Amfenac

Amfenac

SCHEMBL2254

Nc1c(CC(=O)[O-])cccc1C(=O)c1ccccc1.O.[Na+]

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

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

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
Amfenac SCHEMBL3500793 1.00 — —
Amfenac SCHEMBL8347441 0.99 — —
Amfenac SCHEMBL29603368 0.98 — —
Amfenac SCHEMBL9644552 0.98 — —
Amfenac SCHEMBL11459150 0.97 ABCB11 (0.58) —
Amfenac SCHEMBL11467023 0.97 ABCB11 (0.58) —
Amfenac SCHEMBL11460876 0.97 ABCB11 (0.58) —
Amfenac SCHEMBL11726336 0.95 ABCB11 (0.59) —
Amfenac SCHEMBL9747739 0.95 ABCB11 (0.59) —
Amfenac SCHEMBL11730572 0.95 ABCB11 (0.59) —

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

Appears in 5621 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260137680-A1 NOVEL COMPOUNDS SITRYX THERAPEUTICS LTD (GB) 2026-05-21 — — US claimed
US-20260138973-A1 SUBSTITUTED PYRIDINES FOR USE IN TREATING OR PREVENTING INFLAMMATORY DISEASES OR DISEASES ASSOCIATED WITH AN UNDESIRABLE IMMUNE RESPONSE SITRYX THERAPEUTICS LTD (GB) 2026-05-21 — — US claimed
US-12617762-B2 Carboxy derivatives with antiinflamatory properties SITRYX THERAPEUTICS LIMITED (GB) 2026-05-05 — — US claimed
US-20260085061-A1 PHTHALAZINE DERIVATIVES AS PYRUVATE KINASE MODULATORS SITRYX THERAPEUTICS LIMITED (GB) 2026-03-26 — — US claimed
EP-4081511-B3 CARBOXY DERIVATIVES WITH ANTIINFLAMMATORY PROPERTIES SITRYX THERAPEUTICS LTD (GB) 2026-03-04 — — EP claimed
US-12545750-B2 Method for the diimide hydrogenation of emulsified unsaturated polymers PARKER DANE K (US) 2026-02-10 — — US claimed
EP-4634167-A1 SUBSTITUTED PYRIDINES FOR USE IN TREATING OR PREVENTING INFLAMMATORY DISEASES OR DISEASES ASSOCIATED WITH AN UNDESIRABLE IMMUNE RESPONSE Sitryx Therapeutics Limited (GB) 2025-10-22 — — EP claimed
EP-4612132-A1 PHTHALAZINE DERIVATIVES AS PYRUVATE KINASE MODULATORS Sitryx Therapeutics Limited (GB) 2025-09-10 — — EP claimed
EP-4543875-A1 OXADIAZOLE DERIVATIVES, PREPARATION PROCESS THEREOF AND THEIR USE IN TREATING INFLAMMATORY DISEASES Sitryx Therapeutics Limited (GB) 2025-04-30 — — EP claimed
CN-119874621-A Pharmaceutical composition containing pyrazole ether compound and application thereof 上海晓明检测技术服务有限公司 2025-04-25 — — CN claimed
EP-0435362-B1 COMPOSITION COMPRISING NON-STEROIDAL ANTI-INFLAMMATORY AGENT AND EFFECTIVELY NON-ANTIBACTERIAL TETRACYCLINE THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1993-04-21 — — EP claimed
EP-0435362-A1 Composition comprising non-steroidal anti-inflammatory agent and effectively non-antibacterial tetracycline THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1991-07-03 — — EP claimed
EP-0233910-B1 PLANT PROTECTING COMPOSITION INNOFINANCE Altalános Innovácios Pénzintézet (HU) 1990-09-19 — — EP claimed
EP-0225005-B1 ANTI-INFLAMMATORY ANALGESIC ADHESIVE PREPARATION NITTO DENKO CORPORATION (JP) 1990-03-14 — — EP claimed
US-4740374-A Anti-inflammatory analgesic adhesive preparation NITTO ELECTRIC INDUSTRIAL CO., LTD. (JP) 1988-04-26 — — US claimed
EP-0233910-A1 PLANT PROTECTING COMPOSITION. INNOFINANCE ALTALANOS INNOVACI (HU) 1987-09-02 — — EP claimed
EP-0225005-A1 Anti-inflammatory analgesic adhesive preparation NITTO DENKO CORPORATION (JP) 1987-06-10 — — EP claimed
WO-1987000400-A1 PLANT PROTECTING COMPOSITION INNOFINANCE ÁLTALÁNOS INNOVÁCIÓS PÉNZINTÉZET (HU) 1987-01-29 — — WO claimed
US-4221716-A Intermediate and process for the preparation of 7-acylindolin-2-ones A. H. ROBINS COMPANY, INC. (US) 1980-09-09 — — US claimed
US-4126635-A ANTICHOLESTEROL, BLOOD PLATELET AGGREGATION INHIBITION A. H. ROBINS COMPANY, INCORPORATED (US) 1978-11-21 — — US claimed
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