Nhận Dạng Quốc Tế & Đặc Tính Hóa Học
Công thức hóa học
C17H34N4O10
Monoisotopic mass
454.227493328
InChI
InChI=1S/C17H34N4O10/c18-2-6-10(24)12(26)8(21)16(28-6)30-14-5(20)1-4(19)9(23)15(14)31-17-13(27)11(25)7(3-22)29-17/h4-17,22-27H,1-3,18-21H2/t4-,5+,6-,7-,8-,9+,10-,11-,12-,13+,14-,15-,16+,17-/m0/s1
InChI Key
InChIKey=NSKGQURZWSPSBC-NLZFXWNVSA-N
IUPAC Name
(2S,3R,4S,5S,6R)-5-amino-2-(aminomethyl)-6-{[(1S,2S,3R,4S,6R)-4,6-diamino-2-{[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3-hydroxycyclohexyl]oxy}oxane-3,4-diol
Traditional IUPAC Name
ribostamycin
SMILES
NC[C@@H]1O[C@H](O[C@H]2[C@H](N)C[C@H](N)[C@@H](O)[C@@H]2O[C@@H]2O[C@@H](CO)[C@H](O)[C@H]2O)[C@@H](N)[C@H](O)[C@H]1O
pKa (strongest acidic)
12.19
pKa (Strongest Basic)
9.93
Refractivity
100.17 m3·mol-1
Cơ Chế Tác Dụng :
A broad-spectrum antimicrobial isolated from Streptomyces ribosifidicus. [PubChem]
Aminoglycosides work by binding to the bacterial 30S ribosomal subunit (some work by binding to the 50S subunit), inhibiting the translocation of the peptidyl-tRNA from the A-site to the P-site and also causing misreading of mRNA, leaving the bacterium unable to synthesize proteins vital to its growth. However, their exact mechanism of action is not fully known.