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· · COA & SDS available for every product · Same-day shipping on in-stock items Pacritinib citrate , Tyrosine-protein kinase JAK2 inhibitor, CAS No.1228923-42-9, Tyrosine-protein kinase JAK2 inhibitor
Synonyms
Pacritinib citrate | UNII-VJ2PH4NXX7 | Pacritinib citrate [WHO-DD] | Vonjo | Epjevy | SB-1518 CITRATE | CHEMBL5095049 | VJ2PH4NXX7 | 14,19-Dioxa-5,7,27-triazatetracyclo(19.3.1.12,6.18,12)heptacosa-1(25),2,4,6(27),8,10,12(26),16,21,23-decaene, 11-(2-(1-pyr
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Why this grade 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 Synonyms
Pacritinib citrate | UNII-VJ2PH4NXX7 | Pacritinib citrate [WHO-DD] | Vonjo | Epjevy | SB-1518 CITRATE | CHEMBL5095049 | VJ2PH4NXX7 | 14, 19-Dioxa-5, 7, 27-triazatetracyclo(19.3.1.12, 6.18, 12)heptacosa-1(25), 2, 4, 6(27), 8, 10, 12(26), 16, 21, 23-decaene, 11-(2-(1-pyr
Mechanism of action
Tyrosine-protein kinase JAK2 inhibitor
Names and Identifiers Canonical Smiles C1CCN(C1)CCOC2=C3COCC=CCOCC4=CC(=CC=C4)C5=NC(=NC=C5)NC(=C3)C=C2.C(C(=O)O)C(CC(=O)O)(C(=O)O)O IUPAC Name 2-hydroxypropane-1,2,3-tricarboxylic acid;(16E)-11-(2-pyrrolidin-1-ylethoxy)-14,19-dioxa-5,7,27-triazatetracyclo[19.3.1.12,6.18,12]heptacosa-1(24),2(27),3,5,8(26),9,11,16,21(25),22-decaene InChIKey BAHHBHSHSRTKNK-BJILWQEISA-N INCHI 1S/C28H32N4O3.C6H8O7/c1-2-13-32(12-1)14-17-35-27-9-8-25-19-24(27)21-34-16-4-3-15-33-20-22-6-5-7-23(18-22)26-10-11-29-28(30-25)31-26;7-3(8)1-6(13,5(11)12)2-4(9)10/h3-11,18-19H,1-2,12-17,20-21H2,(H,29,30,31);13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/b4-3+; Isomeric SMILES C1CCN(C1)CCOC2=C3COC/C=C/COCC4=CC(=CC=C4)C5=NC(=NC=C5)NC(=C3)C=C2.C(C(=O)O)C(CC(=O)O)(C(=O)O)O Molecular Weight 664.7 Reaxy-Rn 20404913 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20404913&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 acids and derivatives Class Carboxylic acids and derivatives Subclass Tricarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Tricarboxylic acids and derivatives Alternative Parents Phenol ethers Alkyl aryl ethers Alpha hydroxy acids and derivatives N-alkylpyrrolidines Pyrimidines and pyrimidine derivatives Heteroaromatic compounds Tertiary alcohols Trialkylamines Oxacyclic compounds Dialkyl ethers Carboxylic acids Azacyclic compounds Secondary amines Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Not available Substituents Tricarboxylic acid or derivatives - Phenol ether - Alkyl aryl ether - Alpha-hydroxy acid - Hydroxy acid - Pyrimidine - Benzenoid - N-alkylpyrrolidine - Heteroaromatic compound - Pyrrolidine - Tertiary alcohol - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid - Dialkyl ether - Ether - Oxacycle - Azacycle - Secondary amine - Organoheterocyclic compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Alcohol - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. 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.
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