Abstract Biological activity In vitro In vivo Features References
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Trametinib

Abstract Biological activity In vitro In vivo Features References
Product Name
Trametinib
CAS No.
871700-17-3
Chemical Name
Trametinib
Synonyms
CS-30;100836;TraMetinib;CB32514557;GSK-1120212;TraMetinib API;QuMei iMatinib;Trametinib, >=98%;Trametinib Impurity;Mekinist trametinib
CBNumber
CB32514557
Molecular Formula
C26H23FIN5O4
Formula Weight
615.39
MOL File
871700-17-3.mol
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Trametinib Property

Melting point:
300-301 °C
Density 
1.74
form 
White solid.
pka
14.76±0.70(Predicted)
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Safety

Safety Statements 
24/25
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
16292
Product name
Trametinib
Purity
≥95%
Packaging
25mg
Price
$55
Updated
2021/03/22
Cayman Chemical
Product number
16292
Product name
Trametinib
Purity
≥95%
Packaging
50mg
Price
$94
Updated
2021/03/22
Cayman Chemical
Product number
16292
Product name
Trametinib
Purity
≥95%
Packaging
100mg
Price
$110
Updated
2021/03/22
Cayman Chemical
Product number
16292
Product name
Trametinib
Purity
≥95%
Packaging
250mg
Price
$248
Updated
2021/03/22
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Trametinib Chemical Properties,Usage,Production

Abstract

Trametinib (trade name Mekinist) is a cancer drug. It is a MEK inhibitor drug with anti-cancer activity.
Trametinib(Mekinist) is a reversible, highly selective, allosteric inhibitor of mitogen-activated extracellular signal regulated kinase 1 (MEK1) and MEK2 activation and kinase activity. MEK proteins are components of the extracellular signal-related kinase (ERK) pathway. In melanoma and other cancers, this pathway is often activated by mutated forms of BRAF which activates MEK. Trametinib inhibits activation of MEK by BRAF and inhibits MEK kinase activity. Trametinib inhibits growth of BRAF V600 mutant melanoma cell lines and demonstrates anti-tumor effects in BRAF V600 mutant melanoma animal models.
Mekinist is indicated as monotherapy or in combination with Tafinlar (dabrafenib) for the treatment of adult patients with unresectable or metastatic melanoma with a BRAF V600 mutation.

Biological activity

Trametinib (GSK1120212) is a highly specific and potent MEK1/2 inhibitor with IC50 of 0.92 nM/1.8 nM in cell-free assays, no inhibition of the kinase activities of c-Raf, B-Raf, ERK1/2.

In vitro

For the different subtypes of Raf and MEK, with IC50 ranging from 0.92 nM to 3.4 nM,GSK1120212 inhibits the phosphorylation of MBP. GSK1120212 demonstrates no inhibition of the kinase activities of c-Raf, B-Raf, ERK1 and ERK2. In addition, GSK1120212 does not show drastic inhibitory activity against the other 98 kinases. GSK1120212 displays potent inhibitory activity against human colorectal cancer cell lines. HT-29 and COLO205 cells, which are known to have a constitutively active B-Raf mutant, are most sensitive to GSK1120212 with IC50 0.48 nM and 0.52 nM, respectively. The cell lines bearing a K-Ras mutation show a wide range of sensitivity to GSK1120212 with IC50 of 2.2-174 nM. In contrast, COLO320 DM cells, bearing the wild-type gene in both B-Raf and K-Ras, are found to be resistant to GSK1120212 even at 10 μM. GSK1120212 treatment for 24 hours induces cell-cycle arrest at the G1 phase in all sensitive cell lines. Consistently, GSK1120212 treatment leads to upregulation of p15INK4b and/or p27KIP1 in most of the colorectal cancer cell lines. GSK1120212 induces apoptosis both in HT-29 and COLO205 cells, but that COLO205 cells are more sensitive to GSK1120212 than HT-29 cells in terms of apoptosis induction.GSK1120212 blocks tumor necrosis factor-α and interleukin-6 production from peripheral blood mononuclear cells (PBMCs).

In vivo

Oral administration of GSK1120212 at 0.3 mg/kg or 1 mg/kg once daily for 14 days is effective in inhibiting the HT-29 xenograft growth, and 1 mg/kg of GSK1120212 can completely block the tumor increase. The phosphorylation of ERK1/2 is completely inhibited in the established tumor tissues by single oral dose of 1 mg/kg GSK1120212, and both p15INK4b and p27KIP1 protein levels are upregulated after 14 days of treatment with GSK1120212. In the COLO205 xenograft model, tumor regression is observed even at a dose of 0.3 mg/kg. At a dose of 1 mg/kg, a complete regression is obtained in 4 out of 6 mice in which the tumor degenerates to the point that tumor volume is not measurable. Administration of GSK1120212 at 0.1 mg/kg almost completely suppresses adjuvant-induced arthritis (AIA) and type II collagen-induced arthritis (CIA) in Lewis rats or DBA1/J mice, respectively.

