SKL2001 - ≥99% , CAS No.909089-13-0

CAS: 909089-13-0 Cat. No.: S413970 Formule: C14H14N4O3 Poids moléculaire: 286.29 PubChem CID: 16003447
DISPONIBLE À COMMANDE
GRADE & PURITY ≥99%
Synonyms
3-​Isoxazolecarboxamide​,5-​(2-​furanyl)​-​N-​[3-​(1H-​imidazol-​1-​yl)​propyl]​-
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Allemagne (EU)
USA*
Price
Qty
10mg
S413970-10mg
Sur commande · 8–12 semaines
76,27€
50mg
S413970-50mg
Sur commande · 8–12 semaines
235,94€
250mg
S413970-250mg
—
2 En stock
680,22€
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Why this grade

≥99% 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.

Vue d’ensemble

Information

SKL2001 SKL2001 is a novel agonist of the Wnt/β-catenin pathway . It disrupts the Axin/β-catenin interaction.


Targets

Wnt/β-catenin (Cell-free assay)


In vitro

SKL2001 upregulated β-catenin responsive transcription by increasing the intracellular β-catenin protein level and inhibited the phosphorylation of β-catenin at residues Ser33/37/Thr41 and Ser45, which would mark it for proteasomal degradation, without affecting CK1 and GSK-3β enzyme activities. SKL2001 disrupted the Axin/β-catenin interaction, which is a critical step for CK1- and GSK-3β-mediated phosphorylation of β-catenin at Ser33/37/Thr41 and Ser45. The treatment of mesenchymal stem cells with SKL2001 promoted osteoblastogenesis and suppressed adipocyte differentiation, both of which were accompanied by the activation of Wnt/β-catenin pathway. SKL2001 did not affect either NF-κB or p53 reporter activity and inhibits β-catenin phosphorylation without affecting GSK-3β activity.


Cell Research(from reference)

Cell lines:HEK293 reporter and control cell lines 

Concentrations:20 μM 

Incubation Time:15 h 

Specifications

Synonymes
3-​Isoxazolecarboxamide​,5-​(2-​furanyl)​-​N-​[3-​(1H-​imidazol-​1-​yl)​propyl]​-
Spécifications et pureté
≥99%
Mécanismes biochimiques et physiologiques
SKL2001 is a novel agonist of the Wnt/β-catenin pathway. It disrupts the Axin/β-catenin interaction.
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Pureté
≥99%
Propriétés du produit
ALogP
0.929
Nombre de HBD
1
Liaison rotative
6
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504768000
Sourires canoniques
C1=COC(=C1)C2=CC(=NO2)C(=O)NCCCN3C=CN=C3
IUPAC Name
5-(furan-2-yl)-N-(3-imidazol-1-ylpropyl)-1,2-oxazole-3-carboxamide
InChIKey
PQXINDBPUDNMPE-UHFFFAOYSA-N
INCHI
1S/C14H14N4O3/c19-14(16-4-2-6-18-7-5-15-10-18)11-9-13(21-17-11)12-3-1-8-20-12/h1,3,5,7-10H,2,4,6H2,(H,16,19)
Isomères SMILES
C1=COC(=C1)C2=CC(=NO2)C(=O)NCCCN3C=CN=C3
PubChem CID
16003447
Poids moléculaire
286.29

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.

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📊 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
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Carboxylic acid amides
Direct Parent2-heteroaryl carboxamides
Alternative Parents N-substituted imidazoles  Isoxazoles  Heteroaromatic compounds  Furans  Secondary carboxylic acid amides  Oxacyclic compounds  Azacyclic compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 2-heteroaryl carboxamide - N-substituted imidazole - Azole - Furan - Imidazole - Isoxazole - Heteroaromatic compound - Secondary carboxylic acid amide - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 2-heteroaryl carboxamides. These are compounds containing a heteroaromatic ring that carries a carboxamide group.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

1 results found

Lot NumberCertificate TypeDateArticle
H2222156Certificate of AnalysisJun 09, 2025 S413970
Propriétés chimiques et physiques
SolubilitéSolubility (25°C) In vitro DMSO: 57 mg/mL (199.09 mM); Ethanol: 57 mg/mL (199.09 mM); Water: Insoluble;
DMSO (mg/mL) Solubilité maximale57
DMSO (mM) Solubilité maximale199.0988159
Eau (mg/mL) Solubilité maximale<1
Poids moléculaire286.290 g/mol
XLogP30.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count6
Exact Mass286.107 Da
Monoisotopic Mass286.107 Da
Topological Polar Surface Area86.100 Ų
Heavy Atom Count21
Formal Charge0
Complexity355.000
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
Calculateurs de solution
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