Juvidex

Base Information

Chemical Name:Juvidex
CAS No.:723729-16-6
Deprecated CAS:3311-11-3,7683-50-3,136309-77-8,642477-31-4
Molecular Formula:C₆H₁₃O₉P
Molecular Weight:260.138
Hs Code.:
UNII:U2S53JF879
DSSTox Substance ID:DTXSID80957947
Nikkaji Number:J425.349C
Wikidata:Q105285555
Metabolomics Workbench ID:56885

Synonyms:Juvidex;6-O-phosphono-D-mannose;aldehydo-D-mannose 6-phosphate;U2S53JF879;aldehydo-D-mannose 6-(dihydrogen phosphate);(2R,3R,4S,5S)-2,3,4,5-Tetrahydroxy-6-oxohexyl dihydrogen phosphate;[(2R,3R,4S,5S)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxyphosphonic acid;UNII-U2S53JF879;SCHEMBL54511;D-MANNOSE, 6-PHOSPHATE;CHEBI:48042;DTXSID80957947;DB11848;A074F4FA-F19B-4AFA-AF19-0E6F967A7E91;((2R,3S,4S,5S)-3,4,5,6-TETRAHYDROXYTETRAHYDRO-2H-PYRAN-2-YL)METHYL DIHYDROGEN PHOSPHATE

Suppliers and Price of Juvidex

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 0 raw suppliers

Chemical Property of Juvidex

Chemical Property:

XLogP3:-4.5
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:7
Exact Mass:260.02971899
Heavy Atom Count:16
Complexity:263

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(C(C(C(C(C=O)O)O)O)O)OP(=O)(O)O
Isomeric SMILES:C([C@H]([C@H]([C@@H]([C@@H](C=O)O)O)O)O)OP(=O)(O)O
Recent ClinicalTrials:Investigation Into the Safety and Scar-improvement Efficacy of Intradermal Juvidex Dosed Once or Three Times
Recent EU Clinical Trials:A double blind, placebo controlled trial to investigate the efficacy and safety of two concentrations of Juvidex in accelerating the healing of split thickness skin graft donor sites using different dosing regimes

Technology Process of Juvidex

There total 1 articles about Juvidex 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:

: 530-26-7
D-Mannose

: 138-08-9
phosphoenolpyruvic acid

: 79-33-4,106989-11-1,26811-96-1,31587-11-8,26100-51-6
L-Lactic acid

: 723729-16-6
D-mannopyranose 6-phosphate

Guidance literature:: With pyruvate kinase; yeast hexokinase; NAD; lactate dehydrogenase; In water; at 30 ℃; pH=7.5; Concentration; Kinetics; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1016/j.carres.2011.04.011

Reference yield:

: 723729-16-6
D-mannopyranose 6-phosphate

: 530-26-7
D-Mannose

Guidance literature:: With Acinetobacter baumannii recombinant acid phosphatase; nickel dichloride; bovine serum albumin; In water; pH=6; Cooling with ice; Enzymatic reaction;
DOI:10.1371/journal.pone.0252377