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1695-77-8生产厂家

1695-77-8价格

1695-77-8

1695-77-8结构式
1695-77-8结构式
  • 常用中文名:大观霉素
  • 常用英文名:Spectinomycin
  • CAS号:1695-77-8
  • 分子式:C14H24N2O7
  • 分子量:332.35000
  • 相关类别: 原料药 抗生素类药物 氨基糖苷类药
  • 发布时间:2018-06-10 10:41:11
  • 更新时间:2024-01-04 06:12:09
  • 大观霉素是一种广谱抗生素,可抑制多种革兰氏阳性和革兰氏阴性微生物的生长。大观霉素通过选择性靶向细菌核糖体并中断蛋白质合成发挥作用。大观霉素也是td内含子RNA的非竞争性抑制剂[1][2][3][4][5]。

化源商城直购

中文名 大观霉素
英文名 spectinomycin
中文别名 壮观霉素盐酸盐
奇观霉素
英文别名 antibiotic2233wp
EINECS 216-911-3
togamycin
spectinomicina
Spectinomycin
Spectacin
espectinomicina
spectam
trobicin
actinospectacin
描述 大观霉素是一种广谱抗生素,可抑制多种革兰氏阳性和革兰氏阴性微生物的生长。大观霉素通过选择性靶向细菌核糖体并中断蛋白质合成发挥作用。大观霉素也是td内含子RNA的非竞争性抑制剂[1][2][3][4][5]。
相关类别
靶点

bacterial ribosomal subunit[5]

体外研究 大观霉素选择性抑制细胞和大肠杆菌提取物中的蛋白质合成。大观霉素(50μg/mL)可快速可逆地抑制大肠杆菌生长,并立即抑制氨基酸掺入[1]。大观霉素(1μg/mL或3μM)抑制内源性信使RNA或MS-2噬菌体RNA指导的多肽合成,在大肠杆菌提取物中最大抑制率为70-80%[1]。大观霉素通过抑制延伸因子G与核糖体的结合,阻断肽基tRNA从A位点向P位点的移位[2]。大观霉素与16S rRNA中的残基G1064和01192特异性相互作用,并可能使其失活[2]。大观霉素表现出剪接抑制作用,并依赖于pH变化和Mg2+浓度,这表明它和内含子RNA之间存在静电相互作用[3]。
体内研究 大观霉素(20 mg/kg;i.m.;20-100 mg/kg;9 d)在健康雏鸡中显示出安全性[4]。大观霉素(10 mg/kg;静脉注射;单剂量)主要通过肾脏排泄清除,约55%以不变形式排泄到尿液中[5]。大鼠体内大观霉素的药代动力学[5]参数C0(μg/mL)AUC0-∞ (μg•h/mL)Vd(L/kg)CL(L/h/kg)MRT,100 mg/kg给药:肌肉注射(胸肌);9天结果:通过全血计数、生化参数、组织病理学、临床症状、体重增加和饲料转化率(FCR),显示20 mg/kg的生物安全性。产生的轻微毒性为60 mg/kg。
参考文献

[1]. Davies J, et al. Inhibition of protein synthesis by spectinomycin. Science. 1965 Sep 3;149(3688):1096-8.

[2]. Brink MF, et al. Spectinomycin interacts specifically with the residues G1064 and C1192 in 16S rRNA, thereby potentially freezing this molecule into an inactive conformation. Nucleic Acids Res. 1994 Feb 11;22(3):325-31.

[3]. Park IK, et al. Spectinomycin inhibits the self-splicing of the group 1 intron RNA. Biochem Biophys Res Commun. 2000 Mar 16;269(2):574-9.

[4]. Khan EA, et al. Safety evaluation study of lincomycin and spectinomycin hydrochloride intramuscular injection in chickens. Toxicol Rep. 2022 Jan 29;9:204-209.

[5]. Madhura DB, et al. Pharmacokinetic profile of spectinomycin in rats. Pharmazie. 2013 Aug;68(8):675-6.

