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| | 2-(6-Aminohexyl) aminoadenosine-3',5'-cyclic monophosphate Basic information |
| Product Name: | 2-(6-Aminohexyl) aminoadenosine-3',5'-cyclic monophosphate | | Synonyms: | 2-(6-aminohexylamino)adenosine-3’,5’-cyclicmonophosphate,sodiumsalt(2-aha-camp);2-AHA-CAMP;Adenosine, 2-[(6-aminohexyl)amino]-, cyclic 3',5'-(hydrogen phosphate);2-(6-AMINOHEXYL)AMINOADENOSINE-3',5'-CYCLIC MONOP...;2-(6-Aminohexyl) aminoadenosine-3',5'-cyclic monophosphate | | CAS: | 214276-80-9 | | MF: | C16H26N7O6P | | MW: | 443.39 | | EINECS: | | | Product Categories: | | | Mol File: | 214276-80-9.mol |  |
| | 2-(6-Aminohexyl) aminoadenosine-3',5'-cyclic monophosphate Chemical Properties |
| | 2-(6-Aminohexyl) aminoadenosine-3',5'-cyclic monophosphate Usage And Synthesis |
| Uses | 2-AHA-cAMP is an analogue of natural signal molecule cAMP and an activator of cAMP-dependent protein kinase. 2-AHA-cAMP has a free terminal primary amino group, which can be used for coupling to gels or fluorescent dyes[1]. | | Definition | ChEBI: 2-(6-aminohexylamino)-cAMP is a 3',5'-cyclic purine nucleotide that is 3',5'-cyclic AMP in which the hydrogen at position 2 on the purine fragment is replaced by a 6-aminohexylamino group It is a 3',5'-cyclic purine nucleotide, an adenyl ribonucleotide, a secondary amino compound and a primary amino compound. It is functionally related to a 3',5'-cyclic AMP. | | References | [1] Moll D, et al. Biomolecular interaction analysis in functional proteomics. J Neural Transm (Vienna). 2006 Aug;113(8):1015-32. DOI:10.1007/s00702-006-0515-5 |
| | 2-(6-Aminohexyl) aminoadenosine-3',5'-cyclic monophosphate Preparation Products And Raw materials |
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