Meclofenamic Acid

Meclofenamic Acid

SCHEMBL29460464

Cc1ccc(Cl)c(Nc2ccccc2C(=O)[O-])c1Cl.[Na+]

nearest known ligand 0.97

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ALOX5PTGS1PTGS2

The experimentally established mechanism targets of Meclofenamic Acid. 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
PTGS2 known ✓ P35354 13/20 0.97
PTGS1 known ✓ P23219 1/20 0.75
MEN1 O00255 2/20 0.97
MAPK1 P28482 2/20 0.97
KMT2A Q03164 2/20 0.97
GMNN O75496 1/20 0.97
USP2 O75604 1/20 0.97
LMNA P02545 1/20 0.97
CYP1A2 P05177 1/20 0.97
CYP3A4 P08684 1/20 0.97
GAA P10253 1/20 0.97
MAPT P10636 1/20 0.97
THRB P10828 1/20 0.97
CYP2C9 P11712 1/20 0.97
TSHR P16473 1/20 0.97
NFKB1 P19838 1/20 0.97
BLM P54132 1/20 0.97
PMP22 Q01453 1/20 0.97
HIF1A Q16665 1/20 0.97
METTL3 Q86U44 2/20 0.75

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
Meclofenamic Acid SCHEMBL1649454 1.00 PTGS2 (0.97) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL30384019 1.00 PTGS2 (0.97) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL4400214 0.99 PTGS2 (1.00) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL1874563 0.99 PTGS2 (1.00) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL3504 0.99 PTGS2 (1.00) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL30241166 0.99 PTGS2 (1.00) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL18171844 0.94 PTGS2 (0.90) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL1462647 0.88 PTGS2 (0.79) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL1538458 0.87 PTGS2 (0.77) PTGS2MEN1MAPK1KMT2AGMNN
Meclofenamic Acid SCHEMBL8531474 0.87 PTGS2 (0.77) PTGS2MEN1MAPK1KMT2AGMNN

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260137632-A1 NONAQUEOUS PREPARATION FOR PERCUTANEOUS ABSORPTION LEAD CHEMICAL CO., LTD. (JP) 2026-05-21 US disclosed
EP-4656206-A1 NON-AQUEOUS PERCUTANEOUSLY ABSORPTIVE FORMULATION Lead Chemical Co., Ltd. (JP) 2025-12-03 EP disclosed
EP-3856734-B1 REAGENTS AND PROCESS FOR DIRECT C-H FUNCTIONALIZATION STUDIENGESELLSCHAFT KOHLE GGMBH (DE) 2025-09-24 EP disclosed
WO-2025043297-A1 METHOD OF TREATING MYOPIA MCFADDEN SALLY (AU) 2025-03-06 WO disclosed
CN-110573881-B Method for determining interactions between biological cells 艾克斯赛安西娅有限公司 2024-09-03 CN disclosed
US-12065422-B2 Reagents and process for direct C—H functionalization STUDIENGESELLSCHAFT KOHLE GGMBH (DE) 2024-08-20 US disclosed
US-12029717-B2 Methods for treating brain metastasis MEMORIAL SLOAN-KETTERING CANCER CENTER (US) 2024-07-09 US disclosed
EP-3575791-B1 BLOOD TREATMENT METHOD AND BLOOD COLLECTION TUBE ARKRAY INC (JP) 2024-01-10 EP disclosed
EP-3685832-B1 METHODS FOR TREATING BRAIN METASTASIS MEMORIAL SLOAN KETTERING CANCER CENTER (US) 2023-08-30 EP disclosed
US-20230227425-A1 REAGENTS AND PROCESS FOR DIRECT C-H FUNCTIONALIZATION STUDIENGESELLSCHAFT KOHLE MBH (DE) 2023-07-20 US disclosed
US-11608322-B2 Reagents and process for direct C—H functionalization STUDIENGESELLSCHAFT KOHLE MBH (DE) 2023-03-21 US disclosed
CN-110547288-B Blood processing method and blood collection tube 爱科来株式会社 2022-09-02 CN disclosed
US-20220105069-A1 METHODS FOR TREATING BRAIN METASTASIS MEMORIAL SLOAN-KETTERING CANCER CENTER (US) 2022-04-07 US 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 (6 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-20230227425-A1 REAGENTS AND PROCESS FOR DIRECT C-H FUNCTIONALIZATION CFH, DOHH, CTSH PTGS2 3723/4885PTGS1 3936/4885MEN1 2782/4885
US-20220105069-A1 METHODS FOR TREATING BRAIN METASTASIS GJA1, GJB2, EPCAM PTGS2 599/4885PTGS1 359/4885MEN1 894/4885
US-11608322-B2 Reagents and process for direct C—H functionalization CFH, DOHH, CTSH PTGS2 3850/4885PTGS1 4021/4885MEN1 2686/4885
US-20260137632-A1 NONAQUEOUS PREPARATION FOR PERCUTANEOUS ABSORPTION PTGS1, PTGER1, MMP1 PTGS2 12/4885PTGS1 1/4885MEN1 3365/4885
US-12029717-B2 Methods for treating brain metastasis GJA1, GJB2, EPCAM PTGS2 599/4885PTGS1 359/4885MEN1 894/4885
US-12065422-B2 Reagents and process for direct C—H functionalization CFH, DOHH, CTSH PTGS2 3850/4885PTGS1 4021/4885MEN1 2686/4885

“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.