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| description
| - wetenschappelijk artikel (nl)
- наукова стаття, опублікована в лютому 1989 (uk)
- im Februar 1989 veröffentlichter wissenschaftlicher Artikel (de)
- artículu científicu espublizáu en febreru de 1989 (ast)
- artikull shkencor i botuar më 01 shkurt 1989 (sq)
- scientific article published on 01 February 1989 (en)
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| author name string
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| author name string
| - S Takahashi
- I Kaneko
- K Kamoshida
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| rdfs:label
| - Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (en)
- Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (nl)
- Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (sq)
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| skos:prefLabel
| - Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (en)
- Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (nl)
- Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (sq)
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| name
| - Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (en)
- Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (nl)
- Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (sq)
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| title
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| title
| - Complestatin, a potent anti-complement substance produced by Streptomyces lavendulae. I. Fermentation, isolation and biological characterization (en)
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| full work available at URL
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| full work available at URL
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| DOI
| - 10.7164/ANTIBIOTICS.42.236
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| is cites work
of | - The core structure of TMC-95A is a promising lead for reversible proteasome inhibition
- Neuroprotectins A and B, bicyclohexapeptides protecting chick telencephalic neuronal cells from excitotoxicity. I. Fermentation, isolation, physico-chemical properties and biological activity
- Chloropeptins, new anti-HIV antibiotics inhibiting gp120-CD4 binding from Streptomyces sp. I. Taxonomy, fermentation, isolation, and physico-chemical properties and biological activities.
- Synthesis of a TMC-95A ketomethylene analogue by cyclization via intramolecular Suzuki coupling
- Chloropeptins, new anti-HIV antibiotics inhibiting gp120-CD4 binding from Streptomyces sp. II. Structure elucidation of chloropeptin I
- Feglymycin, a novel inhibitor of the replication of the human immunodeficiency virus. Fermentation, isolation and structure elucidation
- Inhibition of human immunodeficiency virus type-1-induced syncytium formation and cytopathicity by complestatin
- A comprehensive review of glycosylated bacterial natural products.
- A Pd(0)-mediated indole (macro)cyclization reaction
- Synthesis of diastereomers of complestatin and chloropeptin I: substrate-dependent atropstereoselectivity of the intramolecular Suzuki-Miyaura reaction
- New antiviral antibiotics, kistamicins A and B. I. Taxonomy, production, isolation, physico-chemical properties and biological activities.
- Structures of TMC-95A-D: novel proteasome inhibitors from Apiospora montagnei sacc. TC 1093
- Synthesis of DEFG ring of complestatin and chloropeptin I: highly atropdiastereoselective macrocyclization by intramolecular Suzuki-Miyaura reaction
- Biosynthesis of L-p-hydroxyphenylglycine, a non-proteinogenic amino acid constituent of peptide antibiotics
- The complestatins as HIV-1 integrase inhibitors. Efficient isolation, structure elucidation, and inhibitory activities of isocomplestatin, chloropeptin I, new complestatins, A and B, and acid-hydrolysis products of chloropeptin I.
- Total synthesis of complestatin: development of a Pd(0)-mediated indole annulation for macrocyclization
- Synthesis and stereochemical determination of complestatin A and B (neuroprotectin A and B)
- Total synthesis of chloropeptin II (complestatin) and chloropeptin I.
- Synthesis of linear tripeptides for right-hand segments of complestatin
- Chloropeptins I and II, novel inhibitors against gp120-CD4 binding from Streptomyces sp.
- Total synthesis of complestatin (chloropeptin II).
- Total synthesis of anti-HIV agent chloropeptin I.
- Isocomplestatin: total synthesis and stereochemical revision
- Enhancement of plasminogen binding and fibrinolysis by chloropeptin I
- Two syntheses of the 16- and 17-membered DEF ring systems of chloropeptin and complestatin
- Detection of novel secondary metabolites.
- Bioactive microbial products: focus upon mechanism of action
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