BIBW2992
BIBW2992 物理性質(zhì)
- 沸點(diǎn) :
- 676.9±55.0 °C(Predicted)
- 比重(密度) :
- 1.380
- 貯蔵溫度 :
- Store at -20°C
- 溶解性:
- ≥24.3 mg/mL in DMSO; insoluble in H2O; ≥42.1 mg/mL in EtOH with ultrasonic
- 外見 :
- solid
- 酸解離定數(shù)(Pka):
- 12.06±0.43(Predicted)
- 色:
- White to off-white
- InChIKey:
- ULXXDDBFHOBEHA-INIZCTEOSA-N
- SMILES:
- C(NC1C(O[C@H]2CCOC2)=CC2C(C=1)=C(NC1=CC=C(F)C(Cl)=C1)N=CN=2)(=O)C=CCN(C)C
- CAS データベース:
- 439081-18-2
安全性情報(bào)
- リスクと安全性に関する聲明
- 危険有害性情報(bào)のコード(GHS)
| 絵表示(GHS) |
|
| 注意喚起語(yǔ) |
警告 |
| 危険有害性情報(bào) |
| コード |
危険有害性情報(bào) |
危険有害性クラス |
區(qū)分 |
注意喚起語(yǔ) |
シンボル |
P コード |
| H302 |
飲み込むと有害 |
急性毒性、経口 |
4 |
警告 |
 |
P264, P270, P301+P312, P330, P501 |
| H315 |
皮膚刺激 |
皮膚腐食性/刺激性 |
2 |
警告 |
 |
P264, P280, P302+P352, P321,P332+P313, P362 |
| H319 |
強(qiáng)い眼刺激 |
眼に対する重篤な損傷性/眼刺激 性 |
2A |
警告 |
 |
P264, P280, P305+P351+P338,P337+P313P |
| H335 |
呼吸器への刺激のおそれ |
特定標(biāo)的臓器毒性、単回暴露; 気道刺激性 |
3 |
警告 |
 |
|
|
| 注意書き |
| P261 |
粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける こと。 |
| P305+P351+P338 |
眼に入った場(chǎng)合:水で數(shù)分間注意深く洗うこと。次にコ ンタクトレンズを著用していて容易に外せる場(chǎng)合は外す こと。その後も洗浄を続けること。 |
|
BIBW2992 価格
| メーカー |
製品番號(hào) |
製品説明 |
CAS番號(hào) |
包裝 |
価格 |
更新時(shí)間 |
購(gòu)入 |
BIBW2992 化學(xué)特性,用途語(yǔ),生産方法
用途
アファチニブ(Afatinib)は、EGFR 遺伝子変異陽(yáng)性の非小細(xì)胞肺癌(NSCLC)の治療に用いられるチロシンキナーゼ阻害薬(英語(yǔ)版)(TKI)の一つである。EGFRおよびerbB-2(HER2)を非可逆的に阻害する。
他國(guó)でも非小細(xì)胞肺癌の治療に用いられる。
説明
In July 2013, the US FDA approved afatinib (also referred to as BIBW- 2992), for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) and with tumors that have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution. Afatinib functions as an irreversible inhibitor by covalently binding directly to the ATP-binding site in the kinase domains of both EGFR(Cys 773) andHER2 (Cys 805;HER-2 is the preferred dimerization partner of EGFR) resulting in downregulation of EGFR signaling. Afatinib is a potent inhibitor of wild-type and mutant forms (L858R) of EGFR (IC
50s of 0.5 and 0.4 nM, respectively), and HER2 (IC
50=14 nM), but about 100-fold more active against the gefitinib resistant L858R– T790M EGFR double mutant, with an IC
50 of 10 nM. Consistent with its in vitro activity, afatinib induces tumor regression in xenograft and transgenic lung cancer models, with superior activity over erlotinib. A synthetic route to afatinib that employs the displacement of a phenylsulfonyl group to install the (S)-3-hydoxytetrahydrofuran ring and a modified Horner–Wadsworth–Emmons reaction with {[4-(3-chloro-4- phenylamino)-7-((S)-tetrahydrofuran-3-yloxy)-quinazolin-6-ylcarbamoyl]- methyl}-phosphonate and dimethylaminoacetaldehyde-hydrogen sulfite adduct to install the eneamide moiety, has been reported.
