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About This Item
Linear Formula:
C10H13N5 · CH3SO3H
CAS Number:
Molecular Weight:
299.35
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
41106305
MDL number:
InChI
1S/C10H13N5.CH4O3S/c11-9-8-10(13-5-12-9)15(6-14-8)7-3-1-2-4-7;1-5(2,3)4/h5-7H,1-4H2,(H2,11,12,13);1H3,(H,2,3,4)
SMILES string
CS(O)(=O)=O.Nc1ncnc2n(cnc12)C3CCCC3
InChI key
AJMDRSJHCYQPQI-UHFFFAOYSA-N
assay
≥98% (HPLC)
form
powder
color
white to beige
mp
180-183 °C (lit.)
solubility
H2O: 5 mg/mL, clear
storage temp.
room temp
Quality Level
Related Categories
Biochem/physiol Actions
A stable, cell-permeable, non-competitive adenylyl cyclase inhibitor that targets the P-site domain.
A stable, cell-permeable, non-competitive adenylyl cyclase inhibitor that targets the P-site domain. IC50 = 100 μM in detergent-dispersed rat brain preparation.
Features and Benefits
This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
wgk
WGK 3
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Yu Zhang et al.
Frontiers in neuroscience, 14, 364-364 (2020-05-16)
Electrical synapses between neurons exhibit a high degree of plasticity, which makes critical contributions to neuronal communication. The GABAergic parvalbumin-expressing (PV+) neurons in the thalamic reticular nucleus (TRN) interact with each other through electrical and chemical synapses. Plasticity of electrical
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Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.
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