Conformational features of peptide fragments of the C-end of histone H1

The conformational possibilities of four synthesized oligopeptides with the amino acid sequences 165–172, 173–184, 152–172, and 152–184 of the C-end of histone H1 of calf thymus above been studied in solution under various conditions by the method of circular dichroism.V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tadchik SSR, Dushanbe. Institute of Cytology, Academy of Sciences of the USSR, Leningrad. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 793–798, November–December, 1990.     

Study of the total histone of the cotton plant of variety 108-F

From two-day etiolated shoots of the cotton plant of variety 108-F we have isolated the total histone and purified it on a column of CM-cellulose. It has been shown by gel electrophoresis and amino acid analysis that the total histone of the cotton plant, like the total histone of wheat, consists of five main fractions, the amount of the lysine-rich fraction A₁ being greater in the cotton plant than in wheat (23% and 19%, respectively), and the amount of arginine-rich fraction A₄ being less (19.2 and 24.3%, respectively). The total histone of the cotton plant is less basic (ratio of basic amino acids to acidic amino acids in the cotton-plant histone 1.24, in wheat histone 1.9, and in calf thymus histone 1.78) but richer in lysine as compared with arginine than the histones of wheat and calf thymus.V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tadzhik SSR, Dushanbe. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 109–112, January–February 1980.     

A comparative study of the histones of some varieties of cotton plant

Tetraploid varieties of the cotton plant belonging to the medium- and thin-fibered types have been studied with respect to their histone/DNA ratio, their content of histone fractions, and the amino acid composition of the total histones. It has been shown that these varieties differ with respect to their contents of the lysine-rich histone fraction Hl, and also by the amounts of certain amino acids in the total histone.V. I. Nikitin Institute of Chemistry, Academy of Sciences of the TadzhSSR, Dushanbe. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 99–102, January–February, 1985.     

Triterpene glycosides from the holothurian Cucumaria frondosa

Two triterpene glycosides have been isolated from an alcoholic extract of the holothurianCucumaria frondosa collected in the Kola littoral, Barents Sea: the main component of the glycoside fraction — frondoside A (I) — and a minor component — frondoside A₁ (II).Pacific Ocean Institute of Bioorganic Chemistry, Far-Eastern Scientific Center, Russian Academy of Sciences, Vladivostok. Murmansk Marine Biological Institute. Russian Academy of Sciences, Dal'nie Zelentsy, Murmansk province. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 260–263, March–April, 1993.     

Synthesis of a fragment of histone H4 with the sequence 14–21

Summary A fragment of histone H4 with the sequence-Gly-Ala-Lys-Arg-His-Arg-Lys-Val- has been synthesized.V. I. Nikitin Institute of Chemistry, Academy of Sciences of the TadzhSSR, Dushanbe. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 48–51, January–February, 1979.     

High-performance liquid chromatography of the phytoecdysteroids ofMelandrium nutans

With the aid of high-performance liquid chromatography, six phytoecdysteroids have been detected in the butanolic fraction of extractive substances from the epigeal part ofMelandrium nutans L. Preparative separation has yielded ecdysterone and polypodine B.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Institute of Physiologically Active Substances, Academy of Sciences of the USSR, Chernogolovka. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 322–324, May–June, 1984.     

Crystal structure investigation of ternary molybdates Li3Ba2Ln3(MoO4)3 (Ln=Gd,Tm)

Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Institute of Physics, Siberian Branch, Russian Academy of Sciences. Buryat Institute of Natural Sciences, Siberian Branch, Russian Academy of Sciences. Translated from Zhurnal Strukturnoi Khimii, Vol. 33, No. 3, pp. 126–130, May–June, 1992.     

