THC Science

Lonazolac
Clinical data
ATC code	M01AB09 (WHO) ;
Identifiers
	IUPAC name [3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl]acetic acid;
CAS Number	53808-88-1 ;
PubChem CID	68706;
ChemSpider	61957 ;
UNII	13097143QI;
KEGG	D07265 ;
ChEBI	CHEBI:76164 ;
CompTox Dashboard (EPA)	DTXSID4046151 ;
ECHA InfoCard	100.053.428
Chemical and physical data
Formula	C17H13ClN2O2
Molar mass	312.75 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES c1ccc(cc1)n2cc(c(n2)c3ccc(cc3)Cl)CC(=O)O;
	InChI InChI=1S/C17H13ClN2O2/c18-14-8-6-12(7-9-14)17-13(10-16(21)22)11-20(19-17)15-4-2-1-3-5-15/h1-9,11H,10H2,(H,21,22) ; Key:XVUQHFRQHBLHQD-UHFFFAOYSA-N ;
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Lonazolac is a nonsteroidal anti-inflammatory drug (NSAID).

Non-steroidal anti-inflammatory drugs (NSAIDs) (primarily M01A and M02A, also N02BA)
pyrazolones / pyrazolidines	Aminophenazone Ampyrone Azapropazone Clofezone Difenamizole Famprofazone Feprazone Kebuzone Metamizole Mofebutazone Morazone Nifenazone Oxyphenbutazone Phenazone Phenylbutazone Propyphenazone Sulfinpyrazone Suxibuzone^‡
salicylates	Aspirin (acetylsalicylic acid)^# Aloxiprin Benorylate Carbasalate calcium Diflunisal Dipyrocetyl Ethenzamide Guacetisal Magnesium salicylate Methyl salicylate Salsalate Salicin Salicylamide Salicylic acid (salicylate) Sodium salicylate
acetic acid derivatives and related substances	Aceclofenac Acemetacin Alclofenac Amfenac Bendazac Bromfenac Bufexamac Bumadizone Diclofenac Difenpiramide Etodolac Felbinac Fenclozic acid Fentiazac Indometacin Indometacin farnesil Isoxepac Ketorolac Lonazolac Mofezolac Oxametacin Prodolic acid Proglumetacin Sulindac Tiopinac Tolmetin Zomepirac^†
oxicams	Ampiroxicam Droxicam Isoxicam Lornoxicam Meloxicam Piroxicam Pivoxicam Tenoxicam
propionic acid derivatives (profens)	Alminoprofen Benoxaprofen^† Carprofen^‡ Dexibuprofen Dexketoprofen Fenbufen Fenoprofen Flunoxaprofen Flurbiprofen Ibuprofen^# Ibuproxam Indoprofen^† Ketoprofen Loxoprofen Miroprofen Naproxen Oxaprozin Pelubiprofen Piketoprofen Pirprofen Suprofen Tarenflurbil Tepoxalin^‡ Tiaprofenic acid Vedaprofen^‡ Zaltoprofen COX-inhibiting nitric oxide donator: Naproxcinod
n-arylanthranilic acids (fenamates)	Azapropazone Clonixin Etofenamate Floctafenine Flufenamic acid Flunixin Flutiazin Glafenine^† Meclofenamic acid Mefenamic acid Morniflumate Niflumic acid Tolfenamic acid
COX-2 inhibitors (coxibs)	Apricoxib Celecoxib (+tramadol) Cimicoxib^‡ Deracoxib^‡ Etoricoxib Firocoxib^‡ Lumiracoxib^† Mavacoxib^‡ Parecoxib Robenacoxib^‡ Rofecoxib^† Valdecoxib^†
other	Aminopropionitrile Benzydamine Chondroitin sulfate Diacerein Fluproquazone Glucosamine Glycosaminoglycan Hyperforin Nabumetone Nimesulide Oxaceprol Proquazone Superoxide dismutase / orgotein Tenidap
NSAID combinations	Ibuprofen/famotidine Ibuprofen/hydrocodone Ibuprofen/oxycodone Ibuprofen/paracetamol Meloxicam/bupivacaine Naproxen/diphenhydramine Naproxen/esomeprazole
Key: underline indicates initially developed first-in-class compound of specific group; ^#WHO-Essential Medicines; ^†withdrawn drugs; ^‡veterinary use.
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Clinical data

ATC code	M01AB09 (WHO)
Identifiers
IUPAC name [3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl]acetic acid
CAS Number	53808-88-1^Y
PubChem CID	68706
ChemSpider	61957^N
UNII	13097143QI
KEGG	D07265^Y
ChEBI	CHEBI:76164^N
CompTox Dashboard (EPA)	DTXSID4046151
ECHA InfoCard	100.053.428
Chemical and physical data
Formula	C₁₇H₁₃ClN₂O₂
Molar mass	312.75 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES c1ccc(cc1)n2cc(c(n2)c3ccc(cc3)Cl)CC(=O)O
InChI InChI=1S/C17H13ClN2O2/c18-14-8-6-12(7-9-14)17-13(10-16(21)22)11-20(19-17)15-4-2-1-3-5-15/h1-9,11H,10H2,(H,21,22)^N Key:XVUQHFRQHBLHQD-UHFFFAOYSA-N^N
^NY (what is this?) (verify)