RK-33 - ≥98% , CAS No.1070773-09-9

CAS: 1070773-09-9 Cat. No.: R413953 Fórmula: C23H20N6O3 Peso molecular: 428.44 PubChem CID: 46184988
Disponível para encomenda
GRADE & PURITY ≥98%
Synonyms
2H-​Diimidazo[4,​5-​d:4',​5'-​f]​[1,​3]​diazepin-​2-​one,3,​7-​dihydro-​3,​7-​bis[(4-​methoxyphenyl)​methyl]​- | RK33 | RK 33 | RK-33 | 3,7-bis(4-methoxybenzyl)-3,7-dihydro-2H-diimidazo[4,5-d:4',5'-f][1,3]diazepin-2-one
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
★
Size
Alemanha (EU)
USA*
Price
Qty
5mg
R413953-5mg
—
5 Em stock

38,96€

58,92€
Gravar 19,96 € (33.87%)
25mg
R413953-25mg
—
1 Em stock

125,74€

189,08€
Gravar 63,34 € (33.50%)
50mg
R413953-50mg
—
1 Em stock

202,10€

303,62€
Gravar 101,53 € (33.44%)
100mg
R413953-100mg
—
1 Em stock

321,84€

483,24€
Gravar 161,40 € (33.40%)
250mg
R413953-250mg
—
1 Em stock

524,03€

786,08€
Gravar 262,06 € (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

Information

RK-33 RK-33 is a first-in-class small molecule inhibitor of DDX3 (a RNA helicase) and causes G1 cell cycle arrest, induces apoptosis, and promotes radiation sensitization in DDX3-overexpressing cells.


Targets

DDX3


In vitro

RK-33 binds specifically to DDX3, but not to the closely related proteins DDX5 and DDX17. RK-33 inhibits cancer growth and radiosensitizes lung cancer cells in a DDX3-dependent manner. RK-33 has no effect on either mitochondrial respiration or ATP generation. RK-33 curbs proliferation and induces apoptosis in a DDX3-dependent fashion. Wnt signaling is mediated by DDX3 and inhibited by RK-33. RK-33 impairs radiation-induced DNA damage repair by inhibiting NHEJ activity.


In vivo

RK-33 in combination with radiation induces tumor regression in multiple mouse models of lung cancer. RK-33, at the dose used, is non-toxic in SCID mice. RK-33-treated mice do not exhibit any discernable morphological changes.


Cell Research(from reference)

Cell lines:MDA-MB-231 cells 

Concentrations:7.5 μM 

Incubation Time:12 h 

Specifications

Sinónimos
2H-​Diimidazo[4,​5-​d:4',​5'-​f]​[1,​3]​diazepin-​2-​one,3,​7-​dihydro-​3,​7-​bis[(4-​methoxyphenyl)​methyl]​- | RK33 | RK 33 | RK-33 | 3,7-bis(4-methoxybenzyl)-3,7-dihydro-2H-diimidazo[4,5-d:4',5'-f][1,3]diazepin-2-one
Especificações e pureza
≥98%
Mecanismos bioquímicos e fisiológicos
RK-33 is a first-in-class small molecule inhibitor of DDX3 (a RNA helicase) and causes G1 cell cycle arrest, induces apoptosis, and promotes radiation sensitization in DDX3-overexpressing cells.
Condições de armazenamento de armazenamento
Store at -20°C,Argon charged
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Pureza
≥98%
Propriedades do produto
ALogP2.687
Ligação rotativa6
Nomes e identificadores
Pubchem Sid488201261
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488201261
Sorrisos canónicosCOC1=CC=C(C=C1)CN2C=NC3=C2N=CN=C4C3=NC(=O)N4CC5=CC=C(C=C5)OC
IUPAC Name5,11-bis[(4-methoxyphenyl)methyl]-3,5,7,9,11,13-hexazatricyclo[8.3.0.02,6]trideca-1(10),2,6,8,12-pentaen-4-one
InChIKeyCOUMZXFUZDBRCZ-UHFFFAOYSA-N
INCHI1S/C23H20N6O3/c1-31-17-7-3-15(4-8-17)11-28-14-26-19-20-22(25-13-24-21(19)28)29(23(30)27-20)12-16-5-9-18(32-2)10-6-16/h3-10,13-14H,11-12H2,1-2H3
SMILES isoméricas COC1=CC=C(C=C1)CN2C=NC3=C2N=CN=C4C3=NC(=O)N4CC5=CC=C(C=C5)OC
PubChem CID 46184988
Peso molecular 428.44

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
ClasseImidazodiazepines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentImidazodiazepines
Alternative Parents Phenoxy compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  1,3-diazepines  N-substituted imidazoles  Heteroaromatic compounds  Azacyclic compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Imidazo-meta-diazepine - Imidazodiazepine - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Meta-diazepine - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Azacycle - Ether - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as imidazodiazepines. These are organic compounds containing an imidazole ring fused to a diazepine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Diazepine is a 7-membered ring consisting of five carbon and two nitrogen atoms.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





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Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot NumberCertificate TypeDataItem
I2617079Certificate of AnalysisSep 29, 2026 R413953
F23281030Certificate of AnalysisApr 03, 2026 R413953
F23281035Certificate of AnalysisApr 03, 2026 R413953
F23281036Certificate of AnalysisApr 03, 2026 R413953
F23281037Certificate of AnalysisApr 03, 2026 R413953
F23281038Certificate of AnalysisApr 03, 2026 R413953
F23281039Certificate of AnalysisApr 03, 2026 R413953
F23281040Certificate of AnalysisApr 03, 2026 R413953
F23281042Certificate of AnalysisApr 03, 2026 R413953
F23281043Certificate of AnalysisApr 03, 2026 R413953
F23281044Certificate of AnalysisApr 03, 2026 R413953

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Propriedades químicas e físicas
SolubilidadeSolubility (25°C) In vitro DMSO: 85 mg/mL (198.39 mM); Water: Insoluble; Ethanol: Insoluble;
SensibilidadeMoisture sensitive.
DMSO (mg/mL) Solubilidade máxima85
DMSO (mM) Solubilidade máxima198.3941742
Água (mg/mL) Solubilidade máxima<1
Peso molecular428.400 g/mol
XLogP32.600
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count5
Rotatable Bond Count6
Exact Mass428.16 Da
Monoisotopic Mass428.16 Da
Topological Polar Surface Area93.700 Ų
Heavy Atom Count32
Formal Charge0
Complexity783.000
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 Count1
Calculadoras de soluções
Revisões

Avaliações dos Clientes

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