Coenzyme A, oxidized lithium salt - ≥85%, high purity , CAS No.31664-36-5

  • ≥85%
Item Number
C463091
Grouped product items
SKUSizeAvailabilityPrice Qty
C463091-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$366.90
C463091-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$882.90

Basic Description

SynonymsCoa disulfide | 5NG | CoA-disulfide | [[(2~{S},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-4-oxidanyl-3-phosphonooxy-oxolan-2-yl]methoxy-oxidanyl-phosphoryl] [(3~{R})-4-[[3-[2-[2-[3-[[(2~{R})-4-[[[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-4-oxidanyl-3-
Specifications & Purity≥85%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

Description

Coenzyme A (CoA, CoASH, HSCoA) is a coenzyme that facilitates enzymatic acyl-group transfer reactions and supports the synthesis and oxidation of fatty acids. CoA is involved in the mechanisms of a wide variety of enzymes. CoA is a thiol compound subject to oxidation. Oxidized CoA may be used to study reduction systems (CoA disulfide reductase (CoADR) systems) that regenerate reduced CoA in vivo. Furthermore, oxidized CoA may be used to study unique functions of this molecule in vivo.

Names and Identifiers

IUPAC Name [[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(3R)-4-[[3-[2-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyldisulfanyl]ethylamino]-3-oxopropyl]amino]-3-hydroxy-2,2-dimethyl-4-oxobutyl] hydrogen phosphate
INCHI InChI=1S/C42H70N14O32P6S2/c1-41(2,15-81-93(75,76)87-91(71,72)79-13-21-29(85-89(65,66)67)27(59)39(83-21)55-19-53-25-33(43)49-17-51-35(25)55)31(61)37(63)47-7-5-23(57)45-9-11-95-96-12-10-46-24(58)6-8-48-38(64)32(62)42(3,4)16-82-94(77,78)88-92(73,74)80-14-22-30(86-90(68,69)70)28(60)40(84-22)56-20-54-26-34(44)50-18-52-36(26)56/h17-22,27-32,39-40,59-62H,5-16H2,1-4H3,(H,45,57)(H,46,58)(H,47,63)(H,48,64)(H,71,72)(H,73,74)(H,75,76)(H,77,78)(H2,43,49,51)(H2,44,50,52)(H2,65,66,67)(H2,68,69,70)/t21-,22-,27-,28-,29-,30-,31+,32+,39-,40-/m1/s1
InChi Key YAISMNQCMHVVLO-ODFVJXNFSA-N
Canonical SMILES CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSSCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=NC6=C(N=CN=C65)N)O)OP(=O)(O)O)O)O
Isomeric SMILES CC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCSSCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=NC6=C(N=CN=C65)N)O)OP(=O)(O)O)O)O
PubChem CID 169341
Molecular Weight 1533.1

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

Flash Point(°F)Not applicable
Flash Point(°C)Not applicable

Safety and Hazards(GHS)

Pictogram(s) GHS05
Signal Danger
Hazard Statements

H315:Causes skin irritation

H318:Causes serious eye damage

Precautionary Statements

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P264:Wash hands [and …] thoroughly after handling.

P362+P364:Take off contaminated clothing and wash it before reuse.

P332+P313:IF SKIN irritation occurs: Get medical advice/attention.

