1-[(1R,2R,3S,4R,5R,6S)-3-carbamimidamido-4-{[(2R,3R,4R,5S)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy}-2,5,6-trihydroxycyclohexyl]guanidine

• ChemBase ID: 953
• Molecular Formular: C21H39N7O12
• Molecular Mass: 581.57406
• Monoisotopic Mass: 581.26566972
• SMILES: [C@@H]1([C@@H]([C@H]([C@@H](O[C@H]1O[C@H]1[C@@H](O[C@@H](C)[C@@]1(C=O)O)O[C@@H]1[C@H]([C@H](O)[C@H]([C@H](O)[C@H]1O)NC(=N)N)NC(=N)N)CO)O)O)NC
• Canonical SMILES: OC[C@@H]1O[C@@H](O[C@H]2[C@H](O[C@H]3[C@H](O)[C@@H](O)[C@@H]([C@H]([C@@H]3NC(=N)N)O)NC(=N)N)O[C@H]([C@]2(O)C=O)C)[C@H]([C@@H]([C@H]1O)O)NC
• InChI: InChI=1S/C21H39N7O12/c1-5-21(36,4-30)16(40-17-9(26-2)13(34)10(31)6(3-29)38-17)18(37-5)39-15-8(28-20(24)25)11(32)7(27-19(22)23)12(33)14(15)35/h4-18,26,29,31-36H,3H2,1-2H3,(H4,22,23,27)(H4,24,25,28)/t5-,6-,7+,8-,9-,10-,11+,12-,13-,14+,15+,16-,17-,18-,21+/m0/s1
• InChIKey: UCSJYZPVAKXKNQ-HZYVHMACSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: 1-[(1R,2R,3S,4R,5R,6S)-3-carbamimidamido-4-{[(2R,3R,4R,5S)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy}-2,5,6-trihydroxycyclohexyl]guanidine
• IUPAC Traditional name: streptomycin; 1-[(1R,2R,3S,4R,5R,6S)-3-carbamimidamido-4-{[(2R,3R,4R,5S)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy}-2,5,6-trihydroxycyclohexyl]guanidine
• Brand Name: Kantrex
• Synonyms: Streptomycin Sesquisulfate Hydrate; Streptomycin a Sulfate; Streptomycin Sulfate; Streptomycin Sulphate; Streptomycin, Sulfate Salt; Streptomycin; Estreptomicina; Streptomisin; Agrept; Agrimycin; Merstep; Streptomycin

Database IDs

• CAS Number: 57-92-1
• PubChem SID: 46506845; 160964416
• PubChem CID: 19649

CALCULATED PROPERTIES

JChem

• Acid pKa: 10.877018
• H Acceptors: 19
• H Donor: 14
• LogD (pH = 5.5): -13.912841
• LogD (pH = 7.4): -12.161263
• Log P: -7.651423
• Molar Refractivity: 149.4707 cm^3
• Polarizability: 52.500404 Å^3
• Polar Surface Area: 331.43 Å^2
• Rotatable Bonds: 9
• Lipinski's Rule of Five: false

ALOGPS 2.1

• Log P: -2.61
• LOG S: -1.66
• Solubility (Water): 1.28e+01 g/l

PROPERTIES

Physical Property

• Hydrophobicity(logP): -6.4

Pharmacology Properties

• Mechanism of Action: Activity increased in alkaline medium binds irreversibly to the bacterial ribosomal 30S subunit; Apoptosis-inducer; Blocks the recognition step in protein-synthesis; Causes misreading of the genetic code; Causes ribosomal dissociation from messenger RNA; Protein synthesis inhibitor

Product Information

• Biological Source: Isol. from Streptomyces griseus
• Application(s): Aminoglycoside antibiotic; Clinically used broad spectrum antibacterial (tuberculostatic) agent

DETAILS

DrugBank - DB01082

• Drug Groups: approved
• Description: Streptomycin is an aminoglycoside antibiotic produced by the soil actinomycete Streptomyces griseus. It acts by binding to the 30S ribosomal subunit of susceptible organisms and disrupting the initiation and elongation steps in protein synthesis. It is bactericidal due to effects that are not fully understood.
• Indication: For the treatment of tuberculosis. May also be used in combination with other drugs to treat tularemia (Francisella tularensis), plague (Yersia pestis), severe M. avium complex, brucellosis, and enterococcal endocarditis (e.g. E. faecalis, E. faecium).
• Pharmacology: Streptomycin is an aminoglycoside antibiotic. Aminoglycosides work by binding to the bacterial 30S ribosomal subunit, causing misreading of t-RNA, leaving the bacterium unable to synthesize proteins vital to its growth. Aminoglycosides are useful primarily in infections involving aerobic, Gram-negative bacteria, such as Pseudomonas, Acinetobacter, and Enterobacter. In addition, some mycobacteria, including the bacteria that cause tuberculosis, are susceptible to aminoglycosides. Infections caused by Gram-positive bacteria can also be treated with aminoglycosides, but other types of antibiotics are more potent and less damaging to the host. In the past the aminoglycosides have been used in conjunction with penicillin-related antibiotics in streptococcal infections for their synergistic effects, particularly in endocarditis. Aminoglycosides are mostly ineffective against anaerobic bacteria, fungi and viruses.
• Toxicity: Nephrotoxic and ototoxic potential. Nephrotoxicity is caused by accumulation of the drug in proximal renal tubular cells, which results in cellular damage. Tubular cells may regenerate despite continued exposure and nephrotoxicity is usually mild and reversible. Streptomycin is the least nephrotoxic of the aminoglycosides owing to the small number of cationic amino groups in its structure. Otoxocity occurs via drug accumulation in the endolymph and perilymph of the inner ear. Accumulation causes irreversible damage to hair cells of the cochlea or summit of the ampullar cristae of the vestibular complex. High frequency hearing loss precedes low frequency hearing loss. Further toxicity may result in retrograde degeneration of the auditory nerve. Vestibular toxicity may result in vertigo, nausea and vomiting, dizziness and loss of balance. ; LD50=430 mg/kg (Orally in rats with Streptomycin Sulfate); Side effects include nausea, vomiting, and vertigo, paresthesia of face, rash, fever, urticaria, angioneurotic edema, and eosinophilia.
• Affected Organisms: Enteric bacteria and other eubacteria
• Absorption: Rapidly absorbed after intramuscular injection with peak serum concentrations attained after 1 - 2 hours. Not absorbed in the GI tract.
• Half Life: 5 - 6 hours in adults with normal renal function
• Elimination: Small amounts are excreted in milk, saliva, and sweat. Streptomycin is excreted by glomerular filtration.
• External Links: Wikipedia; RxList; Drugs.com

REFERENCES

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