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130773-02-3

中文名稱(chēng) 鹽酸奈替康唑
英文名稱(chēng) Neticonazole Hydrochloride
CAS 130773-02-3
分子式 C17H23ClN2OS
分子量 338.9
MOL 文件 130773-02-3.mol
更新日期 2024/07/08 16:38:18
130773-02-3 結(jié)構(gòu)式 130773-02-3 結(jié)構(gòu)式

基本信息

中文別名
鹽酸萘康唑
鹽酸奈康唑
鹽酸奈替康唑
(E)-1-(2-(甲硫基)-1-(2-(戊氧基)苯基)乙烯基)-1H-咪唑鹽酸鹽
英文別名
SS-717
Atolant
Neticonazole hydrochloride
1-[2-methylsulfanyl-1-(2-pentoxyphenyl)ethenyl]imidazole hydrochloride
1-[(E)-2-methylsulfanyl-1-(2-pentoxyphenyl)ethenyl]imidazole,hydrochloride
(E)-1-(2-(Methylthio)-1-(2-(pentyloxy)phenyl)vinyl)-1H-imidazole hydrochloride
long-acting,colorectal,Neticonazole,antifungal,Neticonazole Hydrochloride,Imidazole,anti-cancer,nSMase2,Fungal,secretion,Inhibitor,p-ERK,anti-infection,inhibit,exosome
所屬類(lèi)別
有機(jī)原料:羧酸類(lèi)化合物及衍生物

物理化學(xué)性質(zhì)

熔點(diǎn)145-147°
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO: 250 mg/mL (737.68 mM)
形態(tài)Solid
顏色White to off-white
鹽酸奈替康唑價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2024/11/08HY-128365鹽酸奈替康唑
Neticonazole hydrochloride
130773-02-325mg650元
2024/11/08HY-128365鹽酸奈替康唑
Neticonazole hydrochloride
130773-02-350mg950元
2024/11/08HY-128365鹽酸奈替康唑
Neticonazole hydrochloride
130773-02-3100mg1600元

常見(jiàn)問(wèn)題列表

生物活性
Neticonazole是咪唑類(lèi)抗真菌劑,用于治療皮膚真菌感染。
靶點(diǎn)

Fungal

體外研究

Neticonazole (10 μM; 48 hours; C4-2B cells) treatment decreases the levels of both Alix and Rab27a, and significantly decreases nSMase2 levels. Neticonazole causes a significant inhibition in p-ERK levels.
Neticonazole (0-10 μM) exhibits a potent and dose-dependent inhibition of exosome release from C4-2B cells.
Neticonazole hydrochloride is also an orally active exosome biogenesis and secretion inhibitor.

Western Blot Analysis

Cell Line: C4-2B cells
Concentration: 10 μM
Incubation Time: 48 hours
Result: Decreased the levels of both Alix and Rab27a, and significantly decreased nSMase2 levels.
體內(nèi)研究

Neticonazole (1-100 ng/kg; oral gavage; daily; for 15 days; male C57BL/6 mice) treatment significantly improves the survival of intestinal dysbacteriosis (IDB) mice with colorectal cancer (CRC) xenograft tumors, likely through increasing apoptosis of CRC xenograft tumor cells.

Animal Model: Male C57BL/6 mice (8 weeks old) given ampicillin, neomycin, metronidazole and vancomycin, and injected with SW480 cells
Dosage: 1 ng/kg, 10 ng/kg and 100 ng/kg
Administration: Oral gavage; daily; for 15 days
Result: Significantly improved the survival of IDB mice with CRC xenograft tumors.
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