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Biological activity, and

After an alignment of a set of molecules known to bind to the same receptor a comparative molecular field analysis CoMFA) makes it possible to determine and visuahze molecular interaction regions involved in hgand-receptor binding [51]. Further on, statistical methods such as partial least squares regression PLS) are applied to search for a correlation between CoMFA descriptors and biological activity. The CoMFA descriptors have been one of the most widely used set of descriptors. However, their apex has been reached. [Pg.428]

Comprehensive Catbanion Chemistry, edited by E. Buncel and T. Durst New Synthetic Method< ogy and Biologically Active Substances, edited by Z.-I. Yoshida... [Pg.281]

The correlations between chemical descriptors of molecular properties and biological activity, especially the activity of herbicides and/or plant growth regulators has been described (12). Several alternatives or improvements on the Hansch-Fujita QSAR system have been developed (13—15). [Pg.39]

Naphthalenedicarboxylic Acid. NaphthaUc acid readily dehydrates on heating to 1,8-naphthalenedicarboxyhc acid anhydride [81-84-5] (naphthahc anhydride) (41). The anhydride and its imide naphthaUmide [81-83-4] (R = H) (42) are intermediates for important dyes, pigments, optical bleaches, and biologically active compounds. [Pg.503]

Similar heterogeneous reactions also can occur, but somewhat less efticientiy, in the lower stratosphere on global sulfate clouds (ie, aerosols of sulfuric acid), which are formed by oxidation of SO2 and COS from volcanic and biological activity, respectively (80). The effect is most pronounced in the colder regions of the stratosphere at high latitudes. Indeed, the sulfate aerosols resulting from emptions of El Chicon in 1982 and Mt. Pinatubo in 1991 have been impHcated in subsequent reduced ozone concentrations (85). [Pg.496]

Absorption, metaboHsm, and biological activities of organic compounds are influenced by molecular interactions with asymmetric biomolecules. These interactions, which involve hydrophobic, electrostatic, inductive, dipole—dipole, hydrogen bonding, van der Waals forces, steric hindrance, and inclusion complex formation give rise to enantioselective differentiation (1,2). Within a series of similar stmctures, substantial differences in biological effects, molecular mechanism of action, distribution, or metaboHc events may be observed. Eor example, (R)-carvone [6485-40-1] (1) has the odor of spearrnint whereas (5)-carvone [2244-16-8] (2) has the odor of caraway (3,4). [Pg.237]

Fig. 7. The cycle of stmcmie-based dmg design. The conventional or basic cycle consists of a simple loop between chemical synthesis and biological activity. This cycle is typically initiated through a lead compound. Whereas this cycle remains the core of the dmg discovery process, the resources available... Fig. 7. The cycle of stmcmie-based dmg design. The conventional or basic cycle consists of a simple loop between chemical synthesis and biological activity. This cycle is typically initiated through a lead compound. Whereas this cycle remains the core of the dmg discovery process, the resources available...
Conformational analysis has been used to find and predict conformations which maximize antibiotic activity, using x-ray crystal stmctures coupled with nmr and cd spectra. An early approach utilized the Dale diamond lattice conformational model (480), which was extended to other diamond lattice models (472,481—483). Other studies have reHed on nmr data (225,484—491). However, extensive correlations between conformation and biological activity have not been successful (486,492). [Pg.109]

Efforts have been made to correlate electronic stmcture and biological activity in the tetracycline series (60,61). In both cases, the predicted activities are of the same order as observed in vitro with some exceptions. The most serious drawback to these calculations is the lack of carryover to in vivo antibacterial activity. Attempts have also been made (62) to correlate partition coefficients and antibacterial activity. The stereochemical requirements are somewhat better defined. Thus 4-epitetracycline and 5a-epitetracycline [65517-29-5] C22H24N20g, are inactive (63). The 6-epi compound [19369-52-9] is about one-half as active as the 6a (or natural) configuration. [Pg.180]

Recent publications indicate the cloud-point extraction by phases of nonionic surfactant as an effective procedure for preconcentrating and separation of metal ions, organic pollutants and biologically active compounds. The effectiveness of the cloud-point extraction is due to its high selectivity and the possibility to obtain high coefficients of absolute preconcentrating while analyzing small volumes of the sample. Besides, the cloud-point extraction with non-ionic surfactants insures the low-cost, simple and accurate analytic procedures. [Pg.50]

Contamination of waters with ai senic occurs as a result of a number of industrial activities such as treatment of industrial wastes, fertilizers, pesticides production, mining, metal smelting etc. and natural processes (e.g. weathering of minerals, volcanic and biological activities). [Pg.208]

One of the most important tasks in Analytical chemistry is the effective and express microquantity determination of toxic metals and biologically active organic materials in different objects of environment, raw materials and products of food technology and biotechnology. [Pg.404]