密度 1.43 g/cm3
沸点 583.1ºC at 760 mmHg
熔点 185ºC
分子式 C14H24N2O7
分子量 332.35000
精确质量 332.15800
PSA 129.51000
外观性状 一种白色至淡浅黄色结晶盐酸盐五水化物粉末
蒸汽压 5.05E-16mmHg at 25°C
储存条件 室温
计算化学

1.疏水参数计算参考值(XlogP):-3.1

2.氢键供体数量:5

3.氢键受体数量:9

4.可旋转化学键数量:2

5.互变异构体数量:2

6.拓扑分子极性表面积130

7.重原子数量:23

8.表面电荷:0

9.复杂度:478

10.同位素原子数量:0

11.确定原子立构中心数量:9

12.不确定原子立构中心数量:0

13.确定化学键立构中心数量:0

14.不确定化学键立构中心数量:0

15.共价键单元数量:1

更多

1. 性状:未确定。

2. 密度(g/mL,25/4℃): 未确定

3. 相对蒸汽密度(g/mL,空气=1):未确定

4. 熔点(ºC):未确定

5. 沸点(ºC,常压):未确定

6. 沸点(ºC,5.2kPa): 未确定

7. 折射率: 未确定

8. 闪点(ºC): 未确定

9. 比旋光度(º): 未确定

10. 自燃点或引燃温度(ºC): 未确定

11. 蒸气压(kPa,25ºC): 未确定

12. 饱和蒸气压(kPa,60ºC): 未确定

13. 燃烧热(KJ/mol):未确定

14. 临界温度(ºC): 未确定

15. 临界压力(KPa): 未确定

16. 油水(辛醇/水)分配系数的对数值: 未确定

17. 爆炸上限(%,V/V):未确定

18. 爆炸下限(%,V/V): 未确定

19. 溶解性:未确定

毒理学数据:

急性毒性:大鼠口经LD50:20gm/kg;小鼠口经LD50: >5gm/kg;小鼠静脉LD50:2gm/kg;小鼠腹经LD50: 5724 mg/kg

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UQ0332500
CHEMICAL NAME :
4H-Pyrano(2,3-b)(1,4)benzodioxin-4-one, decahydro-4a,7,9-trihydroxy-2-methyl-6,8- bis(methylamino)-
CAS REGISTRY NUMBER :
1695-77-8
LAST UPDATED :
199706
DATA ITEMS CITED :
10
MOLECULAR FORMULA :
C14-H24-N2-O7
MOLECULAR WEIGHT :
332.40
WISWESSER LINE NOTATION :
T C666 BO DO GV IOTJ E1 HQ KM1 LQ MM1 NQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
BCFAAI Bollettino Chimico Farmaceutico. (Societa Editoriale Farmaceutica, Via Ausonio 12, 20123 Milan, Italy) V.33- 1894- Volume(issue)/page/year: 111,265,1972
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
5724 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
BCFAAI Bollettino Chimico Farmaceutico. (Societa Editoriale Farmaceutica, Via Ausonio 12, 20123 Milan, Italy) V.33- 1894- Volume(issue)/page/year: 111,265,1972
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
20 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AACHAX Antimicrobial Agents and Chemotherapy (1961-70). (Ann Arbor, MI) 1961-70. For publisher information, see AMACCQ. Volume(issue)/page/year: -,507,1961
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85FZAT "Index of Antibiotics from Actinomycetes," Umezawa, H. et al., eds., Tokyo, Univ. of Tokyo Press, 1967 Volume(issue)/page/year: -,105,1967
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AACHAX Antimicrobial Agents and Chemotherapy (1961-70). (Ann Arbor, MI) 1961-70. For publisher information, see AMACCQ. Volume(issue)/page/year: -,507,1961
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>2 gm/kg
TOXIC EFFECTS :
Behavioral - muscle weakness Behavioral - ataxia Gastrointestinal - nausea or vomiting
REFERENCE :
AACHAX Antimicrobial Agents and Chemotherapy (1961-70). (Ann Arbor, MI) 1961-70. For publisher information, see AMACCQ. Volume(issue)/page/year: -,507,1961
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Primate - monkey
DOSE/DURATION :
>500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AACHAX Antimicrobial Agents and Chemotherapy (1961-70). (Ann Arbor, MI) 1961-70. For publisher information, see AMACCQ. Volume(issue)/page/year: -,507,1961
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Mammal - cat
DOSE/DURATION :
>800 mg/kg
TOXIC EFFECTS :
Behavioral - ataxia
REFERENCE :
AACHAX Antimicrobial Agents and Chemotherapy (1961-70). (Ann Arbor, MI) 1961-70. For publisher information, see AMACCQ. Volume(issue)/page/year: -,507,1961
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Unreported
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
>40 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Lungs, Thorax, or Respiration - other changes
REFERENCE :
AACHAX Antimicrobial Agents and Chemotherapy (1961-70). (Ann Arbor, MI) 1961-70. For publisher information, see AMACCQ. Volume(issue)/page/year: -,507,1961 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X7549 No. of Facilities: 14 (estimated) No. of Industries: 1 No. of Occupations: 1 No. of Employees: 432 (estimated) No. of Female Employees: 203 (estimated)

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