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Metabolic Enzyme/Protease
Phosphatase
cyt-PTPε Inhibitor-1 - 98%, high purity , CAS No.428478-94-8

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cyt-PTPε Inhibitor-1 - 98%, high purity , CAS No.428478-94-8

COA

Grade & Purity:

Moligand™

≥98%

Cas Number: 428478-94-8
Molecular Weight: 368.45
PubChem CID: 1418650
PubChem SID: 504760488

In stock

Item Number

C646256

Grouped product items
SKU	Size	Availability	Price
C646256-1mg	1mg	2	$41.90
C646256-5mg	5mg	1	$92.90
C646256-10mg	10mg	1	$135.90
C646256-25mg	25mg	1	$226.90
C646256-50mg	50mg	4	$361.90

View related series

Glucose Metabolism (1943) Metabolic Enzyme/Protease (4860) Phosphatase (222)

Basic Description

Specifications & Purity	Moligand™, ≥98%
Biochemical and Physiological Mechanisms	cyt-PTPε Inhibitor-1 is a potent cytosolic protein tyrosine phosphatase epsilon ( cyt-PTPε ) inhibitor, binds to the catalytic domain of cyt-PTPε, blocks c-Src activation (dephosphorylation of c-Src), and exhibits anti-osteoclastic activity.
Storage Temp	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™
Product Description	cyt-PTPε Inhibitor-1 is a potent cytosolic protein tyrosine phosphatase epsilon (cyt-PTPε) inhibitor, binds to the catalytic domain of cyt-PTPε, blocks c-Src activation (dephosphorylation of c-Src), and exhibits anti-osteoclastic activity.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass N-phenylureas

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	N-phenylureas
Intermediate Tree Nodes	Not available
Direct Parent	N-phenylureas
Alternative Parents	1,3,4-thiadiazol-2-ylureas m-Xylenes Phenoxy compounds Phenol ethers Toluenes Alkyl aryl ethers Heteroaromatic compounds Ureas Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	N-phenylurea - 1,3,4-thiadiazol-2-ylurea - Phenoxy compound - Phenol ether - M-xylene - Xylene - Alkyl aryl ether - Toluene - Azole - Thiadiazole - Heteroaromatic compound - Carbonic acid derivative - Urea - Azacycle - Ether - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as n-phenylureas. These are compounds containing a N-phenylurea moiety, which is structurally characterized by a phenyl group linked to one nitrogen atom of a urea 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

Associated Targets(Human)

Monocyte (474 Activities)

Explore this target

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

PTPRE Tbio Receptor-type tyrosine-protein phosphatase epsilon (68 Activities)

Discover Target: PTPRE

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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504760488
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504760488
IUPAC Name	1-[5-[(2,4-dimethylphenoxy)methyl]-1,3,4-thiadiazol-2-yl]-3-(4-methylphenyl)urea
INCHI	InChI=1S/C19H20N4O2S/c1-12-4-7-15(8-5-12)20-18(24)21-19-23-22-17(26-19)11-25-16-9-6-13(2)10-14(16)3/h4-10H,11H2,1-3H3,(H2,20,21,23,24)
InChIKey	QUSAMXSWOZSTRQ-UHFFFAOYSA-N
Smiles	CC1=CC=C(C=C1)NC(=O)NC2=NN=C(S2)COC3=C(C=C(C=C3)C)C
Isomeric SMILES	CC1=CC=C(C=C1)NC(=O)NC2=NN=C(S2)COC3=C(C=C(C=C3)C)C
PubChem CID	1418650
Molecular Weight	368.45

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

15 results found

Lot Number	Certificate Type	Date	Item
C2513463	Certificate of Analysis	Mar 05, 2025	C646256
C2513683	Certificate of Analysis	Mar 05, 2025	C646256
C2513684	Certificate of Analysis	Mar 05, 2025	C646256
C2513686	Certificate of Analysis	Mar 05, 2025	C646256
C2513687	Certificate of Analysis	Mar 05, 2025	C646256
C2513462	Certificate of Analysis	Mar 05, 2025	C646256
D2419243	Certificate of Analysis	Apr 10, 2024	C646256
D2419244	Certificate of Analysis	Apr 10, 2024	C646256
D2419245	Certificate of Analysis	Apr 10, 2024	C646256
D2419242	Certificate of Analysis	Apr 10, 2024	C646256
D2419246	Certificate of Analysis	Apr 10, 2024	C646256
D2419371	Certificate of Analysis	Apr 10, 2024	C646256
D2419372	Certificate of Analysis	Apr 10, 2024	C646256
D2419374	Certificate of Analysis	Apr 10, 2024	C646256
D2419295	Certificate of Analysis	Apr 10, 2024	C646256

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Chemical and Physical Properties

Solubility	DMSO: 9 mg/mL (24.43 mM)
Molecular Weight	368.500 g/mol
XLogP3	3.900
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	5
Exact Mass	368.131 Da
Monoisotopic Mass	368.131 Da
Topological Polar Surface Area	104.000 Å²
Heavy Atom Count	26
Formal Charge	0
Complexity	459.000
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

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