コビメチニブ
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- ¥3825400
- 化学名: コビメチニブ
- 英語名: XL518
- 別名:コビメチニブ;1-{3,4-ジフルオロ-2-[(2-フルオロ-4-ヨードフェニル)アミノ]ベンゾイル}-3-[(2S)-ピペリジン-2-イル]アゼチジン-3-オール;[3,4-ジフルオロ-2-(2-フルオロ-4-ヨードフェニルアミノ)フェニル][3β-ヒドロキシ-3-[(2S)-2-ピペリジニル]-1-アゼチジニル]メタノン
- CAS番号: 934660-93-2
- 分子式: C21H21F3IN3O2
- 分子量: 531.31
- EINECS:
- MDL Number:MFCD22124461
1物価
選択条件:
ブランド
- 富士フイルム和光純薬株式会社(wako)
パッケージ
- 1g
- 生産者富士フイルム和光純薬株式会社(wako)
- 製品番号W01MAS125087
- 製品説明
- 英語製品説明Cobimetinib
- 包装単位1g
- 価格¥3825400
- 更新しました2024-03-01
- 購入
| 生産者 | 製品番号 | 製品説明 | 包装単位 | 価格 | 更新時間 | 購入 |
|---|---|---|---|---|---|---|
| 富士フイルム和光純薬株式会社(wako) | W01MAS125087 | Cobimetinib |
1g | ¥3825400 | 2024-03-01 | 購入 |
プロパティ
融点 :165 - 166°C
沸点 :565.9±50.0 °C(Predicted)
比重(密度) :1.706
貯蔵温度 :Refrigerator
溶解性 :Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
酸解離定数(Pka) :13.13±0.20(Predicted)
外見 :Solid
色 :Off-White
InChIKey :BSMCAPRUBJMWDF-KRWDZBQOSA-N
SMILES :C(C1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F)(N1CC(O)([C@@H]2CCCCN2)C1)=O
沸点 :565.9±50.0 °C(Predicted)
比重(密度) :1.706
貯蔵温度 :Refrigerator
溶解性 :Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
酸解離定数(Pka) :13.13±0.20(Predicted)
外見 :Solid
色 :Off-White
InChIKey :BSMCAPRUBJMWDF-KRWDZBQOSA-N
SMILES :C(C1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F)(N1CC(O)([C@@H]2CCCCN2)C1)=O
安全情報
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説明
Cobimetinib, codeveloped by Genentech and Exelixis, was approved in August 2015 in Switzerland and November 2015 in the U.S. and Europe for the treatment of unresectable or metastatic BRAFV600 mutationpositive melanoma when used in combination with vemurafenib. Cobimetinib is a potent, highly selective reversible inhibitor of mitogen-activated protein kinases (MEK) 1 and 2,120 which serves to inhibit phosphorylation of ERK1/2,121 disrupting the MAPK pathway which is responsible for cell proliferation, cell survival, and migration.122 Combination of cobimetinib with vemurafenib, an important BRAF inhibitor,123 enables targeting of multiple points on the MAPK pathway, leading to overall enhanced tumor cell apoptosis and response as compared to stand-alone treatment with vemurafenib.124 Specifically, in a representative trial of previously untreated patients with BRAFV600 mutation-positive, unresectable, stage IIIc or IV melanoma, combination of these two therapies led to a significantly improved progression-free survival and overall response rate versus patients treated only with vemurafenib.供給者とメーカー
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