BRACO 19 trihydrochloride - ≥95%(HPLC) , CAS No.1177798-88-7

CAS: 1177798-88-7 Cat. No.: B287457 Peso molecular: 703.14 Número EC: 802-563-5 PubChem CID: 10349800
Disponible para pedir
GRADE & PURITY ≥95%(HPLC)
Synonyms
N,N'-[9[[4-(Dimethylamino)phenyl]amino]-3,6-acridinediyl]bis-1-pyrrolidinepropanamide trihydrochloride
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
10mg
B287457-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
379,90US$
50mg
B287457-50mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.159,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥95%(HPLC) 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
N, N'-[9[[4-(Dimethylamino)phenyl]amino]-3, 6-acridinediyl]bis-1-pyrrolidinepropanamide trihydrochloride
Especificaciones y pureza
≥95%(HPLC)
Mecanismos bioquímicos y fisiológicos
Telomerase inhibitor (IC50= 115 nM). Inhibits expression of human telomerase reverse transcriptase (hTERT), induces cellular senescence and inhibits growth of uterine cancer cellsin vitro. Inhibits growth of uterine tumor xenografts in mice.
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.
Tipo de acción
INHIBITOR
Pureza
≥95%(HPLC)
Nombres e identificadores
Sonrisas canónicasCN(C)C1=CC=C(C=C1)NC2=C3C=CC(=CC3=NC4=C2C=CC(=C4)NC(=O)CCN5CCCC5)NC(=O)CCN6CCCC6.Cl.Cl.Cl
IUPAC NameN-[9-[4-(dimethylamino)anilino]-6-(3-pyrrolidin-1-ylpropanoylamino)acridin-3-yl]-3-pyrrolidin-1-ylpropanamide;trihydrochloride
InChIKeyMJAPNWJRLLDPAB-UHFFFAOYSA-N
INCHI1S/C35H43N7O2.3ClH/c1-40(2)28-11-7-25(8-12-28)38-35-29-13-9-26(36-33(43)15-21-41-17-3-4-18-41)23-31(29)39-32-24-27(10-14-30(32)35)37-34(44)16-22-42-19-5-6-20-42;;;/h7-14,23-24H,3-6,15-22H2,1-2H3,(H,36,43)(H,37,44)(H,38,39);3*1H
Isómeros SMILES CN(C)C1=CC=C(C=C1)NC2=C3C=CC(=CC3=NC4=C2C=CC(=C4)NC(=O)CCN5CCCC5)NC(=O)CCN6CCCC6.Cl.Cl.Cl
PubChem CID 10349800
Peso molecular 703.14

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

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseQuinolines and derivatives
SubclassBenzoquinolines
Intermediate Tree Nodes Not available
Direct ParentAcridines
Alternative Parents 4-aminoquinolines  Beta amino acids and derivatives  N-arylamides  Aniline and substituted anilines  Dialkylarylamines  Aminopyridines and derivatives  N-alkylpyrrolidines  Heteroaromatic compounds  Trialkylamines  Secondary carboxylic acid amides  Secondary amines  Azacyclic compounds  Carbonyl compounds  Hydrocarbon derivatives  Hydrochlorides  Organic oxides  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Acridine - Aminoquinoline - Beta amino acid or derivatives - 4-aminoquinoline - Tertiary aliphatic/aromatic amine - N-arylamide - Dialkylarylamine - Aniline or substituted anilines - Aminopyridine - Monocyclic benzene moiety - Pyridine - N-alkylpyrrolidine - Benzenoid - Heteroaromatic compound - Pyrrolidine - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Secondary amine - Carboxylic acid derivative - Hydrochloride - Amine - Carbonyl group - Organopnictogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as acridines. These are organic compounds containing the acridine moiety, a linear tricyclic heterocycle which consists of two benzene rings joined by a pyridine ring.
External Descriptors hydrochloride
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TERT Tchem Telomerase reverse transcriptase (2428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadSolvent:water, Max Conc. mg/mL: 35.16, Max Conc. mM: 50; Solvent:DMSO, Max Conc. mg/mL: 35.16, Max Conc. mM: 50
Peso molecular703.100 g/mol
XLogP3
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count7
Rotatable Bond Count11
Exact Mass701.278 Da
Monoisotopic Mass701.278 Da
Topological Polar Surface Area92.800 Ų
Heavy Atom Count47
Formal Charge0
Complexity870.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count4
Calculadoras de soluciones
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