Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Hydra system

Currently, only the Hydra system incorporates a measurement of toxicity to the adult to provide a comparison of the sensitivity of the embryo with that of the adult (Johnson et al., 1988). However, the Hydra screen has not been fully validated as being predictive of results in mammals, and has fallen from favor. Thus, a major goal of research directed toward developing an in vitro teratogen screen should be to find a simple yet appropriate measure of toxicity unrelated to development. This would allow the comparison of the dose for a 50% effect (ED50) on developmental toxicity as measured in vitro to an ED50 for adult toxicity in vitro. The validation... [Pg.289]

S CAW-OX Hydra ne Solutions to Control Ocygen Corrosion in Boiler Systems, Olin Corp., Stamford, Coim., 1988. [Pg.295]

Different samples of aqueous solution containing radionuclides of Co and Eu were prepared at different copper sulphate concentrations and constant polymer concentrations (pAM) of 15 mg/1. The addition of salt to the system was done to reduce both the repulsion forces between the radionuclides and the interaction between the polymeric chains [7]. The polymer efficiency for the prepared samples was determined, results are shown in Fig. 15. It is clear that the polymer efficiency for Eu " is higher than for Co. This can be explained by the difference in the tightly bound structured water associated with different cationic species [14,107]. On this basis, we expect that Co is more hydrated than Eu. This is due to the difference in the ionic size. The hydra-... [Pg.130]

Fig. 8.5 The polyp and medusa body forms characteristic of phylum Cnidaria are structurally similar, (a) The polyp form as seen in Hydra, (b) The medusa form is basically an upside-down polyp. The mouths are a primitive muscle system. Note the separation of organs. Fig. 8.5 The polyp and medusa body forms characteristic of phylum Cnidaria are structurally similar, (a) The polyp form as seen in Hydra, (b) The medusa form is basically an upside-down polyp. The mouths are a primitive muscle system. Note the separation of organs.
The function of peptides as first messengers is evolu-tionarily very old. In phylogenetic terms, neuropeptides were established very early as molecules effecting intercellular communication. In coelenterates, such as Hydra, there are many peptides used in neurotransmission, but many of the conventional neurotransmitter systems, such as acetylcholine (ACh), catecholamines and serotonin,... [Pg.318]

Fig. 3. Comparisons of wide-field (A) and confocal fluorescence images (B, mesoglea level C, apical) of rhodamine phalloidin-stained F-actin in a whole-mount hydra tentacle. The hydra was fixed and stained as described in Chapter 18. The bar represents 25 pm. All images were collected with a Nikon (New York) Microphot FX microscope (x40 objective lens). Confocal images were collected with the microscope connected to a Bio-Rad (Hercules, CA) MRC600 laser-scanning confocal system. Fig. 3. Comparisons of wide-field (A) and confocal fluorescence images (B, mesoglea level C, apical) of rhodamine phalloidin-stained F-actin in a whole-mount hydra tentacle. The hydra was fixed and stained as described in Chapter 18. The bar represents 25 pm. All images were collected with a Nikon (New York) Microphot FX microscope (x40 objective lens). Confocal images were collected with the microscope connected to a Bio-Rad (Hercules, CA) MRC600 laser-scanning confocal system.
The amplification of two different macrocyclic receptors for similar diastereomeric compounds has been observed by Sanders and coworkers [13]. A dynamic system of macrocyclic polyhydrazones ranging from dimer to at least undecamer was prepared from the indicated homochiral hydra-zone. Templating with quinine caused the percentage of cyclic tetramer to increase from 63 % to 91 %. The same experiment with quinidine, a diastereomer of quinine, instead amplified the dimer from 9% to 45% (Fig. 5.13). These species were characterized by HPLC and ESI MS. Association... [Pg.164]

Only a limited number of derivatives of this ring system have been reported in literature. The only efficient synthesis utilized azoaroyl-1,2,4-triazines. Thus, condensation of 138 with hydrazines afforded the hydra-zones (139), which give 140 on reflux in acetic acid [85MI2,85PHA(39)504] (Scheme 20). It has been reported that derivatives of 74 were synthesized by cyclization of pyrazoline-4,5-dion-4-isothiosemicarbazones and 4-amidinohydrazones in phenol at 180-200°C (88JPR57). [Pg.247]

Figure 2.15 Perhaps in a 2-D world, only creatures with primitive digestive systems would evolve—like Earthly planaria flatworms or hydra that only have one opening in the digestive system. They eat food and expel 2-D wastes from the same opening. Figure 2.15 Perhaps in a 2-D world, only creatures with primitive digestive systems would evolve—like Earthly planaria flatworms or hydra that only have one opening in the digestive system. They eat food and expel 2-D wastes from the same opening.
Pluto, with a diameter of 2300 km, has now been demoted from the smallest planet to one of the largest Kuiper belt objects. Pluto and its satellite Charon could be considered a binary system because they are closer in size than any other known celestial pair in the solar system and the barycenter of their orbits does not lie within either body. There are also two smaller moons, Nix and Hydra. All four bodies are likely KBOs with similar compositions. Pluto has a thin atmosphere containing N2, with minor CH4, CO, and Ar. Curiously, the face of Pluto oriented towards Charon contains more methane ice, and the opposite face contains more nitrogen and carbon monoxide ice. [Pg.416]

