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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Adenosine, 8-[(4-chlorophenyl)thio]-, cyclic 3',5'-[hydrogen(R)-phosphorothioate]

O[C@@H]1[C@@H]2OP(=S)([O-])OC[C@H]2O[C@H]1n1c(Sc2ccc(cc2)Cl)nc2c1ncnc2N.[Na+] Request for Quotation
Chemical Name: Adenosine, 8-[(4-chlorophenyl)thio]-, cyclic 3',5'-[hydrogen(R)-phosphorothioate]
CAS Number: 129735-01-9
Product Number: AG000TNA(AGN-PC-0PJ21K)
Synonyms:
MDL No: MFCD04113743
Molecular Formula: C16H14ClN5NaO5PS2
Molecular Weight: 509.8594

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Chemical Structure


Rp-8-CPT-cAMPS, a potent cell-permeable cyclic adenosine monophosphate (cAMP) analog, is frequently employed in chemical synthesis for its unique properties and applications. This molecule acts as a competitive antagonist of cAMP-dependent protein kinase A (PKA), thereby inhibiting the activation of PKA signaling pathways. In the realm of chemical synthesis, Rp-8-CPT-cAMPS serves as a valuable tool for studying cellular processes that are regulated by cAMP-mediated signaling.Additionally, Rp-8-CPT-cAMPS is utilized to investigate the role of cAMP in various biochemical pathways and to elucidate the mechanisms underlying cAMP-dependent signaling cascades. Its ability to selectively block the activation of PKA helps researchers discern the specific effects of cAMP on cellular functions, making it an indispensable component in studies related to signal transduction, gene expression, and cell proliferation.Furthermore, Rp-8-CPT-cAMPS has been instrumental in elucidating the intricate interplay between cAMP-dependent signaling pathways and various cellular processes, shedding light on the underlying molecular mechanisms that govern these interactions. Its precise mode of action and high specificity make Rp-8-CPT-cAMPS a valuable asset in chemical synthesis, enabling researchers to manipulate cAMP-dependent pathways with a high degree of control and specificity.