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· · COA & SDS available for every product · Same-day shipping on in-stock items N⁶ benzyl-cAMP - Moligand™ , Activator of protein kinase A, CAS No.32115-08-5, Activator of protein kinase A
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Synonyms
N6-benzyl cyclic AMP | N6 benzyl-cAMP | DTXSID30953994 | (4aR,6R,7R,7aS)-6-[6-(benzylamino)-9H-purin-9-yl]-2,7-dihydroxy-hexahydro-1,3,5,2$l^{5}-furo[3,2-d][1,3,2$l^{5}]dioxaphosphinin-2-one | GTPL5228 | Q27088082 | N(6)-Benzyl-cyclic adenosine 5'-monopho
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Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
N6-benzyl cyclic AMP | N6 benzyl-cAMP | DTXSID30953994 | (4aR, 6R, 7R, 7aS)-6-[6-(benzylamino)-9H-purin-9-yl]-2, 7-dihydroxy-hexahydro-1, 3, 5, 2$l^{5}-furo[3, 2-d][1, 3, 2$l^{5}]dioxaphosphinin-2-one | GTPL5228 | Q27088082 | N(6)-Benzyl-cyclic adenosine 5'-monopho
Specifications & Purity
Moligand™
Mechanism of action
Activator of protein kinase A
Names and Identifiers Canonical Smiles O[C@@H]1[C@@H]2OP(=O)(O)OC[C@H]2O[C@H]1n1cnc2c1ncnc2NCc1ccccc1 IUPAC Name (4aR,6R,7R,7aS)-6-[6-(benzylamino)-9H-purin-9-yl]-2,7-dihydroxy-hexahydro-1,3,5,2$l^{5}-furo[3,2-d][1,3,2$l^{5}]dioxaphosphinin-2-one InChIKey GDDBIAMRTVTOBL-LSCFUAHRSA-N INCHI 1S/C17H18N5O6P/c23-13-14-11(7-26-29(24,25)28-14)27-17(13)22-9-21-12-15(19-8-20-16(12)22)18-6-10-4-2-1-3-5-10/h1-5,8-9,11,13-14,17,23H,6-7H2,(H,24,25)(H,18,19,20)/t11-,13-,14-,17-/m1/s1 Isomeric SMILES C1[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=NC4=C(N=CN=C43)NCC5=CC=CC=C5)O)OP(=O)(O1)O PubChem CID 161733
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 Class Purine nucleotides Subclass Cyclic purine nucleotides Intermediate Tree Nodes Not available Direct Parent 3',5'-cyclic purine nucleotides Alternative Parents Pentose phosphates 6-alkylaminopurines Glycosylamines Monosaccharide phosphates Benzylamines Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams Organic phosphoric acids and derivatives N-substituted imidazoles Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents 3',5'-cyclic purine ribonucleotide - Pentose phosphate - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Benzylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - Imidolactam - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Benzenoid - Pyrimidine - Tetrahydrofuran - Heteroaromatic compound - Azole - Imidazole - Secondary alcohol - Secondary amine - Oxacycle - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Amine - Alcohol - Organonitrogen compound - Aromatic heteropolycyclic compound Description 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.
3D Structure Associated Targets(Human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 419.300 g/mol XLogP3 -0.400 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 10 Rotatable Bond Count 4 Exact Mass 419.099 Da Monoisotopic Mass 419.099 Da Topological Polar Surface Area 141.000 Ų Heavy Atom Count 29 Formal Charge 0 Complexity 639.000 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 1
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