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Defactinib

Product Name
Defactinib
CAS No.
1073154-85-4
Chemical Name
Defactinib
Synonyms
VS6063;VS-6063;VS 6063;CS-1796;PF-941222;Defactinib;Defactinib (VS-6063;VS-6063; PF-04554878;Defactinib free base;PF-04554878 Defactinib
CBNumber
CB82716190
Molecular Formula
C20H21F3N8O3S
Formula Weight
510.49
MOL File
1073154-85-4.mol
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Defactinib Property

Density 
1.495±0.06 g/cm3(Predicted)
storage temp. 
-20°C (des.)
solubility 
Soluble in DMSO (up to at least 25mg/ml)
form 
solid
pka
15.16±0.46(Predicted)
color 
White
Stability:
Stable for 1 year as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChIKey
FWLMVFUGMHIOAA-UHFFFAOYSA-N
SMILES
C(NC)(=O)C1=CC=C(NC2=NC=C(C(F)(F)F)C(NCC3=NC=CN=C3N(C)S(C)(=O)=O)=N2)C=C1
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
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N-Bromosuccinimide Price

Cayman Chemical
Product number
17737
Product name
Defactinib
Purity
≥98%
Packaging
1mg
Price
$37
Updated
2024/03/01
Cayman Chemical
Product number
17737
Product name
Defactinib
Purity
≥98%
Packaging
5mg
Price
$116
Updated
2024/03/01
Cayman Chemical
Product number
17737
Product name
Defactinib
Purity
≥98%
Packaging
10mg
Price
$213
Updated
2024/03/01
Cayman Chemical
Product number
17737
Product name
Defactinib
Purity
≥98%
Packaging
25mg
Price
$353
Updated
2024/03/01
Usbiological
Product number
474093
Product name
Defactinib
Packaging
100mg
Price
$1380
Updated
2021/12/16
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Defactinib Chemical Properties,Usage,Production

Description

Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that plays a vital role in many oncogenic pathways. Defactinib is a dose-dependent inhibitor of FAK, with maximal inhibition of FAK autophosphorylation in cells achieved at 10 μM. It is less effective against the related kinase PYK2. Defactinib restores the chemosensitivity of taxane-resistant cells to paclitaxel , although it is not cytotoxic alone. Defactinib decreases YB-1 phosphorylation and nuclear accumulation in an Akt-dependent manner. It is orally bioavailable, inhibiting FAK and augmenting paclitaxel action in suppressing the growth and number of ovarian cancer cell tumors in mice.

Uses

Defactinib is a selective and orally active FAK inhibitor phase 2. Used in treating cancer patients as it decreases proliferation and increases apoptosis.

in vivo

Defactinib (VS-6063) doses of 25 mg/kg twice a day or greater statistically significantly inhibits pFAK (Tyr397) at 3 hours, with return of expression noted by 24 hours. Therefore, administration of Defactinib at 25 mg/kg twice a day is selected as the dosing schedule for subsequent therapy experiments. For therapy experiments, female nude mice bearing HeyA8 tumors in the peritoneal cavity are randomly divided into 4 groups (n=10 per group): 1) vehicle orally twice daily and phosphate-buffered saline intraperitoneally weekly (control); 2) Defactinib 25 mg/kg orally twice daily; 3) PTX intraperitoneally weekly; and 4) both VDefactinib 25 mg/kg orally twice daily and PTX intraperitoneally weekly. There is an 87.4% reduction in tumor weight by PTX monotherapy in the HeyA8 model, and combination therapy resulted in the greatest tumor weight reduction, with a 97.9% reduction (P=0.05 compared with PTX). In the SKOV3ip1 model, a 92.7% tumor weight reduction is observed in the combination group compared with PTX (P<0.001)[1].

