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· · COA & SDS available for every product · Same-day shipping on in-stock items Home By Target/Pathway/Disease By Disease (DOID) Genetic diseases monogenic disease (DOID:0050177) Glycine, N,N-dimethyl-, 3-(5,6,7,13-tetrahydro-9-((1-methylethoxy)methyl)-5-oxo-12H-indeno(2,1-a)pyrrolo(3,4-c)carbazol-12-yl)propyl ester , Vascular endothelial growth factor receptor inhibitor, CAS No.402857-58-3, Vascular endothelial growth factor receptor inhibitor Glycine, N,N-dimethyl-, 3-(5,6,7,13-tetrahydro-9-((1-methylethoxy)methyl)-5-oxo-12H-indeno(2,1-a)pyrrolo(3,4-c)carbazol-12-yl)propyl ester , Vascular endothelial growth factor receptor inhibitor, CAS No.402857-58-3, Vascular endothelial growth factor receptor inhibitor
Synonyms
CEP-7055 | AD6CBG7OXO | Glycine, N,N-dimethyl-, 3-(5,6,7,13-tetrahydro-9-((1-methylethoxy)methyl)-5-oxo-12H-indeno(2,1-a)pyrrolo(3,4-c)carbazol-12-yl)propyl ester | Glycine, N,N-dimethyl-, 3-[5,6,7,13-tetrahydro-9-[(1-methylethoxy)methyl]-5-oxo-12H-indeno
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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
CEP-7055 | AD6CBG7OXO | Glycine, N, N-dimethyl-, 3-(5, 6, 7, 13-tetrahydro-9-((1-methylethoxy)methyl)-5-oxo-12H-indeno(2, 1-a)pyrrolo(3, 4-c)carbazol-12-yl)propyl ester | Glycine, N, N-dimethyl-, 3-[5, 6, 7, 13-tetrahydro-9-[(1-methylethoxy)methyl]-5-oxo-12H-indeno
Mechanism of action
Vascular endothelial growth factor receptor inhibitor
Product Properties Names and Identifiers Canonical Smiles CC(C)OCC1=CC2=C(C=C1)N(C3=C2C4=C(C5=C3CC6=CC=CC=C65)C(=O)NC4)CCCOC(=O)CN(C)C IUPAC Name 3-[14-oxo-7-(propan-2-yloxymethyl)-3,13-diazahexacyclo[14.7.0.02,10.04,9.011,15.017,22]tricosa-1(16),2(10),4(9),5,7,11(15),17,19,21-nonaen-3-yl]propyl 2-(dimethylamino)acetate InChIKey UHEBDUAFKQHUBV-UHFFFAOYSA-N INCHI 1S/C32H35N3O4/c1-19(2)39-18-20-10-11-26-23(14-20)29-25-16-33-32(37)30(25)28-22-9-6-5-8-21(22)15-24(28)31(29)35(26)12-7-13-38-27(36)17-34(3)4/h5-6,8-11,14,19H,7,12-13,15-18H2,1-4H3,(H,33,37) Isomeric SMILES CC(C)OCC1=CC2=C(C=C1)N(C3=C2C4=C(C5=C3CC6=CC=CC=C65)C(=O)NC4)CCCOC(=O)CN(C)C PubChem CID 9936664 Molecular Weight 525.6
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 Carbazoles Intermediate Tree Nodes Not available Direct Parent Pyrrolocarbazoles Alternative Parents Alpha amino acid esters Fluorenes Isoindolones N-alkylindoles Indoles Substituted pyrroles Heteroaromatic compounds Lactams Secondary carboxylic acid amides Trialkylamines Carboxylic acid esters Monocarboxylic acids and derivatives Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Pyrrolocarbazole - Alpha-amino acid ester - Fluorene - Alpha-amino acid or derivatives - N-alkylindole - Isoindolone - Indole - Isoindoline - Isoindole or derivatives - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Lactam - Secondary carboxylic acid amide - Azacycle - Ether - Dialkyl ether - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxide - Amine - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as pyrrolocarbazoles. These are compounds containing a pyrrolocarbazole moiety, which is a tetracyclic heterocycle which consists of a pyrrole ring fused to a carbazole. 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) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 525.600 g/mol XLogP3 4.500 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 10 Exact Mass 525.263 Da Monoisotopic Mass 525.263 Da Topological Polar Surface Area 72.800 Ų Heavy Atom Count 39 Formal Charge 0 Complexity 895.000 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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