The store will not work correctly when cookies are disabled.
Parece que JavaScript está deshabilitado en su navegador. Para obtener la mejor experiencia en nuestro sitio, asegúrese de activar Javascript en su navegador.
· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items N⁶,2′-O-Dibutyryladenosine 3′,5′ -cyclic monophosphate sodium salt - ≥97%(HPLC) , CAS No.16980-89-5
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
Shipped In
Ice chest + Ice pads
🧪
Why this grade ≥97%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
📋
Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
📚
Literature proof Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general Bucladesine is a membrane permeable selective activator of PKA.
Specifications Sinónimos
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
Especificaciones y pureza
≥97%(HPLC)
Mecanismos bioquímicos y fisiológicos
Cell-permeable analog of cAMP; activates cAMP-dependent protein kinases. Promotes differentiation of dopaminergic neurons (iDA) from hPSCs in combination with other reagents.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 504769482 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504769482 Sonrisas canónicas CCCC(=O)NC1=C2C(=NC=N1)N(C=N2)C3C(C4C(O3)COP(=O)(O4)[O-])OC(=O)CCC.[Na+] 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 InChIKey KRBZRVBLIUDQNG-JBVYASIDSA-M 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 Isómeros 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 Alemania 2 RTECS ES5055500 Peso molecular 491.37 Reaxy-Rn 38305031 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=38305031&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Nucleosides, nucleotides, and analogues Clase Purine nucleotides Subclass Cyclic purine nucleotides Intermediate Tree Nodes Not available Direct Parent 3',5'-cyclic purine nucleotides Alternative Parents Pentose phosphates Glycosylamines Monosaccharide phosphates Purines and purine derivatives N-arylamides Fatty acid esters Organic phosphoric acids and derivatives Fatty amides N-substituted imidazoles Pyrimidines and pyrimidine derivatives Imidolactams Oxolanes Heteroaromatic compounds Carboxylic acid esters Secondary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Organic oxides Organic sodium salts Carbonyl compounds Organic zwitterions Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 3',5'-cyclic purine ribonucleotide - Pentose phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Imidazopyrimidine - Purine - N-arylamide - Fatty acid ester - Fatty amide - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Pyrimidine - Imidolactam - Fatty acyl - Imidazole - Heteroaromatic compound - Azole - Oxolane - Carboxylic acid ester - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Organoheterocyclic compound - Oxacycle - Monocarboxylic acid or derivatives - Organic alkali metal salt - Carboxylic acid derivative - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organic sodium salt - Organic zwitterion - Organic salt - Carbonyl group - Organonitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as 3',5'-cyclic purine nucleotides. These are purine nucleotides in which the oxygen atoms linked to the C3 and C5 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:water, Max Conc. mg/mL: 49.14, Max Conc. mM: 100; Solvent:DMSO, Max Conc. mg/mL: 49.14, Max Conc. mM: 100 Sensibilidad Heat sensitive Peso molecular 491.400 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 11 Rotatable Bond Count 8 Exact Mass 491.118 Da Monoisotopic Mass 491.118 Da Topological Polar Surface Area 167.000 Ų Heavy Atom Count 33 Formal Charge 0 Complexity 765.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 4 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 2
Citations of This Product Referencias 1. Fen Wang, Jinping Zhang, Qian Zhang, Zhangyong Song, Caiyan Xin. (2024) Antifungal activities of Equol against Candida albicans in vitro and in vivo. Virulence, [PMID:39267283 ] [10.1080/21505594.2024.2404256 ] 2. Yaxiu Feng, Xiong Wang, Cien Chen, Di Wang, Changshun Hou, Yiran Wang, Huan Hu, Peiran Chen, LeiYing Qin, Qianya Wan, Xi Yao, Ming-Liang He. (2025) Carbon Quantum Dots Assisted Virus Tracking: From Skin to Brain. ADVANCED MATERIALS, [PMID:40619836 ] [10.1002/adma.202508464 ]
Calculadoras de soluciones Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reseñas Artículos relacionados Adenosine 2′:3′-cyclic monophosphate sodium salt - ≥97% , CAS No.37063-35-7
Adenosine 3',5'-Cyclic Monophosphate（3',5'-cAMP） - Moligand™, ≥99% , Activator of CNGA2;Activator of CNGA3;Activator of HCN1;Activator of HCN2;Activator of protein kinase A, CAS No.60-92-4
1-O-hexadecyl-sn-glycero-2,3-cyclic-phosphate (ammonium salt) - ≥99% , CAS No.799268-68-1
1-oleoyl-sn-glycero-2,3-cyclic-phosphate (ammonium salt) - ≥99% , CAS No.799268-72-7
1-palmitoyl-sn-glycero-2,3-cyclic-phosphate (ammonium salt) - ≥99% , CAS No.799268-71-6
(4R,5R,6S)-4-Nitrobenzyl 3-((diphenoxyphosphoryl)oxy)-6-((R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate - ≥97% , CAS No.90776-59-3
Dibutyryl-cAMP (Bucladesine) - 10mM in DMSO , CAS No.16980-89-5
Uridine-2′,3′-cyclic monophosphate sodium salt - Moligand™, ≥97% , CAS No.15718-50-0
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our
Cookie Policy. Configuración Aceptar todo Rechazar
Shall we send you a message when we have discounts available?
Remind me later Permitir
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corp. All rights reserved.
F2214132