886-52-2

Upstream product

• 836-27-1 1,3-dimethoxy-5-(5-hydroxypentyl)benzene 
• 891-66-7 5-(3,5-Dimethoxy-phenyl)-valeriansaeuremethylester 
• 58545-48-5 (E)-1,3-dimethoxy-5-(pent-1-en-1-yl)benzene 
• 197178-54-4 5-(3,5-dimethoxyphenyl)pentanoic acid ethyl ester 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 38228-28-3 1-(1-hydroxypentyl)-3,5-dimethoxybenzene 

Downstream Products

• 50873-97-7 1,3-dimethoxy-5-(6'-heptynyl)benzene 
• 58545-34-9 1-(5-bromopentyl)benzene-1,3-diol 
• 50873-98-8 C₃₀H₃₈O₄ 
• 171569-34-9 1,3-dimethoxy-5-<14'-(3'',5''-dimethoxyphenyl)-cis-6'-tetradecenyl>benzene 
• 171569-33-8 1,3-dimethoxy-5-<14'-(3'',5''-dimethoxyphenyl)-6'-tetradecynyl>benzene 
• 52483-24-6 1,3-dihydroxy-5-<14'-(3'',5''-dihydroxyphenyl)tetradec-cis-6'-enyl>benzene 
• 21390-07-8 1,3-dimethoxy-5-<14'-(3'',5''-dimethoxyphenyl)tetradecyl>benzene 
• 26050-60-2 1,3-dihydroxy-5-<14'-(3'',5''-dihydroxyphenyl)tetradecyl>benzene 
• 1972-08-3 dronabinol 

Relevant academic research and scientific papers

5-Alkylresorcinol derivatives from the bryozoan Schizomavella mamillata: Isolation, synthesis, and antioxidant Activity

The chemical study of the bryozoan Schizomavella mamillata has led to the isolation of six new 5-alkylresorcinol derivatives, schizols A–F (1–6), whose structures were established by spectrocospic means. Schizol A (1) exhibits a (E)-6-phenylnon-5-enyl moi

Δ9-tetrahydrocannabinol immunochemical studies: Haptens, monoclonal antibodies, and a convenient synthesis of radiolabeled Δ9-tetrahydrocannabinol

Immunopharmacotherapy as an approach to combat drugs of abuse has become an active area of investigation. Marijuana is the most commonly used illicit drug in the U.S. The main active chemical in marijuana is Δ9- tetrahydrocannabinol (Δ9-THC); hence, monoclonal antibodies with high affinity and specificity for Δ9-tetrahydrocannabinol could be valuable immunopharmacotherapeutic intervention and diagnostic tools. We have synthesized immunoconjugates that induce an effective immune response to Δ9-THC and describe a convenient synthesis of radiolabeled Δ9-THC. We demonstrate the value and use of this probe to select anti-Δ9-THC antibodies that bind Δ9-THC with good affinity. The synthetic route to radiolabeled Δ9-THC has enabled the correct assessment of the affinity of these antibodies to their ligand and may facilitate future binding studies between Δ9- THC and its analogues and the cannabinoid receptors.

5-Alkylresorcinols from Hakea trifurcata that cleave DNA

A dichloromethane extract of Hakea trifurcata that mediated relaxation of ?X174 replicative form DNA at micromolar concentrations in the presence of Cu2+ was resolved into six active components by bioassay-guided fractionation. Five of the acti