Luteolin 3'-glucoside

Base Information

• Chemical Name: Luteolin 3'-glucoside
• CAS No.: 5154-41-6
• Molecular Formula: C11H15ClN2O
• Molecular Weight: 448.383
• UNII: NE54EDY436
• ChEMBL ID: CHEMBL1221790
• Metabolomics Workbench ID: 23734
• Nikkaji Number: J503.100A
• Mol file: 5154-41-6.mol

Synonyms:Dracocephaloside;Luteolin 3'-glucoside;Luteolin 3'-O-glucoside;NE54EDY436;UNII-NE54EDY436;Luteolin-3'-o-beta-glucoside;Luteolin 3'-o-beta-D-glucoside;Luteolin 3'-beta-D-glucopyranoside;Luteolin 3'-o-beta-D-glucopyranoside;Luteolin-3'-o-glucuronide (constituent of rosemary) [DSC];4H-1-Benzopyran-4-one, 2-(3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl)-5,7-dihydroxy-;CHEMBL1221790;BDBM226187;Luteolin 3'-O-beta-D-glucoside (17);LUTEOLIN-3'-O-.BETA.-GLUCOSIDE;LUTEOLIN 3'-O-.BETA.-D-GLUCOSIDE;LUTEOLIN 3'-.BETA.-D-GLUCOPYRANOSIDE;LUTEOLIN 3'-O-.BETA.-D-GLUCOPYRANOSIDE;Luteolin-3'-o-glucuronide (constituent of rosemary);Q27284825;4H-1-BENZOPYRAN-4-ONE, 2-(3-(.BETA.-D-GLUCOPYRANOSYLOXY)-4-HYDROXYPHENYL)-5,7-DIHYDROXY-

Chemical Property of Luteolin 3'-glucoside

Chemical Property:

• Vapor Pressure: 0.000709mmHg at 25°C
• Boiling Point: 307.8°Cat760mmHg
• Flash Point: 139.9°C
• Density: 1.173g/cm³
• XLogP3: 0.5
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 4
• Exact Mass: 448.10056145
• Heavy Atom Count: 32
• Complexity: 714

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O
• Isomeric SMILES: C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O

Technology Process of Luteolin 3'-glucoside

There total 2 articles about Luteolin 3'-glucoside 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: 18.0%

2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-on (491-70-3) → 3'-O-(β-D-glucopyranosyl)luteoline (5154-41-6)

Guidance literature:

In dimethyl sulfoxide; for 168h; regioselective reaction; Microbiological reaction;

DOI:10.1016/j.bioorg.2019.01.046

Reference yield:

2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-on (491-70-3) + Sucrose (57-50-1) → Luteolin-4'-O-glucoside + luteolin-3'-O-α-D-glucopyranoside (5154-41-6)

Guidance literature:

With diethylene glycol dimethyl ether; dextransucrase B-512F; In acetate buffer; at 30 ℃; for 7h; pH=5.2;

DOI:10.1016/j.carres.2006.02.008

upstream raw materials:

2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-on

Sucrose