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Z6 SAXS powder pattern from the same material.

Z6a and b. Photodiode circuits Reverse-bias photoconductivity

Z7 Chemical compositions of nonnal shock melts in the sample shocked at 37.6 GPa at loom temperature, and shock partial melts in the 863 C-preheated sample shocked at 22.8 GPa, normalized to the composition of the starting material. Note that shock partial melts are enriched in FeO and Xi02 and depleted in NaaO and FeO . Error bars give 1 sigma of analyses of melts.

Z7 presents data from a molecular sieve chromatographic. separation of plasma proteins according to their molecular weights. This experiment supplies evidence that the change in location of apo E resulted from transfer of this protein from HDI-s to chylomicrons. The data show that, in the fasting subject , the amount of apo E

Z8 A comparison of degradation in the film specimens predicted by the SLP model based on measured and modeled climate data

Z8 Schematic of the OH method of a sessile drop

Z8 Schematic representation of water softening using nanofiltration membrane

Z9 Examples of some transport mechanisms in concrete

Z9 Generalized vaccinia in an infant. From smallpox vaccination adverse reaction. CDC

Z9 Tubular SOFC design

ZACA-lipase-catalyzed kinetic resolution tandem protocol.

Zachariasen s random network model for AjBj glass.

Zachariasen s representation of the atomic arrangement in the crystal of A203.

Zachariasen s representation of the atomic arrangement in the crystal of compounds of the same composition, AjOj. After Ref. .

Zachman Framework.

Zahn s furrow

Zahn viscosity cup.

Zakarian s and Thomson s enantioselective syntheses of -maoecryslal V

Zakhari V. Karaoglanov

Zanamivir , an antiviral drug which inhibits viral sialidases and below the mechanism of hydrolysis of sialosides with the transition state 4 mimed by Zanamivir .

Zanamivir bound into the active site of influenza virus sialidase showing interactions to some of the conserved amino acid residues.

Zanamivir derivatives modified by replacement of the C-7 hydroxyl. Values in parentheses reflect the relative ability of the compounds to inhibit influenza A virus sialidase. The reference value for Zanamivir 1 is 1.0.

Zanamivir derivatives modified through alkylation of the C-7 hydroxyl group. Values in parentheses reflect IC50 values against influenza A virus in a plaque-reduction assay, and are relative to a reference value of 1.0 for Zanamivir .

Zanchetta single-pot processor.

Zanoterone isosteres.



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