RIDADR NONH for all modes of transport

Related Documents

References

1. Gasmi L, McLennan AG.  (2001)  The mouse Nudt7 gene encodes a peroxisomal nudix hydrolase specific for coenzyme A and its derivatives..  Biochem J,  357  (Pt 1): (33-8).  [PMID:11415433] [10.1021/op500134e]
2. H F Gilbert,M D Stewart.  (1981-02-25)  Inactivation of hydroxymethylglutaryl-CoA reductase from yeast by coenzyme A disulfide..  The Journal of biological chemistry,  256  ((4)): (1782-1785).  [PMID:7007371]
3. S B delCardayre,K P Stock,G L Newton,R C Fahey,J E Davies.  (1998-04-16)  Coenzyme A disulfide reductase, the primary low molecular weight disulfide reductase from Staphylococcus aureus. Purification and characterization of the native enzyme..  The Journal of biological chemistry,  273  ((10)): (5744-5751).  [PMID:9488707]
4. S B delCardayre,J E Davies.  (1998-04-16)  Staphylococcus aureus coenzyme A disulfide reductase, a new subfamily of pyridine nucleotide-disulfide oxidoreductase. Sequence, expression, and analysis of cdr..  The Journal of biological chemistry,  273  ((10)): (5752-5757).  [PMID:9488708]
5. J Luba,V Charrier,A Claiborne.  (1999-03-03)  Coenzyme A-disulfide reductase from Staphylococcus aureus: evidence for asymmetric behavior on interaction with pyridine nucleotides..  Biochemistry,  38  ((9)): (2725-2737).  [PMID:10052943]
6. Dennis R Harris,Donald E Ward,Jeremy M Feasel,Kyle M Lancaster,Ryan D Murphy,T Conn Mallet,Edward J Crane.  (2005-02-22)  Discovery and characterization of a Coenzyme A disulfide reductase from Pyrococcus horikoshii. Implications for this disulfide metabolism of anaerobic hyperthermophiles..  The FEBS journal,  272  ((5)): (1189-1200).  [PMID:15720393]
7. T Conn Mallett,Jamie R Wallen,P Andrew Karplus,Hiroaki Sakai,Tomitake Tsukihara,Al Claiborne.  (2006-09-20)  Structure of coenzyme A-disulfide reductase from Staphylococcus aureus at 1.54 A resolution..  Biochemistry,  45  ((38)): (11278-11289).  [PMID:16981688]
8. Rob Ofman,Dave Speijer,René Leen,Ronald J A Wanders.  (2005-09-28)  Proteomic analysis of mouse kidney peroxisomes: identification of RP2p as a peroxisomal nudix hydrolase with acyl-CoA diphosphatase activity..  The Biochemical journal,  393  ((Pt 2)): (537-543).  [PMID:16185196]
9. Farhad Forouhar,In-Sun Lee,Jelena Vujcic,Slavoljub Vujcic,Jianwei Shen,Sergey M Vorobiev,Rong Xiao,Thomas B Acton,Gaetano T Montelione,Carl W Porter,Liang Tong.  (2005-10-08)  Structural and functional evidence for Bacillus subtilis PaiA as a novel N1-spermidine/spermine acetyltransferase..  The Journal of biological chemistry,  280  ((48)): (40328-40336).  [PMID:16210326]
10. Charles S Hummel,Kyle M Lancaster,Edward J Crane.  (2005-10-11)  Determination of coenzyme A levels in Pyrococcus furiosus and other Archaea: implications for a general role for coenzyme A in thermophiles..  FEMS microbiology letters,  252  ((2)): (229-234).  [PMID:16213671]
11. Julie A Boylan,Charles S Hummel,Stéphane Benoit,Jorge Garcia-Lara,Jennifer Treglown-Downey,Edward J Crane,Frank C Gherardini.  (2006-01-05)  Borrelia burgdorferi bb0728 encodes a coenzyme A disulphide reductase whose function suggests a role in intracellular redox and the oxidative stress response..  Molecular microbiology,  59  ((2)): (475-486).  [PMID:16390443]
12. Kevin D Revell,Bart Heldreth,Timothy E Long,Seyoung Jang,Edward Turos.  (2007-01-30)  N-thiolated beta-lactams: Studies on the mode of action and identification of a primary cellular target in Staphylococcus aureus..  Bioorganic & medicinal chemistry,  15  ((6)): (2453-2467).  [PMID:17258460]
13. Jamie R Wallen,Carleitta Paige,T Conn Mallett,P Andrew Karplus,Al Claiborne.  (2008-04-11)  Pyridine nucleotide complexes with Bacillus anthracis coenzyme A-disulfide reductase: a structural analysis of dual NAD(P)H specificity..  Biochemistry,  47  ((18)): (5182-5193).  [PMID:18399646]

Solution Calculators