SCHEMBL4489558

SCHEMBL4489558

CCn1ncccc1=O

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
SCHEMBL10366086 0.88 IDO1 (0.43) —
SCHEMBL4938694 0.83 SLC9A1 (0.42) —
SCHEMBL29649646 0.78 — —
SCHEMBL29649650 0.78 — —
SCHEMBL9963194 0.78 SMN1; SMN2 (0.39) —
SCHEMBL15317758 0.78 IDO1 (0.37) —
SCHEMBL11982364 0.77 IDO1 (0.40) —
SCHEMBL11983401 0.76 RAB9A (0.44) —
SCHEMBL27483881 0.76 ALOX5AP (0.41) —
SCHEMBL12569419 0.75 IDO1 (0.43) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240238423-A9 TETRAHYDROISOQUINOLINE HETEROBIFUNCTIONAL BCL-XL DEGRADERS Treeline Biosciences, Inc. 2024-07-18 — — US disclosed
US-20230382864-A1 PYRIDINONE MK2 INHIBITORS AND USES THEREOF XINTHERA, INC. 2023-11-30 — — US disclosed
US-20230364070-A1 PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER ANTARES THERAPEUTICS, INC. 2023-11-16 — — US disclosed
US-11685719-B2 Pyridinone MK2 inhibitors and uses thereof XINTHERA, INC. (US) 2023-06-27 — — US disclosed
US-20230138663-A1 EAAT2 ACTIVATORS AND METHODS OF USING THEREOF THE BRIGHAM AND WOMEN'S HOSPITAL, INC. 2023-05-04 — — US disclosed
US-20230053465-A1 PYRIDINONE MK2 INHIBITORS AND USES THEREOF XINTHERA, INC. 2023-02-23 — — US disclosed
WO-2023283338-A1 PYRIDINONE MK2 INHIBITORS AND USES THEREOF XINTHERA, INC. (US) 2023-01-12 — — WO disclosed
WO-2022135572-A1 FIVE-MEMBERED RING DERIVATIVE AND MEDICAL USE THEREOF 四川海思科制药有限公司 2022-06-30 — — WO disclosed
US-20170081317-A1 HETEROARYL COMPOUNDS AS IRAK INHIBITORS AND USES THEREOF MERCK PATENT GMBH (DE) 2017-03-23 — — US disclosed
EP-2655357-B1 INDAZOLYL TRIAZOLE DERIVATIVES AS IRAK INHIBITORS MERCK SERONO SA (CH) 2016-06-22 — — EP disclosed
EP-1781635-A4 POTASSIUM CHANNEL INHIBITORS MERCK & CO INC (US) 2009-02-25 — — EP disclosed
US-20090048297-A1 4-AMINO-4-OXOBUTANOYL PEPTIDES AS INHIBITORS OF VIRAL REPLICATION ACHILLION PHARMACEUTICALS (US) 2009-02-19 — — US disclosed
US-20070185092-A1 FACTOR Xa INHIBITORS MILLENNIUM PHARMACEUTICALS, INC. (US) 2007-08-09 — — US disclosed
EP-1781635-A2 POTASSIUM CHANNEL INHIBITORS Merck & Co., Inc. (US) 2007-05-09 — — EP disclosed
WO-2006015159-A2 POTASSIUM CHANNEL INHIBITORS MERCK & CO., INC. (US) 2006-02-09 — — WO disclosed
EP-1411941-A2 PYRIDINONE AND PYRIDAZINONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS Neurocrine Biosciences, Inc. (US) 2004-04-28 — — EP disclosed
WO-2003011293-A2 PYRIDINONE AND PYRIDAZINONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS NEUROCRINE BIOSCIENCES, INC. (US) 2003-02-13 — — WO disclosed
EP-1129097-A1 NOVEL TYPE CONDENSED PYRIDAZINONE COMPOUNDS GYOGYSZERKUTATO INTEZET KFT. (HU) 2001-09-05 — — EP disclosed
WO-2000027851-A1 NOVEL TYPE CONDENSED PYRIDAZINONE COMPOUNDS Gyógyszerkutató Intézet Kft. (HU) 2000-05-18 — — WO disclosed
CN-86102700-A The preparation method of pyridazinone derivative and desinsection thereof, kill mite, nematicide, fungicide composition — 1986-12-17 — — CN disclosed
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