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Product
6-Bnz-8-PIP-cAMP 6-Bnz-8-PIP-cAMP is a stimulator of protein kinase A which has no activated effect on Epac. It can be active to the A site of cAK I in combination with site B I-selective analogues. Grades: ≥ 98% by HPLC. Molecular formula: C22H26N6O7P · Na. Mole weight: 540.4. BOC Sciences 2
6-Bnz-cAMP 6-Bnz-cAMP is a selective activator of cAMP-dependent protein kinase that can be used as an Epac-negative control. Compared to cAMP, it has a superior stability against PDE. Synonyms: N6- Benzoyladenosine- 3', 5'- cyclic monophosphate, sodium salt. Grades: ≥ 98% by HPLC. CAS No. 30275-80-0. Molecular formula: C17H15N5O7P · Na. Mole weight: 455.3. BOC Sciences 3
6-Bnz-cAMP-AM 6-Bnz-cAMP-AM is a precursor of 6-Bnz-cAMP, the specific PKA agonist, which can be used as an Epac-negative control. 6-Bnz-cAMP is released after the metabolism of 6-Bnz-cAMP-AM by esterases. Grades: ≥ 97 % by HPLC for mixture of isomers. Molecular formula: C20H20N5O9P. Mole weight: 505.4. BOC Sciences 2
6-Bnz-cAMP sodium salt 6-Bnz-cAMP sodium salt. Group: Biochemicals. Grades: Purified. CAS No. 1135306-29-4. Pack Sizes: 1mg. US Biological Life Sciences. USBiological 5
Worldwide
6-Bnz-cAMP sodium salt 6-Bnz-cAMP sodium salt is a cell-permeable cAMP analog. 6-Bnz-cAMP selectively activates cAMP-dependent PKA but not Epac signaling pathways [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1135306-29-4. Pack Sizes: 1 mg. Product ID: HY-103322. MedChemExpress MCE
6-Bnz-cAMP sodium salt 6-Bnz-cAMP sodium salt is a cell-permeable cAMP analogue that selectively activates cAMP-dependent PKA but not Epac signaling pathways. It inhibits the proliferation of vascular smooth muscle cell in combination with 8-CPT-2Me-cAMP. Synonyms: N6-Benzoyladenosine-3',5'-cyclic monophosphate sodium salt. Grades: ≥98% by HPLC. CAS No. 1135306-29-4. Molecular formula: C17H15N5NaO7P. Mole weight: 455.29. BOC Sciences 2
Adenosine 3’,5’-cyclic Monophosphate, N6-Benzoyl-, Sodium Salt (6-Bnz-cAMP, Na) A potent cell-permeable activator of cAMP-dependent protein kinase (PKA). Activates both type 1 and type 2 PKA and binds to the cAMP binding site 2 on the regulatory subunit of PKA. It is only slowly metabolized by cyclic nucleotide-dependent phosphodiesterases. Due to its considerably increased lipophilicity, it has sufficient membrane permeability for many biological systems. Group: Biochemicals. Grades: Highly Purified. CAS No. 30275-80-0. Pack Sizes: 10umol. US Biological Life Sciences. USBiological 4
Worldwide
Sp-6-Bnz-cAMPS Sp-6-Bnz-cAMPS is a selective and PDE-resistant stimulator of cAMP-dependent protein kinase, which can be used as an Epac-negative control. Grades: ≥ 98% by HPLC. CAS No. 152218-18-3. Molecular formula: C17H15N5O6PS · Na. Mole weight: 471.4. BOC Sciences 3
6-Bnz-5'-AMP 6-Bnz-5'-AMP is an analogue of adenosine-5'-O-monophosphate and a potential metabolite of N6-Benzoyl-cAMP. Synonyms: N- Benzoyladenosine- 5'- O- monophosphate, sodium salt. Grades: ≥ 97 % by HPLC. CAS No. 40871-55-4. Molecular formula: C17H18N5O8P (free acid). Mole weight: 451.3 (free acid). BOC Sciences 2

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