Nephritogenoside

Base Information

• Chemical Name: Nephritogenoside
• CAS No.: 81276-22-4
• Molecular Formula: C₁₈H₃₂O₁₆
• Molecular Weight: 504.442
• Metabolomics Workbench ID: 49653

Synonyms:nephritogenic glycopeptide;nephritogenic glycoprotein;nephritogenic glycoprotein, human;nephritogenic glycoprotein, mouse;nephritogenic glycoprotein, rat;nephritogenoside;nephritogenoside protein, human;nephritogenoside protein, mouse;nephritogenoside protein, rat

Chemical Property of Nephritogenoside

Chemical Property:

• XLogP3: -7.2
• Hydrogen Bond Donor Count: 11
• Hydrogen Bond Acceptor Count: 16
• Rotatable Bond Count: 11
• Exact Mass: 504.16903493
• Heavy Atom Count: 34
• Complexity: 625

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC(C(C(C(C=O)O)O)O)O)O)O)O)O)O)O)O
• Isomeric SMILES: C([C@@H]1[C@H]([C@@H]([C@H](C(O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC[C@H]([C@H]([C@@H]([C@H](C=O)O)O)O)O)O)O)O)O)O)O)O

Technology Process of Nephritogenoside

There total 7 articles about Nephritogenoside 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:

D-maltose (69-79-4) → isomaltotriose (3371-50-4,6614-36-4,13382-86-0,28245-12-7,32590-17-3,41897-94-3,61433-02-1,74385-45-8,76764-44-8,81276-22-4,111322-08-8,116781-14-7,132617-44-8,132617-45-9) + panose (7485-51-0,32581-31-0,33401-87-5,37070-18-1,58214-47-4,61237-56-7,62733-90-8,63425-90-1,63425-95-6,100676-05-9,112159-73-6,121951-70-0,142924-26-3,25193-53-7) + D-glucose (50-99-7) + isomaltose (499-40-1)

Guidance literature:

With Escherichia coli BL21 recombinant α-glucosidase; In aq. buffer; at 60 - 100 ℃;

DOI:10.3390/molecules24071413

Reference yield:

D-maltose (69-79-4) → isomaltotriose (3371-50-4,6614-36-4,13382-86-0,28245-12-7,32590-17-3,41897-94-3,61433-02-1,74385-45-8,76764-44-8,81276-22-4,111322-08-8,116781-14-7,132617-44-8,132617-45-9) + panose (7485-51-0,32581-31-0,33401-87-5,37070-18-1,58214-47-4,61237-56-7,62733-90-8,63425-90-1,63425-95-6,100676-05-9,112159-73-6,121951-70-0,142924-26-3,25193-53-7) + D-glucose (50-99-7) + isomaltotetraose (35997-20-7,37796-39-7,57674-21-2,61433-03-2,76764-49-3,82085-15-2,116681-43-7,1111-08-6) + isomaltose (499-40-1)

Guidance literature:

With sodium acetate; In water; at 30 ℃; for 20h; pH=5.5;

DOI:10.1007/s10600-009-9185-5

Reference yield:

D-maltose (69-79-4) → isomaltotriose (3371-50-4,6614-36-4,13382-86-0,28245-12-7,32590-17-3,41897-94-3,61433-02-1,74385-45-8,76764-44-8,81276-22-4,111322-08-8,116781-14-7,132617-44-8,132617-45-9) + panose (7485-51-0,32581-31-0,33401-87-5,37070-18-1,58214-47-4,61237-56-7,62733-90-8,63425-90-1,63425-95-6,100676-05-9,112159-73-6,121951-70-0,142924-26-3,25193-53-7) + isomaltose (499-40-1)

Guidance literature:

With culture supernatant of recombinant Pichia pastoris KM₇₁/pPIC₉K-aglu; at 60 ℃; pH=5.5; aq. acetate buffer; Enzymatic reaction;

DOI:10.1021/jf1000502

upstream raw materials:

D-maltose

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