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· · COA & SDS available for every product · Same-day shipping on in-stock items NQTrp - ≥95% , CAS No.185351-19-3
Synonyms
NQTrp, >=98% (HPLC) | DTXSID30717912 | (1,4-dioxo-1,4-dihydronaphthalen-2-yl)-L-tryptophan | 1,4-naphthoquinon-2-yl-l-tryptophan | AKOS027470177 | nqtrp | HY-19738 | (2S)-2-[(1,4-DIOXONAPHTHALEN-2-YL)AMINO]-3-(1H-INDOL-3-YL)PROPANOIC ACID | MS-25694 | N-(
Shipped In
Ice chest + Ice pads
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Why this grade ≥95% 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 Synonyms
NQTrp, >=98% (HPLC) | DTXSID30717912 | (1, 4-dioxo-1, 4-dihydronaphthalen-2-yl)-L-tryptophan | 1, 4-naphthoquinon-2-yl-l-tryptophan | AKOS027470177 | nqtrp | HY-19738 | (2S)-2-[(1, 4-DIOXONAPHTHALEN-2-YL)AMINO]-3-(1H-INDOL-3-YL)PROPANOIC ACID | MS-25694 | N-(
Specifications & Purity
≥95%
Biochemical and Physiological Mechanisms
Potent inhibitor of Aβoligomer and fibril formation (IC50= 50 nM for formation of fibrils from Aβ1-42). Reduces cytotoxicity of Aβoligomers and increases cell viability in neuronal cells. Significantly extends lifespan of Drosophila expressing human Aβ1-4
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504771422 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504771422 Canonical Smiles C1=CC=C2C(=C1)C(=O)C=C(C2=O)NC(CC3=CNC4=CC=CC=C43)C(=O)O IUPAC Name (2S)-2-[(1,4-dioxonaphthalen-2-yl)amino]-3-(1H-indol-3-yl)propanoic acid InChIKey DZZUYZXINNHEGM-SFHVURJKSA-N INCHI 1S/C21H16N2O4/c24-19-10-17(20(25)15-7-2-1-6-14(15)19)23-18(21(26)27)9-12-11-22-16-8-4-3-5-13(12)16/h1-8,10-11,18,22-23H,9H2,(H,26,27)/t18-/m0/s1 Isomeric SMILES C1=CC=C2C(=C1)C(=O)C=C(C2=O)N[C@@H](CC3=CNC4=CC=CC=C43)C(=O)O Molecular Weight 360.36 Reaxy-Rn 25282926 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25282926&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 Indoles and derivatives Subclass Indolyl carboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Indolyl carboxylic acids and derivatives Alternative Parents Naphthoquinones 3-alkylindoles L-alpha-amino acids Quinones Aryl ketones Aralkylamines Substituted pyrroles Vinylogous amides Heteroaromatic compounds Monocarboxylic acids and derivatives Enamines Dialkylamines Carboxylic acids Azacyclic compounds Hydrocarbon derivatives Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Indolyl carboxylic acid derivative - Naphthoquinone - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Naphthalene - 3-alkylindole - Indole - Quinone - Aryl ketone - Aralkylamine - Substituted pyrrole - Benzenoid - Vinylogous amide - Pyrrole - Heteroaromatic compound - Ketone - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Enamine - Azacycle - Monocarboxylic acid or derivatives - Amine - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. These are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring. 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: 36.04, Max Conc. mM: 100 Molecular Weight 360.400 g/mol XLogP3 3.400 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 5 Exact Mass 360.111 Da Monoisotopic Mass 360.111 Da Topological Polar Surface Area 99.300 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 659.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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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