Chemical investigation ofHippopha? rhamnoides. II. Main components of the neutral reaction of the saponification products of an extract of the leaves of the sea buckthorn

The qualitative and quantitative compositions of the neutral fraction of the products of the saponification of a diethyl ether extract of a sea buckthorn leaves have been investigated. Fourteen triterpene compounds and eight aliphatic alcohols have been identified from the results of GLC, CMS, and PMR and also from their melting points.Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Institute of Catalysis, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 514–519, July–August, 1985.     

Synthesis of macrolide pheromones

This review considers pathways for the synthesis of macrocyclic lactones (macrolides) identified as components of pheromones of insects of the order Coleoptera (Cucujidae), genera Cryptolestes and Oryzaephilus —granary pests.Institute of Petrochemistry and Catalysis, Academy of Sciences of the Republic of Bashkortostan, Ufa. Institute of Organic Chemistry, Ufa Scientific Center, Russian Academy of Sciences, Ufa. Institute of Fine Organic Synthesis, Academy of Sciences of the Republic of Bashkortostan, Ufa. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 526–548, July–August, 1995. Original article submitted July 15, 1994.     

Structure of the 1:2 complex formed by the cis-anti-cis diastereomer of dicyclohexano-18-crown-6 with 2-methylbenzenesulfamide

Applied Physics Institute, Moldovian Academy of Sciences. Technical Physics Institute, Ukrainian Academy of Sciences. Translated from Zhurnal Strukturnoi Khimii, Vol. 33, No. 2, pp. 138–144, March–April, 1992.     

Magnetic resonance parameters and structure of substituted stannyloxyphenoxyl radicals: Investigation by means of ESR in the 2-mm band

Institute of Chemical Physics, Russian Academy of Sciences. Institute of Heteroorganic Compounds, Russian Academy of Sciences. Translated from Zhurnal Strukturnoi Khimii, Vol. 33, No. 5, pp. 69–77, September–October, 1992.     

Chemical composition of the low-molecular-mass fraction of Yersinia pseudotuberculosis as a function of the temperature of cultivation

The dependence of the chemical composition of the low-molecular-mass fraction of the microbial cells ofYersinia pseudotuberculosis (str. 2781) on the temperature of cultivation (6 and 37°C) has been investigated.Scientific-Research Institute of Epidemiology and Microbiology, Siberian Branch, Russian Academy of Medical Sciences, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, Nos. 3,4, pp. 312–316, May–August, 1992.     

Crystal structure of 1,2-bis-(phenylseleno)-1,2-dichlorethene

Vladimir State Pedagogical Institute. Institute for Elementorganic Compounds, Russian Academy of Sciences. Irkutsk Institute for Organic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated from Zhurnal Strukturnoi Khimii, Vol. 33, No. 4, pp. 153–154, July–August, 1992.     

New derivatives of (?)-neocembrene from the soft coral Sarcophyton trocheliophorum

A hexane extract of the soft coralSarcophyton trocheliophorum has yielded two new diterpenoids for which the structures of 13S-hydroxy-(–)-neocembrene and 13S-hydroxy-11,12-epoxy-(–)-neocembrene have been established.Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 535–540, July–August, 1988.     

Conformational features of peptide fragments of the C-end of histone H1

The conformational possibilities of four synthesized oligopeptides with the amino acid sequences 165–172, 173–184, 152–172, and 152–184 of the C-end of histone H1 of calf thymus above been studied in solution under various conditions by the method of circular dichroism. V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tadchik SSR, Dushanbe. Institute of Cytology, Academy of Sciences of the USSR, Leningrad. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 793–798, November–December, 1990.     

Insect pheromones and their analogs. XI. Synthesis of 2,6-dimethylhepta-1,6-dien-3-ol acetate — The sex attractant ofPseudococcus comstocki

A new synthesis of 2,6-dimethylhepta-1,6-dien-3-ol acetate (I) — the sex attractant of The Comstock mealybug — has been developed.Institute of Chemistry, Bashkir Branch, Academy of Sciences of the USSR, Ufa. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 259–261, March–April, 1985.