Compound ID | 3155

Update compound information

3-Amino-3-deoxy-α-D-glucopyranosyl-α-D-glucopyranoside

Synonym(s): α,α-3-trehalosamine  |  3-Trehalosamine

Class: Natural product antibiotic

Agent Type: Natural product; Small molecule;
Spectrum of activity: Gram-positive
Mechanism of action: Unknown
Target Pathogen: Active against Staphylococcus aureus, and Streptococcus pneumoniae
Description: Natural product from Nocardiopsis trehalosei; rescues Streptococcus pneumoniae infected mice
Institute where first reported: The Upjohn Company, Kalamazoo
Year first mentioned: 1980
Development status: Experimental
Chemical structure(s):
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Molecular weight: 341.31
Iso. SMILES: C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O)N)O)O
InChI Key: OHNBYBTUSOVUMK-PNKJYEMWSA-N
Can. SMILES: C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@@H]([C@H]([C@@H]([C@@H](CO)O2)O)O)O)O)N)O)O
InChI: InChI=1S/C12H23NO10/c13-5-6(16)3(1-14)21-11(8(5)18)23-12-10(20)9(19)7(17)4(2-15)22-12/h3-12,14-20H,1-2,13H2/t3-,4-,5+,6-,7-,8-,9+,10-,11-,12-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/194651
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/33/7/33_7_690/_article/-char/en

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