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N⁶,2′-O-Dibutyryladenosine 3′,5′-cyclic monophosphate sodium salt - ≥96% (HPLC), powder, high purity , CAS No.16980-89-5

≥95%(HPLC)
powder

CAS#: 16980-89-5
Molecular Weight: 491.37
MDL number: MFCD00005843
PubChem CID: 23663967

Item Number

N464165

Grouped product items
SKU	Size	Availability	Price
N464165-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$28.90
N464165-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$94.90
N464165-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$213.90
N464165-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$769.90
N464165-5×1g	5×1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$3,464.90

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Metabolic Enzyme/Protease (0) Phosphodiesterase (PDE) (0) PKA (0) Stem Cell/Wnt (0)

Basic Description

Synonyms	Dibutyryl cAMP (sodium salt);DBcAMP (sodium salt) \| InChI=1/C6H10O2/c7-6-4-2-1-3-5-8-6/h1-5H \| Actosin \| Adenosine, N-(1-oxobutyl)-, cyclic 3',5'-(hydrogen phosphate) 2'-butanoate, monosodium salt \| Actosin (TN) \| STK803270 \| EINECS 243-065-2 \| MLS0022071
Specifications & Purity	≥95%(HPLC), powder
Biochemical and Physiological Mechanisms	Cell-permeable cAMP analog that activates cAMP dependent protein kinase (PKA).
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads
Product Description	Description Dibutyryl CAMP is a cell-permeable CAMP analogue that activates CAMP dependent protein kinase (PKA) or the CAMP/PKA signaling pathway. Dibutyryl CAMP is used as a morphological differentiation inducer and cell signaling modulator in cells such as Schwann cells. Dibutyrl cAMP is used in a variety of differentiation studies, such as neuron differentiation / neuronal differentiation.

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	sodium;[(4aR,6R,7R,7aR)-6-[6-(butanoylamino)purin-9-yl]-2-oxido-2-oxo-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-7-yl] butanoate
INCHI	InChI=1S/C18H24N5O8P.Na/c1-3-5-11(24)22-16-13-17(20-8-19-16)23(9-21-13)18-15(30-12(25)6-4-2)14-10(29-18)7-28-32(26,27)31-14;/h8-10,14-15,18H,3-7H2,1-2H3,(H,26,27)(H,19,20,22,24);/q;+1/p-1/t10-,14-,15-,18-;/m1./s1
InChi Key	KRBZRVBLIUDQNG-JBVYASIDSA-M
Canonical SMILES	CCCC(=O)NC1=C2C(=NC=N1)N(C=N2)C3C(C4C(O3)COP(=O)(O4)[O-])OC(=O)CCC.[Na+]
Isomeric SMILES	CCCC(=O)NC1=C2C(=NC=N1)N(C=N2)[C@H]3[C@@H]([C@H]4[C@H](O3)COP(=O)(O4)[O-])OC(=O)CCC.[Na+]
WGK Germany	2
RTECS	ES5055500
PubChem CID	23663967
Molecular Weight	491.37

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Safety and Hazards(GHS)

WGK Germany	2
RTECS	ES5055500
Merck Index	1463

Reviews

References

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