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lindenenol

$180

  • Brand : BIOFRON

  • Catalogue Number : AV-H23025

  • Specification : 98%

  • CAS number : 26146-27-0

  • Formula : C15H18O2

  • Molecular Weight : 230.3

  • PUBCHEM ID : 497203

  • Volume : 20mg

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Catalogue Number

AV-H23025

Analysis Method

HPLC,NMR,MS

Specification

98%

Storage

2-8°C

Molecular Weight

230.3

Appearance

Powder

Botanical Source

Lindera aggregata( Sims) Kosterm.

Structure Type

Sesquiterpenoids

Category

Standards;Natural Pytochemical;API

SMILES

CC1=COC2=C1C(C3C(=C)C4CC4C3(C2)C)O

Synonyms

Cycloprop(2,3)indeno(5,6-b)furan-4-ol, 4,4a,5,5a,6,6a,6b,7-octahydro-3,6b-dimethyl-5-methylene-, (4R,4aS,5aS,6aR,6bS)-/Cycloprop[2,3]indeno[5,6-b]furan-4-ol, 4,4a,5,5a,6,6a,6b,7-octahydro-3,6b-dimethyl-5-methylene-, (4R,4aS,5aS,6aR,6bS)-/Linderenol/(4R,4aS,5aS,6aR,6bS)-3,6b-Dimethyl-5-methylene-4,4a,5,5a,6,6a,6b,7-octahydrocyclopropa[2,3]indeno[5,6-b]furan-4-ol/Linderene

IUPAC Name

(1S,2R,9S,10R,12S)-4,9-dimethyl-13-methylidene-6-oxatetracyclo[7.4.0.03,7.010,12]trideca-3(7),4-dien-2-ol

Applications

Density

1.2±0.1 g/cm3

Solubility

Methanol; Acetontrile; Ethyl Acetate; DMSO

Flash Point

114.3±24.6 °C

Boiling Point

265.4±30.0 °C at 760 mmHg

Melting Point

145-147℃ (methanol )

InChl

InChI=1S/C15H18O2/c1-7-6-17-11-5-15(3)10-4-9(10)8(2)13(15)14(16)12(7)11/h6,9-10,13-14,16H,2,4-5H2,1,3H3/t9-,10-,13-,14+,15+/m1/s1

InChl Key

XRDJYSVGPBJZSG-PSDLAXTLSA-N

WGK Germany

RID/ADR

HS Code Reference

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:26146-27-0) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

30642244

Abstract

Background
The apomictic reproductive mode of Brachiaria (syn. Urochloa) forage species allows breeders to faithfully propagate heterozygous genotypes through seed over multiple generations. In Brachiaria, reproductive mode segregates as single dominant locus, the apospory-specific genomic region (ASGR). The AGSR has been mapped to an area of reduced recombination on Brachiaria decumbens chromosome 5. A primer pair designed within ASGR-BABY BOOM-like (BBML), the candidate gene for the parthenogenesis component of apomixis in Pennisetum squamulatum, was diagnostic for reproductive mode in the closely related species B. ruziziensis, B. brizantha, and B. decumbens. In this study, we used a mapping population of the distantly related commercial species B. humidicola to map the ASGR and test for conservation of ASGR-BBML sequences across Brachiaria species.

Results
Dense genetic maps were constructed for the maternal and paternal genomes of a hexaploid (2n = 6x = 36) B. humidicola F1 mapping population (n = 102) using genotyping-by-sequencing, simple sequence repeat, amplified fragment length polymorphism, and transcriptome derived single nucleotide polymorphism markers. Comparative genomics with Setaria italica provided confirmation for x = 6 as the base chromosome number of B. humidicola. High resolution molecular karyotyping indicated that the six homologous chromosomes of the sexual female parent paired at random, whereas preferential pairing of subgenomes was observed in the apomictic male parent. Furthermore, evidence for compensated aneuploidy was found in the apomictic parent, with only five homologous linkage groups identified for chromosome 5 and seven homologous linkage groups of chromosome 6. The ASGR mapped to B. humidicola chromosome 1, a region syntenic with chromosomes 1 and 7 of S. italica. The ASGR-BBML specific PCR product cosegregated with the ASGR in the F1 mapping population, despite its location on a different carrier chromosome than B. decumbens.

