3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-(gamma-glutamylamino)hexopyranoside

Base Information

Chemical Name:3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-(gamma-glutamylamino)hexopyranoside
CAS No.:106372-52-5
Molecular Formula:C₃₂H₃₆N₂O₁₃
Molecular Weight:656.643
Hs Code.:

3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-(gamma-glutamylamino)hexopyranoside

Synonyms:5,12-Naphthacenedione,8-acetyl-10-[[3-[(4-amino-4-carboxy-1-oxobutyl)amino]-2,3,6-trideoxy-a-L-lyxo-hexopyranosyl]oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-,[8S-[8a,10a(R*)]]-

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Chemical Property of 3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-(gamma-glutamylamino)hexopyranoside

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:966.1°Cat760mmHg
Flash Point:538.1°C
Density:1.56g/cm³

Purity/Quality:

Safty Information:

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MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-(gamma-glutamylamino)hexopyranoside

There total 1 articles about 3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-(gamma-glutamylamino)hexopyranoside 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:

: 128960-77-0
glutathione

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daunorubicin

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γ-glyamyl daunomycin

Guidance literature:: With GGT; In various solvent(s); at 25 ℃; for 25h; pH=8.5; Enzymatic reaction;
DOI:10.1002/(SICI)1098-2280(1998)32:4<377::AID-EM12>3.0.CO;2-1