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A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse

[Image: see text] An improved synthesis of a haptenic heroin surrogate 1 (6-AmHap) is reported. The intermediate needed for the preparation of 1 was described in the route in the synthesis of 2 (DiAmHap). A scalable procedure was developed to install the C-3 amido group. Using the Boc protectng grou...

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Autores principales: Sulima, Agnieszka, Jalah, Rashmi, Antoline, Joshua F. G., Torres, Oscar B., Imler, Gregory H., Deschamps, Jeffrey R., Beck, Zoltan, Alving, Carl R., Jacobson, Arthur E., Rice, Kenner C., Matyas, Gary R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767880/
https://www.ncbi.nlm.nih.gov/pubmed/29236495
http://dx.doi.org/10.1021/acs.jmedchem.7b01427
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author Sulima, Agnieszka
Jalah, Rashmi
Antoline, Joshua F. G.
Torres, Oscar B.
Imler, Gregory H.
Deschamps, Jeffrey R.
Beck, Zoltan
Alving, Carl R.
Jacobson, Arthur E.
Rice, Kenner C.
Matyas, Gary R.
author_facet Sulima, Agnieszka
Jalah, Rashmi
Antoline, Joshua F. G.
Torres, Oscar B.
Imler, Gregory H.
Deschamps, Jeffrey R.
Beck, Zoltan
Alving, Carl R.
Jacobson, Arthur E.
Rice, Kenner C.
Matyas, Gary R.
author_sort Sulima, Agnieszka
collection PubMed
description [Image: see text] An improved synthesis of a haptenic heroin surrogate 1 (6-AmHap) is reported. The intermediate needed for the preparation of 1 was described in the route in the synthesis of 2 (DiAmHap). A scalable procedure was developed to install the C-3 amido group. Using the Boc protectng group in 18 allowed preparation of 1 in an overall yield of 53% from 4 and eliminated the necessity of preparing the diamide 13. Hapten 1 was conjugated to tetanus toxoid and mixed with liposomes containing monophosphoryl lipid A as an adjuvant. The 1 vaccine induced high anti-1 IgG levels that reduced heroin-induced antinociception and locomotive behavioral changes following repeated subcutaneous and intravenous heroin challenges in mice and rats. Vaccinated mice had reduced heroin-induced hyperlocomotion following a 50 mg/kg heroin challenge. The 1 vaccine-induced antibodies bound to heroin and other abused opioids, including hydrocodone, oxycodone, hydromorphone, oxymorphone, and codeine.
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spelling pubmed-57678802018-01-16 A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse Sulima, Agnieszka Jalah, Rashmi Antoline, Joshua F. G. Torres, Oscar B. Imler, Gregory H. Deschamps, Jeffrey R. Beck, Zoltan Alving, Carl R. Jacobson, Arthur E. Rice, Kenner C. Matyas, Gary R. J Med Chem [Image: see text] An improved synthesis of a haptenic heroin surrogate 1 (6-AmHap) is reported. The intermediate needed for the preparation of 1 was described in the route in the synthesis of 2 (DiAmHap). A scalable procedure was developed to install the C-3 amido group. Using the Boc protectng group in 18 allowed preparation of 1 in an overall yield of 53% from 4 and eliminated the necessity of preparing the diamide 13. Hapten 1 was conjugated to tetanus toxoid and mixed with liposomes containing monophosphoryl lipid A as an adjuvant. The 1 vaccine induced high anti-1 IgG levels that reduced heroin-induced antinociception and locomotive behavioral changes following repeated subcutaneous and intravenous heroin challenges in mice and rats. Vaccinated mice had reduced heroin-induced hyperlocomotion following a 50 mg/kg heroin challenge. The 1 vaccine-induced antibodies bound to heroin and other abused opioids, including hydrocodone, oxycodone, hydromorphone, oxymorphone, and codeine. American Chemical Society 2017-12-13 2018-01-11 /pmc/articles/PMC5767880/ /pubmed/29236495 http://dx.doi.org/10.1021/acs.jmedchem.7b01427 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Sulima, Agnieszka
Jalah, Rashmi
Antoline, Joshua F. G.
Torres, Oscar B.
Imler, Gregory H.
Deschamps, Jeffrey R.
Beck, Zoltan
Alving, Carl R.
Jacobson, Arthur E.
Rice, Kenner C.
Matyas, Gary R.
A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse
title A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse
title_full A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse
title_fullStr A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse
title_full_unstemmed A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse
title_short A Stable Heroin Analogue That Can Serve as a Vaccine Hapten to Induce Antibodies That Block the Effects of Heroin and Its Metabolites in Rodents and That Cross-React Immunologically with Related Drugs of Abuse
title_sort stable heroin analogue that can serve as a vaccine hapten to induce antibodies that block the effects of heroin and its metabolites in rodents and that cross-react immunologically with related drugs of abuse
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767880/
https://www.ncbi.nlm.nih.gov/pubmed/29236495
http://dx.doi.org/10.1021/acs.jmedchem.7b01427
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