Naproxen

Naproxen

SCHEMBL29350675

COc1ccc2cc([C@@H](C)C(=O)O)ccc2c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

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

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 3/20 1.00
PTGS1 known ✓ P23219 3/20 1.00
AKR1C3 P42330 11/20 1.00
AKR1C2 P52895 11/20 1.00
TSHR P16473 2/20 1.00
CDC42 P60953 1/20 1.00
RAC1 P63000 1/20 1.00
CYP1A2 P05177 1/20 1.00
SLC22A6 Q4U2R8 1/20 1.00
LMNA P02545 1/20 0.71
MAPT P10636 1/20 0.71
CYP2C9 P11712 1/20 0.71
TDP1 Q9NUW8 1/20 0.69
L3MBTL1 Q9Y468 1/20 0.69
AKR1C1 Q04828 1/20 0.65
APP P05067 1/20 0.58
CYP2C19 P33261 1/20 0.58

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
Naproxen SCHEMBL29360045 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL215236 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL28834409 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL616149 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL42434 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL29359528 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL29350704 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL3046 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL10029028 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR
Naproxen SCHEMBL30346195 1.00 AKR1C3 (1.00) AKR1C3AKR1C2PTGS2PTGS1TSHR

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 70 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117534557-B Preparation method of D, L-naproxen 江苏八巨药业有限公司 2025-01-24 CN claimed
WO-2024075139-A1 A PROCESS FOR PREPARATION OF FINERENONE AND INTERMEDIATES THEREOF MAITHRI DRUGS PRIVATE LIMITED (IN) 2024-04-11 WO claimed
CN-117534557-A Preparation method of D, L-naproxen 江苏八巨药业有限公司 2024-02-09 CN claimed
WO-2024026354-A2 METHODS AND COMPOSITIONS FOR USE IN TREATING AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE (ARPKD) THE GENERAL HOSPITAL CORPORATION (US) 2024-02-01 WO claimed
CN-110573495-B Trans-isomeric heterocyclic compounds and process for preparing same 浙江医药股份有限公司新昌制药厂 2023-04-11 CN claimed
CN-218459490-U Feeding device of D, L-naproxen bromination reation kettle 江苏八巨药业有限公司 2023-02-10 CN claimed
US-12377072-B2 Modulators of GTPases and their use UNM RAINFOREST INNOVATIONS (US) 2025-08-05 US disclosed
CN-120082607-A Method for splitting chiral acid/alcohol through enzymatic esterification-hydrolysis cascade 华南理工大学 2025-06-03 CN disclosed
US-12319952-B2 Method for enzymatic resolution of chiral substances SOUTH CHINA UNIVERSITY OF TECHNOLOGY (CN) 2025-06-03 US disclosed
CN-120058595-A Chiral amine reagent, preparation method thereof and application thereof in chiral drug resolution and analysis 安徽医科大学 2025-05-30 CN disclosed
CN-120009432-A Method for detecting 9 antipyretic analgesic drugs in feed 北京市兽药饲料监测中心 2025-05-16 CN disclosed
CN-116250539-B Ternary weeding composition containing fenpyrazamine and application thereof 青岛清原化合物有限公司 2025-03-18 CN disclosed
CN-119613243-A Preparation method for converting naproxen impurity into naproxen racemate 江苏八巨药业有限公司 2025-03-14 CN disclosed
US-11459295-B2 2-beta-naphthyl-acetic acid analogs as AKR1C3 inhibitors and methods of using same THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2022-10-04 US disclosed
CN-115043721-A Preparation method of alpha-substituted chiral carboxylic acid compound 山东师范大学 2022-09-13 CN disclosed
EP-3527573-B9 SYNTHESIS OF POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS GILEAD SCIENCES INC (US) 2022-07-06 EP disclosed
CN-110903189-B Synthesis method of chiral 2-aryl propionate 大连大学 2022-06-21 CN disclosed
CN-114394983-A Synthesis of polycyclic carbamoylpyridone compounds 吉利德科学公司 2022-04-26 CN disclosed
CN-112048527-B Method for splitting chiral substance by double enzyme combination 华南理工大学 2022-04-22 CN disclosed
CN-110698499-B Chiral silver nanocluster and preparation and application thereof 安徽大学 2022-01-25 CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11459295-B2 2-beta-naphthyl-acetic acid analogs as AKR1C3 inhibitors and methods of using same AKR1C3, AKR1C2, AKR1A1 PTGS2 294/4885PTGS1 408/4885AKR1C3 1/4885
US-12377072-B2 Modulators of GTPases and their use CDC42, RAC1, ROCK1 PTGS2 2977/4885PTGS1 1972/4885AKR1C3 2474/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.