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Possible atropisomers linked by metals.

Possible average structures for Wijodak SESC-3 short-contact-time

Possible aziridinium ion intermediate 103 in the nucleophilic substitution of chlorine in Michael adducts of type 91

Possible B hydride valence structures.

Possible Ba sites in BaFe2S4. Sites for Ba, twelve coordinated by S face-capped tetragonal prism

Possible band organizations in conducting solids

Possible basal plane oxygen orderings in YBa2Cu306 5. Filled and open circles are occupied and unoccupied oxygen 0 with permission from JAI

Possible base pairing of isochromenone structures with guanine

Possible base stacked conformations for dinucleoside phosphates. Reprinted from V.A. Bloomfield, D.M. Crothers, and I. Tinoco, Jr.

Possible base-catalysed hydrolysis mechanism of NeuNAcOAr.

Possible base-pairing interactions for the quadruplex homodimer. Hoogsteen pairings of the parallel stranded PtDNA duplex requires protonation of the GC pair. Adapted from Ref. .

Possible base-pairing scheme for 34 and four cytosine-containing derivatives. Reproduced with permission from Ref. . Copyright 2000, Wiley-VCH.

POSSIBLE BEHAVIOUR OF A GASSY SYSTEM DURING RELIEF

Possible benefit of abnormal grain growth for pore shrinkage

Possible BI2 and NO complexes A-C and their spectra.

Possible bifunctional approach to Michael components of the organocatalyst 145a

Possible bifunctional interaction of the zwitterionic intermediate of the aza-MBH reaction with the chiral anion of a CIL-312, which contains a hydrogen-bond donor.

Possible binding interactions of fipronil with side chains of residues A2, T6 and L9 in the NCA site. Fipronil was docked into a model of the NCA binding site of a homopentameric mammalian CABAa-jSj receptor, after Ref , using the Schrddinger Suite 2006 Induced Fit Docking protocol Clide version 4.0, Schrddinger, LLC, New York, 2005 Prime version 1.5, Schrddinger, LLC, New York, 2005.

Possible binding mode of the dye rhodamine to peptides immobilized on polyethylene glycol-polystyrene beads the peptides bear acetoxymethyl end groups.

Possible binding modes for 2,2 -dipyridyl dithiocarbamate.

Possible binding modes for 3,5-dimethyIpyrazoIe dithiocaibamate.

Possible binding modes for AP-guanylhistamine.

Possible binding modes for the dithiocarbamate derived from phenylhydrazine.

Possible binding modes of amino acid side chains. The coordinated metal ion is indicated by the circle labeled M.

Possible binding modes of armed crown ether.



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