SCHEMBL1194001

SCHEMBL1194001

O=C(O)c1ccc(S(F)(F)(F)(F)F)cc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 3/20 0.60
▸ TP53 P04637 1/20 0.60
▸ AKR1C3 P42330 3/20 0.53
▸ AKR1C2 P52895 3/20 0.53
▸ SRD5A2 P31213 3/20 0.52
▸ CA1 P00915 2/20 0.50
▸ CA2 P00918 2/20 0.50
▸ CA12 O43570 1/20 0.50
▸ CA3 P07451 1/20 0.50
▸ TYR P14679 1/20 0.50
▸ DRD1 P21728 1/20 0.50
▸ CA4 P22748 1/20 0.50
▸ CA6 P23280 1/20 0.50
▸ CA5A P35218 1/20 0.50
▸ CA7 P43166 1/20 0.50
▸ CA9 Q16790 1/20 0.50
▸ CA14 Q9ULX7 1/20 0.50
▸ CA5B Q9Y2D0 1/20 0.50
▸ BCL2L1 Q07817 1/20 0.48
▸ BAD Q92934 1/20 0.48

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
Terephthalic Acid SCHEMBL1010632 0.81 TSHR (0.92) TSHRTP53SRD5A2CA1CA2
SCHEMBL16161046 0.80 AKR1C3 (0.41) TSHRTP53AKR1C3AKR1C2CA1
SCHEMBL21585246 0.79 ALDH1A1 (0.61) TSHRTP53AKR1C3AKR1C2SRD5A2
SCHEMBL8045036 0.78 ALDH1A1 (0.43) TSHRTP53AKR1C3AKR1C2CA1
SCHEMBL3539246 0.78 PARP10 (0.48) TSHRAKR1C3AKR1C2CA1CA2
SCHEMBL8737307 0.78 MAPT (0.48) AKR1C3AKR1C2ALDH1A1SMN1; SMN2
Terephthalic Acid SCHEMBL175823 0.78 TSHR (1.00) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL2511919 0.78 TSHR (1.00) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL5053781 0.78 TSHR (1.00) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL1655 0.78 TSHR (1.00) TSHRTP53SRD5A2CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110770271-B Method for preparing functionalized fluorinated monomers, fluorinated monomers and compositions for preparing same 埃特纳科技有限公司 2023-04-18 — — CN claimed
US-20090036704-A1 Process for Preparing 4-Pentafluorosulfanylbenzoylguanidines SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2009-02-05 — — US claimed
US-7449594-B2 Process for preparing 4-pentafluorosulfanylbenzoylguanidines SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2008-11-11 — — US claimed
US-20070106094-A1 Process For Preparing 4-Pentafluorosulfanylbenzoylguanidines SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-05-10 — — US claimed
US-7126026-B2 Process for preparing 4-pentafluorosulfanylbenzoylguanidines SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2006-10-24 — — US claimed
US-20050131070-A1 Process for preparing 4-pentafluorosulfanylbenzoylguanidines AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2005-06-16 — — US claimed
EP-4558500-A1 IMIDAZOPYRIDINE COMPOUNDS, PREPARATION THEREOF AND THERAPEUTIC USES THEREOF Sanofi (FR) 2025-05-28 — — EP disclosed
CN-118791407-A Sulfinylamino group benzamide and process for preparing same Sulfonylamino benzamide derivatives 奥索生物公司 2024-10-18 — — CN disclosed
CN-118638096-A Sulfinylamino group benzamide and process for preparing same Sulfonylamino benzamide derivatives 奥索生物公司 2024-09-13 — — CN disclosed
CN-112204008-B Sulfonylaminobenzamides and sulfonylaminobenzamide derivatives 奥索生物公司 2024-07-05 — — CN disclosed
WO-2024017977-A1 IMIDAZOPYRIDINE COMPOUNDS, PREPARATION THEREOF AND THERAPEUTIC USES THEREOF SANOFI (FR) 2024-01-25 — — WO disclosed
EP-3796975-B1 SULFONYLAMINOBENZAMIDE DERIVATIVES ORSOBIO INC (US) 2023-08-30 — — EP disclosed
US-11390610-B2 Piperazine derivatives as MAGL inhibitors HOFFMANN-LA ROCHE INC. (US) 2022-07-19 — — US disclosed
US-20070179191-A1 OXADIAZOLONES AND DERIVATIVES THEREOF AS PPAR DELTA AGONISTS SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-08-02 — — US disclosed
EP-1740583-A1 OXADIAZOLONE DERIVATIVES AS PPAR DELTA AGONISTS Sanofi-Aventis Deutschland GmbH (DE) 2007-01-10 — — EP disclosed
WO-2005097786-A1 OXADIAZOLONE DERIVATIVES AS PPAR DELTA AGONISTS SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2005-10-20 — — WO disclosed
US-20030216476-A1 Pentafluorosulfanylbenzoylguanidines, processes for their preparation, their use as medicaments or diagnostic aids, and medicaments comprising them AVENTIS PHARMA DEUTSHCHLAND GMBH (DE) 2003-11-20 — — US disclosed
US-6140528-A ALKYL PENTAFLUOROSULFANYL-SUBSTITUTED-BENZOATES RHONE-POULENC AGRICULTURE LTD (GB) 2000-10-31 — — US disclosed
US-6013805-A USED AS HERBICIDES RHONE-POULENC AGRICULTURE LTD (GB) 2000-01-11 — — US disclosed
US-5849928-A Herbicidal isoxazole and 2-cyano-1,3-dione compounds RHONE-POULENC AGRICULTURE LIMITED (GB) 1998-12-15 — — 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-20070179191-A1 OXADIAZOLONES AND DERIVATIVES THEREOF AS PPAR DELTA AGONISTS PPARD, PPARA, PPARG TSHR 680/4885TP53 3150/4885AKR1C3 1404/4885
US-11390610-B2 Piperazine derivatives as MAGL inhibitors MAGI3, PYM1, MAG TSHR 3028/4885TP53 3649/4885AKR1C3 2867/4885
US-20090036704-A1 Process for Preparing 4-Pentafluorosulfanylbenzoylguanidines NHERF1, SLC9A1, SLC5A1 TSHR 465/4885TP53 4774/4885AKR1C3 1284/4885
US-20050131070-A1 Process for preparing 4-pentafluorosulfanylbenzoylguanidines NHERF1, SLC9A1, SLC5A1 TSHR 465/4885TP53 4774/4885AKR1C3 1284/4885
US-20030216476-A1 Pentafluorosulfanylbenzoylguanidines, processes for their preparation, their use as medicaments or diagnostic aids, and medicaments comprising them TNNI3, TNNT2, SDHB TSHR 2514/4885TP53 3255/4885AKR1C3 2694/4885
US-20070106094-A1 Process For Preparing 4-Pentafluorosulfanylbenzoylguanidines PAH, NCEH1, PNMT TSHR 376/4885TP53 4322/4885AKR1C3 2080/4885

“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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