Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D05UWI
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| Former ID |
DNC002844
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| Drug Name |
Parecoxib
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| Synonyms |
Parecoxib; SC-69124; Dynastat; Valus-P; Vorth-P; SC 69124; UNII-9TUW81Y3CE; 9TUW81Y3CE; Parecoxib [USAN:INN:BAN]; CHEBI:73038; N-((p-(5-methyl-3-phenyl-4-isoxazolyl)phenyl)sulfonyl)propionamide; Parocoxib; N-[4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)phenyl]sulfonylpropanamide; Propanamide, N-((4-(5-methyl-3-phenyl-4-isoxazolyl)phenyl)sulfonyl)-; N-[4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzenesulfonyl]propanamide; N-{[4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)phenyl]sulfonyl}propanamide; parecoxibum; Valdecoxib Impurity J; Parecoxib (
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| Drug Type |
Small molecular drug
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| Structure |
 |
Download2D MOL |
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| Formula |
C19H18N2O4S
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| Canonical SMILES |
CCC(=O)NS(=O)(=O)C1=CC=C(C=C1)C2=C(ON=C2C3=CC=CC=C3)C
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| InChI |
1S/C19H18N2O4S/c1-3-17(22)21-26(23,24)16-11-9-14(10-12-16)18-13(2)25-20-19(18)15-7-5-4-6-8-15/h4-12H,3H2,1-2H3,(H,21,22)
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| InChIKey |
TZRHLKRLEZJVIJ-UHFFFAOYSA-N
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| CAS Number |
CAS 198470-84-7
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| PubChem Compound ID | ||||
| PubChem Substance ID |
10238678, 14828797, 17397807, 29300637, 49829565, 50067919, 76546468, 99444910, 104236927, 104409301, 129337106, 135076077, 137039042, 137244309, 142086609, 160969477, 162169241, 174528197, 177749133, 178100244, 179225992, 198980232, 210275621, 210281280, 211536041, 223794316, 226400424, 249867344, 252553762
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| ChEBI ID |
CHEBI:73038
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| ADReCS Drug ID | BADD_D01674 | |||
| SuperDrug ATC ID |
M01AH04
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| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Lactotransferrin (LTF) | Target Info | Inhibitor | [1] |
| NetPath Pathway | TGF_beta_Receptor Signaling Pathway | |||
| TCR Signaling Pathway | ||||
| Reactome | ROS production in response to bacteria | |||
| Amyloid formation | ||||
| WikiPathways | Latent infection of Homo sapiens with Mycobacterium tuberculosis | |||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. | |||
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