SCHEMBL52755

SCHEMBL52755

CN(CCF)C(=O)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
SCHEMBL51563 0.84 EPHX2 (0.30)
SCHEMBL25240125 0.82 BCHE (0.33)
SCHEMBL3763074 0.82 NPC1 (0.36)
SCHEMBL211520 0.78
SCHEMBL1131981 0.78
SCHEMBL25180839 0.77 CYP2C9 (0.35)
SCHEMBL28903229 0.77 NOS3 (0.38)
SCHEMBL21815374 0.77 NOS3 (0.38)
SCHEMBL211519 0.76
Hydrochloric Acid SCHEMBL11895625 0.76

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11932647-B2 Cyclic iminopyrimidine derivatives as kinase inhibitors ABM THERAPEUTICS CORPORATION (US) 2024-03-19 US disclosed
EP-3684772-B1 CYCLIC IMINOPYRIMIDINE DERIVATIVES AS KINASE INHIBITORS ABM THERAPEUTICS CORP (US) 2023-12-06 EP disclosed
US-11254680-B2 Cyclic iminopyrimidine derivatives as kinase inhibitors ABM THERAPEUTICS CORPORATION (US) 2022-02-22 US disclosed
US-11225485-B2 2022-01-18 US disclosed
US-20200247813-A1 CYCLIC IMINOPYRIMIDINE DERIVATIVES AS KINASE INHIBITORS ABM THERAPEUTICS CORPORATION (US) 2020-08-06 US disclosed
EP-3684772-A1 CYCLIC IMINOPYRIMIDINE DERIVATIVES AS KINASE INHIBITORS ABM Therapeutics Corporation (US) 2020-07-29 EP disclosed
WO-2019060611-A1 CYCLIC IMINOPYRIMIDINE DERIVATIVES AS KINASE INHIBITORS ABM THERAPEUTICS, INC. (KY) 2019-03-28 WO disclosed
US-9328120-B2 6-cycloalkyl-pyrazolopyrimidinones for the treatment of CNS disorders BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2016-05-03 US disclosed
EP-2280981-B1 BRIDGED HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2014-04-23 EP disclosed
US-8129398-B2 HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2012-03-06 US disclosed
EP-2280981-A1 BRIDGED HETEROCYCLES AS HIV INTEGRASE INHIBITORS Bristol-Myers Squibb Company (US) 2011-02-09 EP disclosed
US-7737166-B2 Antifungal bicyclic hetero ring compounds DAIICHI SANKYO COMPANY, LIMITED (JP) 2010-06-15 US disclosed
US-20090253677-A1 HIV Integrase Inhibitors BRISTOL-MYERS SQUIBB COMPANY 2009-10-08 US disclosed
WO-2009117540-A1 BRIDGED HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2009-09-24 WO disclosed
US-20090143353-A1 such as 2-tert-Butyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile hydrochloride, a 1,6-beta-glucan synthetase inhibitor having potent growth inhibition, used treating a fungal infections; fungicides DAIICHI SANKYO COMPANY, LIMITED (JP) 2009-06-04 US disclosed
EP-1932837-A1 BICYCLO HETEROCYCLIC COMPOUND HAVING ANTIFUNGAL ACTION Daiichi Sankyo Company, Limited (JP) 2008-06-18 EP disclosed