Big Chemical Encyclopedia

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

Articles Figures Tables About

Guanylate

The ANP leceptoi exists in two forms, ANP and ANPg, both of which have been cloned. These membrane-bound guanylate cyclases have a single transmembrane domain, an intracellular protein kinase-like domain, and a catalytic cyclase domain, activation of which results in the accumulation of cychc guanosine monophosphate (cGMP). A third receptor subtype (ANP ) has been identified that does not have intrinsic guanylate cyclase activity and may play a role in the clearance of ANP. [Pg.528]

Clindamycin 3-phosphate [28708-34-17, antibacterially inactive in vitro, and the ribonucleotides clindamycin 3-(5 -cytidylate) [31186-90-0], clindamycin 3-(5 -adenylate) [31186-91-1], clindamycin 3-(5 -uridylate) [36010-69-2], and clindamycin 3-(5 -guanylate) [36010-70-5], all inactive in vitro, can be generated... [Pg.90]

Although the stmctures of ribavirin and selenazofutin are similar, they appear to exert their antiviral action at different enzyme sites along the same biochemical pathway. Selenazofutin forms the nicotinamide adenosiae dinucleotide (NAD) analogue, which inhibits IMP dehydrogenase by binding ia place of the NAD cofactor, and hence this potent reduction of guanylate pools is responsible for the antiviral effect of selenazofutin. [Pg.313]

DMTr = 4,4 -dimethoxytrityl Bj, 83, B3, B4 = adenyl, cytidyl, guanyl, thymidyl... [Pg.664]

Synthesis of l-guanyl-3-methylpyrazole (29) (86% yield) from pyrazole 13 and aqueous cyanamide has been claimed (94GEP4237687). [Pg.167]

The same compound (28) can be prepared from an A -guanyl or A -nitroguanyl derivative of 3-aminopropanol. ° Also A -(3-hydroxy-... [Pg.324]

Lefkowitz, R. J., Mullikin, D., and Caron, M. G. (1976). Regulation of P-adrenergic receptors by guanyl-5 -yl imidodiphosphate and other purine nucleotides. J. Biol. Chem. 251 4686-4692. [Pg.57]

Adaptor Proteins. Figure 1 Adaptor protein domains. A scheme of the domain structures of some well-characterized adaptor proteins is shown. Descriptions of domain characteristics are in main text except C2, binds to phospholipids GTPase activating protein (GAP) domain, inactivates small GTPases such as Ras Hect domain, enzymatic domain of ubiquitin ligases and GUK domain, guanylate kinase domain. For clarity, not all domains contained within these proteins are shown. [Pg.15]

A second class of neuronal calcium sensors is formed by the guanylate cyclase-activating protein (GCAP). The GCAPs are expressed only in the photoreceptor cells of the retina of vertebrates. Recoverins and GCAPs have antagonistic roles in phototransduction. [Pg.293]

A half-sandwich titanacarborane guanidinate complex is formed on treatment of the corresponding amide precursor with 1,3-dicyclohexylcarbodiimide (Scheme 106). The compounds have been employed as catalysts for the guanylation of amines (cf. Section V.C). ... [Pg.261]


See other pages where Guanylate is mentioned: [Pg.217]    [Pg.389]    [Pg.53]    [Pg.227]    [Pg.450]    [Pg.457]    [Pg.457]    [Pg.518]    [Pg.518]    [Pg.564]    [Pg.280]    [Pg.305]    [Pg.484]    [Pg.312]    [Pg.123]    [Pg.240]    [Pg.253]    [Pg.532]    [Pg.271]    [Pg.474]    [Pg.474]    [Pg.333]    [Pg.333]    [Pg.10]    [Pg.17]    [Pg.149]    [Pg.571]    [Pg.643]    [Pg.668]    [Pg.1144]    [Pg.328]    [Pg.579]    [Pg.336]    [Pg.51]    [Pg.6]    [Pg.328]    [Pg.328]   
See also in sourсe #XX -- [ Pg.280 ]

See also in sourсe #XX -- [ Pg.80 ]




SEARCH



1 -guanyl-32,5-dimethylpyrazole

3 ,5 -Cyclic guanylate

Azides, guanyl synthesis

Carbon monoxide guanylate cyclase activation

Cyclic Guanylate cyclase

Cytoplasmic guanylate cyclase

Disodium guanylate

Guanosine-2 -monophosphate Guanylic acid

Guanosine-5 -phosphate Guanylic acid

Guanyl aminotetrazole

Guanyl azide

Guanyl cyclase

Guanyl cyclases, transmembrane

Guanyl formation

Guanyl nucleotide exchange factor

Guanyl nucleotide receptor

Guanyl nucleotide-binding protein

Guanyl nucleotides

Guanyl radical

Guanyl soluble

Guanyl transferase

Guanyl urea

Guanyl-thiourea

Guanylate catabolism

Guanylate cyclase

Guanylate cyclase activation

Guanylate cyclase assay

Guanylate cyclase by nitric oxide

Guanylate cyclase cerebellum

Guanylate cyclase effects

Guanylate cyclase heme oxygenase

Guanylate cyclase moieties

Guanylate cyclase nitric oxide-mediated activation

Guanylate cyclase pathway

Guanylate cyclase radicals

Guanylate cyclase receptor system

Guanylate cyclase recombinant

Guanylate cyclase subunits

Guanylate cyclase-activating proteins

Guanylate deamination

Guanylate kinase

Guanylate kinase, inhibitors

Guanylate kinase, structure

Guanylate reductase

Guanylate synthesis from inosinate

Guanylate synthetase

Guanylate synthetase mechanism

Guanylate-binding protein 1, human

Guanylating reagents

Guanylation

Guanylation

Guanylic 2-deoxy

Guanylic acid

Guanylic acid 5 -phosphate

Guanylic acid hydrolysis

Guanylic acid sodium salt

Guanylic acid synthesis

Guanylic acid system

Guanylic acid, 35 -cyclic phosphate

Hormone-activated guanylate cyclase

Inosinate formation from guanylate

Inosine from guanylic acid

Insulin Guanylate cyclase

Kinases guanylate kinase

L-Guanyl-3,5-dimethylpyrazole

MAGUK (membrane-associated guanylate

Membrane-associated guanylate kinase

Membrane-associated guanylate kinase inverted-2 (MAGI

Nitric oxide guanyl cyclase activated

Of guanylic acid

Platelet activation guanyl cyclase

Receptors with guanylate cyclase activity

Retinal guanylate cyclase gene

Sodium 5 -Guanylate

Soluble guanylate cyclase

Soluble guanylate cyclase activation

Soluble guanylate cyclase activation mechanism

Soluble guanylate cyclase activation production

Soluble guanylate cyclase activation synthesis

© 2024 chempedia.info