Piroxicam

Piroxicam

SCHEMBL8908556

CN1C(C(=O)Nc2ccccn2)=C(O)c2ccccc2S1(=O)=O.[NaH]

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

The experimentally established mechanism targets of Piroxicam. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS1 known ✓ P23219 5/20 0.98
PTGS2 known ✓ P35354 3/20 0.98
KDM4E B2RXH2 3/20 0.98
USP2 O75604 3/20 0.98
CYP2C9 P11712 2/20 0.98
CYP1A2 P05177 1/20 0.98
CYP3A4 P08684 1/20 0.98
CYP2D6 P10635 1/20 0.98
ALOX15 P16050 1/20 0.98
NFKB1 P19838 1/20 0.98
CYP2C19 P33261 1/20 0.98
BLM P54132 1/20 0.98
SLC22A6 Q4U2R8 1/20 0.98
SLC22A8 Q8TCC7 1/20 0.98
MAPK1 P28482 1/20 0.95
GAA P10253 1/20 0.68
LMNA P02545 2/20 0.66
KDR P35968 1/20 0.66
ABCB11 O95342 2/20 0.64
POLB P06746 1/20 0.64

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Piroxicam SCHEMBL28536166 0.99 PTGS1 (1.00) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL29352427 0.99 PTGS1 (1.00) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL29396075 0.99 PTGS1 (1.00) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL15741898 0.99 PTGS1 (1.00) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL2680486 0.99 PTGS1 (1.00) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL13462 0.99 PTGS1 (1.00) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL6759456 0.98 KDM4E (1.00) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL6942519 0.98 PTGS1 (0.98) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL5084571 0.98 PTGS1 (0.98) PTGS1KDM4EUSP2PTGS2CYP2C9
Piroxicam SCHEMBL27394226 0.98 PTGS1 (0.98) PTGS1KDM4EUSP2PTGS2CYP2C9

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115190878-B Crystalline hydrates of JAK inhibitor compounds 施万生物制药研发IP有限责任公司 2024-10-29 CN disclosed
CN-117064898-A Application of pirenoxine sodium in preparing antitumor drug 江西中医药大学 2023-11-17 CN disclosed
CN-112739697-B Dimethylaminoazetidine amides as JAK inhibitors 施万生物制药研发IP有限责任公司 2023-10-20 CN disclosed
CN-112703037-B 5-to 7-membered heterocyclic amides as JAK inhibitors 施万生物制药研发IP有限责任公司 2023-10-20 CN disclosed
CN-116507327-A Chewable formulations 礼蓝动物保健有限公司 2023-07-28 CN disclosed
US-5641504-A TRANSDERMAL DRUG DELIVERY ALZA CORPORATION (US) 1997-06-24 US disclosed
US-5378730-A Transdermal delivery of lidocaine ALZA CORPORATION (US) 1995-01-03 US disclosed
WO-1992020377-A1 SKIN PERMEATION ENHANCER COMPOSITIONS USING GLYCEROL MONOLINOLEATE ALZA CORPORATION (US) 1992-11-26 WO disclosed
EP-0123520-B1 PROCESS FOR PREPARING BASE SALTS OF PIROXICAM DEPOSITED ON A PHARMACEUTICALLY-ACCEPTABLE CARRIER PFIZER INC. (US) 1988-08-17 EP disclosed
EP-0123520-A1 Process for preparing base salts of piroxicam deposited on a pharmaceutically-acceptable carrier PFIZER INC. (US) 1984-10-31 EP disclosed