67463-64-3 Usage
Description
(1S,3S)-3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 3-amino-2,3,6-trideoxy-alpha-L-xylo-hexopyranoside hydrochloride (1:1) is a complex organic molecule with a tetracycline backbone, featuring an acetyl group, multiple hydroxyl groups, a methoxy group, and an amino sugar moiety. The hydrochloride addition results in the formation of a salt, indicating that this compound may have potential applications in the pharmaceutical industry, particularly as an antibiotic or for other therapeutic uses due to its intricate chemical structure and functional groups.
Uses
Used in Pharmaceutical Industry:
(1S,3S)-3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 3-amino-2,3,6-trideoxy-alpha-L-xylo-hexopyranoside hydrochloride (1:1) is used as a potential antibiotic for its ability to target and disrupt bacterial protein synthesis, thereby inhibiting bacterial growth. The presence of the tetracycline backbone suggests that it may be effective against a range of bacterial infections.
Additionally, due to the presence of various functional groups such as hydroxyl and methoxy groups, this compound may also be used for other therapeutic purposes, including the treatment of specific conditions or diseases where these functional groups can interact with biological targets to produce a desired effect.
Check Digit Verification of cas no
The CAS Registry Mumber 67463-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67463-64:
(7*6)+(6*7)+(5*4)+(4*6)+(3*3)+(2*6)+(1*4)=153
153 % 10 = 3
So 67463-64-3 is a valid CAS Registry Number.
67463-64-3Relevant articles and documents
HEMISYNTHESE DE NOUVEAUX GLICOSIDES ANALOGUES DE LA DAUNORUBICINE
Boivin, Jean,Montagnac, Alain,Monneret, Claude,Pais, Mary
, p. 223 - 242 (2007/10/02)
Seven daunorubicin analogs containing α-L-, α-D-, and β-D-glicosidic linkages, in which the natural occuring sugar (L-daunosamine) was replaced by diastereomeric 3-amino-2,3,6-trideoxyhexoses (3-epi-L-daunosamine, D-acosamine, D-daunosamine, D-ristosamine, and 3-epi-D-daunosamine), were prepared.In all cases, glycosidation with daunomycinone was performed in the presence of p-toluenesulfonic acid starting from 1-O-acetyl-2,3,6-trideoxy-4-O-p-nitrobenzoyl-3-trifluoro-acetamidohexopyranoses (prepared from the corresponding methyl 3-amino-2,3,6-trideoxyhexopyranosides) or from 1,5-anhydro-2,3,6-trideoxy-4-O-p-nitrobenzoyl-3-trifluoroacetamidohex-1-enitols (prepared from glycosals or pseudoglycals, the 3-amino group being introduced by substitution with sodium azide and subsequent reduction).Glycosidation was followed by removal of the protecting groups.
