7179-49-9
中文名称
盐酸林可霉素(一水物)
英文名称
Lincomycin hydrochloride monohydrate
CAS
7179-49-9
EINECS 编号
212-726-7
分子式
C18H37ClN2O7S
MDL 编号
MFCD00167245
分子量
461.01
MOL 文件
7179-49-9.mol
更新日期
2024/04/24 11:42:39
7179-49-9 结构式
基本信息
中文别名
盐酸林可霉素6-(1-甲-反-丙基-L-2-吡咯烷甲酰氨基)-1-硫代-6,8-二脱氧-D-赤式-A-D-半乳辛吡喃糖苷盐酸
洁霉素盐酸盐
林可霉素
盐酸洁霉素
林可霉素盐酸盐
6,8-二脱氧-6-(1-甲基-4-丙基-L-2-吡咯烷甲酰氨基)-1-硫代-D-赤式-alpha-D-半乳辛吡喃糖苷盐酸盐(一水物)
盐酸林可霉素(一水物)
英文别名
LINCOCIN HYDROCHLORIDE MONOHYDRATElincomycin hydrochloride bp98
LINCOMYCIN HYDROCHLORIDE MONOHYDRATE
lincorex
methyl (2s-trans)-6,8-dideoxy-6-[[(1-methyl-4-propylpyrrolidin-2-yl)carbonyl]amino]-1-thio-d-erythro-alpha-d-galacto-octopyranoside monohydrochloride
d-erythro-d-galacto-octopyranoside,methyl6,8-dideoxy-6-(1-methyl-4-propyl-2-pyrrolidinecarboxamido)-1-thio-,monohydrochloride,hemihydrate
frademicina
lincocinhydrochloridehydrate
lincomycin,hydrochloride,hemihydrate
lincomycin,hydrochloridehydrate
methyl6,8-dideoxy-6-(1-methyl-4-propyl-2-d-erythro-d-galacto-octopyranosid
mycivin
pyrrolidinecarboxamido)-1-thio-,monohydrochloride,hemihydrate
waynecomycin
LINCOMYCIN HYDROCHLORIDE, HYDRATE, VETRA
LINCOMYCINHYDROCHLORIDE,MONOHYDRATE,USP
Lincocin
Lincomycin hydrochloride BP98
Lincomycin hydrochloride monohydrate
Lincorex
物理化学性质
外观性状白色结晶性粉未，微臭，味苦。该药抗菌谱广，无过敏性，穿透力强，是髓炎等骨科病的首选抗菌药物。
熔点156-158°
比旋光度D25 +143° (water)
储存条件2-8°C
溶解度Very soluble in water, slightly soluble in ethanol (96 per cent), very slightly soluble in acetone.
形态neat
Merck5500
InChIKeyLFZGYTBWUHCAKF-DCNJEFSFSA-N
盐酸林可霉素(一水物)价格(试剂级)
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2024/01/16 | L0166 | 盐酸林可霉素一水合物 Lincomycin Hydrochloride Monohydrate | 7179-49-9 | 5G | 1035元 |
| 2024/01/16 | L0166 | 盐酸林可霉素一水合物 Lincomycin Hydrochloride Monohydrate | 7179-49-9 | 25G | 1990元 |
| 2024/01/16 | S5295 | 盐酸林可霉素(一水物) Lincomycin Hydrochloride Monohydrate | 7179-49-9 | 25mg | 794.47元 |
常见问题列表
生物活性
Lincomycin hydrochloride monohydrate 是窄谱抗生素, 具有与红霉素相似的效力, 对革兰氏阳性球菌具有很好的作用效果, 主要抑制细菌细胞蛋白质的合成。体内研究
Lincomycin (25 and 50 mg/kg, intravenously) depresses neuromuscular transmission to a degree which depended on stimulation frequencies in the rabbit sciatic nerve-gastrocnemius muscle preparation.
| Animal Model: | Adult albino New Zealand rabbits weighing 2.5-3.5 kg. |
| Dosage: | 25 and 50 mg/kg. |
| Administration: | Intravenously. |
| Result: | Depressed neuromuscular transmission. |