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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 1,3-Dipropylxanthine - Moligand™ , Antagonist of A 2A receptor;Antagonist of A 2B receptor, CAS No.31542-62-8, Antagonist of A 2A receptor;Antagonist of A 2B receptor
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
BDBM82032 | AKOS016004647 | Calcium chloride, anhydrous, free-flowing, Redi-Dri(TM), ACS reagent, >=96% | PDSP2_000326 | 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dipropyl- | J-018455 | GTPL427 | MJVIGUCNSRXAFO-UHFFFAOYSA-N | 1,3-dipropyl-3,7-dihydro-1h-purine
Shipped In
Ice chest + Ice pads
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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 Store at -20°C Ships Ice chest + Ice pads 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.
Descripción general 1,3-Dipropylxanthine is a caffeine analog and phosphodiesterase inhibitor that has some selectivity for A2 adenosine receptors.
Specifications Sinónimos
BDBM82032 | AKOS016004647 | Calcium chloride, anhydrous, free-flowing, Redi-Dri(TM), ACS reagent, >=96% | PDSP2_000326 | 1H-Purine-2, 6-dione, 3, 7-dihydro-1, 3-dipropyl- | J-018455 | GTPL427 | MJVIGUCNSRXAFO-UHFFFAOYSA-N | 1, 3-dipropyl-3, 7-dihydro-1h-purine
Especificaciones y pureza
Moligand™
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.
Mecanismo de acción
Antagonist of A 2A receptor;Antagonist of A 2B receptor
Nombres e identificadores Sonrisas canónicas CCCN1C2=C(C(=O)N(C1=O)CCC)NC=N2 IUPAC Name 1,3-dipropyl-7H-purine-2,6-dione InChIKey MJVIGUCNSRXAFO-UHFFFAOYSA-N INCHI 1S/C11H16N4O2/c1-3-5-14-9-8(12-7-13-9)10(16)15(6-4-2)11(14)17/h7H,3-6H2,1-2H3,(H,12,13) Isómeros SMILES CCCN1C2=C(C(=O)N(C1=O)CCC)NC=N2 Peso molecular 236.27 Reaxy-Rn 253265 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=253265&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 Organoheterocyclic compounds Clase Imidazopyrimidines Subclass Purines and purine derivatives Intermediate Tree Nodes Not available Direct Parent Xanthines Alternative Parents 6-oxopurines Alkaloids and derivatives Pyrimidones Vinylogous amides Imidazoles Heteroaromatic compounds Ureas Lactams Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Xanthine - 6-oxopurine - Purinone - Alkaloid or derivatives - Pyrimidone - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Azacycle - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety. 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 Soluble in Chloroform, Dichloromethane, DMF, Ethyl Acetate and Methanol Punto de fusión (°C) 204-206°C (lit.) Peso molecular 236.270 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 4 Exact Mass 236.127 Da Monoisotopic Mass 236.127 Da Topological Polar Surface Area 69.300 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 321.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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