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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Doxercalciferol - Moligand™, ≥98% , Vitamin D receptor agonist, CAS No.54573-75-0, Vitamin D receptor agonist
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. ≥98% Synonyms
1-Hydroxyergocalciferol | 1.alpha.-Hydroxyvitamin D2 | AKOS005146517 | DOXERCALCIFEROL [USAN] | DOXERCALCIFEROL [VANDF] | TSA-840 | D82103 | GTPL2790 | 1alpha-hydroxyvitamin D2 / 1alpha-hydroxyergocalciferol | BRN 4716774 | H05BX03 | (1R,3S,5Z)-5-[(2E)-2-
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98% 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.
Specifications Sinónimos
1-Hydroxyergocalciferol | 1.alpha.-Hydroxyvitamin D2 | AKOS005146517 | DOXERCALCIFEROL [USAN] | DOXERCALCIFEROL [VANDF] | TSA-840 | D82103 | GTPL2790 | 1alpha-hydroxyvitamin D2 / 1alpha-hydroxyergocalciferol | BRN 4716774 | H05BX03 | (1R, 3S, 5Z)-5-[(2E)-2-
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Vitamin D2analog that acts as a vitamin D receptor activator (VDRA).
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
Vitamin D receptor agonist
Propiedades del producto Nombres e identificadores Pubchem Sid 504763332 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504763332 Sonrisas canónicas CC(C)C(C)C=CC(C)C1CCC2C1(CCCC2=CC=C3CC(CC(C3=C)O)O)C IUPAC Name (1R,3S,5Z)-5-[(2E)-2-[(1R,3aS,7aR)-1-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol InChIKey HKXBNHCUPKIYDM-CGMHZMFXSA-N INCHI 1S/C28H44O2/c1-18(2)19(3)9-10-20(4)25-13-14-26-22(8-7-15-28(25,26)6)11-12-23-16-24(29)17-27(30)21(23)5/h9-12,18-20,24-27,29-30H,5,7-8,13-17H2,1-4,6H3/b10-9+,22-11+,23-12-/t19-,20+,24+,25+,26-,27-,28+/m0/s1 Isómeros SMILES C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]\2[C@@]1(CCC/C2=C\C=C/3\C[C@H](C[C@@H](C3=C)O)O)C WGK Alemania 3 PubChem CID 5281107 Peso molecular 412.65
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 Lipids and lipid-like molecules Clase Steroids and steroid derivatives Subclass Vitamin D and derivatives Intermediate Tree Nodes Not available Direct Parent Vitamin D and derivatives Alternative Parents Triterpenoids Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Triterpenoid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound Descripción This compound belongs to the class of organic compounds known as vitamin d and derivatives. These are compounds containing a secosteroid backbone, usually secoergostane or secocholestane. External Descriptors Vitamin D2 and derivatives 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:ethanol, Max Conc. mg/mL: 20.63, Max Conc. mM: 50; Solvent:DMSO, Max Conc. mg/mL: 4.13, Max Conc. mM: 10 Sensibilidad Heat Sensitive Punto de fusión (°C) 140 °C Peso molecular 412.600 g/mol XLogP3 6.300 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 5 Exact Mass 412.334 Da Monoisotopic Mass 412.334 Da Topological Polar Surface Area 40.500 Ų Heavy Atom Count 30 Formal Charge 0 Complexity 712.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 7 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 3 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 3 Covalently-Bonded Unit Count 1
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 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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