Isolation and structural determination of a new macrolide, makinolide, from the newly isolated Streptomyces sp. MK-30

Shinya Kodani; Ayako Murao; Michitaka Hidaki; Kanna Sato; Naoto Ogawa

doi:10.1038/ja.2012.24

Isolation and structural determination of a new macrolide, makinolide, from the newly isolated Streptomyces sp. MK-30

The Journal of Antibiotics ◽

10.1038/ja.2012.24 ◽

2012 ◽

Vol 65 (6) ◽

pp. 331-334 ◽

Cited By ~ 6

Author(s):

Shinya Kodani ◽

Ayako Murao ◽

Michitaka Hidaki ◽

Kanna Sato ◽

Naoto Ogawa

Keyword(s):

Structural Determination ◽

Streptomyces Sp

Isolation and Structural Determination of Phepropeptins A, B, C, and D, New Proteasome Inhibitors, Produced by Streptomyces sp.

The Journal of Antibiotics ◽

10.7164/antibiotics.54.874 ◽

2001 ◽

Vol 54 (11) ◽

pp. 874-881 ◽

Cited By ~ 14

Author(s):

RYUICHI SEKIZAWA ◽

ISAO MOMOSE ◽

NAOKO KINOSHITA ◽

HIROSHI NAGANAWA ◽

MASA HAMADA ◽

...

Keyword(s):

Proteasome Inhibitors ◽

Structural Determination ◽

Streptomyces Sp

Structural Determination of Hypnosin, a Spore Germination Inhibitor of Phytopathogenic Streptomyces sp. Causing Root Tumor in Melon (Cucumis sp.)

Journal of Agricultural and Food Chemistry ◽

10.1021/jf072719x ◽

2007 ◽

Vol 55 (26) ◽

pp. 10622-10627 ◽

Cited By ~ 4

Author(s):

Yuu Aoki ◽

Masahiro Yoshida ◽

Hiroshi Kawaide ◽

Hiroshi Abe ◽

Masahiro Natsume

Keyword(s):

Spore Germination ◽

Structural Determination ◽

Germination Inhibitor ◽

Streptomyces Sp

ChemInform Abstract: Isolation and Structural Determination of Phepropeptins A, B, C, and D, New Proteasome Inhibitors, Produced by Streptomyces sp.

ChemInform ◽

10.1002/chin.200217194 ◽

2010 ◽

Vol 33 (17) ◽

pp. no-no

Author(s):

Ryuichi Sekizawa ◽

Isao Momose ◽

Naoko Kinoshita ◽

Hiroshi Naganawa ◽

Masa Hamada ◽

...

Keyword(s):

Proteasome Inhibitors ◽

Structural Determination ◽

Streptomyces Sp

Isolation and structural determination of cyclic lipopeptide from cultured freshwater cyanobacterium Oscillatoria sp. (UIC 10045)

Planta Medica ◽

10.1055/s-0032-1320744 ◽

2012 ◽

Vol 78 (11) ◽

Author(s):

S Luo ◽

HS Kang ◽

AM Krunic ◽

J Yang ◽

SM Swanson ◽

...

Keyword(s):

Structural Determination ◽

Cyclic Lipopeptide ◽

Freshwater Cyanobacterium

ROTATIONAL SPECTRA AND STRUCTURAL DETERMINATION OF HCCNCS

Proceedings of the 72nd International Symposium on Molecular Spectroscopy ◽

10.15278/isms.2017.rf08 ◽

2017 ◽

Author(s):

Wenhao Sun ◽

Jennifer van Wijngaarden ◽

Rebecca Davis

Keyword(s):

Structural Determination ◽

Rotational Spectra

Structural Determination of A Transcribing RNA Polymerase II Complex

10.21236/ada367567 ◽

1999 ◽

Author(s):

Averall Gnatt

Keyword(s):

Rna Polymerase ◽

Rna Polymerase Ii ◽

Structural Determination

Structural Determination of Certain Novel ER Complexes

10.21236/ada434775 ◽

2004 ◽

Author(s):

Ya-Ling Wu ◽

Geoffrey L. Greene

Keyword(s):

Structural Determination

Phytochemical Constituents of Annona reticulata and their Cytotoxic Activity

Letters in Organic Chemistry ◽

10.2174/1570178616666190724123004 ◽

2020 ◽

Vol 17 (3) ◽

pp. 206-210

Author(s):

Ty Viet Pham ◽

Thang Quoc Le ◽

Anh Tuan Le ◽

Hung Quoc Vo ◽

Duc Viet Ho

Keyword(s):

Cytotoxic Activity ◽

Cell Lines ◽

Structural Determination ◽

Phytochemical Investigation ◽

Ic50 Values ◽

Phytochemical Constituents ◽

First Time ◽

Annona Reticulata

A phytochemical investigation of the leaves of Annona reticulata led to the isolation and structural determination of β-sitosterol (1), ent-pimara-8(14),15-dien-19-oic acid (2), ent-pimara- 8(14),15-dien-19-ol (3), quercetin (4), quercetin 3-O-α-L-arabinopyranoside (5), and a mixture of quercetin 3-O-β-D-galactopyranoside (6a) and quercetin 3-O-β-D-glucopyranoside (6b). Of these, compounds 2 and 3 were isolated from the genus Annona for the first time. Compound 3 showed strong cytotoxicity against SK-LU-1 and SW626 cell lines with IC50 values of 17.64 ± 1.07 and 19.79 ± 1.41 μg mL-1, respectively.

NMR-based identification of the phenolic profile of fruits of Lycium barbarum (goji berries). Isolation and structural determination of a novel N-feruloyl tyramine dimer as the most abundant antioxidant polyphenol of goji berries

Food Chemistry ◽

10.1016/j.foodchem.2015.08.129 ◽

2016 ◽

Vol 194 ◽

pp. 1254-1259 ◽

Cited By ~ 57

Author(s):

Martino Forino ◽

Luciana Tartaglione ◽

Carmela Dell’Aversano ◽

Patrizia Ciminiello

Keyword(s):

Structural Determination ◽

Lycium Barbarum ◽

Phenolic Profile ◽

Goji Berries

Structural Determination of the Hydrofullerene C60D36 by Neutron Diffraction

Acta Crystallographica Section B Structural Science ◽

10.1107/s0108768198000093 ◽

1998 ◽

Vol 54 (3) ◽

pp. 345-350 ◽

Cited By ~ 8

Author(s):

L. E. Hall ◽

D. R. McKenzie ◽

R. L. Davis ◽

M. I. Attalla ◽

A. M. Vassallo

Keyword(s):

Neutron Diffraction ◽

Density Function ◽

Diffraction Data ◽

Fourier Transformation ◽

Structural Determination ◽

Molecular Models ◽

Reduced Density ◽

C Nmr

A mixture of C60D36 with 24.5 \pm 4.5% C60 by weight has been analysed by neutron diffraction techniques. The diffraction data was converted to a reduced density function G(r) by Fourier transformation. The C60 component of the G(r) was subtracted out. This enabled a comparison for five molecular models of C60D36, with symmetries T, Th , S 6 and two D 3 d isomers, with the experimental G(r). This specimen of C60D36 was found to be best described by a T symmetry isomer, in agreement with 13C NMR and IR data for C60H36 [Attalla et al. (1993). J. Phys. Chem. pp. 6329–6331].