4 Results for "

Sancycline

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "Sancycline" in MCE Product Catalog:

Cat. No.: HY-17466
CAS No.: 808-26-4
Synonyms: Bonomycin; 6-Demethyl-6-deoxytetracycline
Sancycline (6-Demethyl-6-deoxytetracycline) acts by reversibly binding to the 30 S ribosomal subunit and inhibiting protein translation by blocking entry of aminoacyl-tRNA into the ribosome a site similar to tetracycline (HY-A0107). Sancycline, four linearly fused six-membered rings with four stereocenters, is a rare semi-synthetic tetracycline (HY-A0107) prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of Declomycin .
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Cat. No.: HY-17466A
CAS No.: 6625-20-3
Synonyms: Bonomycin hydrochloride; 6-Demethyl-6-deoxytetracycline hydrochloride
Sancycline (6-Demethyl-6-deoxytetracycline) hydrochloride acts by reversibly binding to the 30 S ribosomal subunit and inhibiting protein translation by blocking entry of aminoacyl-tRNA into the ribosome a site similar to tetracycline (HY-A0107). Sancycline hydrochloride, four linearly fused six-membered rings with four stereocenters, is a rare semi-synthetic tetracycline (HY-A0107) prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of Declomycin .
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Cat. No.: HY-17466R
CAS No.: 808-26-4
Synonyms: Bonomycin (Standard); 6-Demethyl-6-deoxytetracycline (Standard)
Sancycline (Standard) is the analytical standard of Sancycline. This product is intended for research and analytical applications. Sancycline (6-Demethyl-6-deoxytetracycline) acts by reversibly binding to the 30 S ribosomal subunit and inhibiting protein translation by blocking entry of aminoacyl-tRNA into the ribosome a site similar to tetracycline (HY-A0107). Sancycline, four linearly fused six-membered rings with four stereocenters, is a rare semi-synthetic tetracycline (HY-A0107) prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of Declomycin[1][2][3].
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Cat. No.: HY-W701232
CAS No.: 906364-48-5
epi-Sancycline (hydrochloride) is a class of biochemical reagents used for glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology .
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