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22189-32-8 molecular structure
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(1R,3S,5R,8R,10R,11S,12S,13R,14S)-8,12,14-trihydroxy-5-methyl-11,13-bis(methylamino)-2,4,9-trioxatricyclo[8.4.0.03,8]tetradecan-7-one pentahydrate dihydrochloride

ChemBase ID: 132811
Molecular Formular: C14H36Cl2N2O12
Molecular Mass: 495.34784
Monoisotopic Mass: 494.16452996
SMILES and InChIs

SMILES:
C[C@@H]1CC(=O)[C@]2([C@@H](O1)O[C@@H]1[C@H]([C@@H]([C@@H]([C@@H]([C@H]1O2)NC)O)NC)O)O.O.O.O.O.O.Cl.Cl
Canonical SMILES:
CN[C@H]1[C@H](O)[C@H]2O[C@@H]3O[C@H](C)CC(=O)[C@@]3(O[C@@H]2[C@H]([C@H]1O)NC)O.O.O.O.O.O.Cl.Cl
InChI:
InChI=1S/C14H24N2O7.2ClH.5H2O/c1-5-4-6(17)14(20)13(21-5)22-12-10(19)7(15-2)9(18)8(16-3)11(12)23-14;;;;;;;/h5,7-13,15-16,18-20H,4H2,1-3H3;2*1H;5*1H2/t5-,7-,8+,9+,10+,11-,12-,13+,14+;;;;;;;/m1......./s1
InChIKey:
DCHJOVNPPSBWHK-UXXUFHFZSA-N

Cite this record

CBID:132811 http://www.chembase.cn/molecule-132811.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(1R,3S,5R,8R,10R,11S,12S,13R,14S)-8,12,14-trihydroxy-5-methyl-11,13-bis(methylamino)-2,4,9-trioxatricyclo[8.4.0.03,8]tetradecan-7-one pentahydrate dihydrochloride
IUPAC Traditional name
prospec pentahydrate dihydrochloride
Synonyms
Spectinomycin dihydrochloride pentahydrate
大观霉素 二盐酸盐 五水合物
壮观霉素 二盐酸盐 五水合物
CAS Number
22189-32-8
EC Number
244-554-3
MDL Number
MFCD00150886
Beilstein Number
5684150
PubChem SID
24899474
24899581
24899822
24899532
162227088
24888387
PubChem CID
30971

