SCHEMBL4687548

SCHEMBL4687548

O=C(Cc1ccccc1)Nc1nccs1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FFAR2 O15552 1/20 0.74
▸ LMNA P02545 3/20 0.68
▸ USP2 O75604 1/20 0.68
▸ TSHR P16473 1/20 0.68
▸ SCN3A Q9NY46 1/20 0.65
▸ RAB9A P51151 3/20 0.65
▸ SMN1; SMN2 Q16637 3/20 0.65
▸ NPC1 O15118 2/20 0.65
▸ TP53 P04637 1/20 0.65
▸ THRB P10828 1/20 0.65
▸ HPGD P15428 1/20 0.65
▸ KDM4E B2RXH2 1/20 0.65
▸ POLB P06746 1/20 0.63
▸ L3MBTL1 Q9Y468 1/20 0.62
▸ ROCK2 O75116 1/20 0.61
▸ ROCK1 Q13464 1/20 0.61
▸ ALDH1A1 P00352 3/20 0.60
▸ MAPK1 P28482 1/20 0.60
▸ HRH1 P35367 1/20 0.60
▸ GAA P10253 1/20 0.59

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
Hydrochloric Acid SCHEMBL29855979 0.98 FFAR2 (0.72) FFAR2LMNAUSP2TSHRSCN3A
SCHEMBL13694245 0.85 MAPK8 (0.63) FFAR2LMNAUSP2TSHRRAB9A
SCHEMBL1458948 0.85 PKM (0.67) LMNAUSP2TSHRRAB9ASMN1; SMN2
SCHEMBL27874867 0.85 RAB9A (0.62) FFAR2LMNAUSP2TSHRSCN3A
SCHEMBL31207176 0.84 FFAR2 (0.64) FFAR2LMNAUSP2TSHRSCN3A
SCHEMBL23657933 0.83 PRKACA (0.61) FFAR2LMNAUSP2TSHRRAB9A
SCHEMBL11627595 0.83 ROCK1 (0.61) FFAR2LMNAUSP2TSHRSCN3A
SCHEMBL1358311 0.82 KDM4E (0.67) FFAR2LMNAUSP2TSHRRAB9A
SCHEMBL18956343 0.82 ALDH1A1 (0.70) LMNAUSP2TSHRRAB9ASMN1; SMN2
SCHEMBL29911992 0.82 ALDH1A1 (0.65) FFAR2LMNAUSP2TSHRRAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115160311-B Difunctional compound for EGFR degradation and application thereof 北京康辰药业股份有限公司 2024-03-15 — — CN claimed
CN-115109055-B Difunctional compound for EGFR degradation and application thereof 北京康辰药业股份有限公司 2023-11-28 — — CN claimed
CN-115160311-A Bifunctional compound for EGFR degradation and application thereof 北京康辰药业股份有限公司 2022-10-11 — — CN claimed
CN-115109055-A Bifunctional compound for EGFR degradation and application thereof 北京康辰药业股份有限公司 2022-09-27 — — CN claimed
CN-100506807-C Amide derivatives as GK activators NOVO NORDISK AS (DK) 2009-07-01 — — CN claimed
CN-101434585-A Amide derivatives as GK activators NOVO NORDISK AS (DK) 2009-05-20 — — CN claimed
CN-1286835-C Phenylacetamido-thiazole derivatives, process for their preparation and their use as antitumor agents PHARMACIA ITALIA SPA (IT) 2006-11-29 — — CN claimed
EP-1724270-A2 Phenylacetamido-thiazole derivatives, process for their preparation and their use as antitumor agents Pfizer Italia S.r.l. (IT) 2006-11-22 — — EP claimed
EP-1406899-B1 PHENYLACETAMIDO-THIAZOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS ANTITUMOR AGENTS PFIZER ITALIA SRL (IT) 2006-11-15 — — EP claimed
US-20040235919-A1 Phenylacetamido-thiazole derivatives, process for the preparation and their use as antitumor agents PFIZER ITALIA S.R.I. (IT) 2004-11-25 — — US claimed
CN-1531535-A Phenylacetamido-thiazole derivatives, process for their preparation and their use as antitumor agents — 2004-09-22 — — CN claimed
EP-1406899-A2 PHENYLACETAMIDO-THIAZOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS ANTITUMOR AGENTS Pharmacia Italia S.p.A. (IT) 2004-04-14 — — EP claimed
WO-2003008365-A2 PHENYLACETAMIDO-THIAZOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS ANTITUMOR AGENTS PHARMACIA ITALIA S.P.A. (IT) 2003-01-30 — — WO claimed
EP-0815108-A1 CYCLIC UREA HIV PROTEASE INHIBITORS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1998-01-07 — — EP claimed
US-5683999-A Cyclic urea HIV protease inhibitors THE DUPONT MERCK PHARMACEUTICAL COMPANY (US) 1997-11-04 — — US claimed
US-12622909-B2 Allosteric EGFR inhibitors and methods of use thereof DANA-FARBER CANCER INSTITUTE, INC. (US) 2026-05-12 — — US disclosed
US-20250388573-A1 FUSED BICYCLIC EGFR INHIBITORS AND METHODS OF USE THEREOF DANA FARBER CANCER INST INC (US) 2025-12-25 — — US disclosed
US-5683999-A Cyclic urea HIV protease inhibitors THE DUPONT MERCK PHARMACEUTICAL COMPANY (US) 1997-11-04 — — US disclosed
EP-0772606-A1 SUBSTITUTED THIAZOLES FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1997-05-14 — — EP disclosed
WO-1996003392-A1 SUBSTITUTED THIAZOLES FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1996-02-08 — — WO 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 (3 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-12622909-B2 Allosteric EGFR inhibitors and methods of use thereof EGFR, ERBB3, ERBB2 FFAR2 564/4885LMNA 4706/4885USP2 2262/4885
US-20250388573-A1 FUSED BICYCLIC EGFR INHIBITORS AND METHODS OF USE THEREOF EGFR, ERBB2, ERBB3 FFAR2 660/4885LMNA 4146/4885USP2 3259/4885
US-20040235919-A1 Phenylacetamido-thiazole derivatives, process for the preparation and their use as antitumor agents CDK2, CDK1, CDKN1A FFAR2 4127/4885LMNA 3198/4885USP2 4174/4885

“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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