SCHEMBL1309996

SCHEMBL1309996

CC(O)Cc1ccsc1

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
SCHEMBL18579637 1.00
SCHEMBL9071081 1.00
SCHEMBL23829867 0.83 MME (0.47)
SCHEMBL680803 0.82
SCHEMBL27504736 0.80 MME (0.43)
SCHEMBL5304252 0.79 TAAR1 (0.50)
SCHEMBL4205089 0.79 DRD2 (0.42)
SCHEMBL5536860 0.78
SCHEMBL18875010 0.78
SCHEMBL12251318 0.78 TAAR1 (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 36 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250382306-A1 HETEROCYCLIC COMPOUND AS TAAR1 LIGAND AGONIST Shandong luye pharmaceutical co ltd (CN) 2025-12-18 US disclosed
EP-4545534-A1 HETEROCYCLIC COMPOUND AS TAAR1 LIGAND AGONIST Shandong Luye Pharmaceutical Co., Ltd. (CN) 2025-04-30 EP disclosed
WO-2025049326-A1 TRICYCLIC HETEROAROMATIC INHIBITORS OF KLK5 BIOCRYST PHARMACEUTICALS, INC. (US) 2025-03-06 WO disclosed
WO-2023246872-A1 HETEROCYCLIC COMPOUND AS TAAR1 LIGAND AGONIST 山东绿叶制药有限公司 2023-12-28 WO disclosed
CN-110337440-B Compounds useful for inhibition of ROR-gamma-t 伊莱利利公司 2021-08-03 CN disclosed
US-11008336-B2 Compounds useful for inhibiting RORγt ELI LILLY AND COMPANY (US) 2021-05-18 US disclosed
US-11008336-B2 Compounds useful for inhibiting RORγt ELI LILLY AND COMPANY (US) 2021-05-18 US disclosed
EP-3589638-B1 COMPOUNDS USEFUL FOR INHIBITING ROR-GAMMA-T LILLY CO ELI (US) 2021-04-07 EP disclosed
EP-3589638-B1 COMPOUNDS USEFUL FOR INHIBITING ROR-GAMMA-T LILLY CO ELI (US) 2021-04-07 EP disclosed
CN-108026112-B Compounds for inhibition of ROR-gamma-T 伊莱利利公司 2020-04-10 CN disclosed
US-20170066781-A1 COMPOUNDS USEFUL FOR INHIBITING ROR-GAMMA-T LILLY CO ELI (US) 2017-03-09 US disclosed
US-20170066781-A1 COMPOUNDS USEFUL FOR INHIBITING ROR-GAMMA-T LILLY CO ELI (US) 2017-03-09 US disclosed
US-8053378-B2 Modified phenolic resin, epoxy resin composition containing the same, and prepreg containing the composition MITSUI CHEMICALS, INC. (JP) 2011-11-08 US disclosed
CN-101084250-B Modified phenol resin, epoxy resin composition containing the same, and prepreg using the composition MITSUI CHEMICALS INC 2011-06-15 CN disclosed
US-20080044667-A1 Modified Phenolic Resin, Epoxy Resin Composition Containing the Same, and Prepreg Containing the Composition MITSUI CHEMICALS, INC. (JP) 2008-02-21 US disclosed
CN-101084250-A Modified phenol resin, epoxy resin composition containing the same, and prepreg using the composition MITSUI CHEMICALS INC (JP) 2007-12-05 CN disclosed
US-5679670-A CONTROLLING INTRAOCULAR PRESSURE ALCON LABORATORIES, INC. (US) 1997-10-21 US disclosed
US-5378703-A FOR CONTROLLING INTRAOCULAR PRESSURE ALCON LABORATORIES, INC. (US) 1995-01-03 US disclosed
CN-1019489-B Process for preparing optically active furoimidazole-2, 4-diones HOFFMANN LA ROCHE (CH) 1992-12-16 CN disclosed
CN-85105078-A The manufacture method of lactone 1986-12-31 CN disclosed