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 8.576982  H Acceptors
H Donor LogD (pH = 5.5) -5.963829 
LogD (pH = 7.4) -3.421742  Log P -2.3693373 
Molar Refractivity 75.4362 cm3 Polarizability 31.587643 Å3
Polar Surface Area 129.51 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
H2O: soluble50 mg/mL, clear, faintly yellow expand Show data source
Apperance
powder expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
2 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
2-8°C expand Show data source
Purity
≥98.0% (AT) expand Show data source
Grade
Biotechnology Performance Certified expand Show data source
VETRANAL™, analytical standard expand Show data source
Salt Data
2 HCl, 5 H2O expand Show data source
Potency
≥603 μg per mg expand Show data source
Suitability
cell culture tested expand Show data source
suitable for cell culture expand Show data source
Impurities
endotoxin, tested expand Show data source
Sterility
γ-irradiated expand Show data source
Empirical Formula (Hill Notation)
C14H24N2O7 · 2HCl · 5H2O expand Show data source
Classification
Rare Genuine Natural Compounds expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 85555 external link
Other Notes
Aminoglycoside antibiotic. Interaction of antibiotics with functional sites in 16S ribosomal RNA5
Application
Spectinomycin is used in antibiotic resistance and sensitivity studies in various species such as Escherichia coli, Borrelia burgdorferi, and Neisseria gonorrhoeae 1,2,3.
Biochem/physiol Actions
Spectinomycin binds to the 30S subunit of the bacterial ribosome thereby inhibiting protein synthesis 4.
Sigma Aldrich - S1317 external link
Biochem/physiol Actions
Mode of Action: Inhibits protein synthesis (elongation) by interfering with peptidyl tRNA translocation. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria (Gonnococcus only).Mode of Resistance: Mutation in rpsE (the gene for ribosomal protein S5) prevents binding of spectinomycin.
Spectinomycin is a broad spectrum antibiotic that inhibits protein synthesis (elongation) by binding to the bacterial 30S ribosomal subunit and interfering with peptidyl tRNA translocation. Resistance to spectinomycin is conferred by aminoglycoside-3′-adenyltransferase gene (aadA). It is effective against Gram-negative and Gram-positive bacteria. Mutation in rpsE (the gene for ribosomal protein S5) prevents binding of spectinomycin.
Application
Spectinomycin is an aminocyclitol antibiotic produced by Streptomyces spectabilis. It is used to treat acute gonorrheal urethritis and proctitis in the male and acute gonorrheal cervicitis and proctitis in the female1. It is used to mark cell layers in order to monitor cell fate during leaf development2. Spectinomycin is used as a selection marker in plant related transformation systems for plant cells that contain the marker gene Spcr. Spectinomycin is also used for amplification of low copy number plasmid carrying replicons such as Col E1, pMB1 (pBR322 and its derivatives), and p15A/rep (pACYC and its derivatives). The replication of these plasmids relies on long-lived enzymes supplied by the host. Addition of spectinomycin to the plasmid containing cells inhibits replication of the host, while the plasmids continue to replicate for 10-15 hours. The copy number of the plasmid can increase 100-fold, from 20-30 copies to 3000 copies as in the case of ColE1. Spectinomycin is used to study respiratory tract infections of cattle caused by Pasteurella multocida and Mannheimia haemolytica3. Spectinomycin dihydrochloride pentahydrate has been used to generate plants deficient for the plastid-encoded RNA polymerase (PEP) on MS-agar medium4.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich - S4014 external link
Application
Recommended for use in cell culture applications at 7.5-20 mg/L and as a selection agent for transformed plant cells that contain the selectable marker gene Spcr.
Biochem/physiol Actions
作用方式:通过干扰肽基 tRNA 的转位抑制蛋白质合成(延伸)。 抗菌谱:革兰氏阴性和革兰氏阳性菌(仅包括淋球菌)。 抗性机理:rpsE(核糖体蛋白 S5 的基因)的突变可阻止壮观霉素的结合。
Reconstitution
Prepare stock solutions should be prepared (water 10 mg/ml) and filter sterilized. Stock solutions can be stored at 2-8 °C for several weeks or at -20 °C for extended periods.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich - S2647 external link
Biochem/physiol Actions
作用方式:通过干扰肽基 tRNA 的转位抑制蛋白质合成(延伸)。 抗菌谱:革兰氏阴性和革兰氏阳性菌(仅包括淋球菌)。 抗性机理:rpsE(核糖体蛋白 S5 的基因)的突变可阻止壮观霉素的结合。
Reconstitution
直接在小瓶中用无菌水配制储存液 (10mg/mL)。储存液在 2-8°C 下可保存数周,在 -20°C 下可长期保存。
Application
Spectinomycin dihydrochloride pentahydrate is an antibiotic used as a selection agent in molecular biological and microbiological applications.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich - S9007 external link
Application
Used as a selection agent for transformed plant cells that contain the selectable marker gene Spcr and to inhibit bacterial protein synthesis at the level of peptidy tRNA translocation.
Biochem/physiol Actions
作用方式:通过干扰肽基 tRNA 的转位抑制蛋白质合成(延伸)。 抗菌谱:革兰氏阴性和革兰氏阳性菌(仅包括淋球菌)。 抗性机理:rpsE(核糖体蛋白 S5 的基因)的突变可阻止壮观霉素的结合。
Spectinomycin is a broad spectrum antibiotic that inhibits protein synthesis (elongation) by binding to the bacterial 30S ribosomal subunit and interfering with peptidyl tRNA translocation. Resistance to spectinomycin is conferred by aminoglycoside-3′-adenyltransferase gene (aadA). It is effective against Gram-negative and Gram-positive bacteria. Mutation in rpsE (the gene for ribosomal protein S5) prevents binding of spectinomycin.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Sigma Aldrich - 46738 external link
Legal Information
VETRANAL is a trademark of Sigma-Aldrich Co. LLC

REFERENCES

REFERENCES

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