Clanfenur is a substituted benzoylphenylurea, an analogue of the pesticide fenfluramide, with potential antineoplastic activity. Clanfenur can bind to the colchicine-binding site on β-tubulin, inhibit microtubule polymerization, and thus prevent tumor cell replication .

Specifications

Synonyms

N-((4-Chlorophenyl)carbamoyl)-2-(dimethylamino)-6-fluorobenzamide

Specifications & Purity

Moligand™, ≥98%

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Moligand™

Action Type

INHIBITOR

Purity

≥98%

Names and Identifiers

Canonical Smiles	CN(C)C1=C(C(=CC=C1)F)C(=O)NC(=O)NC2=CC=C(C=C2)Cl
IUPAC Name	N-[(4-chlorophenyl)carbamoyl]-2-(dimethylamino)-6-fluorobenzamide
InChIKey	SRLPZQAEBMZCIJ-UHFFFAOYSA-N
INCHI	1S/C16H15ClFN3O2/c1-21(2)13-5-3-4-12(18)14(13)15(22)20-16(23)19-11-8-6-10(17)7-9-11/h3-9H,1-2H3,(H2,19,20,22,23)
Isomeric SMILES	CN(C)C1=C(C(=CC=C1)F)C(=O)NC(=O)NC2=CC=C(C=C2)Cl
Alternate CAS	51213-99-1
NSC Number	603108
MeSH Entry Terms	1-(2-fluoro-6-dimethylaminobenzoyl)-3-(4-chlorophenyl)urea;clanfenur
Molecular Weight	335.76

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

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📊 Datasheet

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass N-phenylureas
      - Level5 N-acyl-phenylureas
        Level6 N-benzoyl-N'-phenylureas

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	N-phenylureas
Intermediate Tree Nodes	N-acyl-phenylureas
Direct Parent	N-benzoyl-N'-phenylureas
Alternative Parents	2-aminobenzamides 2-halobenzoic acids and derivatives Aniline and substituted anilines Benzoyl derivatives Dialkylarylamines Chlorobenzenes Fluorobenzenes Aryl chlorides Aryl fluorides Vinylogous amides Vinylogous halides Ureas Amino acids and derivatives Organochlorides Organofluorides Carbonyl compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	N-benzoyl-n'-phenylurea - Aminobenzamide - Aminobenzoic acid or derivatives - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - 2-aminobenzamide - Benzoic acid or derivatives - Tertiary aliphatic/aromatic amine - Benzoyl - Dialkylarylamine - Aniline or substituted anilines - Halobenzene - Fluorobenzene - Chlorobenzene - Aryl fluoride - Aryl chloride - Aryl halide - Vinylogous amide - Vinylogous halide - Amino acid or derivatives - Urea - Tertiary amine - Carbonic acid derivative - Carboxylic acid derivative - Organic nitrogen compound - Organofluoride - Carbonyl group - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organic oxygen compound - Organohalogen compound - Organochloride - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as n-benzoyl-n'-phenylureas. These are n-acyl-phenylureas that have the acyl group substituted by a phenyl group.
External Descriptors	Not available
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. DOI: 10.1186/s13321-016-0174-y

3D Structure

Associated Targets(Human)

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

Discover Target: GLP1R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Item
F2523451	Certificate of Analysis	Dec 11, 2024	C694232
F2523452	Certificate of Analysis	Dec 11, 2024	C694232
F2523454	Certificate of Analysis	Dec 11, 2024	C694232
F2523468	Certificate of Analysis	Dec 11, 2024	C694232
F2523470	Certificate of Analysis	Dec 11, 2024	C694232
F2523474	Certificate of Analysis	Dec 11, 2024	C694232
F2523476	Certificate of Analysis	Dec 11, 2024	C694232
F2523477	Certificate of Analysis	Dec 11, 2024	C694232

Molecular Weight	335.760 g/mol
XLogP3	3.900
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	3
Exact Mass	335.084 Da
Monoisotopic Mass	335.084 Da
Topological Polar Surface Area	61.400 Å²
Heavy Atom Count	23
Formal Charge	0
Complexity	428.000
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

Clanfenur - Moligand™, ≥98% , CAS No.51213-99-1

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Storage & shipping

Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

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