Dihydroflavine-adenine dinucleotide

Base Information

Chemical Name:Dihydroflavine-adenine dinucleotide
CAS No.:1910-41-4
Molecular Formula:C27H35 N9 O15 P2
Molecular Weight:787.574
Hs Code.:
DSSTox Substance ID:DTXSID301343006
Nikkaji Number:J792.632D
Wikidata:Q27102690,Q27113979
Metabolomics Workbench ID:37656

Synonyms:1,5-dihydro-FAD;FADH2

Suppliers and Price of Dihydroflavine-adenine dinucleotide

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
Packaging
price

Total 3 raw suppliers

Chemical Property of Dihydroflavine-adenine dinucleotide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：388.35000
Density:2.09g/cm³
LogP:-1.36600
XLogP3:-4.8
Hydrogen Bond Donor Count:11
Hydrogen Bond Acceptor Count:21
Rotatable Bond Count:13
Exact Mass:787.17278544
Heavy Atom Count:53
Complexity:1520

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C=C1C)N(C3=C(N2)C(=O)NC(=O)N3)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
Isomeric SMILES:CC1=CC2=C(C=C1C)N(C3=C(N2)C(=O)NC(=O)N3)C[C@@H]([C@@H]([C@@H](COP(=O)(O)OP(=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=NC6=C(N=CN=C65)N)O)O)O)O)O
General Description **Conclusion:** [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [[(2R,3S,4S)-5-(7,8-dimethyl-2,4-dioxo-1,5-dihydrobenzo[g]pteridin-10-yl)-2,3,4-trihydroxypentoxy]-hydroxyphosphoryl] hydrogen phosphate, also known as reduced flavin adenine dinucleotide (FADH₂), is a biologically active, reduced form of FAD that serves as a redox cofactor. It can be catalytically generated from FAD using hydrogen (H₂) as a reductant, as demonstrated by platinum cluster catalysts and Escherichia coli hydrogenase 1 (Hyd1), which facilitate the non-native reduction of flavins for applications such as alkene hydrogenation. This reduced cofactor plays a critical role in electron transfer processes in enzymatic reactions.

Technology Process of Dihydroflavine-adenine dinucleotide

There total 2 articles about Dihydroflavine-adenine dinucleotide 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:

: 146-14-5,887565-61-9
flavin adenine dinucleotide

: 1910-41-4
flavin adenine dinucleotide fully reduced neutral

Guidance literature:: With phosphate buffer; hydrogen; Na2 anchored onto OAE-SEPHADEX anion exchanger; at 20 ℃; for 1.66667h;
DOI:10.1039/cc9960000207

Reference yield:

: 91200-63-4,103775-60-6,84366-81-4,146-14-5
flavin-adenin dinucleotide, disodium salt

: 1910-41-4
flavin adenine dinucleotide fully reduced neutral

Guidance literature:: With hydrogen; hydrogenase 1 from Escherichia coli; In aq. buffer; at 25 ℃; under 750.075 Torr; pH=8; Kinetics; Glovebox; Enzymatic reaction;
DOI:10.1002/anie.202101186