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Results for "

phenyl β d glucopyranoside

" in TargetMol Product Catalog
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    TargetMol | Cell_Research_Reagents
4-[2-(3,5-Dimethoxyphenyl)ethyl]phenyl 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
TN63991338076-61-1
4-[2-(3,5-Dimethoxyphenyl)ethyl]phenyl 6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside showed cytotoxic activities to Hela and hep2 cell lines.
  • $390
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Phenyl 4,6-O-Benzylidene-1-thio-β-D-glucopyranoside
Phenyl 4,6-O-Benzylidene-1-thio-β-D-glucopyranoside, Phenyl 4,6-O-benzylidene-1-thio-beta-D-glucopyranoside
TSW-0026787508-17-6
Phenyl 4,6-O-Benzylidene-1-thio-β-D-glucopyranoside is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.
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MNP-Glc
MNP-Glc, 2-Methoxy-4-(2-nitroethenyl)phenyl β-D-glucopyranoside
TXB-0010070622-80-9
MNP-Glc is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.
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4-(3-oxobutyl)phenyl 6-O-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-O-(3,4,5-trihydroxybenzoyl)-b-D-glucopyranoside
TN5281105274-16-6
4-(3-oxobutyl)phenyl 6-O-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-O-(3,4,5-trihydroxybenzoyl)-b-D-glucopyranoside is a natural product for research related to life sciences. The catalog number is TN5281 and the CAS number is 105274-16-6.
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Phenyl-β-D-glucopyranoside
PHENYL-B-D-GLUCOPYRANOSIDE
TN67471464-44-4
Phenyl-β-D-glucopyranoside (PHENYL-B-D-GLUCOPYRANOSIDE) is a component of Phellodendron amurense with anti-cancer and anti-inflammatory activities.
  • $29
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Phenyl-1-thio-β-D-glucopyranoside
TSW-001182936-70-1
Phenyl-1-thio-β-D-glucopyranoside has potential applications in glycobiology research.
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7-10 days
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Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside
TSW-00248197005-22-4
Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside is a biochemical reagent commonly used in glycobiology studies. Glycobiology focuses on the structure, synthesis, biology, and evolution of sugars, involving carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.
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