Antibiotic Z-1159-2

Base Information

Chemical Name:Antibiotic Z-1159-2
CAS No.:55484-62-3
Molecular Formula:C17H33N3O11
Molecular Weight:455.4574
Hs Code.:
DSSTox Substance ID:DTXSID00970830
Nikkaji Number:J87.133H
Wikidata:Q82954094
Mol file:55484-62-3.mol

Synonyms:Antibiotic Z-1159-2;55484-62-3;Z-1159-2;D-Streptamine, O-2-amino-2-deoxy-alpha-D-glucopyranosyl-(1-4)-O-(beta-D-xylofuranosyl-(1-5))-2-deoxy-;DTXSID00970830;C17H33N3O11;AKOS040745571;(2R,3S,4R,5R,6S)-5-amino-6-[(1R,2R,3S,4R,6S)-4,6-diamino-2-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxycyclohexyl]oxy-2-(hydroxymethyl)oxane-3,4-diol;LS-146947;4,6-Diamino-3-hydroxy-2-(pentofuranosyloxy)cyclohexyl 2-amino-2-deoxyhexopyranoside

Suppliers and Price of Antibiotic Z-1159-2

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of Antibiotic Z-1159-2

Chemical Property:

Vapor Pressure:1.82E-28mmHg at 25°C
Boiling Point:784.9°Cat760mmHg
Flash Point:428.5°C
PSA：0.00000
Density:1.64g/cm³
LogP:0.00000
XLogP3:-6.1
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:6
Exact Mass:455.21150888
Heavy Atom Count:31
Complexity:592

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(C(C(C(C1N)OC2C(C(C(C(O2)CO)O)O)N)OC3C(C(C(O3)CO)O)O)O)N
Isomeric SMILES:C1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)N)O[C@H]3[C@@H]([C@H]([C@H](O3)CO)O)O)O)N

Technology Process of Antibiotic Z-1159-2

There total 8 articles about Antibiotic Z-1159-2 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%

: 918800-32-5
C₄₆H₄₇N₉O₁₈

: 55781-25-4,55484-62-3
6'-hydroxyl-ribostamycin

Guidance literature:: C₄₆H₄₇N₉O₁₈; With ethanol; methylamine; for 8h;

With sodium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 0.166667h;

With trimethylphosphane; In tetrahydrofuran; water; for 5h;

Reference yield: 62.0%

: 289505-18-6
(2R,3S,4R,5R,6S)-5-Azido-6-[(1R,2R,3S,4R,6S)-4,6-diazido-2-((2S,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yloxy)-3-hydroxy-cyclohexyloxy]-2-hydroxymethyl-tetrahydro-pyran-3,4-diol

: 55781-25-4,55484-62-3
6'-hydroxyl-ribostamycin

Guidance literature:: With sodium hydroxide; trimethylphosphane; In tetrahydrofuran; water; at 20 ℃; for 10h;
DOI:10.1016/S0040-4039(00)00586-4

Reference yield:

: 534-47-4,11030-86-7
Paromamine

: 55781-25-4,55484-62-3
6'-hydroxyl-ribostamycin

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / trifluoromethanesulfonyl azide; Et₃N; CuSO₄ / CH₂Cl₂; methanol; H₂O

2: 65 percent / pyridine / -6 °C

3: 85 percent / BF₃*Et₂O / CH₂Cl₂

4: MeNH₂ / ethanol

5: PMe₃; aq. NaOH / tetrahydrofuran / 20 °C

With pyridine; sodium hydroxide; triflic azide; boron trifluoride diethyl etherate; copper(II) sulfate; triethylamine; methylamine; trimethylphosphane; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;
DOI:10.1016/j.bmcl.2006.09.013