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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Poly(Disperse Red 13 acrylate) - Moligand™ , Activator of IP 3R1;Activator of IP 3R2;Activator of IP 3R3, CAS No.142656-03-9, Activator of IP 3R1;Activator of IP 3R2;Activator of IP 3R3
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
(1R,2R,3S,4R,5R,6S)-3,5,6-trihydroxycyclohexane-1,2,4-triyl tris[dihydrogen (phosphate)] | 1D-myo-Inositol 1,4,5-trisphosphate | inositol 1,4,5-trisphosphate | Inositol triphosphate (6CI,7CI) | CMC_10501 | d-myo-inositol-1,4,5-triphosphate | 1btn | CMC_72
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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 Sinónimos
(1R, 2R, 3S, 4R, 5R, 6S)-3, 5, 6-trihydroxycyclohexane-1, 2, 4-triyl tris[dihydrogen (phosphate)] | 1D-myo-Inositol 1, 4, 5-trisphosphate | inositol 1, 4, 5-trisphosphate | Inositol triphosphate (6CI, 7CI) | CMC_10501 | d-myo-inositol-1, 4, 5-triphosphate | 1btn | CMC_72
Especificaciones y pureza
Moligand™
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Activator of IP 3R1;Activator of IP 3R2;Activator of IP 3R3
Nombres e identificadores Sonrisas canónicas C1(C(C(C(C(C1OP(=O)(O)O)O)OP(=O)(O)O)OP(=O)(O)O)O)O IUPAC Name [(1R,2S,3R,4R,5S,6R)-2,3,5-trihydroxy-4,6-diphosphonooxycyclohexyl] dihydrogen phosphate InChIKey MMWCIQZXVOZEGG-XJTPDSDZSA-N INCHI 1S/C6H15O15P3/c7-1-2(8)5(20-23(13,14)15)6(21-24(16,17)18)3(9)4(1)19-22(10,11)12/h1-9H,(H2,10,11,12)(H2,13,14,15)(H2,16,17,18)/t1-,2+,3+,4-,5-,6-/m1/s1 Isómeros SMILES [C@H]1([C@@H]([C@H]([C@@H]([C@H]([C@@H]1OP(=O)(O)O)O)OP(=O)(O)O)OP(=O)(O)O)O)O CAS alternativo 85166-31-0 Términos de entrada MeSH 1,4,5-InsP3;1,4,5-IP3;Inositol 1,4,5-Triphosphate;Inositol 1,4,5-Trisphosphate;Myo-Inositol 1,4,5-Trisphosphate;Myoinositol 1,4,5-Triphosphate Peso molecular 420.1 Reaxy-Rn 8514194 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8514194&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 Organic oxygen compounds Clase Organooxygen compounds Subclass Alcohols and polyols Intermediate Tree Nodes Cyclic alcohols and derivatives - Cyclitols and derivatives Direct Parent Inositol phosphates Alternative Parents Monoalkyl phosphates Cyclohexanols Polyols Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic homomonocyclic compounds Substituents Inositol phosphate - Monoalkyl phosphate - Cyclohexanol - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as inositol phosphates. These are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. External Descriptors myo-inositol trisphosphate 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 chloroform: soluble; toluene: soluble Punto de inflamación (°F) Not applicable Punto de inflamación (°C) Not applicable Punto de fusión (°C) Tg74℃ (onset) Peso molecular 420.100 g/mol XLogP3 -7.000 Hydrogen Bond Donor Count 9 Hydrogen Bond Acceptor Count 15 Rotatable Bond Count 6 Exact Mass 419.962 Da Monoisotopic Mass 419.962 Da Topological Polar Surface Area 261.000 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 574.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 6 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
Calculadoras de soluciones Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
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Reconstitution Calculator Reseñas Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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