SCHEMBL2820745

SCHEMBL2820745

FC(F)(F)c1cnc[nH]1

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL27617871 0.70 — —
SCHEMBL28018128 0.67 PARP1 (0.43) —
SCHEMBL14415970 0.66 HRH4 (0.44) —
SCHEMBL26068453 0.66 ALDH1A1 (0.43) —
SCHEMBL14857108 0.64 HRH4 (0.43) —
SCHEMBL12261150 0.63 HRH4 (0.39) —
SCHEMBL7194641 0.61 IDO1 (0.59) —
Hydrochloric Acid SCHEMBL27554053 0.61 — —
Hydrochloric Acid SCHEMBL27259157 0.61 — —
SCHEMBL1801743 0.61 HRH3 (0.46) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10224485-B2 Process for preparing a crystalline organic semiconductor material BASF SE (DE) 2019-03-05 — — US claimed
US-20170012208-A1 ORGANIC SEMICONDUCTOR FORMULATIONS USINVEST LLC 2017-01-12 — — US claimed
CN-102124002-B Novel phenylimidazole derivatives as pde10a enzyme inhibitors LUNDBECK & CO AS H 2014-06-25 — — CN claimed
CN-102124002-A Novel phenylimidazole derivatives as pde10a enzyme inhibitors LUNDBECK & CO AS H 2011-07-13 — — CN claimed
EP-4720162-A1 MAIN CHAIN CATIONIC OLIGO(IMIDAZOLIUM) FORMS N-HETEROCYCLIC CARBENE FOR EFFECTIVE BACTERIAL KILLING IN COMPLEX ENVIRONMENT Nanyang Technological University (SG) 2026-04-08 — — EP disclosed
EP-4650345-A1 HETEROCYCLIC COMPOUND AND USE THEREOF IN MEDICINE Kangbaida (Sichuan) Biotechnology Co., Ltd. (CN) 2025-11-19 — — EP disclosed
WO-2025236011-A1 COMPOSITIONS FOR PHOSPHOROUS-AZOLE EXCHANGE CHEMISTRY AND USE THEREOF TO TARGET FUNCTIONAL PROTEIN SITES BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2025-11-13 — — WO disclosed
US-20250098679-A1 HERBICIDAL PYRIDONE DERIVATIVES SYNGENTA CROP PROTECTION AG (CH) 2025-03-27 — — US disclosed
WO-2025043225-A2 DEGRADERS OF CYCLIN-DEPENDENT KINASE 2 GENENTECH, INC. (US) 2025-02-27 — — WO disclosed
WO-2024248739-A1 MAIN CHAIN CATIONIC OLIGO(IMIDAZOLIUM) FORMS N-HETEROCYCLIC CARBENE FOR EFFECTIVE BACTERIAL KILLING IN COMPLEX ENVIRONMENT NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2024-12-05 — — WO disclosed
EP-4448509-A1 HERBICIDAL PYRIDONE DERIVATIVES Syngenta Crop Protection AG (CH) 2024-10-23 — — EP disclosed
WO-2024149242-A1 HETEROCYCLIC COMPOUND AND USE THEREOF IN MEDICINE 成都百裕制药股份有限公司 2024-07-18 — — WO disclosed
EP-2213668-A2 Imidazoles as aldosterone synthase inhibitors Novartis AG (CH) 2010-08-04 — — EP disclosed
US-20100048562-A1 ORGANIC COMPOUNDS NOVARTIS AG (CH) 2010-02-25 — — US disclosed
US-20100048562-A1 ORGANIC COMPOUNDS NOVARTIS AG (CH) 2010-02-25 — — US disclosed
US-20100048562-A1 ORGANIC COMPOUNDS NOVARTIS AG (CH) 2010-02-25 — — US disclosed
CN-101605777-A Imidazoles as aldosterone synthase inhibitors NOVARTIS AG (CH) 2009-12-16 — — CN disclosed
EP-2094680-A2 IMIDAZOLES AS ALDOSTERONE SYNTHASE INHIBITORS Novartis AG (CH) 2009-09-02 — — EP disclosed
WO-2008076336-A2 IMIDAZOLES AS ALDOSTERONE SYNTHASE INHIBITORS NOVARTIS AG (CH) 2008-06-26 — — WO disclosed
WO-2008076336-A2 IMIDAZOLES AS ALDOSTERONE SYNTHASE INHIBITORS NOVARTIS AG (CH) 2008-06-26 — — WO disclosed
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