使用
BIBW2992 (Afatinib, Tomtovok, Tovok) irreversibly inhibits EGFR/HER2 including EGFRwt, EGFRL858R, EGFRL858R/T790M and HER2 with IC50 of 0.5 nM, 0.4 nM, 10 nM and 14 nM, respectively.
BIBW2992 上流と下流の製品情報(bào)
原材料
準(zhǔn)備製品
BIBW2992 生産企業(yè)
Global( 429)Suppliers
439081-18-2(BIBW2992)キーワード:
- 439081-18-2
- Tovok
- Afatinb
- (S)-N-(4-((3-Chloro-4-fluorophenyl)amino)-7-((tetrahydrofuran-3-yl)oxy)quinazolin-6-yl)-4-(dim
- Tovok, BIBW 2992
- BIBW 2992;TOVOK
- BIBW2992 Afatinib
- Afatinib (BIBW 2992)
- ToMtovok
- (S,E)-N-(4-(3-chloro-4-fluorophenylaMino)-7-(tetrahydrofuran-3-yloxy)quinazolin-6-yl)-4-(diMethylaMino)but-2-enaMide
- (E)-N-(7-((S)-tetrahydrofuran-3-yloxy)-4-(3-chloro-4-fluorophenylaMino)quinazolin-6-yl)-4-(diMethylaMino)but-2-enaMide
- (S)-N-(4-((3-Chloro-4-fluorophenyl)amino)-7-((tetrahydrofuran-3-yl)oxy)quinazolin-6-yl)-4-(dimeth
- (S,E)-N-(4-(3-chloro-4-fluorophenylaMino)-7-(tetrahydrofuran-2-yloxy)quinazolin-6-yl)-4-(diMethylaMino)but-2-enaMide
- (S)-N-(4-((3-Chloro-4-fluorophenyl)aMino)-7-((tetrahydrofuran- 3-yl)oxy)quinazolin-6-yl)-4-(diMethylaMino)but-2-enaMide
- BIBW 2992 N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-[[(3S)-tetrahydro-3-furanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-2-butenamide
- Afatinib, Free Base
- Tofacitinib and its interMediate
- Afatinib, >=99%
- Afatinib (BIBW 2992)r
- Afatinib (BIBW 2992) powder
- (E/Z)-Afatinib
- Afatinib(cis-trans isomerismtautomers)
- Afatinib(W.S)
- AFATINIB; BIBW2992;BIBW-2292
- BIBW-2292
- CS-95
- TOVOK (BIBW-2992, Afatinib)
- [14C]Afatinib
- [14C] (S)-N-(4-((3-Chloro-4-fluorophenyl)amino)-7-((tetrahydrofuran-3-yl)oxy)quinazolin-6-yl)-4-(dim
- 2-Butenamide, N-[4-[(3-chloro-4-fluorophenyl)amino]-7-[[(3S)-tetrahydro-3-furanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-
- Cancer Treatment Afatinib CAS
- N-[4-[(3-クロロ-4-フルオロフェニル)アミノ]-7-[[(S)-テトラヒドロフラン-3-イル]オキシ]-6-キナゾリニル]-4-(ジメチルアミノ)-2-ブテンアミド
- BIBW2992
- N-{4-[(3-クロロ-4-フルオロフェニル)アミノ]-7-[(3S)-オキソラン-3-イルオキシ]キナゾリン-6-イル}-4-(ジメチルアミノ)ブタ-2-エンアミド
- ジオトリフ