storage

Store at -20°C

References

[1] SUZANNE F JONES. A phase I study of VS-6063, a second-generation focal adhesion kinase inhibitor, in patients with advanced solid tumors.[J]. Investigational New Drugs, 2015, 33 5: 1100-1107. DOI:10.1007/s10637-015-0282-y
[2] VIHREN N KOLEV. Inhibition of FAK kinase activity preferentially targets cancer stem cells.[J]. Oncotarget, 2017: 51733-51747. DOI:10.18632/oncotarget.18517
[3] FABRIZIO MARCUCCI  François L  Cristiano Rumio. Anti-Cancer Stem-like Cell Compounds in Clinical Development - An Overview and Critical Appraisal.[J]. Frontiers in Oncology, 2016: 115. DOI:10.3389/fonc.2016.00115
[4] J. RING. FAK/PYK2 inhibitors defactinib and VS-4718 enhance immune checkpoint inhibitor efficacy[J]. Journal for Immunotherapy of Cancer, 2015, 3 1: P354-P354. DOI:10.1186/2051-1426-3-s2-p354
[5] HONG JIANG. Targeting focal adhesion kinase renders pancreatic cancers responsive to checkpoint immunotherapy[J]. Nature Medicine, 2016, 22 8: 851-860. DOI:10.1038/nm.4123

Defactinib Preparation Products And Raw materials

Raw materials

Preparation Products

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Defactinib Suppliers

Deyang Sino Biotech. Co., LTD
Tel
+86-19182167371 +86-19182167371;
Email
service@synlord.com
Country
China
ProdList
110
Advantage
58
Nantong Hanfang Biotechnology Co. , Ltd.
Tel
hanfangpharma@126.com; 18616537568
Email
hanfangpharma@126.com
Country
China
ProdList
29965
Advantage
58
Shanghai Boyle Chemical Co., Ltd.
Tel
Fax
86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2922
Advantage
55
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6003
Advantage
61
Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Fax
+86-10-82967029
Email
2355560935@qq.com
Country
China
ProdList
12000
Advantage
60
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4747
Advantage
58
Haoyuan Chemexpress Co., Ltd.
Tel
021-58950125
Fax
(86) 21-58955996
Email
info@chemexpress.com
Country
China
ProdList
7552
Advantage
61
ShangHai Caerulum Pharma Discovery Co., Ltd.
Tel
18149758185
Email
sales-cpd@caerulumpharma.com
Country
China
ProdList
3506
Advantage
58
Shandong Juntai Pharmaceutical Co., LTD.
Tel
15853135817
Fax
0531-66958526
Email
sales@h2opharm.com
Country
China
ProdList
201
Advantage
55
AdooQ Bioscience CHINA
Tel
025-58849295 18951903616;
Fax
025-68650336
Email
info@adooq.cn
Country
China
ProdList
2990
Advantage
60
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View Lastest Price from Defactinib manufacturers

Career Henan Chemical Co
Product
Defactinib 1073154-85-4
Price
US $1.00/KG
Min. Order
1KG
Purity
97%
Supply Ability
200kg
Release date
2020-02-01

1073154-85-4, DefactinibRelated Search:


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  • VS-6063
  • Defactinib(PF-04554878)
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  • N-Methyl-4-[[4-[[[3-[methyl(methylsulfonyl)amino]-2-pyrazinyl]methyl]amino]-5-(trifluoromethyl)-2-pyrimidinyl]amino]benzamide
  • N-METHYL-4-(4-((3-(N-METHYLMETHYL SULFON
  • N-methyl-4-[[4-[[3-[methyl(methylsulfonyl)amino]pyrazin-2-yl]methylamino]-5-(trifluoromethyl)pyrimidin-2-yl]amino]benzamide
  • Defactinib (VS-6063
  • N-methyl-4-(4-((3-(N-methylmethylsulfonamido)pyrazin-2-yl)methylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)benzamide
  • VS-6063; PF-04554878
  • PF-04554878 Defactinib
  • N-methyl-4-((4-(((3-(N-methylmethylsulfonamido)pyrazin-2-yl)methyl)amino)-5-(trifluoromethyl)pyrimidin-2-yl)amino)benzamide Defactinib(PF-04554878)(VS-6063)
  • VS-6063; VS6063; VS 6063; PF04554878; PF-04554878; PF 04554878
  • CS-1796
  • Benzamide, N-methyl-4-[[4-[[[3-[methyl(methylsulfonyl)amino]-2-pyrazinyl]methyl]amino]-5-(trifluoromethyl)-2-pyrimidinyl]amino]-
  • Defactinib free base
  • Defactinib, FAK inhibitor
  • Defactinib, 10 mM in DMSO
  • PF-941222
  • 1073154-85-4
  • C20H21F3N8O3S
  • Inhibitors
  • API