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Key Documents

B2557

Sigma-Aldrich

8-Bromo-2′-monobutyryladenosine-3′,5′-cyclic monophosphorothioate, Rp-isomer

>97% (HPLC), solid

Synonym(s):

Rp-8-Br-MB-cAMPS

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About This Item

Empirical Formula (Hill Notation):
C14H16BrN5O6PSNa
Molecular Weight:
516.24
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.77

Quality Level

Assay

>97% (HPLC)

form

solid

packaging

vial of 5 μmol (2.5 mg solid)

solubility

water: soluble

storage temp.

−20°C

SMILES string

CCCC(=O)O[C@@H]1[C@@H]2O[P@](O)(=S)OC[C@H]2O[C@H]1n3c(Br)nc4c(N)ncnc34

InChI

1S/C14H17BrN5O6PS/c1-2-3-7(21)25-10-9-6(4-23-27(22,28)26-9)24-13(10)20-12-8(19-14(20)15)11(16)17-5-18-12/h5-6,9-10,13H,2-4H2,1H3,(H,22,28)(H2,16,17,18)/t6-,9-,10-,13-,27-/m1/s1

InChI key

KWTXVSKODFLFLA-WJCFKVOZSA-N

Application

Lipophilic precursor that is more lipophilic and membrane-permeable compared to Rp-8-Br-cAMPS.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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V Ruiz-Velasco et al.
Circulation research, 82(5), 557-565 (1998-04-07)
Cyclic nucleotides are known to modify voltage-gated (L-type) Ca2+ channel activity in vascular smooth muscle cells, but the exact mechanism(s) underlying these effects is not well defined. The purpose of the present study was to investigate the modulatory role of

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