Osilodrostat

Osilodrostat

SCHEMBL1037475

N#Cc1ccc(C2CCc3cncn32)c(F)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CYP11B1

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

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
CYP11B1 known ✓ P15538 7/20 1.00
CYP11B2 P19099 17/20 1.00
CYP19A1 P11511 8/20 1.00
KCNH2 Q12809 2/20 1.00
CYP17A1 P05093 1/20 1.00
HRH1 P35367 1/20 1.00

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
Osilodrostat SCHEMBL30395982 1.00 CYP11B2 (1.00) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
Osilodrostat SCHEMBL12460772 1.00 CYP11B2 (1.00) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
Osilodrostat SCHEMBL1037474 1.00 CYP11B2 (1.00) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
Osilodrostat SCHEMBL14761109 0.99 CYP11B2 (0.98) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
Osilodrostat SCHEMBL16280483 0.99 CYP11B2 (0.98) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
Osilodrostat SCHEMBL13837602 0.93 CYP11B2 (0.87) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
Osilodrostat SCHEMBL15128942 0.93 CYP11B2 (0.87) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
Osilodrostat SCHEMBL30395736 0.93 CYP11B2 (0.87) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
SCHEMBL1039611 0.93 CYP11B2 (1.00) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1
SCHEMBL1040487 0.92 CYP11B2 (1.00) CYP11B2CYP19A1CYP11B1KCNH2CYP17A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2836228-B1 COMBINATION OF SOMATOSTATIN-ANALOGS WITH 11BETA-HYDROXYLASE INHIBITORS NOVARTIS AG (CH) 2024-03-20 EP claimed
US-20200030442-A1 COMBINATION THERAPIES CAO ZHU ALEXANDER (US) 2020-01-30 US claimed
US-20170340733-A1 COMBINATION THERAPIES NOVARTIS AG (CH) 2017-11-30 US claimed
EP-3233918-A1 COMBINATION THERAPIES Novartis AG (CH) 2017-10-25 EP claimed
WO-2016100882-A1 COMBINATION THERAPIES NOVARTIS AG (CH) 2016-06-23 WO claimed
US-20160176883-A1 Forms and salts of a dihydropyrrolo[1,2c]imidazolyl aldosterone synthase or aromatase inhibitor NOVARTIS AG (CH) 2016-06-23 US claimed
US-9334276-B2 Forms and salts of a dihydropyrrolo[1,2c]imidazolyl aldosterone synthase or aromatase inhibitor NOVARTIS AG (CH) 2016-05-10 US claimed
US-9333234-B2 Combination of somatostatin-analogs with 11beta-hydroxylase inhibitors NOVARTIS AG (CH) 2016-05-10 US claimed
EP-2804863-B1 NEW FORMS AND SALTS OF A DIHYDROPYRROLO[1,2-C]IMIDAZOLYL ALDOSTERONE SYNTHASE OR AROMATASE INHIBITOR NOVARTIS AG (CH) 2015-12-02 EP claimed
US-20150087588-A1 COMBINATION OF SOMATOSTATIN-ANALOGS WITH 11BETA-HYDROXYLASE INHIBITORS NOVATIS AG (CH) 2015-03-26 US claimed
EP-2836228-A1 COMBINATION OF SOMATOSTATIN-ANALOGS WITH 11BETA-HYDROXYLASE INHIBITORS Novartis AG (CH) 2015-02-18 EP claimed
US-20140364470-A1 New forms and salts of a dihydropyrrolo[1,2c]imidazolyl aldosterone synthase or aromatase inhibitor NOVARTIS AG (CH) 2014-12-11 US claimed
EP-2804863-A1 NEW FORMS AND SALTS OF A DIHYDROPYRROLO[1,2-C]IMIDAZOLYL ALDOSTERONE SYNTHASE OR AROMATASE INHIBITOR Novartis AG (CH) 2014-11-26 EP claimed
EP-2256118-B1 Condensed imidazolo derivatives for the inhibition of aromatase and the treatment of aldosterone related diseases NOVARTIS AG (CH) 2014-10-29 EP claimed
US-8835646-B2 Organic compounds NOVARTIS AG (CH) 2014-09-16 US claimed
US-20130287789-A1 Organic Compounds NOVARTIS AG (CH) 2013-10-31 US claimed
WO-2013153129-A1 COMBINATION OF SOMATOSTATIN-ANALOGS WITH 11BETA-HYDROXYLASE INHIBITORS NOVARTIS AG (CH) 2013-10-17 WO claimed
WO-2013109514-A1 NEW FORMS AND SALTS OF A DIHYDROPYRROLO[1,2-C]IMIDAZOLYL ALDOSTERONE SYNTHASE OR AROMATASE INHIBITOR NOVARTIS AG (CH) 2013-07-25 WO claimed
EP-1919916-B1 CONDENSED IMIDAZOLO DERIVATIVES FOR THE INHIBITION OF ALDOSTERONE SYNTHASE AND AROMATASE NOVARTIS AG (CH) 2013-04-03 EP claimed
US-8314097-B2 Organic compounds NOVARTIS AG (CH) 2012-11-20 US 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-20200030442-A1 COMBINATION THERAPIES BRCA1, TP53, VHL CYP11B1 2056/4885CYP11B2 1506/4885CYP19A1 1005/4885
US-20170340733-A1 COMBINATION THERAPIES BRCA1, TP53, VHL CYP11B1 2056/4885CYP11B2 1506/4885CYP19A1 1005/4885
US-20140364470-A1 New forms and salts of a dihydropyrrolo[1,2c]imidazolyl aldosterone synthase or aromatase inhibitor CYP19A1, CYP21A2, CYP17A1 CYP11B1 8/4885CYP11B2 13/4885CYP19A1 1/4885
US-20150087588-A1 COMBINATION OF SOMATOSTATIN-ANALOGS WITH 11BETA-HYDROXYLASE INHIBITORS SSTR5, CRH, SSTR2 CYP11B1 9/4885CYP11B2 10/4885CYP19A1 121/4885
US-20160176883-A1 Forms and salts of a dihydropyrrolo[1,2c]imidazolyl aldosterone synthase or aromatase inhibitor CYP21A2, CYP19A1, NR5A1 CYP11B1 8/4885CYP11B2 15/4885CYP19A1 2/4885
US-20130287789-A1 Organic Compounds CYP19A1, CYP17A1, HSD17B11 CYP11B1 5/4885CYP11B2 14/4885CYP19A1 1/4885

“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.