SCHEMBL769541

SCHEMBL769541

CC(C)(C)c1cc(NC(=O)Oc2ccccc2)no1

nearest known ligand 0.64

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ RAF1 P04049 9/20 0.64
▸ MAPK13 O15264 1/20 0.64
▸ MAPK12 P53778 1/20 0.64
▸ MAPK11 Q15759 1/20 0.64
▸ MAPK14 Q16539 1/20 0.64
▸ RAB9A P51151 4/20 0.63
▸ NPC1 O15118 3/20 0.63
▸ MEN1 O00255 2/20 0.63
▸ KMT2A Q03164 2/20 0.63
▸ FLT3 P36888 4/20 0.55
▸ MAPT P10636 1/20 0.54
▸ HTT P42858 1/20 0.54
▸ NPSR1 Q6W5P4 1/20 0.54
▸ POLB P06746 1/20 0.54
▸ EGFR P00533 1/20 0.52
▸ SMN1; SMN2 Q16637 1/20 0.51

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
SCHEMBL1015499 0.89 RAF1 (0.52) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL769245 0.87 RAF1 (0.50) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL1015351 0.87 RAF1 (0.50) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL11293751 0.87 RAF1 (0.50) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL770045 0.87 RAF1 (0.50) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL4903102 0.86 RAF1 (0.48) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL1011493 0.86 RAF1 (0.49) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL17732309 0.86 RAF1 (0.49) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL1012213 0.85 RAF1 (0.48) RAF1MAPK13MAPK12MAPK11MAPK14
SCHEMBL13611455 0.84 RAF1 (0.50) RAF1MAPK13MAPK12MAPK11MAPK14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4724439-A1 HETEROARYL DERIVATIVES AS DDRS INHIBITORS Chiesi Farmaceutici S.p.A. (IT) 2026-04-15 — — EP disclosed
EP-4662206-A1 GSPT1 DEGRADER COMPOUNDS Captor Therapeutics S.A. (PL) 2025-12-17 — — EP disclosed
WO-2024251855-A1 HETEROARYL DERIVATIVES AS DDRS INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2024-12-12 — — WO disclosed
US-12115152-B2 Pan-RAF kinase inhibitor and use thereof Tarapeutics Science Inc. (CN) 2024-10-15 — — US disclosed
US-12091413-B2 Inhibitors of NEK7 kinase Halia Therapeutics, Inc. (US) 2024-09-17 — — US disclosed
WO-2024165577-A1 GSPT1 DEGRADER COMPOUNDS CAPTOR THERAPEUTICS S.A. (PL) 2024-08-15 — — WO disclosed
EP-4146348-B1 INHIBITORS OF NEK7 KINASE HALIA THERAPEUTICS INC (US) 2024-07-03 — — EP disclosed
US-20240158394-A1 NEK7 INHIBITORS Halia Therapeutics, Inc. 2024-05-16 — — US disclosed
WO-2024059200-A1 NEK7 INHIBITORS Halia Therapeutics, Inc. (US) 2024-03-21 — — WO disclosed
US-20230416259-A1 INHIBITORS OF NEK7 KINASE HALIA THERAPEUTICS INC (US) 2023-12-28 — — US disclosed
EP-1436265-A2 CHEMICAL COMPOUNDS SmithKline Beecham Corporation (US) 2004-07-14 — — EP disclosed
EP-1432714-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2004-06-30 — — EP disclosed
EP-1425284-A2 FURO- AND THIENOPYRIMIDINE DERIVATIVES AS ANGIOGENESIS INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 2004-06-09 — — EP disclosed
WO-2004043379-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2004-05-27 — — WO disclosed
WO-2003072541-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2003-09-04 — — WO disclosed
WO-2003029209-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2003-04-10 — — WO disclosed
WO-2003022852-A2 FURO-AND THIENOPYRIMIDINE DERIVATIVES AS ANGIOGENESIS INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 2003-03-20 — — WO disclosed
EP-0144098-A1 Cyclic ureas of isoxazole SHIONOGI & CO., LTD. (JP) 1985-06-12 — — EP disclosed
EP-0114456-A2 Acylated isoxazolyl ureas, their preparation, herbicidal formulations containing the same, and a herbicidal method SHIONOGI & CO., LTD. (JP) 1984-08-01 — — EP disclosed
EP-0044185-A2 Imidazolidinone derivatives ELI LILLY AND COMPANY (US) 1982-01-20 — — EP 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 (4 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-12091413-B2 Inhibitors of NEK7 kinase NEK7, NEK1, NEK5 RAF1 274/4885MAPK13 409/4885MAPK12 713/4885
US-12115152-B2 Pan-RAF kinase inhibitor and use thereof BRAF, RAF1, ARAF RAF1 2/4885MAPK13 36/4885MAPK12 71/4885
US-20240158394-A1 NEK7 INHIBITORS NEK7, NEK5, NEK1 RAF1 944/4885MAPK13 670/4885MAPK12 1037/4885
US-20230416259-A1 INHIBITORS OF NEK7 KINASE NEK7, NEK1, NEK5 RAF1 274/4885MAPK13 409/4885MAPK12 713/4885

“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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