Synthesis and structure–activity relationships of phenylpropanoid amides of serotonin on tyrosinase inhibition (Q83539643)

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scientific article published on February 13, 2011

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English	Synthesis and structure–activity relationships of phenylpropanoid amides of serotonin on tyrosinase inhibition	scientific article published on February 13, 2011

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

title

Synthesis and structure-activity relationships of phenylpropanoid amides of serotonin on tyrosinase inhibition (English)

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

Synthesis and structure–activity relationships of phenylpropanoid amides of serotonin on tyrosinase inhibition (English)

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Crossref

DOI

10.1016/J.BMCL.2011.02.028

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https://api.crossref.org/works/10.1016/J.BMCL.2011.02.028

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26 November 2024

author name string

Toshiyuki Takahashi

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1

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

Mitsuo Miyazawa

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2

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

language of work or name

English

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National Center for Biotechnology Information

PubMed publication ID

21377874

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21377874

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26 November 2024

publication date

13 February 2011

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

full work available at URL

https://api.elsevier.com/content/article/PII:S0960894X11002125?httpAccept=text/xml

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DOI

10.1016/J.BMCL.2011.02.028

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https://api.crossref.org/works/10.1016/J.BMCL.2011.02.028

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26 November 2024

https://api.elsevier.com/content/article/PII:S0960894X11002125?httpAccept=text/plain

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Crossref

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10.1016/J.BMCL.2011.02.028

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26 November 2024

published in

Bioorganic & Medicinal Chemistry Letters

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

volume

21

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

issue

7

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Europe PubMed Central

PubMed publication ID

21377874

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

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24 January 2020

page(s)

1983-1986

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Europe PubMed Central

PubMed publication ID

21377874

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24 January 2020

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Inhibitory effects of active compounds isolated from safflower (Carthamus tinctorius L.) seeds for melanogenesis

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Dimethyl sulfide, a volatile flavor constituent, is a slow-binding inhibitor of tyrosinase

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10.1016/J.BMCL.2011.02.028

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Tyrosinase inhibitors from Bolivian medicinal plants

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Use of a free radical method to evaluate antioxidant activity

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Effects of wine phenolics and sorghum tannins on tyrosinase activity and growth of melanoma cells

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Inhibitory effects of esculetin on melanin biosynthesis

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Analogues of N-hydroxycinnamoylphenalkylamides as inhibitors of human melanocyte-tyrosinase

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Phenylethylamide and phenylmethylamide derivatives as new tyrosinase inhibitors

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Free radicals and antioxidants in food and in vivo: what they do and how they work

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Food preservatives sodium sulfite and sorbic acid suppress mitogen-stimulated peripheral blood mononuclear cells.

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Antioxidants and vitamins in cosmetics

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Serotomide and safflomide modulate forskolin-stimulated cAMP formation via 5-HT1 receptor

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Biosynthesis and biotechnological production of serotonin derivatives

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Antioxidative Compounds Isolated from Safflower (Cartthamus tinctorius L.) Oil Cake

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Tyrosinase Inhibitory and Anti-Tumor Promoting Activities of Compounds Isolated from Safflower (Carthamus Tinctorius L.) and Cotton (Gossypium Hirsutum L.) Oil Cakes

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Serotonin derivative, N-(p-Coumaroyl)serotonin, isolated from safflower (Carthamus tinctorius L.) oil cake augments the proliferation of normal human and mouse fibroblasts in synergy with basic fibroblast growth factor (bFGF) or epidermal growth fac

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N-[(Dihydroxyphenyl)acyl]serotonins as potent inhibitors of tyrosinase from mouse and human melanoma cells

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Serotonin derivatives, major safflower (Carthamus tinctorius L.) seed antioxidants, inhibit low-density lipoprotein (LDL) oxidation and atherosclerosis in apolipoprotein E-deficient mice

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The chemistry of indoles. CIII. Simple syntheses of serotonin, N-methylserotonin, bufotenine, 5-methoxy-N-methyltryptamine, bufobutanoic acid, N-(indol-3-yl)methyl-5-methoxy-N-methyltryptamine, and lespedamine based on 1-hydroxyindole chemistry

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24

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10.1016/J.BMCL.2011.02.028

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26 November 2024

Identifiers

DOI

10.1016/J.BMCL.2011.02.028

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21377874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

PubMed publication ID

21377874

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21377874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21377874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

 

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