2’3′-cGAMP sodium salt CAS#: 1441190-66-4; ChemWhat Code: 1491587

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

Identification

Product Name2’3′-cGAMP sodium salt
IUPAC Name2-amino-9-[(1R,6R,8R,9R,10S,15R,17R,18R)-8-(6-aminopurin-9-yl)-3,9,12,18-tetrahydroxy-3,12-dioxo-2,4,7,11,13,16-hexaoxa-3λ5,12λ5-diphosphatricyclo[13.2.1.06,10]octadecan-17-yl]-1H-purin-6-one
Molecular Structure
CAS Registry Number 1441190-66-4
EINECS NumberNo data available
MDL NumberNo data available
Beilstein Registry NumberNo data available
Synonyms2’3′-cGAMPCGAMP2′,3′-cGAMP2′-3′-cyclic-GMP-AMP2’,3’-cGAMPcyclic [G(2′,5′)pA(3′,5′)p]cyclic GMP-AMP
Molecular FormulaC20H24N10O13P2
Molecular Weight674.417
InChIInChI=1S/C20H24N10O13P2/c21-14-8-15(24-3-23-14)29(4-25-8)18-11(32)12-7(41-18)2-39-45(36,37)43-13-10(31)6(1-38-44(34,35)42-12)40-19(13)30-5-26-9-16(30)27-20(22)28-17(9)33/h3-7,10-13,18-19,31-32H,1-2H2,(H,34,35)(H,36,37)(H2,21,23,24)(H3,22,27,28,33)/t6-,7-,10-,11-,12-,13-,18-,19-/m1/s1
InChI KeyXRILCFTWUCUKJR-INFSMZHSSA-N
Canonical SMILESNc1nc2c(ncn2[C@@H]2O[C@@H]3COP(=O)(O)O[C@H]4C@@HC@HO[C@@H]4COP(=O)(O)O[C@@H]2[C@@H]3O)c(=O)[nH]1
Patent Information
Patent IDTitlePublication Date
WO2020/1787703’3′-CYCLIC DINUCLEOTIDES AND PRODRUGS THEREOF2020
WO2019/222500METHODS OF MODULATING ACTIVITY OF A CYCLIC DINUCLEOTIDE (CDN) WITH A CDN TRANSPORTER-MODULATING AGENT2019

Physical Data

AppearanceWhite powder
SolubilityNo data available
Flash PointNo data available
Refractive indexNo data available
SensitivityNo data available
Chromatographic data
HPLC (High performance liquid chromatography)
TLC (Thin layer chromatography)

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)Temperature (NMR Spectroscopy), °C Frequency (NMR Spectroscopy), MHz
HSQC (Heteronuclear Single Quantum Coherence), Spectrum1H, 13Cwater-d2, aq. phosphate buffer35300
HMBC (Heteronuclear Multiple Bond Coherence), Spectrum1H, 13Cwater-d2, aq. phosphate buffer3575
COSY (Correlation Spectroscopy), Spectrum1H, 1Hwater-d2, aq. phosphate buffer35
2’3′-cGAMP sodium salt CAS#: 1441190-66-4 NMR
Description (Mass Spectrometry)
liquid chromatography mass spectrometry (LCMS), spectrum
liquid chromatography mass spectrometry (LCMS), electrospray ionisation (ESI), spectrum

Route of Synthesis (ROS)

Route of Synthesis (ROS) of 2’3′-cGAMP sodium salt CAS# 1441190-66-4
Route of Synthesis (ROS) of 2’3′-cGAMP sodium salt CAS# 1441190-66-4
ConditionsYield
With DL-dithiothreitol; full length cyclic GMP-AMP synthase; sodium chloride; magnesium chloride; dsDNA In glycerol at 37℃; for 0.666667h; Catalytic behavior; Kinetics; Reagent/catalyst; Enzymatic reaction;

Safety and Hazards

GHS Hazard StatementsNot Classified

Other Data

TransportationNONH for all modes of transport
Under the room temperature and away from light
HS CodeNo data available
StorageStorage at -20 °
Shelf Life1 year
Market PriceUSD
Druglikeness
Lipinski rules component
Molecular Weight674.417
logP-4.491
HBA23
HBD7
Matching Lipinski Rules1
Veber rules component
Polar Surface Area (PSA)344.98
Rotatable Bond (RotB)2
Matching Veber Rules1
Use Pattern
Innate immunity research: Serves as a potent STING (Stimulat r of Interferon Genes) pathway agonist, widely used to study innate immune responses in humans and animals.
Cancer research: Activates the immune system, supporting stuies on tumor immunotherapy.
Vaccine adjuvant: Investigated for its potential to enhance vaccine efficacy.
Antiviral studies: Used in exploring mechanisms against DNA viruses and some RNA viruses.
Drug development: Employed as a candidate molecule or tool compound for developing novel immunomodulatory therapies.

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