NSC 405020 - 10mM in DMSO , CAS No.7497-07-6

CAS: 7497-07-6 Cat. No.: N425823 Fórmula: C12H15Cl2NO Peso molecular: 260.16 Número CE: 804-136-9
Disponível para encomenda
GRADE & PURITY 10mM in DMSO
Synonyms
DS-10698 | BCP08049 | 3,4-Dichloro-N-(2-pentanyl)benzamide | CCG-267051 | EX-A190 | NSC405020 | NSC-405020 | FT-0721918 | DTXSID80323865 | HMS3653L08 | HY-15827 | s8072 | NCGC00386282-11 | SW219617-1 | 3,4-Dichloro-N-(1-methylbutyl)benzamide | 3,4-Dichlor
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Alemanha (EU)
USA*
Price
Qty
1ml
N425823-1ml
—
2 Em stock

143,09€

209,91€
Gravar 66,82 € (31.83%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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.

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Literature proof

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

Visão geral

NSC 405020 is a noncatalytic inhibitor of MT1-MMP, directly interacts with PEX domain of MT1-MMP, affects PEX homodimerization but not catalytic activity of MT1-MMP.

Specifications

Sinónimos
DS-10698 | BCP08049 | 3,4-Dichloro-N-(2-pentanyl)benzamide | CCG-267051 | EX-A190 | NSC405020 | NSC-405020 | FT-0721918 | DTXSID80323865 | HMS3653L08 | HY-15827 | s8072 | NCGC00386282-11 | SW219617-1 | 3,4-Dichloro-N-(1-methylbutyl)benzamide | 3,4-Dichlor
Especificações e pureza
10mM in DMSO
Mecanismos bioquímicos e fisiológicos
NSC405020 is a PEX inhibitor targeting the PEX domain of MT1-MMP that repressed tumor growth and caused a fibrotic DPEX-like tumor phenotype in vivo. NSC405020 does not inhibit the catalytic activity of MMP-2.MT1-MMP (Membrane type-1 matrix metalloprotein
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Tipo de ação
INHIBITOR
Nomes e identificadores
Pubchem Sid528766325
Sorrisos canónicosCCCC(C)NC(=O)C1=CC(=C(C=C1)Cl)Cl
IUPAC Name3,4-dichloro-N-pentan-2-ylbenzamide
InChIKeyARDYECYBETXQFD-UHFFFAOYSA-N
INCHI1S/C12H15Cl2NO/c1-3-4-8(2)15-12(16)9-5-6-10(13)11(14)7-9/h5-8H,3-4H2,1-2H3,(H,15,16)
SMILES isoméricas CCCC(C)NC(=O)C1=CC(=C(C=C1)Cl)Cl
Peso molecular 260.16
Reaxy-Rn 2453936
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2453936&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Halobenzoic acids and derivatives
Direct Parent4-halobenzoic acids and derivatives
Alternative Parents 3-halobenzoic acids and derivatives  Benzamides  Dichlorobenzenes  Benzoyl derivatives  Aryl chlorides  Secondary carboxylic acid amides  Organooxygen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents 4-halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - Benzamide - Benzoyl - 1,2-dichlorobenzene - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Organochloride - Aromatic homomonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as 4-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 4-position of the benzene ring.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
MMP14 Tchem Matrix metalloproteinase 14 (1592 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
Peso molecular260.160 g/mol
XLogP34.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count4
Exact Mass259.053 Da
Monoisotopic Mass259.053 Da
Topological Polar Surface Area29.100 Ų
Heavy Atom Count16
Formal Charge0
Complexity235.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
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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