Succinyl coenzyme A sodium salt
≥85%
Manufacturer: Sigma Aldrich
CAS Number: 108347-97-3
Synonym(S): Succinyl CoA sodium salt
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 MG | S1129-5-MG | In Stock | ₹ 28,567.18 |
| 25 MG | S1129-25-MG | In Stock | ₹ 94,556.38 |
S1129 - 5 MG
In Stock
Quantity
1
Base Price: ₹ 28,567.18
GST (18%): ₹ 5,142.092
Total Price: ₹ 33,709.272
Quality Level
200
Assay
≥85%
form
powder
solubility
water: 50 mg/mL, clear, colorless
storage temp.
−20°C
SMILES string
[Na+].[Na+].CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)([O-])=O)n2cnc3c(N)ncnc23)C(O)C(=O)NCCC(=O)NCCSC(=O)CCC([O-])=O
InChI
1S/C25H40N7O19P3S/c1-25(2,20(38)23(39)28-6-5-14(33)27-7-8-55-16(36)4-3-15(34)35)10-48-54(45,46)51-53(43,44)47-9-13-19(50-52(40,41)42)18(37)24(49-13)32-12-31-17-21(26)29-11-30-22(17)32/h11-13,18-20,24,37-38H,3-10H2,1-2H3,(H,27,33)(H,28,39)(H,34,35)(H,43,44)(H,45,46)(H2,26,29,30)(H2,40,41,42)/p-2/t13-,18-,19-,20?,24-/m1/s1
InChI key
VNOYUJKHFWYWIR-FZEDXVDRSA-L
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Sigma Aldrich Fine Chemicals Biosciences Succinyl coenzyme A sodium salt | 108347-97-3 | MFCD00057770 | 25 mg | Sigma Aldrich Fine Chemicals Biosciences | ₹ 1,00,960.80 | |
 | Succinyl-Coenzyme A (sodium) | ChemScene | ₹ 17,967.60 - ₹ 51,336.00 | |
 | 108347-97-3 | Coenzyme A, S-(hydrogen butanedioate), xsodium salt | A2B Chem | ₹ 4,363.56 - ₹ 29,004.84 |
Related Products
Description
- Application: Succinyl coenzyme A sodium salt has been used: for the nonenzymatic succinylation of lysine in vitro[1], as a substrate for adipic acid biosynthesis in recombinant E. coli [2] in isocitrate dehydrogenase (ICDH) treatment for the succinylation of proteins[3]as a substrate to study the specificity and kinetics of enzymes such as acetate:succinate CoA-transferase and 5-aminolevulinate synthase (ALA synthase)
- Biochem/physiol Actions: Succinyl CoA is an intermediate in the citric acid cycle.[4] It is formed by α-ketoglutarate dehydrogenase by the decarboxylation of α-ketoglutarate. Succinyl CoA is also formed from propionyl CoA during the β-oxidation of odd-chain fatty acids.[5] Succinyl CoA serves as a precursor in heme synthesis. It is also required for the oxidation of ketone bodies.
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
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Quality Level: 200
Assay: ≥85%
form: powder
solubility: water: 50 mg/mL, clear, colorless
storage temp.: −20°C
SMILES string: [Na+].[Na+].CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)([O-])=O)n2cnc3c(N)ncnc23)C(O)C(=O)NCCC(=O)NCCSC(=O)CCC([O-])=O
InChI: 1S/C25H40N7O19P3S/c1-25(2,20(38)23(39)28-6-5-14(33)27-7-8-55-16(36)4-3-15(34)35)10-48-54(45,46)51-53(43,44)47-9-13-19(50-52(40,41)42)18(37)24(49-13)32-12-31-17-21(26)29-11-30-22(17)32/h11-13,18-20,24,37-38H,3-10H2,1-2H3,(H,27,33)(H,28,39)(H,34,35)(H,43,44)(H,45,46)(H2,26,29,30)(H2,40,41,42)/p-2/t13-,18-,19-,20?,24-/m1/s1
InChI key: VNOYUJKHFWYWIR-FZEDXVDRSA-L
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