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497061-48-0

中文名稱 DC_AC50
英文名稱 3-amino-N-(2-bromo-4,6-difluorophenyl)-6,7-dihydro-5H-cyclopenta[b]thieno[3,2-e]pyridine-2-carboxamide
CAS 497061-48-0
分子式 C17H12BrF2N3OS
分子量 424.26
MOL 文件 497061-48-0.mol
更新日期 2026/06/09 18:09:49
497061-48-0 結(jié)構(gòu)式 497061-48-0 結(jié)構(gòu)式

基本信息

中文別名
化合物DC_AC50
英文別名
DC_AC50
DC_AC50 (DC-AC50
DC_AC50 >=98% (HPLC)
3-amino-N-(2-bromo-4,6-difluorophenyl)-6,7-dihydro-5H-cyclopenta[b]thieno[3,2-e]pyridine-2-carboxamide
5H-Cyclopenta[b]thieno[3,2-e]pyridine-2-carboxamide, 3-amino-N-(2-bromo-4,6-difluorophenyl)-6,7-dihydro-

物理化學(xué)性質(zhì)

沸點(diǎn)485.1±45.0 °C(Predicted)
密度1.759±0.06 g/cm3(Predicted)
儲(chǔ)存條件2-8°C
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)8.80±0.70(Predicted)
形態(tài)粉末
顏色白色至淺棕色
InChI1S/C17H12BrF2N3OS/c18-10-5-8(19)6-11(20)14(10)23-16(24)15-13(21)9-4-7-2-1-3-12(7)22-17(9)25-15/h4-6H,1-3,21H2,(H,23,24)
InChIKeyDFNOJNBNTVQPCA-UHFFFAOYSA-N
SMILESNC1=C(C(NC2=C(Br)C=C(F)C=C2F)=O)SC3=NC4=C(CCC4)C=C31

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)有害 (GHS07)
GHS07
警示詞警告
危險(xiǎn)性描述H315-H319-H335
防范說明P305+P351+P338
WGK GermanyWGK 3
存儲(chǔ)類別11 - Combustible Solids
危險(xiǎn)性類別Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

圖譜信息

DC_AC50價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2026/06/05HY-107636DC_AC50497061-48-01 mg386元
2026/06/05HY-107636DC_AC50
DC_AC50
497061-48-05mg850元
2026/06/05HY-107636DC_AC50497061-48-010 mM * 1 mLin DMSO935元

常見問題列表

生物活性
DC_AC50 是 Atox1 和 CCS (銅伴侶蛋白) 的雙抑制劑。抑制細(xì)胞內(nèi)銅伴侶可作為減少/防止獲得性化療耐藥的一種策略。
體外研究

DC_AC50 exhibits IC 50 values of 9.88 μM, 12.57 μM, 5.96 μM and 6.68 μM in Canine Abrams, Canine D1, human HOS and human MG63) cells, respectively.
DC_AC50 (0-10 μM)-treated cells are significantly less mitotically active, as demonstrated by decreased expression of phospho-histone H3 and cell cycle analysis.
DC_AC50 (10 μM) potentiates carboplatin-induced apoptosis in OSA cells and decreasesclonogenic survival.
DC_AC50 induces cell cycle arrest at both the 3 and 10 μM doses and DC_AC50 induces increase S phase cells dose-independently.
DC_AC50 (3 μM) inhibits the migration and of canine and human OSA cells.
DC_AC50 (2.5-10 μM) is highly efficient at inhibiting cancer cell proliferation (human lung cancer H1299 cells, leukaemia cancer K562 cells, breast cancer MDA-MB-231 cells and head and neck cancer 212LN cells) in a dose-dependent manner. DC_AC50 fails to exhibit any notable inhibition of the cell proliferation of human normal epithelial lung BEAS-2B cells or breast MCF-10A cells as control cells.

Cell Viability Assay

Cell Line: Canine OSA (Abrams, D1 and human OSA (HOS, MG63) cells.
Concentration: 0-10 μM.
Incubation Time: 72 h.
Result: Dose-dependently decreased viability of OSA cells.

Apoptosis Analysis

Cell Line: Abrams and HOS cells.
Concentration: 1, 3 and 10 μM (10 μM Carboplatin).
Incubation Time: 24 h.
Result: Potentiated carboplatin-induced apoptosis.
"497061-48-0" 相關(guān)產(chǎn)品信息
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