8-pCPT-2-O-Me-cAMP-AM 13C6
| Chemical Name | 8-pCPT-2-O-Me-cAMP-AM 13C6 |
|---|---|
| Alternate Names | Adenosine Stable Isotopes, Stable Isotopes of Adenosine |
| CAT No. | CS-EK-00324 |
| CAS Registry# | 1152197-23-3 unlabeled |
| Category | Stable Isotopes |
| Stock | Enquire |
| Mol. Wt. | Not Available |
| Mol. For. | Not Available |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Adenosine |
| Canonical Smiles | CC(=O)OCOP1(=O)OCC2C(O1)C(C(O2)N3C4=NC=NC(=C4N=C3SC5=CC=C(C=C5)Cl)N)OC |
| InchIKey | FZMWUFYPEVDWPA-SILPBKOMSA-N |
| Inchl | InChI=1S/C20H21ClN5O8PS/c1-10(27)30-9-32-35(28)31-7-13-15(34-35)16(29-2)19(33-13)26-18-14(17(22)23-8-24-18)25-20(26)36-12-5-3-11(21)4-6-12/h3-6,8,13,15-16,19H,7,9H2,1-2H3,(H2,22,23,24)/t13-,15-,16-,19-,35?/m1/s1 |
| IUPAC | [(4aR,6R,7R,7aR)-6-[6-amino-8-(4-chlorophenyl)sulfanylpurin-9-yl]-7-methoxy-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-2-yl]oxymethyl acetate |
| Controlled | No |
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| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
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[13C6]-8-(4-Chlorophenylthio)-2'-O-methyladenosine 3',5'-(acetyloxy)methyl)-cyclic monophosphate is a complex chemical compound that is used for various research purposes. The compound contains 13 carbon atoms, which are all isotopically labeled with carbon-13. This isotope labeling is essential for tracking the compound during experiments and research studies.
The compound is a cyclic monophosphate derivative of 8-(4-Chlorophenylthio)-2'-O-methyladenosine, which is a potent inhibitor of cAMP-dependent protein kinase (PKA). The addition of the cyclic monophosphate group to the molecule increases its potency as a PKA inhibitor and also enhances its cellular permeability.
The acetyloxy group present in the compound is also essential for its function as it allows the compound to cross the cell membrane and reach its target site. The compound is commonly used in biochemistry and pharmacology research to study the role of PKA in various cellular processes.
In conclusion, [13C6]-8-(4-Chlorophenylthio)-2'-O-methyladenosine 3',5'-(acetyloxy)methyl)-cyclic monophosphate is a highly specialized chemical compound that is used for research purposes. Its isotopic labeling, cyclic monophosphate group, and acetyloxy group make it an ideal tool for studying the role of PKA in various cellular processes.
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Related Compounds
Adenosine 15N | Adenosine-5' 13C | Adenosine-3' 13C | Adenosine-3’,5’-cyclic-13C5 Monophosphate | Adenosine-1' 13C | Adenosine 13C5 | Adenosine-13C5 cyclic monophosphate sodium salt | Adenosine-2-d1 | Adenosine-2' 13C | N6-(N-Threonylcarbonyl)adenosine-13C4,15N | N6-Methyladenosine-d3 | Adenosine-13C10 15N5 | Adenosine 5'-Monophosphate 13C5 | Adenosine 15N N1-Oxide |