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Guanosine 5′-[β,γ-imido]triphosphate trisodium salt hydrate_Molecular_structure_CAS_148892-91-5)
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Guanosine 5′-[β,γ-imido]triphosphate trisodium salt hydrate

Catalog No. G0635 Name Sigma Aldrich
CAS Number 148892-91-5 Website http://www.sigmaaldrich.com
M. F. C10H14N6Na3O13P3 Telephone 1-800-521-8956
M. W. 588.141153 Fax
Purity ≥85% (HPLC) Email
Storage Chembase ID: 155143

SYNONYMS

IUPAC name
trisodium hydrogen {[({[(2R,3S,4R,5R)-5-(2-amino-6-hydroxy-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)phosphinato]amino}phosphonate
IUPAC Traditional name
trisodium hydrogen ({[(2R,3S,4R,5R)-5-(2-amino-6-hydroxypurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxyphosphinato)aminophosphonate
Synonyms
Gpp(NH)p
5′-Guanylyl-imidodiphosphate trisodium salt hydrate
β:γ-Imidoguanosine 5′-triphosphate trisodium salt hydrate
GMP-PNP

DATABASE IDS

MDL Number MFCD00084770
CAS Number 148892-91-5
PubChem SID 24895020

PROPERTIES

Empirical Formula (Hill Notation) C10H14N6Na3O13P3 · xH2O
Purity ≥85% (HPLC)
Shipped in dry ice
Apperance white powder
Solubility H2O: soluble50 mg/mL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36/37
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Application
Non-hydrolyzable analog of GTP; the preferred GTP analog to activate ADP-ribosylation factor.
Guanosine 5′-[β,γ-imido]triphosphate (GMP-PNP, Gpp(NH)p) is a non-hydrolyzable analog of GTP that binds and irreversibly activates G proteins. Gpp(NH)p is used in a variety of applications that involve GTP binding, including GTP-activation, GTP-inhibition, GTP transport, GTP hydrolysis, and GTP structure stabilization. Since a cycle of GTP binding, hydrolysis, and release is required for the initiation of protein translocation across the endoplasmic reticulum, guanosine 5′-[β,γ-imido]triphosphate is often used in studies of protein synthesis. Gpp(NH)p is used to activate ADP-ribosylation factors and to modulate G proteins involved in cell signaling, protein synthesis and other metabolic processes.
Biochem/physiol Actions
Binds and irreversibly activates G proteins.1 Since a cycle of GTP binding, hydrolysis, and release is required for the initiation of protein translocation across the endoplasmic reticulum, this non-hydrolyzable GTP analog is often used in studies of protein synthesis.2,3
Description (简体中文)
Application
Non-hydrolyzable analog of GTP; the preferred GTP analog to activate ADP-ribosylation factor.
Guanosine 5′-[β,γ-imido]triphosphate (GMP-PNP, Gpp(NH)p) is a non-hydrolyzable analog of GTP that binds and irreversibly activates G proteins. Gpp(NH)p is used in a variety of applications that involve GTP binding, including GTP-activation, GTP-inhibition, GTP transport, GTP hydrolysis, and GTP structure stabilization. Since a cycle of GTP binding, hydrolysis, and release is required for the initiation of protein translocation across the endoplasmic reticulum, guanosine 5′-[β,γ-imido]triphosphate is often used in studies of protein synthesis. Gpp(NH)p is used to activate ADP-ribosylation factors and to modulate G proteins involved in cell signaling, protein synthesis and other metabolic processes.
Biochem/physiol Actions
Binds and irreversibly activates G proteins.1 Since a cycle of GTP binding, hydrolysis, and release is required for the initiation of protein translocation across the endoplasmic reticulum, this non-hydrolyzable GTP analog is often used in studies of protein synthesis.2,3

REFERENCES