SCHEMBL2049672

SCHEMBL2049672

OCc1ccc2nccn2c1

nearest known ligand 0.68

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ KEAP1 Q14145 1/20 0.68
▸ DYRK1A Q13627 2/20 0.49
▸ DAO P14920 1/20 0.47
▸ MEN1 O00255 1/20 0.46
▸ CYP1A2 P05177 1/20 0.46
▸ KMT2A Q03164 1/20 0.46
▸ CPB2 Q96IY4 1/20 0.46
▸ RET P07949 2/20 0.45
▸ MERTK Q12866 5/20 0.43
▸ NAMPT P43490 5/20 0.42
▸ AXL P30530 4/20 0.41
▸ FLT3 P36888 4/20 0.41
▸ TYRO3 Q06418 1/20 0.40
▸ MET P08581 1/20 0.40
▸ HDAC1 Q13547 1/20 0.40

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
SCHEMBL14554770 0.81 KEAP1 (0.68) KEAP1DYRK1ADAOMEN1CYP1A2
SCHEMBL74518 0.81 KEAP1 (0.68) KEAP1DYRK1ADAOMEN1CYP1A2
SCHEMBL25804613 0.81 KEAP1 (0.68) KEAP1DYRK1ADAOMEN1CYP1A2
SCHEMBL6092812 0.81 KEAP1 (1.00) KEAP1DYRK1ADAOMEN1CYP1A2
SCHEMBL2535366 0.81 KEAP1 (0.68) KEAP1DYRK1ADAOMEN1CYP1A2
SCHEMBL24494597 0.81 KEAP1 (0.68) KEAP1DYRK1ADAOMEN1CYP1A2
SCHEMBL14638413 0.81 KEAP1 (0.68) KEAP1DYRK1ADAOMEN1CYP1A2
Hydrochloric Acid SCHEMBL17184538 0.79 KEAP1 (0.96) KEAP1DYRK1ADAOMEN1CYP1A2
Ammonia Solution, Strong SCHEMBL28922912 0.79 KEAP1 (0.66) KEAP1DYRK1ADAOMEN1CYP1A2
Hydrochloric Acid SCHEMBL23201169 0.79 KEAP1 (0.96) KEAP1DYRK1ADAOMEN1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119661811-A Latent accelerator based on anhydride-tertiary amine dynamic ion pair, preparation method and application thereof 江南大学 2025-03-21 — — CN claimed
US-9139567-B2 Arylpyrazole ethers as inhibitors of leukotriene A4 hydrolase BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2015-09-22 — — US claimed
US-20140221373-A1 ARYLPYRAZOLE ETHERS AS INHIBITORS OF LEUKOTRIENE A4 HYDROLASE BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2014-08-07 — — US claimed
EP-2734516-A1 ARYLPYRAZOLE ETHERS AS INHIBITORS OF LEUKOTRIENE A4 HYDROLASE Boehringer Ingelheim International GmbH (DE) 2014-05-28 — — EP claimed
US-20130216498-A1 IMIDAZOPYRIDINE DERIVATIVES AS JAK INHIBITORS ALMIRALL, S.A. (ES) 2013-08-22 — — US claimed
WO-2013012844-A1 ARYLPYRAZOLE ETHERS AS INHIBITORS OF LEUKOTRIENE A4 HYDROLASE BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2013-01-24 — — WO claimed
EP-2516436-A1 IMIDAZOPYRIDINE DERIVATIVES AS JAK INHIBITORS Almirall S.A. (ES) 2012-10-31 — — EP claimed
WO-2011076419-A1 IMIDAZOPYRIDINE DERIVATIVES AS JAK INHIBITORS ALMIRALL, S.A. (ES) 2011-06-30 — — WO claimed
CN-119661811-A Latent accelerator based on anhydride-tertiary amine dynamic ion pair, preparation method and application thereof 江南大学 2025-03-21 — — CN disclosed
WO-2024153595-A1 CHROMANE DERIVATIVES AS EGFR SELECTIVE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2024-07-25 — — WO disclosed
CN-112867715-B 5-azaindazole derivatives as adenosine receptor antagonists 默克专利股份公司 2024-03-05 — — CN disclosed
EP-4289838-A2 ARYLMETHOXY ISOINDOLINE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME Celgene Corporation (US) 2023-12-13 — — EP disclosed
EP-3599236-B1 ARYLMETHOXY ISOINDOLINE DERIVATIVES AND COMPOSITIONS COMPRISING AND METHODS OF USING THE SAME CELGENE CORP (US) 2023-08-23 — — EP disclosed
EP-3870582-B1 5-AZAINDAZOLE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS MERCK PATENT GMBH (DE) 2023-07-19 — — EP disclosed
WO-2008014219-A2 THIOZOLIDINEDIONE DERIVATIVES AS P13 KINASE INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 2008-01-31 — — WO disclosed
EP-1813613-A1 NOVEL FUSED IMIDAZOLE DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 2007-08-01 — — EP disclosed
US-5606061-A HYPOTENSIVE AGENTS, ANTIASTHMATICS EISAI CO., LTD. (JP) 1997-02-25 — — US disclosed
US-5498634-A TREATING HYPERTENSION, ANGINA, ATP-SENSITIVE POTASSIUM CHANNEL AND ASTHMA EISAI CO., LTD. (JP) 1996-03-12 — — US disclosed
US-5444066-A Thioformamide derivatives having hypotensive activity EISAI CO., LTD. (JP) 1995-08-22 — — US disclosed
EP-0609442-A1 THIOFORMAMIDE DERIVATIVE Eisai Co., Ltd. (JP) 1994-08-10 — — 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 (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-20130216498-A1 IMIDAZOPYRIDINE DERIVATIVES AS JAK INHIBITORS JAK1, JAK2, JAK3 KEAP1 2612/4885DYRK1A 1291/4885DAO 1916/4885
US-20140221373-A1 ARYLPYRAZOLE ETHERS AS INHIBITORS OF LEUKOTRIENE A4 HYDROLASE LTA4H, LTC4S, LTB4R KEAP1 316/4885DYRK1A 3341/4885DAO 940/4885

“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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