The held of marine natural products chemistry, which encompasses the study of the chemical structures and biological activities of secondary metabolites produced by marine plants, animals, and microorganisms, began in earnest in the early 1960s. " This is in stark contrast to the study of terrestrial plant natural... [Pg.61]

The organization of Part Two is according to structural type. The first section, Chapter Seven, is concerned with the synthesis of macrocyclic compounds. Syntheses of a number of heterocyclic target structures appear in Chapter Eight. Sesquiterpenoids and polycyclic higher isoprenoids are dealt with in Chapters Nine and Ten, respectively. The remainder of Part Two describes syntheses of prostanoids (Chapter Eleven) and biologically active acyclic polyenes including leukotrienes and other eicosanoids (Chapter Twelve). [Pg.99]

Modem Methods for the Introduction of Fluonne into Organic Molecules An Approach to Compounds with Altered Chemical and Biological Activities... [Pg.19]

Carbon-Fluorine Compounds Chemistry, Biochemistry, and Biological Activities A Ciba Foundation Symposium, Elsevier Amsterdam, 1972... [Pg.1018]

The Knorr pyrazole synthesis has been extensively utilized in the preparation of a number of pyrazoles as metal chelators, photographic dyes, herbicides, and biologically active... [Pg.297]

The use of the Hammett equation has also been extended to several new types of applications. Since these are not germane to the subject matter of the present chapter, we wiU simply mention work on applications to ethylenic and acetylenic compounds the various applications to physical properties, such as infrared frequencies and intensities, ultraviolet spectra, polarographic half-wave potentials, dipole moments,NMR and NQR spectra,and solubility data and applications to preparative data and biological activity. [Pg.212]

As described above, the chemistry of 1,2-dithietaiies is far from being developed. Tlierefore, development of excellent synthetic methods of 1,2-dithietanes is truly desired in order to understand their intrinsic nature associated with chemical reactivities, structure, and biological activities. [Pg.249]

Tire purpose of this chapter is to review the chemistry of the nitro-1,5-, -1,6-, -1,7-, and -1,8-naphthyridines (1) [nitro-2,6- and nitro-2,7-naph-thyridines (2) are unknown], with special attention to the results obtained in the laboratories of both authors. Tliis article mainly refers to the synthesis and reactivity of the nitronaphthyridines their physical and spectroscopic properties and biological activity are only covered briefly. For the convenience of the reader a table listing melting points of (di-)nitronaph-thyridines and some derivatives is included (Table III). Tire literature to about 1998 has been covered. [Pg.286]

Because of the number of citations, only selected imidazoquinolines are described, and biological activity is mentioned only briefly. The largest increase in the number of citations was caused by the discovery of the antibacterial properties of nalidixic acid type drugs. Efforts to prepare the bioisosters, for example of oxolinic acid, intensified in the early 1970s, and the discovery of the carcinogenic properties of 2-aminoimidazoquinolines followed in the early 1980s. These azoloquinolines can be considered as benzene-separated deazapurines. [Pg.191]

Synthesis and biological activity of glycosidopyrrole analogs of gancyclovir 97F281. [Pg.235]

Chemistry and biological activity of artemisinin (sesquiterpene y-lactone with oxepane fragment and transannular peroxide bridge) and related antimalari-als 99H(51)1681. [Pg.239]

Chemistry, physicochemical properties, and biological activities of N -oxygenated adenines 99H(51)1971. [Pg.261]


See other pages where Biological activity, and is mentioned: [Pg.495]    [Pg.224]    [Pg.70]    [Pg.387]    [Pg.263]    [Pg.272]    [Pg.272]    [Pg.276]    [Pg.420]    [Pg.103]    [Pg.82]    [Pg.123]    [Pg.273]    [Pg.286]    [Pg.56]    [Pg.340]    [Pg.360]    [Pg.538]    [Pg.61]    [Pg.261]    [Pg.262]   
See also in sourсe #XX -- [ Pg.40 , Pg.41 , Pg.42 , Pg.43 , Pg.44 , Pg.45 , Pg.46 , Pg.47 ]




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Biological and Lipid Antioxidant Activity of Selenium

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Chirality, and biological activity

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Natural Products and Biologically Active Compounds

Natural and Synthetic Biologically Active Heterocycles

Natural and synthetic biologically-active

Naturally Occurring and Biologically Active Isoxazoles

Occurrence, Structure, and Biological Activity

Origin and Biological Activity

Other biological materials and biologically active substances

PG Structure and Biological Activities

Partition coefficients and biological activity

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References on Biological Activities of MDP and Derivatives

Relationships between Chemical Structure and Biological Activity

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Structural Biology and Structure-Activity Relationship Studies

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Syntheses of natural products and biologically active compounds

Synthesis and biological activities of condensed

The Law of Mass Action, binding sites and receptors—understanding why specific, potent biological activity is a rare property for any one chemical to possess

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