(Q103812501)

(2S)-2-[[(2S)-1-[(2S)-2-[[(2S,3R)-2-[[(2R,3R)-3-amino-2-hydroxydecanoyl]amino]-3-methylpentanoyl]-methylamino]-4-methylpentanoyl]pyrrolidine-2-carbonyl]amino]-3-(4-hydroxyphenyl)propanoic acid

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(2S)-2-[[(2S)-1-[(2S)-2-[[(2S,3R)-2-[[(2R,3R)-3-amino-10-chloro-2-hydroxydecanoyl]amino]-3-methylpentanoyl]-methylamino]-4-methylpentanoyl]pyrrolidine-2-carbonyl]amino]-3-(4-hydroxyphenyl)propanoic acid

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(2S)-1-[(2S)-2-[[(2S,3R)-2-[[(2R,3R)-3-amino-10,10-dichloro-2-hydroxydecanoyl]amino]-3-methylpentanoyl]-methylamino]-4-methylpentanoyl]pyrrolidine-2-carboxylic acid

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1 reference

(2R)-1-[(2R)-2-[[(2S,3S)-2-[[(2S,3S)-3-amino-10-chloro-2-hydroxydecanoyl]amino]-3-methylpentanoyl]-methylamino]-4-methylpentanoyl]pyrrolidine-2-carboxylic acid

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(2R)-1-[(2R)-2-[[(2S,3S)-2-[[(2S,3S)-3-amino-10,10-dichloro-2-hydroxydecanoyl]amino]-3-methylpentanoyl]-methylamino]-4-methylpentanoyl]pyrrolidine-2-carboxylic acid

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(2S)-2-[[(2R)-1-[(2R)-2-[[(2S,3S)-2-[[(2S,3S)-3-amino-2-hydroxydecanoyl]amino]-3-methylpentanoyl]-methylamino]-4-methylpentanoyl]pyrrolidine-2-carbonyl]amino]-3-(4-hydroxyphenyl)propanoic acid

1 reference

(2S)-2-[[(2R)-1-[(2R)-2-[[(2S,3S)-2-[[(2S,3S)-3-amino-10,10-dichloro-2-hydroxydecanoyl]amino]-3-methylpentanoyl]-methylamino]-4-methylpentanoyl]pyrrolidine-2-carbonyl]amino]-3-(4-hydroxyphenyl)propanoic acid

1 reference

1 reference

(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2R,3R)-2-hydroxy-3-(methylamino)decanoyl]amino]-3-methylbutanoyl]-methylamino]-3-methylbutanoyl]-methylamino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-(4-hydroxyphenyl)propanoic acid

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Keishi Ishida

1

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

Taku Kato

2

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

Masahiro Murakami

3

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

Masayuki Watanabe

4

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

Mariyo F. Watanabe

5

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

publication date

October 2000

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16 September 2022

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

volume

56

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

issue

44

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

3 December 2020

page(s)

8643-8656

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/S0040-4020(00)00770-5

Microginin, an angiotensin-converting enzyme inhibitor from the blue-green alga Microcystis aeruginosa

3 December 2020

cites work

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Microginins 299-A and -B, leucine aminopeptidase inhibitors from the cyanobacterium Microcystis aeruginosa (NIES-299)

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Four new microginins, linear peptides from the cyanobacterium Microcystis aeruginosa

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Theonellamides A-E, cytotoxic bicyclic peptides, from a marine sponge Theonella sp.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Production of actinonin, an inhibitor of aminopeptidase M, by actinomycetes

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Amastatin, an inhibitor of aminopeptidase A, produced by actinomycetes

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Leuhistin, a new inhibitor of aminopeptidase M, produced by Bacillus laterosporus BMI156-14F1. I. Taxonomy, production, isolation, physico-chemical properties and biological activities.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Leuhistin, a new inhibitor of aminopeptidase M, produced by Bacillus laterosporus BMI156-14F1. II. Structure determination of leuhistin

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Biosynthetic study of leuhistin, a new inhibitor of aminopeptidase M.

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Bestatin, an inhibitor of aminopeptidase B, produced by actinomycetes

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

The structure of bestatin

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Enhancement of delayed-type hypersensitivity by bestatin, an inhibitor of aminopeptidase B and leucine aminopeptidase

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Inhibition of aminopeptidase B and leucine aminopeptidase by bestatin and its stereoisomer

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Structure determination and refinement of bovine lens leucine aminopeptidase and its complex with bestatin.

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Leucine aminopeptidase: bestatin inhibition and a model for enzyme-catalyzed peptide hydrolysis

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https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Inhibition of bovine lens leucine aminopeptidase by bestatin: number of binding sites and slow binding of this inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

K-26, a novel inhibitor of angiotensin I converting enzyme produced by an actinomycete K-26

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

K-13, a novel inhibitor of angiotensin I converting enzyme produced by Micromonospora halophytica subsp. exilisia. I. Fermentation, isolation and biological properties

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

K-13, a novel inhibitor of angiotensin I converting enzyme produced by Micromonospora halophytica subsp. exilisia. II. Structure determination

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Design of potent competitive inhibitors of angiotensin-converting enzyme. Carboxyalkanoyl and mercaptoalkanoyl amino acids

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

A new class of angiotensin-converting enzyme inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Kallidin- and bradykinin-degrading pathways in human heart: degradation of kallidin by aminopeptidase M-like activity and bradykinin by neutral endopeptidase

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Kawaguchipeptin A, a novel cyclic undecapeptide from cyanobacterium Microcystis aeruginosa (NIES-88)

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Bruceantin, a new potent antileukemic simaroubolide from Brucea antidysenterica

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Results of a large scale screen of microalgae for the production of protease inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Spectrophotometric assay and properties of the angiotensin-converting enzyme of rabbit lung

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

X-ray structure determination of (2S, 3R)-3-amino-2-hydroxy-4-phenylbutanoic acid, a new amino acid component of bestatin.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2800%2900770-5

7 January 2021

Identifiers

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