
Common name
1-phenyl-3-(trifluoromethyl)pyrazole
IUPAC name
1-phenyl-3-(trifluoromethyl)pyrazole
SMILES
FC(F)(F)c1nn(cc1)c2ccccc2
Common name
1-phenyl-3-(trifluoromethyl)pyrazole
IUPAC name
1-phenyl-3-(trifluoromethyl)pyrazole
SMILES
FC(F)(F)c1nn(cc1)c2ccccc2
INCHI
InChI=1S/C10H7F3N2/c11-10(12,13)9-6-7-15(14-9)8-4-2-1-3-5-8/h1-7H
FORMULA
C10H7F3N2

Common name
1-phenyl-3-(trifluoromethyl)pyrazole
IUPAC name
1-phenyl-3-(trifluoromethyl)pyrazole
Molecular weight
213.179
clogP
1.320
clogS
-2.764
Frequency
0.0003
HBond Acceptor
0
HBond Donor
1
Total PolarSurface Area
19.67
Number of Rings
2
Rotatable Bond
2
Drug ID | Common name | Structure CAS | Compound class | Therapeutic area |
---|---|---|---|---|
FDBD00355 | Celecoxib |
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Antineoplastic Agents; Cyclooxygenase 2 Inhibitors; Antineoplastic and Immunomodulating Agents; Musculo-Skeletal System; Antiinflammatory and Antirheumatic Products, Non-Steroids; Antiinflammatory and Antirheumatic Products; Coxibs; Cytochrome P-450 CYP2C9 Inhibitors; Cytochrome P-450 CYP2C9 Inducers; CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; | For relief and management of osteoarthritis (OA), rheumatoid arthritis (RA), juvenile rheumatoid arthritis (JRA), ankylosing spondylitis, acute pain, primary dysmenorrhea and oral adjunct to usual care for patients with familial adenomatous polyposis. |
1 ,
1
FRAGNAME | PDBID | SIMILIRITY | XSCORE | SMILE | HAC |
---|---|---|---|---|---|
1oq5_ligand_2_4.mol2 | 1oq5 | 1 | -6.81 | C(F)(F)(F)c1cc[n+]([nH]1)c1ccccc1 | 15 |
4ehr_ligand_2_40.mol2 | 4ehr | 0.724138 | -6.36 | C(O)c1cc[n+](c2ccccc2)[nH]1 | 13 |
4ehr_ligand_2_21.mol2 | 4ehr | 0.707317 | -6.48 | c1(ccccc1)[n+]1c(C)cc[nH]1 | 12 |
4ehr_ligand_3_94.mol2 | 4ehr | 0.670213 | -6.61 | C(O)c1cc(C)[n+](c2ccccc2)[nH]1 | 14 |
2nnq_ligand_2_20.mol2 | 2nnq | 0.663265 | -8.01 | c1cc(ccc1)c1cc[n+]([nH]1)c1ccccc1 | 17 |
4r5t_ligand_2_9.mol2 | 4r5t | 0.650602 | -7.36 | Cc1ccc([n+]2[nH]ccc2)cc1 | 12 |
100 ,
11