(Q42165810)

English

Phenolic modification as an approach to improve the pharmacology of the 3-acyloxy-2-benzylpropyl homovanillic amides and thioureas, a promising class of vanilloid receptor agonists and analgesics

scientific article published on April 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Phenolic modification as an approach to improve the pharmacology of the 3-acyloxy-2-benzylpropyl homovanillic amides and thioureas, a promising class of vanilloid receptor agonists and analgesics (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

1 reference

based on heuristic

inferred from title

author name string

Jeewoo Lee

1

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Jiyoun Lee

2

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Myung-Sim Kang

3

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Kang-Pil Kim

4

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Suk-Jae Chung

5

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Peter M Blumberg

6

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Jung-Bum Yi

7

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Young Ho Park

8

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

language of work or name

0 references

publication date

1 April 2002

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Bioorganic & Medicinal Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

1171-1179

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Euphorbium: modern research on its active principle, resiniferatoxin, revives an ancient medicine.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel natural vanilloid receptor agonists: new therapeutic targets for drug development

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Vanilloid receptors: new insights enhance potential as a therapeutic target

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Similarities and differences in the structure-activity relationships of capsaicin and resiniferatoxin analogues

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis and Evaluation of Phorboid 20-Homovanillates: Discovery of a Class of Ligands Binding to the Vanilloid (Capsaicin) Receptor with Different Degrees of Cooperativity

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinct structure-activity relations for stimulation of 45Ca uptake and for high affinity binding in cultured rat dorsal root ganglion neurons and dorsal root ganglion membranes.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Resiniferatoxin-amide and analogues as ligands for protein kinase C and vanilloid receptors and determination of their biological activities as vanilloids

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analog of capsaicin, the irritant constituent in red pepper

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

3-Acyloxy-2-phenalkylpropyl amides and esters of homovanillic acid as novel vanilloid receptor agonists

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

N-(3-Acyloxy-2-benzylpropyl)-N'-(4-hydroxy-3-methoxybenzyl) thiourea derivatives as potent vanilloid receptor agonists and analgesics

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Analogues of capsaicin with agonist activity as novel analgesic agents: structure-activity studies. 4. Potent, orally active analgesics

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

N-(3-acyloxy-2-benzylpropyl)-N'-dihydroxytetrahydrobenzazepine and tetrahydroisoquinoline thiourea analogues as vanilloid receptor ligands

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2801%2900387-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0968-0896(01)00387-X

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

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