Dehydroisoandrosterone 3-glucuronide

Base Information

Chemical Name:Dehydroisoandrosterone 3-glucuronide
CAS No.:5716-14-3
Molecular Formula:C25H36O8
Molecular Weight:464.55
Hs Code.:
DSSTox Substance ID:DTXSID30408434,DTXSID201290600
Mol file:5716-14-3.mol

Synonyms:5716-14-3;Dehydroisoandrosterone 3-glucuronide;6-[(10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid;DHEA glucuronide;DTXSID30408434;DTXSID201290600;3331-64-4;FT-0635817;NS00009039

Suppliers and Price of Dehydroisoandrosterone 3-glucuronide

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

IsoSciences
DehydroepiandrosteroneGlucuronide ≥97%
1mg
$ 239.00

American Custom Chemicals Corporation
DEHYDROISOANDROSTERONE 3-GLUCURONIDE 95.00%
5MG
$ 799.78

AHH
Dehyroisoandrosterone3-glucuronide 98%
0.05g
$ 525.00

Total 4 raw suppliers

Chemical Property of Dehydroisoandrosterone 3-glucuronide

Chemical Property:

PSA：133.52000
LogP:1.23000
Storage Temp.:−20°C
XLogP3:1.9
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:464.24101810
Heavy Atom Count:33
Complexity:855

Purity/Quality:

97% ^*data from raw suppliers

DehydroepiandrosteroneGlucuronide ≥97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CC12CCC3C(C1CCC2=O)CC=C4C3(CCC(C4)OC5C(C(C(C(O5)C(=O)O)O)O)O)C

Technology Process of Dehydroisoandrosterone 3-glucuronide

There total 8 articles about Dehydroisoandrosterone 3-glucuronide 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: 100.0%

: (E)-17-carboxymethoxyimino-dehydroepiandrosterone 3-β-D-glucuronide

: 5716-14-3
Dehydroepiandrosterone 3-glucuronide

Guidance literature:: With titanium(III) chloride; ammonium acetate; water; acetic acid; In 1,4-dioxane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/jo101914s

Reference yield: 94.0%

: 777038-38-7
α-D-glucuronyl fluoride

: 53-43-0
dehydroepiandrosterone

: 5716-14-3
Dehydroepiandrosterone 3-glucuronide

Guidance literature:: With Escherichia coli β-glucuronidase E504G mutant; In aq. phosphate buffer; tert-butyl alcohol; at 37 ℃; for 48h; pH=7.5; Enzymatic reaction;
DOI:10.1039/c4ob00984c

Reference yield: 26.0%

: 1-deoxy-1-fluoro-α-D-glucopyranuronic acid ammonium salt

: 53-43-0
dehydroepiandrosterone

: 5716-14-3
Dehydroepiandrosterone 3-glucuronide

Guidance literature:: With Escherichia coli glucuronylsynthase mutant E₅₀₄G; n-dodecyl β-D-glucopyranosyl-(1->4)-β-D-glucopyranoside; at 20 ℃; for 96h; pH=7.5; aq. phosphate buffer;
DOI:10.1021/ol8002767