Fomesafen

Fomesafen

SCHEMBL527125

CS(=O)(=O)[N-]C(=O)c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-].[Na+]

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Fomesafen. 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
▸ THRB known ✓ P10828 1/20 0.38
▸ TDP1 Q9NUW8 3/20 0.70
▸ MEN1 O00255 2/20 0.70
▸ KMT2A Q03164 2/20 0.70
▸ TTR P02766 1/20 0.70
▸ PPOX P50336 1/20 0.70
▸ FFAR1 O14842 5/20 0.43
▸ LMNA P02545 4/20 0.41
▸ POLB P06746 2/20 0.41
▸ MAPT P10636 2/20 0.41
▸ CCR6 P51684 1/20 0.41
▸ NPSR1 Q6W5P4 1/20 0.41
▸ GPR55 Q9Y2T6 1/20 0.41
▸ SMN1; SMN2 Q16637 3/20 0.40
▸ HPGD P15428 1/20 0.40
▸ FLT1 P17948 1/20 0.39
▸ FLT4 P35916 1/20 0.39
▸ KDR P35968 1/20 0.39
▸ ALDH1A1 P00352 1/20 0.39
▸ PYGL P06737 1/20 0.39

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
Fomesafen SCHEMBL466794 0.85 TDP1 (0.70) TDP1MEN1KMT2ATTRPPOX
Acifluorfen SCHEMBL9720252 0.85 TDP1 (0.86) TDP1MEN1KMT2ATTRPPOX
SCHEMBL11004074 0.85 MEN1 (0.73) TDP1MEN1KMT2ATTRPPOX
Acifluorfen SCHEMBL39453 0.84 TDP1 (0.82) TDP1MEN1KMT2ATTRPPOX
SCHEMBL6752643 0.84 MEN1 (0.82) TDP1MEN1KMT2ATTRPPOX
Acifluorfen SCHEMBL3690938 0.84 TDP1 (0.98) TDP1MEN1KMT2ATTRPPOX
Acifluorfen SCHEMBL29352750 0.84 TDP1 (0.82) TDP1MEN1KMT2ATTRPPOX
Acifluorfen SCHEMBL29471425 0.84 TDP1 (0.82) TDP1MEN1KMT2ATTRPPOX
Acifluorfen SCHEMBL30370086 0.84 TDP1 (0.82) TDP1MEN1KMT2ATTRPPOX
SCHEMBL9755520 0.84 TDP1 (0.71) TDP1MEN1KMT2ATTRPPOX

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4337017-A1 HERBICIDE/SAFENER COMBINATION BASED ON SAFENERS FROM THE CLASS OF SUBSTITUTED [(1,5-DIPHENYL-1H-1,2,4-TRIAZOL-3-YL)OXY]ACETIC ACIDS AND THEIR SALTS Bayer Aktiengesellschaft (DE) 2024-03-20 — — EP claimed
WO-2022152728-A1 HERBICIDAL COMPOSITIONS BAYER AKTIENGESELLSCHAFT (DE) 2022-07-21 — — WO claimed
WO-2026098491-A1 TRANSGENIC GLYCINE MAX EVENT KA-6G2Ø16-7 AND DETECTION METHOD THEREFOR 青岛清原种子科学有限公司 2026-05-15 — — WO disclosed
CN-118266468-B Weeding composition containing protoporphyrinogen oxidase inhibitor and application thereof 青岛恒宁生物科技有限公司 2026-05-15 — — CN disclosed
EP-4617275-A1 OXABICYCLOALKANE COMPOUNDS, PREPARATION METHOD THEREFOR, AND HERBICIDAL COMPOSITION AND USE THEREOF Qingdao KingAgroot Chemical Compound Co., Ltd. (CN) 2025-09-17 — — EP disclosed
US-20250230462-A1 PPO2 POLYPEPTIDE HAVING TOLERANCE TO PPO INHIBITOR HERBICIDE AND APPLICATION QINGDAO KINGAGROOT CHEMICAL COMPOUND CO., LTD. (CN) 2025-07-17 — — US disclosed
WO-2025118900-A1 USE OF HEMG PPO ENZYME IN GENERATING OR IMPROVING TOLERANCE TO PPO-INHIBITING HERBICIDES 青岛清原种子科学有限公司 2025-06-12 — — WO disclosed
US-12325646-B2 Fertigation water treatment UNIVERSITY OF GUELPH (CA) 2025-06-10 — — US disclosed
CN-120118937-A Use of HemG PPO enzymes for producing or increasing tolerance to PPO-inhibiting herbicides 青岛清原种子科学有限公司 2025-06-10 — — CN disclosed
US-20250024837-A1 PESTICIDE SYSTEM BANISH, MICHELE 2025-01-23 — — US disclosed
US-20240368618-A1 PPO POLYPEPTIDES TOLERANT TO PPO-INHIBITING HERBICIDES AND USE THEREOF QINGDAO KINGAGROOT CHEMICAL COMPOUND CO., LTD. (CN) 2024-11-07 — — US disclosed
EP-2196089-A1 Fungicidal Compositions Sygenta Participations AG. (CH) 2010-06-16 — — EP disclosed
EP-2196088-A1 Fungicidal Compositions Syngenta Participations AG (CH) 2010-06-16 — — EP disclosed
EP-2193715-A1 Fungicidal Compositions Sygenta Participations AG. (CH) 2010-06-09 — — EP disclosed
EP-2193714-A1 Fungicidal Compositions Sygenta Participations AG. (CH) 2010-06-09 — — EP disclosed
EP-2193717-A1 Fungicidal Compositions Sygenta Participations AG. (CH) 2010-06-09 — — EP disclosed
EP-2193716-A1 Fungicidal Compositions Syngenta Participations AG (CH) 2010-06-09 — — EP disclosed
EP-2150113-A1 FUNGICIDAL COMPOSITIONS Syngeta Participations AG (CH) 2010-02-10 — — EP disclosed
WO-2008131901-A1 FUNGICIDAL COMPOSITIONS SYNGENTA PARTICIPATIONS AG (CH) 2008-11-06 — — WO disclosed
US-20060276339-A1 Methods and compositions for increasing the efficacy of biologically-active ingredients BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM 2006-12-07 — — 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 (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-20060276339-A1 Methods and compositions for increasing the efficacy of biologically-active ingredients ENPP1, ENPP3, SMPD1 THRB 4526/4885TDP1 696/4885MEN1 1618/4885
US-20250024837-A1 PESTICIDE SYSTEM ACHE, PFAS, FPGS THRB 4104/4885TDP1 100/4885MEN1 4754/4885

“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.

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