319426-63-6

Basic information

• Product Name: TETRACYCLINE 10-O-B-D-GALACTOPYRANOSIDE
• Synonyms: TETRACYCLINE 10-O-B-D-GALACTOPYRANOSIDE;TETRACYCLINE 10-O-BETA-D-GALACTOPYRANOSIDE;Tetracycline10-O--D-Galactopyranoside;Tetracycline 10-O-β-D-Galactopyranopyranoside;Tetracycline Galactoside
• CAS NO: 319426-63-6
• Molecular Formula: C28H34N2O13
• Molecular Weight: 606.58
• Mol File: 319426-63-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 975.4oC at 760 mmHg
• Flash Point: 543.7oC
• Appearance: /
• Density: 1.71g/cm3
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.738
• Storage Temp.: −20°C
• CAS DataBase Reference: TETRACYCLINE 10-O-B-D-GALACTOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: TETRACYCLINE 10-O-B-D-GALACTOPYRANOSIDE(319426-63-6)
• EPA Substance Registry System: TETRACYCLINE 10-O-B-D-GALACTOPYRANOSIDE(319426-63-6)

Safety Data

• Hazard Codes: Xn
• Statements: 33-36/37/38-63-64
• Safety Statements: 22-36/37/39-45
• Hazardous Substances Data: 319426-63-6(Hazardous Substances Data)

Usage

Uses

Tetracycline 10-O-b-D-galactopyranoside is a tetracycline analog.

InChI:InChI=1/C28H34N2O13/c1-27(40)9-5-4-6-12(42-26-22(36)21(35)18(32)13(8-31)43-26)14(9)19(33)15-10(27)7-11-17(30(2)3)20(34)16(25(29)39)24(38)28(11,41)23(15)37/h4-6,10-11,13,17-18,21-22,26,31-32,34-37,40-41H,7-8H2,1-3H3,(H2,29,39)/t10-,11-,13+,17-,18-,21-,22+,26+,27+,28-/m0/s1

Upstream product

• 60-54-8 tetracycline 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 

Relevant articles and documents

Compositions and methods for targeted enzymatic release of cell regulatory compounds

Novel pro-drugs and methods for their use to alter the growth and biological characteristics of living cells, tissues, or whole organisms are described. The methods allow for selective activation of the pro-drugs at or near transformant host cells expressing a gene for an enzyme that activates the pro-drugs. Pro-drugs according to a preferred embodiment of the invention are conjugates of a bioactive compound and a chemical group that is capable of being cleaved from the bioactive compound by action of an enzyme. Methods according to this invention include, (a) introducing into targeted cells a gene encoding an enzyme and (b) administering a pro-drug, wherein the enzyme releases the pro-drug from conjugation. In a preferred embodiment of the invention, the gene encoding the enzyme is a marker gene.