Flavitan

Base Information

• Chemical Name: Flavitan
• CAS No.: 146-14-5
• Molecular Formula: C27H33 N9 O15 P2
• Molecular Weight: 785.558
• Hs Code.: 29349990
• NSC Number: 112207
• DSSTox Substance ID: DTXSID70859284
• Wikidata: Q32039181
• ChEMBL ID: CHEMBL3580425
• Mol file: 146-14-5.mol

Synonyms:Dinucleotide, Flavin-Adenine;FAD;Flavin Adenine Dinucleotide;Flavin-Adenine Dinucleotide;Flavitan

Chemical Property of Flavitan

Chemical Property:

• Appearance/Colour: solid
• Boiling Point: °Cat760mmHg
• PKA: 1.13±0.50(Predicted)
• Flash Point: °C
• PSA: 382.55000
• Density: 2.08g/cm³
• LogP: -1.79440
• Storage Temp.: −20°C
• XLogP3: -5
• Hydrogen Bond Donor Count: 9
• Hydrogen Bond Acceptor Count: 20
• Rotatable Bond Count: 13
• Exact Mass: 785.15713538
• Heavy Atom Count: 53
• Complexity: 1560

Purity/Quality:

99% ^*data from raw suppliers

FlavineAdenineDinucleotide ^*data from reagent suppliers

Safty Information:

• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=NC6=C(N=CN=C65)N)O)O)O)O)O
• Uses: The prosthetic group of certain flavoproteins including D-amino acid oxidase, glucose oxidase, glycine oxidase, fumaric hydrogenase, histaminase, and xanthine oxidase. Riboflavin kinase tumor necrosis factor receptor 1 NADPH oxidase Labelled Flavine Adenine xidase. Riboflavin kinase tumor necrosis factor receptor 1 NADPH oxidase The prosthetic group of certain flavoproteins including D-amino acid oxidase, glucose oxidase, glycine oxidase, fumaric hydrogenase, histaminase, and xanthine oxidase. Riboflavin kinase tumor necrosis factor receptor 1 NADPH oxidase.

Technology Process of Flavitan

There total 9 articles about Flavitan 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:

5'-adenosine monophosphate (61-19-8,24937-83-5,67583-85-1) → flavin adenine dinucleotide (146-14-5,887565-61-9)

Guidance literature:

With pyridine; di-p-tolylcarbodiimide;

DOI:10.1021/ja01629a136

Reference yield:

flavin adenine dinucleotide fully reduced neutral (1910-41-4) → flavin adenine dinucleotide (146-14-5,887565-61-9)

Guidance literature:

With Artemisone; In acetonitrile;

DOI:10.1002/cmdc.201000508

Reference yield:

→ flavin adenine dinucleotide (146-14-5,887565-61-9)

Guidance literature:

With pyridine; 2-monochlorophenol; beim Behandeln unter Lichtausschluss;

DOI:10.1021/ja01547a073

upstream raw materials:

Flavin mononucleotide

ATP

5'-adenosine monophosphate

flavin adenine dinucleotide fully reduced neutral

Downstream raw materials:

flavin adenine dinucleotide fully reduced neutral

lumiflavin

5'-adenosine monophosphate

Flavin mononucleotide

Refernces

• 1、 DeLuca,Kaplan. "-". . p. 6,7. Retrieved 1958.
• 2、 Haynes, Richard K.,Cheu, Kwan-Wing,Tang, Maggie Mei-Ki,Chen, Min-Jiao,Guo, Zu-Feng,Guo, Zhi-Hong,Coghi, Paolo,Monti, Diego. "Reactions of Antimalarial Peroxides with Each of Leucomethylene Blue and Dihydroflavins: Flavin Reductase and the Cofactor Model Exemplified". experimental part. p. 279 - 291. Retrieved 2012/01/12.