SCHEMBL269227

SCHEMBL269227

[CH2]CCc1ccc[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
SCHEMBL269445 0.86
SCHEMBL4687381 0.84 GPR84 (0.35)
SCHEMBL7172295 0.84 MAOA (0.42)
SCHEMBL499775 0.82 GPR84 (0.38)
SCHEMBL3391747 0.82 GPR84 (0.38)
SCHEMBL10538535 0.79 MAOA (0.38)
SCHEMBL7003873 0.79 GPR84 (0.41)
SCHEMBL211078 0.79
SCHEMBL79201 0.78 MAOA (0.47)
SCHEMBL25422764 0.77

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210316288-A1 HYBRID MATERIAL AND METHOD FOR THE PRODUCTION THEREOF UNIVERSITE PIERRE ET MARIE CURIE (FR) 2021-10-14 US claimed
EP-1979355-B1 SPIRO IMIDAZOLE DERIVATIVES AS PPAR MODULATORS IRM LLC (BM) 2010-08-18 EP claimed
US-20090137610-A1 SPIRO IMIDOZOLE DERIVATIVES AS PPAR MODULATORS IRM LLC (BM) 2009-05-28 US claimed
EP-1979355-A1 SPIRO IMIDAZOLE DERIVATIVES AS PPAR MODULATORS IRM LLC (BM) 2008-10-15 EP claimed
WO-2007087448-A1 SPIRO IMIDAZOLE DERIVATIVES AS PPAR MODULATORS IRM LLC (BM) 2007-08-02 WO claimed
EP-0832898-A2 Substituted amino acid derivatives BAYER AG (DE) 1998-04-01 EP claimed
EP-0825989-A1 SUBSTITUTED OXAZOLES FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1998-03-04 EP claimed
WO-1996036617-A1 SUBSTITUTED OXAZOLES FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1996-11-21 WO claimed
CN-108948019-B Focal adhesion kinase inhibitors and uses thereof 广东东阳光药业有限公司 2022-07-08 CN disclosed
US-20210316288-A1 HYBRID MATERIAL AND METHOD FOR THE PRODUCTION THEREOF UNIVERSITE PIERRE ET MARIE CURIE (FR) 2021-10-14 US disclosed
EP-3750892-A1 NOVEL 5-CYCLOPROPYL-FURO[3,4-C]PYRIDINE-3,4(1H,5H)-DIONE 1,1' SUBSTITUTED DERIVATIVES AND THEIR USES Yerevan State University (AM) 2020-12-16 EP disclosed
US-10201525-B2 Tetrazole-substituted arylamides as PX2 and PX2/3 antagonists ROCHE PALO ALTO LLC (US) 2019-02-12 US disclosed
WO-2018209343-A1 NOVEL METHODS, COMPOUNDS, AND COMPOSITIONS: SMALL MOLECULE ANTICANCER AGENTS RAJUR SHARANAPPA BASAPPA (US) 2018-11-15 WO disclosed
CN-108368606-A The method of generation for thin inoranic membrane 巴斯夫欧洲公司 2018-08-03 CN disclosed
WO-1996036617-A1 SUBSTITUTED OXAZOLES FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1996-11-21 WO disclosed
WO-1996028418-A1 SULFONYLALKANOYLAMINO HYDROXYETHYLAMINO SULFONAMIDE RETROVIRAL PROTEASE INHIBITORS G.D. SEARLE & CO. (US) 1996-09-19 WO disclosed
CN-1098716-A Vasopressin antagonists and oxytocin antagonists OTSUKA CHEMICAL CO LTD (JP) 1995-02-15 CN disclosed
EP-0620003-A1 VASOPRESSIN ANTAGONIST AND OXYTOCIN ANTAGONIST OTSUKA PHARMACEUTICAL CO., LTD. (JP) 1994-10-19 EP disclosed
US-5321032-A Peptide compounds and pharmaceutical compositions thereof FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1994-06-14 US disclosed
EP-0515681-A1 PEPTIDE COMPOUND FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1992-12-02 EP disclosed