Compound ID | 1014

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Mannosidostreptomycin (Streptomycin analogue)

Synonym(s): Streptomycin B  |  Mannosidestreptomycin

Class: Aminoglycoside

Details of activity: Cited as resistant to bacterial "R factors"
Description: Smith, D H et al. 1969. "Mannosidostreptomycin: a biologically active streptomycin analogue resistant to R factor adenylation".
Year first mentioned: 1969
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 743.72
Iso. SMILES: C[C@H]1[C@@]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H]([C@@H]([C@H]2O)O)N=C(N)N)O)N=C(N)N)O[C@H]3[C@H]([C@@H]([C@H]([C@@H](O3)CO)O[C@@H]4[C@H]([C@H]([C@@H]([C@@H](O4)CO)O)O)O)O)NC)(C=O)O
InChI Key: HQXKELRFXWJXNP-ABOIPUQESA-N
Can. SMILES: C[C@H]1[C@](C=O)([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H]([C@@H]([C@H]2O)O)N=C(N)N)O)N=C(N)N)O[C@H]3[C@H]([C@@H]([C@H]([C@H](CO)O3)O[C@@H]4[C@H]([C@H]([C@@H]([C@H](CO)O4)O)O)O)O)NC)O
InChI: InChI=1S/C27H49N7O17/c1-6-27(45,5-37)21(24(46-6)50-20-10(34-26(30)31)13(39)9(33-25(28)29)14(40)17(20)43)51-22-11(32-2)15(41)19(8(4-36)48-22)49-23-18(44)16(42)12(38)7(3-35)47-23/h5-24,32,35-36,38-45H,3-4H2,1-2H3,(H4,28,29,33)(H4,30,31,34)/t6-,7-,8-,9+,10-,11-,12+,13+,14-,15-,16-,17+,18-,19-,20+,21-,22-,23+,24-,27+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/76971547
Citation:

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