Conclusions
The first dense molecular maps of B. humidicola provide strong support for cytogenetic evidence indicating a base chromosome number of six in this species. Furthermore, these results show conservation of the ASGR across the Paniceae in different chromosomal backgrounds and support postulation of the ASGR-BBML as candidate genes for the parthenogenesis component of apomixis.

Electronic supplementary material
The online version of this article (10.1186/s12864-018-5392-4) contains supplementary material, which is available to authorized users.

KEYWORDS

Apomixis, Apospory, Parthenogenesis, BABY BOOM, Aneuploidy, Segmental allopolyploidy, Genotyping-by-sequencing, Molecular karyotyping, Urochloa, Brachiaria

Title

Translocation of a parthenogenesis gene candidate to an alternate carrier chromosome in apomictic Brachiaria humidicola

Author

Margaret Worthington,corresponding author1,5 Masumi Ebina,2 Naoki Yamanaka,3 Christopher Heffelfinger,4 Constanza Quintero,1 Yeny Patricia Zapata,1 Juan Guillermo Perez,1 Michael Selvaraj,1 Manabu Ishitani,1 Jorge Duitama,1,6 Juan Fernando de la Hoz,1,7 Idupulapati Rao,1,8 Stephen Dellaporta,4 Joe Tohme,1 and Jacobo Arango1

Publish date

2019 Jan 14.

PMID

27184859

Abstract

Nitrogen-doped (N-doped) graphene has been prepared by a simple one-step hydrothermal approach using hexamethylenetetramine (HMTA) as single carbon and nitrogen source. In this hydrothermal process, HMTA pyrolyzes at high temperature and the N-doped graphene subsequently self-assembles on the surface of MgO particles (formed by the Mg powder reacting with H2O) during which graphene synthesis and nitrogen doping are simultaneously achieved. The as-synthesized graphene with incorporation of nitrogen groups possesses unique structure including thin layer thickness, high surface area, mesopores and vacancies. These structural features and their synergistic effects could not only improve ions and electrons transportation with nanometer-scale diffusion distances but also promote the penetration of electrolyte. The N-doped graphene exhibits high reversible capacity, superior rate capability as well as long-term cycling stability, which demonstrate that the N-doped graphene with great potential to be an efficient electrode material. The experimental results provide a new hydrothermal route to synthesize N-doped graphene with potential application for advanced energy storage, as well as useful information to design new graphene materials.

In the past decade, graphene has attracted wide attentions due to its fascinating characters and broad applications1,2 such as in catalysis, water splitting, energy storage and solar cells. These applications of graphene are closely associated with their intrinsic two-dimensional (2-D) crystal structure formed by sp2 hybridized carbon1. In the past few years, many researchers have demonstrated that the physical and chemical properties of graphene could be tailored and improved by heteroatom doping on graphene sheets at edges, vacancies, pores and strained regions3,4. The doping of heteroatoms into the pristine graphene sheets would lead to structural and electronic disorders, which could further result in changes of graphene properties, including Fermi level, bandgap, localized electronic state, thermal stability, electrical conductivity, and magnetic property5. New or improved properties could be obtained by altering the type and content of various dopant atoms6,7.

Nitrogen (1s22s22p3)3 is the next element to carbon (1s22s22p2) in the periodic table with only one less valence electron, which possesses higher electronegativity of N (χ = 3.04) than that of C (χ = 2.55). The doping of N would create polarization in the sp2 carbon network, thereby further influence the chemical and physical properties of graphene. Previous reports demonstrated that N doping is efficient in tuning the characters of graphene materials: the bandgap opening and charge-carrier concentration could be induced by only 0.4 at% doping of graphitic N8; pyrrolic N-doping at the edge sites of graphene nanoribbons (GNR) would create strong magnetic moments9; the work function of graphene could be reduced by graphitic and pyridinic N-doping10,11. In this case, nitrogen doping is a useful route for decorating graphene because N-doping easily manipulates local electronic for the potential application including electronic devices8, biosensors12 and catalysts13. Moreover, the nitrogen doped local electronic structures allow for enhanced binding with ions in the solution which is beneficial for lithium ion batteries14. Nitrogen-doping would improve the pore affinity to aqueous electrolyte and reduce the electric resistance which would further promote the electrochemical performance of graphene electrode15,16. For example, nitrogen-doped graphene nanosheets prepared by heat treatment of graphite oxide under an ammonia atmosphere at 800 °C exhibited a high reversible capacity 900 mAh/g at current of 42 mA/g17; nitrogen-doped holey graphene hollow microspheres synthesized by a template sacrificing method also exhibited high reversible capacities and rate performances18.

