GUANOSINE 3′:5′-CYCLIC MONOPHOSPHATE SODIUM SALT CAS#: 40732-48-7; ChemWhat Code: 97108

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameGUANOSINE 3′:5′-CYCLIC MONOPHOSPHATE SODIUM SALT CAS#: 40732-48-7
Molecular StructureGUANOSINE-35-CYCLIC-MONOPHOSPHATE-SODIUM-SALT-CAS-40732-48-7
CAS Registry Number 40732-48-7
MDL NumberMFCD00038424
Synonyms40732-48-7
cyclic gmp
Guanosine 3′,5′-cyclic monophosphate sodium salt
Sodium guanosine cyclic monophosphate
Guanosine Monophosphate Monosodium Salt
Guanosine, cyclic 3′,5′-(hydrogen phosphate), monosodium salt
MFCD00038424
6WYT1TNR45
3′,5′-Cyclic GMP monosodium salt
Monosodium-GMP
GUANOSINE3:5-CYCLICMONOPHOSPHATESODIUMSALT
Guanosine-3′:5′-cyclic monophosphate monosodium salt
Cyclic GMP (sodium)
SODIUM 3′,5′-CYCLIC GMP ANION
sodium;9-[(4aR,6R,7R,7aS)-7-hydroxy-2-oxido-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-2-amino-1H-purin-6-one
sodium;9-[(4aR,6R,7R,7aS)-7-hydroxy-2-oxido-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-2-amino-3H-purin-6-one
Cyclic gmp sodium salt
UNII-6WYT1TNR45
EINECS 255-056-0
Cyclic 3′,5′-Guanosine Monophosphate Monosodium Salt
3′,5′-cGMP-Na
CYCLIC GMP, SODIUM SALT
DTXSID10961153
AKOS037646872
AS-71285
NS00074094
G76861
Guanosine 3′,5′-cyclophosphate monosodium salt
Guanosine 3:5-cyclic monophosphate sodium salt
guanosine 3′,5′-cyclic-monophosphate sodium salt
Guanosine 3’5′-cyclic Monophosphate, Sodium Salt
GUANOSINE 3, 5′-MONOPHOSPHATE, SODIUM SALT
Q27265640
Guanosine 3′,5′-cyclic monophosphate sodium salt, >=99.0% (HPLC)
Guanosine 3′,5′-cyclic monophosphate sodium salt, >=99% (HPLC), powder
Guanosine 3′,5′-cyclic Monophosphate, Sodium Salt – CAS 40732-48-7
GUANOSINE, CYCLIC 3′,5′-(HYDROGEN PHOSPHATE), SODIUM SALT (1:1)
Sodium (4aR,6R,7R,7aS)-6-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-7-hydroxytetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-2-olate 2-oxide
sodium (4aR,6R,7R,7aS)-6-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-7-hydroxy-2-oxo-hexahydro-2??-furo[3,2-d][1,3,2]dioxaphosphinin-2-olate
Molecular FormulaC10H11N5NaO7P
Molecular Weight367.19
InChIInChI=1S/C10H12N5O7P.Na/c11-10-13-7-4(8(17)14-10)12-2-15(7)9-5(16)6-3(21-9)1-20-23(18,19)22-6;/h2-3,5-6,9,16H,1H2,(H,18,19)(H3,11,13,14,17);/q;+1/p-1/t3-,5-,6-,9-;/m1./s1
InChI KeyKMPIYXNEROUNOG-GWTDSMLYSA-M
Isomeric SMILESC1[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=NC4=C3N=C(NC4=O)N)O)OP(=O)(O1)[O-].[Na+]

Physical Data

AppearanceWhite powder

Spectra

No data available


Route of Synthesis (ROS)

No data available


Safety and Hazards

GHS Hazard StatementsNot Classified

Source: European Chemicals Agency (ECHA)
License Note: Use of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is acknowledged as the source: “Source: European Chemicals Agency, http://echa.europa.eu/”. Such acknowledgement must be included in each copy of the material. ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions: Links can only be made to webpages that provide a link to the Legal Notice page.
License URL: https://echa.europa.eu/web/guest/legal-notice
Record Name: (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate
URL: https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/213446
Description: The information provided here is aggregated from the “Notified classification and labelling” from ECHA’s C&L Inventory. Read more: https://echa.europa.eu/information-on-chemicals/cl-inventory-database


Other Data

HS Code
Storage-20℃, sealed well and away from light
Shelf Life1 year
Market Price
Use Pattern
Sodium Guanosine-3′,5′-Cyclic Monophosphate (cGMP-Na) has several important applications in biochemistry, pharmacology, and biotechnology.
1. Signal Transduction Research
cGMP acts as an intracellular second messenger, playing a critical role in various biological signal transduction processes, such as smooth muscle relaxation, vasodilation, and neural signaling.
It is widely used to study guanylate cyclase activity and cGMP-dependent signaling pathways.
2. Pharmacological Studies
Used to investigate the effects of drugs targeting cGMP-related pathways, such as treatments for hypertension, erectile dysfunction (e.g., mechanisms of phosphodiesterase-5 inhibitors), and cardiovascular diseases.
Aids in new drug development and the evaluation of drug effects on cGMP-related processes.
3. Enzymology Research
Serves as a substrate for cGMP-dependent protein kinases and phosphodiesterases, enabling studies of enzyme mechanisms and their regulatory functions.
4. Cellular and Molecular Biology
Facilitates research on cGMP’s role in cell proliferation, differentiation, and apoptosis.
Applied in cellular models or tissue culture experiments to explore signaling pathway regulation.

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