101565-95-1

Basic information

• Product Name: meta-METHOXYTOPOLIN RIBOSIDE (MemTR)
• Synonyms: meta-METHOXYTOPOLIN RIBOSIDE (MemTR);N-[(3-Methoxyphenyl)methyl]-adenosine;N6-(m-Methoxybenzyl)adenosine
• CAS NO: 101565-95-1
• Molecular Formula: C₁₈H₂₁N₅O₅
• Molecular Weight: 387.38984
• Mol File: 101565-95-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 162-163℃
• Appearance: /
• CAS DataBase Reference: meta-METHOXYTOPOLIN RIBOSIDE (MemTR)(CAS DataBase Reference)
• NIST Chemistry Reference: meta-METHOXYTOPOLIN RIBOSIDE (MemTR)(101565-95-1)
• EPA Substance Registry System: meta-METHOXYTOPOLIN RIBOSIDE (MemTR)(101565-95-1)

Safety Data

• Hazardous Substances Data: 101565-95-1(Hazardous Substances Data)

Usage

Description

Meta-METHOXYTOPOLIN RIBOSIDE (MemTR) is a compound that has been identified for its potential applications in various fields, particularly in the study of plant growth regulators and their impact on plant development.

Uses

Used in Plant Biology Research:
Meta-METHOXYTOPOLIN RIBOSIDE (MemTR) is used as a research compound for studying the influence of plant growth regulators on shoot proliferation and secondary metabolite production in micropropagated Huernia hystrix. This application helps researchers understand the role of growth regulators in plant development and may lead to advancements in plant breeding and cultivation techniques.

Upstream product

• 824-98-6 m-methoxybenzyl chloride 
• 58-61-7 adenosine 
• 5071-96-5 3-METHOXYBENZYLAMINE 
• 2004-06-0 6-Chloropurine riboside 

Relevant articles and documents

Preparation, biological activity and endogenous occurrence of N6-benzyladenosines

Cytokinin activity of forty-eight 6-benzyladenosine derivatives at both the receptor and cellular levels as well as their anticancer properties were compared in various in vitro assays. The compounds were prepared by the condensation of 6-chloropurine rib

Synthesis of substituted-benzyl and sugar-modified analogues of 6-N-(4- nitrobenzyl)adenosine and their interactions with 'ES' nucleoside transport systems

Four classes of 6-X-benzylated purine nucleosides, (i) 6-N-(substituted- benzyl)adenosines, (ii) 6-N-(4-nitrobenzyl)adenine nucleosides with modified sugars, (iii) 6-N(S)-(4-azidobenzyl) derivatives of adenosine, 6-thioinosine, and 6-thioguanosine, and (iv) 6-N-{4-N-[acyl(sulfonyl)amino]benzyl} adenosines, were synthesized and their binding interactions with 'es-NT' (equilibrative, inhibitor-sensitive nucleoside transport) systems were studied. Several tight-binding analogues were found.