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180200-66-2

中文名稱 水合加替沙星
英文名稱 Gatifloxacin sesquihydrate
CAS 180200-66-2
分子式 C19H24FN3O5
分子量 393.42
MOL 文件 180200-66-2.mol
更新日期 2024/12/16 11:38:06
180200-66-2 結構式 180200-66-2 結構式

基本信息

中文別名
加替沙星水合
水合加替沙星
加替沙星水合物
加替沙星羧酸乙酯
加替沙星 USP標準品
1-環(huán)丙基-6-氟-4-氧代-8-甲氧基-7-(3-甲基
1-環(huán)丙基-6-氟-8-甲氧基-7-(3-甲基哌嗪-1-基)-4-氧代3-喹啉羧酸
1-環(huán)丙基-6-氟-8-甲氧基-7-(3-甲基哌嗪-1-基)-4-氧代-3-喹啉羧酸
1-環(huán)丙基-6-氟-8-甲氧基-7-(3-甲基-1- 哌嗪)-4-氧代-喹啉-3-羧酸
1-環(huán)丙基-6-氟-8-甲氧基-7-(3-甲基哌嗪-1-基)-4-氧代-1,4-二氫3-喹啉羧酸
英文別名
TEQUIN
(+-)-1-C
AKOS NCG1-0010
Gatifloxacin Tablet
Gatifloxacin (300 mg)
Gatifloxacin Monohydrate
Gatifloxacin sesquihydrate
Gatifloxacin formic acid ethyl ester
Gatifloxacin sesquihydrate USP/EP/BP
Gatifloxacin sesquihydrate Micronized
所屬類別
原料藥:喹諾酮類藥

物理化學性質

沸點684℃
RTECS號VB1983600
儲存條件Keep in dark place,Inert atmosphere,2-8°C
溶解度溶于 1N NaOH,濃度為 10mg/ml
形態(tài)neat
BRN14390028
InChIInChI=1S/C19H22FN3O4.H2O/c1-10-8-22(6-5-21-10)16-14(20)7-12-15(18(16)27-2)23(11-3-4-11)9-13(17(12)24)19(25)26;/h7,9-11,21H,3-6,8H2,1-2H3,(H,25,26);1H2
InChIKeyIJOOSVJZBQQMBV-UHFFFAOYSA-N
SMILESO(C1C(N2CCNC(C)C2)=C(F)C=C2C(=O)C(C(=O)O)=CN(C3CC3)C=12)C.O

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302+H312+H332
危險品標志Xn
危險類別碼20/21/22
安全說明36/37
WGK Germany1

常見問題列表

生物活性
Gatifloxacin sesquihydrate (AM-1155 sesquihydrate) 是一種有效的氟喹諾酮類抗生素 (antibiotic),具有廣譜抗菌活性。Gatifloxacin sesquihydrate (AM-1155 sesquihydrate) 可抑制細菌 II 型拓撲異構酶 (type II topoisomerases) (IC50=13.8 μg/ml; 金黃色葡萄球菌拓撲異構酶 IV) 和大腸桿菌 DNA 解旋酶 (IC50=0.109 μg/ml)。Gatifloxacin sesquihydrate (AM-1155 sesquihydrate) 在動物模型中,可用于細菌性結膜炎的研究。
靶點

Topoisomerase II

36.7 μM (IC 50 )

體外研究

Gatifloxacin sesquihydrate is against S. aureus MS5935 topoisomerase IV, E. coli NIHJ JC-2 DNA gyrase and HeLa cell topoisomerase II with IC 50 values of 13.8 μg/ml, 0.109 μg/ml, and 265 μg/ml, respectively.Gatifloxacin sesquihydrate is against S. aureus MS5935 topoisomerase IV, E. coli NIHJ JC-2 DNA gyrase and HeLa cell topoisomerase II with MIC values of 0.05 μg/ml, 0.0063 μg/ml, and 122 μg/ml, respectively.Gatifloxacin sesquihydrate exhibits antibacterial activities for wild-type strains (MS5935, MS5952, MR5867 and MR6009) the first-, second-, third-, and fourth-step mutants with MIC values of 0.05 to 0.10 μg/ml, 0.20 μg/ml, 1.56 to 3.13 μg/ml, 1.56 to 6.25 μg/ml, and 50 to 200 μg/ml, respectively. Gatifloxacin sesquihydrate displays the most potent activity against the second- and third-step mutants (MS5952, MR5867 and MR6009) except for the second-step mutant of strain MS5935.Gatifloxacin sesquihydrate has potent activity against norA transformant NY12 (MIC, 0.39 μg/ml).Gatifloxacin sesquihydrate (20-100 μM; 72 hours) significantly decreases insulin content to 60% at Day 1, and continues to be reduced to 50.1% and 44.7% at Day 3 by 20 μM and 100 μM Gatifloxacin sesquihydrate, respectively.

體內研究

Gatifloxacin sesquihydrate (subcutaneous injection; 100 mg/kg; 3 times a day; 30 days) significantly decreases the number of lesions in mouse footpad with Nocardia brasiliensis .

Animal Model: Female BALB/c mice with Nocardia brasiliensis in the right hind footpad
Dosage: 100 mg/kg
Administration: Subcutaneous injection; 3 times a day; 30 days
Result: Reduced the production of lesions in mice.
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