anti-tumor activity in a mouse medulloblastoma model with ic50 of 8.9 nm. pf-5274857 also shows significant dose-dependent tumor growth inhibition (tgi) and induces tumor regression. in skin tissue, downregulation of gli1 and gli2 is also observed with a similar time course by pf-52748571.

target

Smoothened

References

1. rohner a, spilker me, lam jl, et al. effective targeting of hedgehog signaling in a medulloblastoma model with pf-5274857, a potent and selective smoothened antagonist that penetrates the blood-brain barrier. molecular cancer therapeutics.2012;11(1):57-65.

pf-5274857 Preparation Products And Raw materials

Raw materials

Preparation Products

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pf-5274857 Suppliers

Jinan Trio PharmaTech Co., Ltd.
Tel
+86 (531) 88811783
Fax
+86 (531) 55696010 QQ 1762738062
Email
sales@trio-pharmatech.com (International market)
Country
China
ProdList
1856
Advantage
62
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
meilunui@163.com
Country
China
ProdList
4727
Advantage
58
NCE Biomedical Co.,Ltd.
Tel
4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
Fax
+86-27-87599188
Country
China
ProdList
1493
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
Shanghai Witofly Chemical Co.,Ltd
Tel
Email
sales@witofly.com
Country
China
ProdList
2864
Advantage
52
Shanghai HuanChuan Industry Co.,Ltd.
Tel
021-61478794
Fax
021-61478794
Email
sales@hcshhai.com
Country
China
ProdList
9793
Advantage
50
Shanghai JiYi Biotechnology Co. Ltd.
Tel
13621943973
Fax
-
Email
sales@shjiyipharmatech.com
Country
China
ProdList
1166
Advantage
55
LETOPHARM LIMITED
Tel
+86-21-5821 5861
Fax
+86-21-5106 2861
Email
sales@letopharm.com
Country
China
ProdList
2384
Advantage
58
Shanghai Lollane Biological Technology Co.,Ltd.
Tel
021-52996696,15000506266 15000506266
Fax
+86-21-52996696
Country
China
ProdList
4456
Advantage
55
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View Lastest Price from pf-5274857 manufacturers

Career Henan Chemical Co
Product
pf-5274857 1373615-35-0
Price
US $1.00/KG
Min. Order
1KG
Purity
95%~99%
Supply Ability
per week 100kg
Release date
2019-09-05

1373615-35-0, pf-5274857Related Search:


  • pf-5274857
  • PF5274857;PF 5274857
  • CS-601
  • PF-5274857;PF 5274857;PF5274857
  • 1-(4-(5-chloro-4-(3,5-diMethylpyridin-2-yl)pyridin-2-yl)piperazin-1-yl)-3-(Methylsulfonyl)propan-1-one
  • 1-[4-(5′-Chloro-3,5-dimethyl-2,4′-bipyridin-2′-yl)piperazin-1-yl] -3- (methylsulfonyl)propan-1-one hydrochloride
  • PF-5274857 hydrochloride
  • 1-[4-(5'-Chloro-3,5-dimethyl[2,4'-bipyridin]-2'-yl)-1-piperazinyl]-3-(methylsulfonyl)-1-propanone
  • 1-(4-(5-Chloro-4-(3,5-dimethylpyridin-2-yl)pyridin-2-yl)piperazin-1-yl)-3-(methylsulfonyl)prop
  • 1-Propanone, 1-[4-(5'-chloro-3,5-dimethyl[2,4'-bipyridin]-2'-yl)-1-piperazinyl]-3-(methylsulfonyl)-
  • pf-5274857 USP/EP/BP
  • PF-5274857 freebase
  • 1-(4-(5'-Chloro-3,5-dimethyl-[2,4'-bipyridin]-2'-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one
  • inhibit,driven,PF 5274857,PF5274857,metastasis,pathway,Smo,PF-5274857,Smoothened,Inhibitor,brain,tumor
  • 1-(4-(5'-Chloro-3,5-dimethyl-[2,4'-bipyridin]-2'-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one
  • 1373615-35-0
  • 373615-35-0
  • 73615-35-0
  • C20H25ClN4O3S
  • Inhibitors