4-[(5s)-5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n-[(4r)-2-ethyl-3-oxo-1,2-oxazolidin-4-yl]-2-methylbenzamide (CED0285059)

Record Information

Version

1.0

Creation Date

2026-08-30 16:20:47 UTC

Update Date

2026-08-30 16:20:47 UTC

Accession Number

CHEM330475

Identification

Common Name

4-[(5s)-5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n-[(4r)-2-ethyl-3-oxo-1,2-oxazolidin-4-yl]-2-methylbenzamide

Class

Small Molecule

Description

4-[(5s)-5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n-[(4r)-2-ethyl-3-oxo-1,2-oxazolidin-4-yl]-2-methylbenzamide has the chemical formula C23H19Cl2F4N3O4. With an average molecular weight of 548.30 g/mol, 4-[(5s)-5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-n-[(4r)-2-ethyl-3-oxo-1,2-oxazolidin-4-yl]-2-methylbenzamide is a heavy molecule.

Contaminant Type

Not Available

Chemical Structure

MOL SDF PDB SMILES InChI

Synonyms

Not Available

Chemical Formula

C₂₃H₁₉Cl₂F₄N₃O₄

Average Molecular Mass

Not Available

Monoisotopic Mass

547.069 g/mol

CAS Registry Number

1309959-62-3

IUPAC Name

Not Available

Traditional Name

Not Available

SMILES

CCN1C(=O)C(CO1)NC(=O)C2=C(C=C(C=C2)C3=NOC(C3)(C4=CC(=C(C(=C4)Cl)F)Cl)C(F)(F)F)C

InChI Identifier

InChI=1S/C23H19Cl2F4N3O4/c1-3-32-21(34)18(10-35-32)30-20(33)14-5-4-12(6-11(14)2)17-9-22(36-31-17,23(27,28)29)13-7-15(24)19(26)16(25)8-13/h4-8,18H,3,9-10H2,1-2H3,(H,30,33)/t18-,22+/m1/s1

InChI Key

WLSQDEYDCAGPIR-GCJKJVERSA-N

Chemical Taxonomy

Classification

Not classified

Biological Properties

Status

Detected and Not Quantified

Origin

Not Available

Cellular Locations

Not Available

Biofluid Locations

Not Available

Tissue Locations

Not Available

Applications

Not Available

Biological Roles

Not Available

Chemical Roles

Not Available

Organoleptic Effects

Not Available

Physical Properties

State

Not Available

Appearance

Not Available

Experimental Properties

Property	Value
Melting Point	Not Available
Boiling Point	Not Available
Solubility	Not Available

Predicted Properties

Not Available

Spectra

Not Available

Toxicity Profile

Mechanism of Toxicity

Not Available

Carcinogenicity (IARC Classification)

Not Available

Minimum Risk Level

Not Available

Symptoms

Not Available

Treatment

Not Available

Toxicity Values

Toxicity Value	Unit	Value Range	Organism	Dose Descriptor	Route of Exposure	Predicted or Experimental	Reference
8512.0	Log mg/kg	[4800:15000]	Rat	LD50	oral	predicted	Not Available

Health Effects

Health Effect	Relationship	Direction	Reference

Exposure Sources

Source ID	Source	Sector	Reference
10	Insecticides	Agriculture & land management	Not Available
596	Acaricides	Agriculture & land management	Not Available
600	Herbicides And Algicides	Agriculture & land management	Not Available
603	Nematocides	Agriculture & land management	Not Available
604	Pest Attractants	Agriculture & land management	Not Available
605	Pest Repellants	Agriculture & land management	Not Available
606	Plant Growth Regulators	Agriculture & land management	Not Available

Pathways

0 pathways

No pathways found

No metabolic pathways have been associated with this synthetic chemical

Targets

Structure	Protein	UniProt ID	Organism	Relationship	Details
Click to view 3D structure	Apoptotic protease-activating factor 1	O14727	Humans	Predicted (SEA)	72.789
Click to view 3D structure	Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1	Q9GZU7	Humans	Predicted (SEA)	269.981
Click to view 3D structure	DNA dC->dU-editing enzyme APOBEC-3G	Q9HC16	Humans	Predicted (SEA)	29.8163
Click to view 3D structure	Induced myeloid leukemia cell differentiation protein Mcl-1	Q07820	Humans	Predicted (SEA)	672.384
Click to view 3D structure	Small ubiquitin-related modifier 1	P63165	Humans	Predicted (SEA)	208.247
Click to view 3D structure	Penicillin-binding protein 2x	P14677	Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4)	Predicted (SEA)	10.1204
Click to view 3D structure	DNA (cytosine-5)-methyltransferase 1	P26358	Humans	Predicted (SEA)	360.13
Click to view 3D structure	Glycoprotein G	Q9IH62	Henipavirus nipahense	Predicted (SEA)	58.2312
Click to view 3D structure	Histone acetyltransferase KAT5	Q92993	Humans	Predicted (SEA)	21.5642
Click to view 3D structure	Voltage-gated inwardly rectifying potassium channel KCNH2	Q12809	Humans	Predicted (SEA)	5832.07
Click to view 3D structure	Histone acetyltransferase KAT7	O95251	Humans	Predicted (SEA)	44.3741
Click to view 3D structure	Cytochrome P450 3A4	P08684	Humans	Predicted (SEA)	5908.83
Click to view 3D structure	Cannabinoid receptor 2	P34972	Humans	Predicted (SEA)	1504.59
Click to view 3D structure	Cannabinoid receptor 1	P21554	Humans	Predicted (SEA)	1847.05
Click to view 3D structure	A disintegrin and metalloproteinase with thrombospondin motifs 7	Q1EHB3	Rattus norvegicus	Predicted (SEA)	26.0016
Click to view 3D structure	A disintegrin and metalloproteinase with thrombospondin motifs 12	P58397	Humans	Predicted (SEA)	26.0016
Click to view 3D structure	A disintegrin and metalloproteinase with thrombospondin motifs 7	Q68SA9	Mus musculus	Predicted (SEA)	26.0016
Click to view 3D structure	Cytochrome P450 2D6	P10635	Humans	Predicted (SEA)	5740.68
Click to view 3D structure	Beta-adrenergic receptor kinase 1	P25098	Humans	Predicted (SEA)	859.845
Click to view 3D structure	Mitogen-activated protein kinase 9	P45984	Humans	Predicted (SEA)	4813.11
Click to view 3D structure	Histone acetyltransferase KAT6A	Q92794	Humans	Predicted (SEA)	116.385
Click to view 3D structure	Cytochrome P450 2C9	P11712	Humans	Predicted (SEA)	6406.29
Click to view 3D structure	RAF proto-oncogene serine/threonine-protein kinase	P04049	Humans	Predicted (SEA)	2879.8
Click to view 3D structure	Tyrosine-protein kinase JAK2	O60674	Humans	Predicted (SEA)	5468.44
Click to view 3D structure	Mitogen-activated protein kinase 14	Q16539	Humans	Predicted (SEA)	4926.77