“…The title compound, C(13)H(13)BN(2)O, is one in a series of 1,3,2-benzodiaza­boroles featuring a 2-meth­oxy­phenyl substitution at the 2-position in the nitro­gen–boron heterocyle. …”
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“…The title compound, C(4)H(6)N(2)S(3), has two very similar mol­ecules per asymmetric unit. …”
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“…In the present study, Eu(3+)- and Dy(3+)-codoped uniform-shaped Y(2)O(3) submicron particles were prepared using the urea homogeneous precipitation method. …”
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“…Our study showed that PTX3 plasma levels are influenced by three PTX3 polymorphisms. …”
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“…Dimethylfumarate (DMF), an immune modulator and antioxidant, may function as an inhibitor of STAT3 and an activator of Nrf2. This study examined whether DMF inhibits adipogenic differentiation of 3T3-L1 preadipocytes by inhibiting STAT3 or activating Nrf2. …”
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“…Synthesis of phosphatidylinositol-3-phosphate (PI3P) by Vps34, a class III phosphatidylinositol 3-kinase (PI3K), is critical for the initial steps of autophagosome (AP) biogenesis. …”
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“…The title compound, [FeZr(2)(C(5)H(5))(4)Cl(2)(C(13)H(18)B(2))], is a heteronuclear complex that consists of a [3]ferrocenophane moiety substituted at each cyclo­penta­dienyl (Cp) ring by a BH(3) group; the BH(3) group is bonded via two H atoms to the Zr atom of the zirconocene chloride moiety in a bidentate fashion. …”
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“…Here we describe the conformational effects of AP sites substituted for 2′-deoxyadenosine in the first (ap7), second (ap13) or third (ap19) loop of the quadruplex formed in K(+) by the human telomere DNA 5′-d[AG(3)(TTAG(3))(3)]. CD spectra and electrophoresis reveal that the presence of AP sites does not hinder the formation of intramolecular quadruplexes. …”
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“…In the title compound, C(26)H(33)NO(2) [systematic name: (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(pyridin-3-yl)-2,3,4,7,8,9,10,11,12,13,14,15-dodeca­hydro-1H-cyclo­penta­[a]phenanthren-3-yl acetate], the steroid A, B, C and D rings adopt chair, half-chair, chair and envelope conformations, respectively. …”
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“…The hybrid halide perovskite CH(3)NH(3)PbI(3) has enabled solar cells to reach an efficiency of about 20%, demonstrating a pace for improvements with no precedents in the solar energy arena. …”
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“…CH(3)NH(3)PbI(3) was found to exhibit inverse solubility at high temperatures in γ-butyrolactone. …”
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“…Here, we report on the graphoepitaxial liquid-solid growth of nanowires of the photovoltaic compound CH(3)NH(3)PbI(3) in open nanofluidic channels. The guided growth, visualized in real-time with a simple optical microscope, undergoes through a metastable solvatomorph formation in polar aprotic solvents. …”
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“…As a model study presented in this work, in situ synchrotron radiation x-ray diffraction was combined with microscopy and gravimetric analysis to study the degradation process of CH(3)NH(3)PbI(3) in moisture, and the results reveal that: 1) intermediate monohydrated CH(3)NH(3)PbI(3)·H(2)O is detected in the degradation process of CH(3)NH(3)PbI(3) and the final decomposition products are PbI(2) and aqueous CH(3)NH(3)I; 2) the aqueous CH(3)NH(3)I could hardly further decompose into volatile CH(3)NH(2), HI or I(2); 3) the moisture disintegrate CH(3)NH(3)PbI(3) and then alter the distribution of the decomposition products, which leads to an incompletely-reversible reaction of CH(3)NH(3)PbI(3) hydrolysis and degrades the photoelectric properties. …”
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“…Its crystal structure is unique, with relatively strongly bound layers extending parallel to (020), defined by YO(8), CuO(4) and TeO(3) polyhedra, while the NO(3) (−) anions and one third of the water mol­ecules lie between those layers. …”
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“…Thus, we employed biochemical and structural biology approaches to investigate the interaction of the ING3 PHD finger (ING3(PHD)) with the active transcription mark H3K4me3. …”
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“…An unprecedentedly stable CH(3)NH(3)PbI(3) film synthesized by a modified chemical vapor transport method is demonstrated. …”
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“…Here we describe our bottom-up approach, showing that the bacterial type III effector AvrRxo1 of plant pathogens is an authentic phosphotransferase that produces two novel metabolites by phosphorylating nicotinamide/nicotinic acid adenine dinucleotide at the adenosine 3′-hydroxyl group. …”
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