Adenosine 3′,5′-diphosphate disodium salt
≥96%
Manufacturer: Sigma Aldrich
CAS Number: 75431-54-8
Synonym(S): 3′-phosphoadenosine 5′-phosphate, 3′-phosphorylated nucleotide, PAP, 3′-Phosphoadenosine 5′-phosphate
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 10 MG | A5763-10-MG | In Stock | ₹ 24,269.65 |
| 25 MG | A5763-25-MG | In Stock | ₹ 56,852.90 |
| 100 MG | A5763-100-MG | In Stock | ₹ 1,57,211.48 |
A5763 - 10 MG
In Stock
Quantity
1
Base Price: ₹ 24,269.65
GST (18%): ₹ 4,368.537
Total Price: ₹ 28,638.187
biological source
synthetic (inorganic)
Quality Level
200
Assay
≥96%
form
powder
solubility
water: 25 mg/mL, clear, colorless to very faintly yellow
storage temp.
−20°C
SMILES string
[Na].Nc1ncnc2n(cnc12)C3OC(COP(O)(O)=O)C(OP(O)(O)=O)C3O
InChI
1S/C10H15N5O10P2.Na.H/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7(25-27(20,21)22)4(24-10)1-23-26(17,18)19;;/h2-4,6-7,10,16H,1H2,(H2,11,12,13)(H2,17,18,19)(H2,20,21,22);;
InChI key
ISROZYFZEAVMSP-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | 75431-54-8 | 3'-Adenylic acid,5'-(dihydrogen phosphate), disodium salt (9CI) | A2B Chem | ₹ 3,422.40 - ₹ 18,737.64 |
Related Products
Description
- General description: 3′-phosphoadenosine 5′-phosphate (PAP), a 3′-phosphorylated nucleotide is found in almost all organisms and is obtained as a by-product of sulfur and lipid metabolism.[1]
- Application: Adenosine 3′,5′-diphosphate disodium salt has been used: to spot sample on cellulose high-performance thin-layer chromatography (HPTLC) plates in two-dimensional thin layer chromatography[2]in enzyme activity assay to study the activities of HOS2/FIERY1 wild typehos2 mutant and fiery1?2 mutant protein against 3′-phosphoadenosine 5′-phosphate (PAP)[3]as a standard for the quantification of phosphoadenosines[4]
- Biochem/physiol Actions: 3′-phosphoadenosine 5′-phosphate (PAP) is capable of blocking exoribonucleases (XRNs) activity in the nucleus and cytosol. It stimulates stomatal closure and can serve as a secondary messenger during abscisic acid (ABA) signaling.[5] It is capable of blocking RNA catabolism. Hence it may serve as a physiological modulator of poly (ADP-ribose) polymerase 1 (PARP1) activity.[1]
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
biological source: synthetic (inorganic)
Quality Level: 200
Assay: ≥96%
form: powder
solubility: water: 25 mg/mL, clear, colorless to very faintly yellow
storage temp.: −20°C
SMILES string: [Na].Nc1ncnc2n(cnc12)C3OC(COP(O)(O)=O)C(OP(O)(O)=O)C3O
InChI: 1S/C10H15N5O10P2.Na.H/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7(25-27(20,21)22)4(24-10)1-23-26(17,18)19;;/h2-4,6-7,10,16H,1H2,(H2,11,12,13)(H2,17,18,19)(H2,20,21,22);;
InChI key: ISROZYFZEAVMSP-UHFFFAOYSA-N
biological source: __
Quality Level: 100
Assay: ≥98.0%
form: powder or crystals
solubility: water: soluble 132 g/L at 20 °C
storage temp.: __
SMILES string: N.N.OP(O)(O)=O
InChI: 1S/2H3N.H3O4P/c;;1-5(2,3)4/h2*1H3;(H3,1,2,3,4)
InChI key: MNNHAPBLZZVQHP-UHFFFAOYSA-N
biological source: __
Quality Level: 100
Assay: ≥98.0%
form: powder or crystals
solubility: water: soluble 132 g/L at 20 °C
storage temp.: __
SMILES string: N.N.OP(O)(O)=O
InChI: 1S/2H3N.H3O4P/c;;1-5(2,3)4/h2*1H3;(H3,1,2,3,4)
InChI key: MNNHAPBLZZVQHP-UHFFFAOYSA-N
