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G8378

Sigma-Aldrich

Guanosine 5′-tetraphosphate tris salt

from Saccharomyces cerevisiae, ~95%

Sinônimo(s):

G-tetra-P

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About This Item

Fórmula empírica (Notação de Hill):
C10H17N5O17P4
Número CAS:
103213-27-0
Peso molecular:
603.16
Número MDL:
MFCD00058646
Código UNSPSC:
41106305
ID de substância PubChem:
329799979

fonte biológica

Saccharomyces cerevisiae

Ensaio

~95%

forma

solid

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

NC(CO)(CO)CO.NC1=Nc2c(ncn2[C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]3O)C(=O)N1

InChI

1S/C10H17N5O17P4.C4H11NO3/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(29-9)1-28-34(22,23)31-36(26,27)32-35(24,25)30-33(19,20)21;5-4(1-6,2-7)3-8/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H,24,25)(H,26,27)(H2,19,20,21)(H3,11,13,14,18);6-8H,1-3,5H2/t3-,5-,6-,9-;/m1./s1

chave InChI

ZEHPDAAYQIAYON-GWTDSMLYSA-N

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Ações bioquímicas/fisiológicas

Guanosine 5′-tetraphosphate (G-tetra-P) may be used as a substrate to study the specificity and kinetics of polyphosphatases (triphosphate tunnel metalloenzymes (TTMs)) and exopolyphosphatases. Also used as an inhibitor to study the kinetics and mechanism of various guanylate cyclases. Guanosine 5′-tetraphosphate may be used in various studies with adenosine-5′-tetraphosphate.

Pictogramas

Health hazard
GHS08

Palavra indicadora

Warning

Frases de perigo

H371

Classificações de perigo

STOT SE 2

Órgãos-alvo

Eyes,Central nervous system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Faylene A Lunn et al.
The Journal of biological chemistry, 283(4), 2010-2020 (2007-11-16)
Cytidine 5'-triphosphate synthase catalyzes the ATP-dependent formation of CTP from UTP using either NH(3) or l-glutamine (Gln) as the source of nitrogen. GTP acts as an allosteric effector promoting Gln hydrolysis but inhibiting Gln-dependent CTP formation at concentrations of >0.15
T V Kulakovskaya et al.
Biochemistry. Biokhimiia, 62(9), 1051-1052 (1998-02-11)
A cytosolic preparation of Saccharomyces cerevisiae is capable of hydrolyzing adenosine-5'-tetraphosphate and guanosine-5'-tetraphosphate with activities which are 1.5-2 times greater than that with polyP15. The apparent K(m) values for hydrolysis of adenosine-5'-tetraphosphate and guanosine-5'-tetraphosphate are 100 and 80 microM, respectively.
Ruchi Jain et al.
The Journal of biological chemistry, 283(45), 31047-31057 (2008-09-11)
Triphosphate tunnel metalloenzymes (TTMs) are a superfamily of phosphotransferases with a distinctive active site located within an eight-stranded beta barrel. The best understood family members are the eukaryal RNA triphosphatases, which catalyze the initial step in mRNA capping. The RNA
Jianmin Fang et al.
The Journal of biological chemistry, 282(44), 32501-32510 (2007-09-11)
We report the cloning, expression, purification, and characterization of the Trypanosoma cruzi exopolyphosphatase (TcPPX). The product of this gene (TcPPX), has 383 amino acids and a molecular mass of 43.1 kDa. TcPPX differs from most exopolyphosphatases in its preference for
A Garger et al.
Visual neuroscience, 18(4), 625-632 (2002-02-07)
The second messenger systems involved in the final stages of the phototransduction cascade in Limulus photoreceptors remain unclear. Excised patches of transducing membrane contain cGMP-gated channels, suggesting the involvement of cGMP in the excitation process. To further explore this possibility

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