Setanaxib

Setanaxib

SCHEMBL1302603

CN(C)c1cccc(-c2c3c(=O)n(-c4ccccc4Cl)[nH]c3cc(=O)n2C)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NOX1NOX4

The experimentally established mechanism targets of Setanaxib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ NOX4 known ✓ Q9NPH5 20/20 1.00
▸ NOX1 known ✓ Q9Y5S8 5/20 1.00
▸ CYBB P04839 5/20 1.00
▸ NOX5 Q96PH1 4/20 1.00
▸ CYP3A4 P08684 2/20 0.50
▸ CYP2C8 P10632 1/20 0.50
▸ CYP2C9 P11712 1/20 0.50
▸ CYP2C19 P33261 1/20 0.50

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
Setanaxib SCHEMBL29375704 1.00 NOX4 (1.00) NOX4CYBBNOX1NOX5CYP3A4
Setanaxib SCHEMBL29362127 1.00 NOX4 (1.00) NOX4CYBBNOX1NOX5CYP3A4
SCHEMBL16612593 0.87 NOX4 (0.77) NOX4CYBBNOX1NOX5CYP3A4
SCHEMBL16612522 0.86 NOX4 (0.75) NOX4CYBBNOX1NOX5CYP3A4
SCHEMBL1302255 0.85 NOX4 (0.74) NOX4CYBBNOX1NOX5
SCHEMBL16612222 0.85 NOX4 (0.74) NOX4CYBBNOX1NOX5CYP3A4
SCHEMBL14931735 0.84 NOX4 (0.72) NOX4CYBBNOX1NOX5CYP3A4
SCHEMBL29523003 0.84 NOX4 (0.72) NOX4CYBBNOX1NOX5CYP3A4
SCHEMBL1302943 0.83 NOX4 (0.72) NOX4CYBBNOX1NOX5CYP3A4
SCHEMBL14931788 0.82 NOX4 (0.69) NOX4CYBBNOX1NOX5CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE50878-E1 Pyrazolo pyridine derivatives as NADPH oxidase inhibitors CALLIDITAS THERAPEUTICS SUISSE SA (CH) 2026-05-05 — — US claimed
US-20260021079-A1 NOX INHIBITORS FOR USE IN THE TREATMENT OF ALPORT SYNDROME CALLIDITAS THERAPEUTICS SUISSE SA (CH) 2026-01-22 — — US claimed
US-20240358687-A1 USE OF NOX INHIBITORS FOR TREATMENT OF CANCER CALLIDITAS THERAPEUTICS SUISSE SA (CH) 2024-10-31 — — US claimed
US-12011436-B2 Use of NOX inhibitors for treatment of cancer CALLIDITAS THERAPEUTICS SUISSE SA (CH) 2024-06-18 — — US claimed
WO-2023217764-A1 NOX INHIBITORS FOR USE IN THE TREATMENT OF ALPORT SYNDROME CALLIDITAS THERAPEUTICS SUISSE SA (CH) 2023-11-16 — — WO claimed
US-20220259302-A1 METHODS AND COMPOSITIONS FOR THE IMPROVEMENT OF LYSOSOMAL FUNCTION AND TREATMENT OF NEURODEGENERATIVE DISEASE UNIV VANDERBILT (US) 2022-08-18 — — US claimed
EP-3946297-A1 HYALURONIC ACID NANOPARTICLES COMPRISING NADPH OXIDASES INHIBITORS AND USES IN TREATING CANCER Emory University (US) 2022-02-09 — — EP claimed
US-20210177811-A1 USE OF NOX INHIBITORS FOR TREATMENT OF CANCER CALLIDITAS THERAPEUTICS SUISSE SA (CH) 2021-06-17 — — US claimed
US-20200354445-A1 METHODS AND COMPOSITIONS FOR THE IMPROVEMENT OF LYSOSOMAL FUNCTION AND TREATMENT OF NEURODEGENERATIVE DISEASE VANDERBILT UNIVERSITY 2020-11-12 — — US claimed
WO-2020205937-A1 HYALURONIC ACID NANOPARTICLES COMPRISING NADPH OXIDASES INHIBITORS AND USES IN TREATING CANCER EMORY UNIVERSITY (US) 2020-10-08 — — WO claimed
EP-2860179-B1 Pyrazolo pyridine derivatives as NADPH oxidase inhibitors GENKYOTEX SUISSE SA (CH) 2018-03-14 — — EP claimed
WO-2016189501-A1 PROCESS FOR THE PREPARATION OF A NADPH OXIDASE INHIBITOR AND ITS POLYMORPHS AND USES THEREOF GENKYOTEX SA (CH) 2016-12-01 — — WO claimed
EP-3098220-A1 PROCESS FOR THE PREPARATION OF A NADPH OXIDASE INHIBITOR AND ITS POLYMORPHS AND USES THEREOF GenKyoTex SA (CH) 2016-11-30 — — EP claimed
US-20150290208-A1 PYRAZOLO PYRIDINE DERIVATIVES AS NADPH OXIDASE INHIBITORS CALLIDITAS THERAPEUTICS SUISSE SA (CH) 2015-10-15 — — US claimed
US-9096588-B2 Pyrazolo pyridine derivatives as NADPH oxidase inhibitors GENKYOTEX SA (CH) 2015-08-04 — — US claimed
WO-2015049655-A1 COMPOUNDS USEFUL FOR THE TREATMENT OF PDE5 INHIBITOR-POORLY RESPONSIVE ERECTILE DYSFUNCTION GENKYOTEX SA (CH) 2015-04-09 — — WO claimed
EP-2857399-A1 Compounds useful for the treatment of PDE5 inhibitor-poorly responsive erectile dysfunction GenKyoTex SA (CH) 2015-04-08 — — EP claimed
US-20110269757-A1 PYRAZOLO PYRIDINE DERIVATIVES AS NADPH OXIDASE INHIBITORS GENKYOTEX SA (CH) 2011-11-03 — — US claimed
EP-2344492-A1 PYRAZOLO PYRIDINE DERIVATIVES AS NADPH OXIDASE INHIBITORS GenKyoTex SA (CH) 2011-07-20 — — EP claimed
WO-2010035221-A1 PYRAZOLO PYRIDINE DERIVATIVES AS NADPH OXIDASE INHIBITORS GENKYOTEX SA (CH) 2010-04-01 — — WO claimed

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-20150290208-A1 PYRAZOLO PYRIDINE DERIVATIVES AS NADPH OXIDASE INHIBITORS NOX1, NOX4, CYBB NOX4 2/4885NOX1 1/4885CYBB 3/4885
US-20110269757-A1 PYRAZOLO PYRIDINE DERIVATIVES AS NADPH OXIDASE INHIBITORS NOX1, NOX4, CYBB NOX4 2/4885NOX1 1/4885CYBB 3/4885
US-20260021079-A1 NOX INHIBITORS FOR USE IN THE TREATMENT OF ALPORT SYNDROME NOX1, NOX5, NOX4 NOX4 3/4885NOX1 1/4885CYBB 6/4885
US-12011436-B2 Use of NOX inhibitors for treatment of cancer NOX1, NOX5, NOX3 NOX4 5/4885NOX1 1/4885CYBB 6/4885
US-20240358687-A1 USE OF NOX INHIBITORS FOR TREATMENT OF CANCER NOX1, NOX5, NOX3 NOX4 5/4885NOX1 1/4885CYBB 6/4885
US-20210177811-A1 USE OF NOX INHIBITORS FOR TREATMENT OF CANCER NOX1, NOX5, NOX3 NOX4 5/4885NOX1 1/4885CYBB 6/4885

“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.

Send feedback