SCHEMBL1027196

SCHEMBL1027196

N#Cc1cc[nH]c(=O)c1

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
SCHEMBL6209834 0.79 — —
SCHEMBL21333512 0.77 — —
SCHEMBL2671435 0.69 ATIC (0.60) —
SCHEMBL3574426 0.69 IMPDH2 (0.58) —
SCHEMBL28489960 0.69 GRM5 (0.64) —
SCHEMBL30500463 0.69 HAO1 (0.38) —
Hydrochloric Acid SCHEMBL7004520 0.67 GRM5 (0.62) —
SCHEMBL6042142 0.67 NOTUM (0.77) —
SCHEMBL9199411 0.65 — —
SCHEMBL91366 0.65 IMPDH2 (1.00) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110263610-A1 COMPOUNDS AND COMPOSITIONS AS ITPKB INHIBITORS IRM LLC (BM) 2011-10-27 — — US claimed
EP-4685143-A1 DOUBLE REGULATOR FOR MGLUR5 AND HDAC6 AND USE THEREOF Vivozon,Inc. (KR) 2026-01-28 — — EP disclosed
US-12312345-B2 Fluoroalkyl-oxadiazoles and uses thereof TENAYA THERAPEUTICS, INC. (US) 2025-05-27 — — US disclosed
US-20250092040-A1 AKT1 MODULATORS ALTEROME THERAPEUTICS, INC. 2025-03-20 — — US disclosed
WO-2025011476-A1 INDAZOLE DERIVATIVE OR PHARMACEUTICAL SALT THEREOF AND USE THEREOF 浙江大学 2025-01-16 — — WO disclosed
CN-119219609-A Indazole derivative or pharmaceutically acceptable salt thereof and application thereof 浙江大学 2024-12-31 — — CN disclosed
WO-2024196136-A1 DOUBLE REGULATOR FOR MGLUR5 AND HDAC6 AND USE THEREOF 주식회사 비보존 2024-09-26 — — WO disclosed
US-20240239797-A1 AKT1 MODULATORS ALTEROME THERAPEUTICS, INC. 2024-07-18 — — US disclosed
US-20240239797-A1 AKT1 MODULATORS ALTEROME THERAPEUTICS, INC. 2024-07-18 — — US disclosed
US-20240228469-A1 PCSK9 INHIBITORS AND METHODS OF USE THEREOF ASTRAZENECA AB (SE) 2024-07-11 — — US disclosed
US-20110034697-A1 PROCESS FOR PREPARING 2-HYDROXY-4-SUBSTITUTED PYRIDINES YUKI GOSEI KOGYO CO., INC. (JP) 2011-02-10 — — US disclosed
US-20110027864-A1 PROCESS FOR PREPARING 2-HYDROXY-4-SUBSTITUTED PYRIDINES YUKI GOSEI KOGYO CO., INC. (JP) 2011-02-03 — — US disclosed
EP-2274302-A2 COMPOUNDS AND COMPOSITIONS AS ITPKB INHIBITORS IRM LLC (BM) 2011-01-19 — — EP disclosed
US-7803585-B2 Process for preparing 2-Hydroxy-4-Substituted Pyridines YUKI GOSEI KOGYO CO., LTD. (JP) 2010-09-28 — — US disclosed
EP-1959951-B1 HETEROARYL SUBSTITUTED PIPERIDINE DERIVATIVES AS L-CPT1 INHIBITORS HOFFMANN LA ROCHE (CH) 2009-12-23 — — EP disclosed
WO-2009123948-A2 COMPOUNDS AND COMPOSITIONS AS ITPKB INHIBITORS IRM LLC (BM) 2009-10-08 — — WO disclosed
CN-101321525-A Heteroaryl substituted piperidine derivatives as L-CPT1 inhibitors HOFFMANN LA ROCHE (CH) 2008-12-10 — — CN disclosed
US-20080286843-A1 Process for Preparing 2-Hydroxy-Substituted Pyridines YUKI GOSEI KOGYO CO., INC. (JP) 2008-11-20 — — US disclosed
WO-2007075783-A2 SUBSTITUTED ISOQUINOLINE-1,3(2H,4H)-DIONES, 1-THIOXO-1,4-DIHYDRO-2H-ISOQUINOLINE-3-ONES AND 1,4-DIHYDRO-3(2H)-ISOQUINOLONES AND USE THEREOF AS KINASE INHIBITOR WYETH (US) 2007-07-05 — — WO disclosed
EP-1801102-A1 PROCESS FOR PRODUCTION OF 2-HYDROXY-4-SUBSTITUTED PYRIDINES YUKI GOSEI KOGYO CO., LTD. (JP) 2007-06-27 — — EP disclosed
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