Caution. Never add the acid before the system is filled with vapor, as high concns of hydra-zoic acid may cause explns if air is present. Be careful to avoid leakage of acid vapor, as HNj is very poisonous... [Pg.614]

The electrochemical generation of a nitrilimine provides an entrance to a wide range of heterocyclic systems via anodic oxidation of aldehyde hydra-zones. The same reaction was used for annelation of various heterocyclic systems,86 e.g., substituted pyridines, quinolines, isoquinolines, indoles, imidazoles, benzimidazoles, and benzotriazoles. [Pg.261]

Cnidaria (coelenterates) have the simplest known nervous system. Simple amidated tetrapeptides, some of which are also found in molluscs, are among their neurotransmitters.331 EGRFamide and l-3- phenyllactyl-LRNamide are found in some sea anemones.332 When a hydra (Fig. 1-13) is cut into two pieces, one containing a head and one a foot, each piece reforms the missing end. The decapeptide head activator (Table 30-5) diffuses upward from the foot end and induces formation of a head. Similarly, a hormone produced by head cells... [Pg.1758]

It was interesting that a few Algols, namely, U Cep (Plavec 1983), RW Tauri (Plavec and Dobias 1983) and TT Hydrae, U Sge and UX Monocerotis (Plavec et al. 1984) were observed with the IUE satellite at principal eclipse. And on these images the resonance doublets of C IV, Si IV and N V are displayed in emission and, as far as intensities and sequence of intensities go, they behave like in the rest of the close binary systems, that is, C IV is the strongest feature of the three. [Pg.202]

Very primitive multicellular organisms, such as the hydra (e.g., Chlorohydra viriiissima, the ultimate simple feeding tube), have nervous systems that may only use simple proteins as neurotransmitters, suggesting that these proteins were the first signaling molecules used by primordial nervous systems. If we extract a few of these proteins from the brain of a typical Hydra and inject them in human neurons, they will actually produce similar signaling responses from those neurons. [Pg.131]

In fact, the proteins used by hydra in their nervous systems are identical to some of the proteins that our brains use to help us think and feel. These proteins are called neuropeptides. A neuropeptide is like a string of beads, and each bead is an amino acid. Neuropeptides may be assembled from only a few... [Pg.131]

For example liquid gas generators are described in which carbon-free compounds are used and which can also be reacted to form working gases without any slag, e.g. systems consisting of hydrazine/hydra-zine nitrate. [Pg.57]

Many heterocyclic bases can be oxidized to A-oxides with sodium perborate and acetic acid in the absence of metal catalysts.352 Use of a smaller excess of oxidant leads to diazo compounds.353 Aliphatic amines can be converted to nitroso products. Sodium perborate/acetic acid systems can also cleave hydra-zones, regenerating carbonyl compounds which have been protected by hydrazine formation.354... [Pg.146]

Similarly to the asymmetric synthesis by imines and oxazoline, there is also a chiral hydrazone, (S)-l-amino-2-(methoxymethyl)pyrrolidine 51a, which gives chiral hydra-zones on reaction with aldehydes and ketones104, and is able to form an intermolecular chelate with the methoxy group. Enders and coworkers used this system for enantioselec-tive aldol reaction105, and for synthesis of chiral ketone104 and aldehyde106 (equation 30). [Pg.1522]

Another example of a B-N-N system is that obtained by reaction of l,l-dimethyl-2,2-bis(trimethylstannyl)hydra-zine with dichloro-mesityl-borane giving, after removal of the solvents and sublimation of the Me3SnCl, the 2,2-bis(chloromesitylboryl)-l,l-dimethylhydrazine 12 as a colorless powder this compound possesses a diazoboratir-ane subsystem <1999EJI1765>. Compound 12 was characterized by multinuclear ( H, B) NMR and infrared... [Pg.517]

The use of sodium acetate trideuteriohydrate causes the selective incorporation of deuterium at the 8 carbon of the original unsaturated tosyl hydra-zone. This datum alone, however, does not warrant a clear distinction between the various possibilities open to this system, as Scheme 8.3 shows. [Pg.202]


See other pages where Hydra system is mentioned: [Pg.294]    [Pg.130]    [Pg.319]    [Pg.620]    [Pg.197]    [Pg.302]    [Pg.767]    [Pg.198]    [Pg.188]    [Pg.39]    [Pg.102]    [Pg.942]    [Pg.567]    [Pg.21]    [Pg.181]    [Pg.274]    [Pg.35]    [Pg.339]    [Pg.300]    [Pg.155]    [Pg.188]    [Pg.350]    [Pg.350]    [Pg.2305]    [Pg.517]   
See also in sourсe #XX -- [ Pg.289 ]




SEARCH



Hydra

© 2024 chempedia.info