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· · COA & SDS available for every product · Same-day shipping on in-stock items 9-Oxo-10(9H)-acridineacetic acid - ≥98%(HPLC) , CAS No.38609-97-1
Synonyms
10-Carboxymethyl-10H-acridine-9-one sodium salt | CRIDANIMOD [WHO-DD] | 10-carboxymethyl-9-acridanone;10-CMA;XBIO-101;9-Oxo-10(9H)-acridineacetic acid | CBDivE_005011 | 10-(Carboxymethyl)-9(10H)acridone | 10-(Carboxymethyl)-9(10H)-acridone | 2-(9-oxo-10-a
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice 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.
Overview 9-Oxo-10(9H)-acridineacetic acid and its analogs,as interferon inducers,are used for studying their potential activity.
Specifications Synonyms
10-Carboxymethyl-10H-acridine-9-one sodium salt | CRIDANIMOD [WHO-DD] | 10-carboxymethyl-9-acridanone;10-CMA;XBIO-101;9-Oxo-10(9H)-acridineacetic acid | CBDivE_005011 | 10-(Carboxymethyl)-9(10H)acridone | 10-(Carboxymethyl)-9(10H)-acridone | 2-(9-oxo-10-a
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
STING agonist; murine-selective (Kd= 3.5 μM). Triggers type I IFN response in murine macrophages, with no effect on human STING signaling.
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504753564 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504753564 Canonical Smiles C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3N2CC(=O)O IUPAC Name 2-(9-oxoacridin-10-yl)acetic acid InChIKey UOMKBIIXHQIERR-UHFFFAOYSA-N INCHI 1S/C15H11NO3/c17-14(18)9-16-12-7-3-1-5-10(12)15(19)11-6-2-4-8-13(11)16/h1-8H,9H2,(H,17,18) Isomeric SMILES C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3N2CC(=O)O WGK Germany 3 RTECS AR7190000 Molecular Weight 253.25 Beilstein 227508 Reaxy-Rn 227508 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=227508&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 Class Quinolines and derivatives Subclass Benzoquinolines Intermediate Tree Nodes Acridines Direct Parent Acridones Alternative Parents Hydroquinolones Hydroquinolines Alpha amino acids and derivatives Pyridines and derivatives Benzenoids Vinylogous amides Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Acridone - Dihydroquinolone - Alpha-amino acid or derivatives - Dihydroquinoline - Pyridine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as acridones. These are acridines containing a ketone group attached to the C9 carbon atom of the acridine 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 25.32, Max Conc. mM: 100 Melt Point(°C) 289°C Molecular Weight 253.250 g/mol XLogP3 2.700 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 2 Exact Mass 253.074 Da Monoisotopic Mass 253.074 Da Topological Polar Surface Area 57.600 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 356.000 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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