To date, N-doped graphene materials can be obtained by various methods including plasma method14, arc-discharge approach19, chemical vapor deposition (CVD)20 and thermal anealing method21,22. Among these methods, nitrogen-containing functional groups could be doped by reacting with nitrogen-containing reagents (urea, NH3 and nitric acid)23,24 or through carbonizing/activating of nitrogen-rich carbon precursors, such as pentachloropyridine25, polypyrrole26 and pyrimidine27. These methods either require high quality equipment or involve several steps during synthesis process, which are obstacles for large scale fabrication. One step hydrothermal carbonization is a traditional method which is an important technique for the preperation of various carbonaceous materials and hybrids. Recent studies have shown that hydrothermal method is an efficient method for large-scale preparation of graphene: graphene oxide(GO) prepared by oxidation of graphite powder according to the modified Hummers’ method was further reduced by a nitrogen containing reductant and finally transferred into N-doped graphene28,29.

In this paper, we developed a novel one-step hydrothermal method using HMTA as single carbon and nitrogen source. Briefly, HMTA pyrolyzes in high temperature and the N-doped graphene subsequently self-assembles on the surface of MgO particles (formed by the Mg powder reacting with H2O). During this in-situ approach, graphene synthesis and nitrogen doping are simultaneously achieved. The as-synthesized graphene with nitrogen-containing functional groups possesses an average thickness of 4-10 nm with interconnected mesoporous system. The high surface area, mesopores and vacancies of the N-doped graphene are particularly beneficial for the reversibly storage of lithium ions. These structural features and their synergistic effects would promote ions and electrons transportation with nanometer-scale diffusion distances as well as be favorable to the penetration of electrolyte. Extensive research carried out on lithium ion batteries demonstrate that the N-doped graphene electrode exhibits high reversible capacity, superior rate capability as well as long-term cycling stability (above 600 mAh/g after 50 cycles at current of 100 mA/g, above 500 mAh/g after 150 cycles at current of 200 mA/g), which suggest its great potential to be an efficient electrode material candidate.

Title

One-pot hydrothermal synthesis of Nitrogen-doped graphene as high-performance anode materials for lithium ion batteries

Author

Zheng Xing,1 Zhicheng Ju,a,1 Yulong Zhao,1 Jialu Wan,1 Yabo Zhu,1 Yinghuai Qiang,b,1 and Yitai Qian2

Publish date

2016 May 17.

PMID

22674577

Abstract

Segregation of the bacterial multidrug resistance plasmid TP228 requires the centromere-binding protein ParG, the parH centromere, and the Walker box ATPase ParF. The cycling of ParF between ADP- and ATP-bound states drives TP228 partition; ATP binding stimulates ParF polymerization, which is essential for segregation, whereas ADP binding antagonizes polymerization and inhibits DNA partition. The molecular mechanism involved in this adenine nucleotide switch is unclear. Moreover, it is unknown how any Walker box protein polymerizes in an ATP-dependent manner. Here, we describe multiple ParF structures in ADP- and phosphomethylphosphonic acid adenylate ester (AMPPCP)-bound states. ParF-ADP is monomeric but dimerizes when complexed with AMPPCP. Strikingly, in ParF-AMPPCP structures, the dimers interact to create dimer-of-dimer “units” that generate a specific linear filament. Mutation of interface residues prevents both polymerization and DNA segregation in vivo. Thus, these data provide insight into a unique mechanism by which a Walker box protein forms polymers that involves the generation of ATP-induced dimer-of-dimer building blocks.

KEYWORDS

ATP, ATPases, Bacteria, Biophysics, X-ray Crystallography

Title

Structural Mechanism of ATP-induced Polymerization of the Partition Factor ParF

Author

Maria A. Schumacher,‡,1 Qiaozhen Ye,§ Madhuri T. Barge,¶ Massimiliano Zampini,? Daniela Barill?,¶,2 and Finbarr Hayes?,3

Publish date

2012 Jun 6