Features

More potent than PD0325901 or AZD6244.

References

https://en.wikipedia.org/wiki/Trametinib
https://www.novartisoncology.com/news/product-portfolio/mekinist

Uses

Used in the systematic treatment of advanced cutaneous melanoma. An EGFR kinase inhibitor.

Uses

antiprotozoal

Definition

ChEBI: A pyridopyrimidine that is used (as its dimethyl sulfoxide addition compound) for the treatment of patients with unresectable or metastatic melanoma with BRAF V600E or V600K mutations, and who have not received prior BRAF inhibitor treatment.

Indications

MEK, also known as MAPK, is a dual specificity threonine/tyrosine kinase that is a key node in the Raf–Ras–MEK signaling pathway. Small-molecule MEK inhibitors represent the largest group of type III allosteric inhibitors that do not bind to the ATP binding pocket. As of December 2016, besides the FDA-approved MEK1/2 inhibitors trametinib (Mekinist(R), GlaxoSmithKline) and cobimetinib (Cotellic(R), Roche), over 10 MEK inhibitors are currently in clinical trials. Trametinib was approved by FDA in 2013 for the treatment of patients with either B-Raf V600E or V600K mutated metastatic melanoma. Considering the fact that MEK and Raf are different kinases along the same pathway of Ras–Raf–MEK/ERK signaling cascade, combination strategies using both MEK and B-Raf inhibitors were utilized to overcome the observed progression using single-agent trametinib, which usually occurs within 7months. FDA approved the combination of trametinib and dabrafenib for the treatment of B-Raf V600E/K mutated metastatic melanoma in January 2014 and the combination of cobimetinib and vemurafenib for the same type of indication. Although significant improvement in progression-free survival was observed using MEK/B-Raf combination strategy, the incidence of some common adverse effects, such as vomiting, diarrhea, nausea, rash, and pyrexia, also increased.

Clinical Use

Trametinib (GSK1120212) is an oral MEK inhibitor which has demonstrated excellent results in combination therapy for BRAF-mutated melanoma and is FDA approved in combination with BRAF inhibitors for that indication. Trametinib was evaluated initially as a single agent in KRAS mutant NSCLC in comparison with docetaxel and pemetrexed. Results as a single agent were not impressive, with an ORR of only 12% in these patients.

Trametinib Preparation Products And Raw materials

Raw materials

Preparation Products

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Trametinib Suppliers

Guangzhou Tomums Life Science Co., Ltd.
Tel
020-31155029-
Fax
020-31155029
Email
sales@tomums.cn
Country
China
ProdList
4704
Advantage
58
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399-
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4575
Advantage
55
Shanghai Drjart Biological Co., Ltd.
Tel
Email
tianxiao549423850@163.com
Country
China
ProdList
118
Advantage
58
Jurong Coupling Biotechnology Co., Ltd.
Tel
Email
278191416@qq.com
Country
China
ProdList
150
Advantage
58
Hubei Junxian Biotechnology Co., Ltd
Email
3464928989@qq.com
Country
China
ProdList
46
Advantage
58
Bono Kangyuan (Beijing) Pharmaceutical Technology Co., Ltd
Tel
01056380788-8515
Email
wch013@bionna.cn
Country
CHINA
ProdList
49
Advantage
58
Ningbo Risheng Pharmaceutical Technology Co., Ltd.
Tel
Fax
0574-89132888
Email
2928184953@qq.com
Country
China
ProdList
40
Advantage
58
Wuhan Bo Jin Biotechnology Co.,Ltd.
Tel
Email
2709603029@qq.com
Country
China
ProdList
78
Advantage
58
Shanghai Boyle Chemical Co., Ltd.
Fax
86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2926
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833- ;010-82848833-
Fax
86-10-82849933
Email
jkinfo@jkchemical.com;market6@jkchemical.com
Country
China
ProdList
96815
Advantage
76
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View Lastest Price from Trametinib manufacturers

Zhuozhou Wenxi import and Export Co., Ltd
Product
Trametinib 871700-17-3
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-10
Zhuozhou Wenxi import and Export Co., Ltd
Product
Trametinib 871700-17-3
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-09
BOC Sciences
Product
Trametinib 871700-17-3
Price
US $199.00/mg
Min. Order
1g
Purity
≥98%
Supply Ability
10kg
Release date
2020-05-13

871700-17-3, TrametinibRelated Search:


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