5,372 research outputs found
AdS. Klein-Gordon equation
I propose a generalization of the Klein-Gordon equation in the frame-work of AdS space-time and exhibit a four parameter family of solutions among which there is a two parameter family of time-dependent bound states
New Stereoselective Route to the Epoxyquinol Core of Manumycin-Type Natural Products. Synthesis of Enantiopure (+)-Bromoxone, (−)-LL-C10037α, and (+)-KT 8110
A practical route is decribed for the preparation of the C7N core of manumycin-type compounds.
Starting from p-benzoquinone, optically pure compounds in both forms can be prepared via
enzymatic resolution of a derived diacetoxy conduritol. A diepoxy aminoinositol is accessible which
can function for formation of enantiopure epoxyquinones and quinols. Examples are given for
acylation reactions of this amine with several acyl derivatives. With this approach (−)-LL-C10037α
and quinones such as (+)-KT-8110 with 5R,6S-configuration can be synthesized through oxidation.
In addition a short route to (+)-bromoxone is described. Most steps include simple epoxide formation
and cleavage reactions which all can be carried out in a high stereoselective manner
New Stereoselective Route to the Epoxyquinol Core of Manumycin-Type Natural Products. Synthesis of Enantiopure (+)-Bromoxone, (−)-LL-C10037α, and (+)-KT 8110
A practical route is decribed for the preparation of the C7N core of manumycin-type compounds.
Starting from p-benzoquinone, optically pure compounds in both forms can be prepared via
enzymatic resolution of a derived diacetoxy conduritol. A diepoxy aminoinositol is accessible which
can function for formation of enantiopure epoxyquinones and quinols. Examples are given for
acylation reactions of this amine with several acyl derivatives. With this approach (−)-LL-C10037α
and quinones such as (+)-KT-8110 with 5R,6S-configuration can be synthesized through oxidation.
In addition a short route to (+)-bromoxone is described. Most steps include simple epoxide formation
and cleavage reactions which all can be carried out in a high stereoselective manner
Trias orationum panegyricarum, laureatis honoribus reverendorum nobilium ac eruditorum dd. aa. ll. & philosophiae neo-magistrorum, promotore r. p. Francisco Szekely e Soc. Jesu aa. ll. & philosophiae doctore, ejusdemque professore emerito p. t. seniore, in alma Universitate Cassoviensi creatorum dedicata, a rhetoribus academicis Cossoviensibus, anno M. DC. LXXXXII. die [ ] mensis augusti
Trias orationum panegyricarum, laureatis honoribus reverendorum nobilium ac eruditorum dd. aa. ll. & philosophiae neo-magistrorum, promotore r. p. Francisco Szekely e Soc. Jesu aa. ll. & philosophiae doctore, ejusdemque professore emerito p. t. seniore, in alma Universitate Cassoviensi creatorum dedicata, a rhetoribus academicis Cossoviensibus, anno M. DC. LXXXXII. die [ ] mensis augusti [resursă electronică] . - Cassoviae [Kassa] : excudit Johannes Klein, [1692]. - [15] fol. ; 8°
Natalia LL - artystka neoawangardowa
The paper shows Natalia Lach-Lachowicz (Natalia LL) as a neo avant-garde artist whose works in a specific maximalistic way are very close to the main currents of avant-garde trends: new mediality (photography), minimalism, conceptualism, performance, bodyart, pop-art, and feminist art. The author of the article concentrates mainly on the mutual influences of conceptualism, consumptionism, and feminism in Natalia LL’s works and pays attention to the emancipatory potential of her works of the seventies and the eighties
Levinson's theorem for the Klein-Gordon equation in one dimension
In terms of the modified Sturm-Liouville theorem, the Levinson theorem for the one-dimensional Klein-Gordon equation with a symmetric potential V(x) is established.
It is shown that the number N+ (N-) of bound states with even (odd) parity is related to the phase shift of the scattering states with the same parity at zero momentum as
and
The solution of the one-dimensional Klein-Gordon equation with the energy
M or is called as a
half bound state if it is finite but does not decay fast enough at infinity to
be square integrable
Energy flux in isotropic turbulence under large variations of external forcing
We investigate the response of energy flux in isotropic turbulence to step-function like perturbation in external forcing at large length scales. From both physical experiments and direct numerical simulations, we measured the evolution of the Eulerian velocity structure functions, such as , , before and after the perturbation in forcing. In both cases, we observed the cascade of the energy excess at large scales cascade through scales to the dissipative range, which can be used to study the dynamics of the cascade, and in particular, to estimate the relevant time scales
Epigenetic mechanisms do not control viral latency III in primary effusion lymphoma cells infected with a recombinant Epstein-Barr virus.
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Some rhetorical strategies in later nineteenth-century laboring-class poetry
Structural and functional analysis of the pro-domain of human cathelicidin, LL-37
Cathelicidins form a family of small host defense peptides distinct from another class of cationic antimicrobial peptides, the defensins. They are expressed as large precursor molecules with a highly conserved pro-domain known as the cathelin-like domain (CLD). CLDs have high degrees of sequence homology to cathelin, a protein isolated from pig leukocytes and belonging to the cystatin family of cysteine protease inhibitors. In this report, we describe for the first time the X-ray crystal structure of the human CLD (hCLD) of the sole human cathelicidin, LL-37. The structure of hCLD, determined at 1.93 Å resolution, shows the cystatin-like fold and is highly similar to the structure of the CLD of the pig cathelicidin, protegrin-3. We assayed the in vitro antibacterial activities of hCLD, LL-37 and the precursor form, pro-cathelicidin (also known as hCAP18), and we found that the unprocessed protein inhibited the growth of Gramnegative bacteria with efficiencies comparable to the mature peptide, LL-37. In addition, the antibacterial activity of LL-37 was not inhibited by hCLD intermolecularly, since exogenously added hCLD had no effect on the bactericidal activity of the mature peptide. hCLD itself lacked antimicrobial function and did not inhibit the cysteine protease, cathepsin L. Our results contrast with previous reports of hCLD activity. A comparative structural analysis between hCLD and the cysteine protease inhibitor stefin A showed why hCLD is unable to function as an inhibitor of cysteine proteases. In this respect, the cystatin scaffold represents an ancestral structural platform from which proteins evolved divergently, with some losing inhibitory functions
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