SCHEMBL420617

SCHEMBL420617

O=C1C=C(CO)CO1

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
SCHEMBL419742 0.76
SCHEMBL979771 0.76
SCHEMBL7303886 0.74 CA1 (0.35)
SCHEMBL18845026 0.73
SCHEMBL9423576 0.71
SCHEMBL7343487 0.70 CA1 (0.36)
SCHEMBL981029 0.70 CALM1 (0.42)
SCHEMBL21556785 0.69 CA1 (0.39)
SCHEMBL17967787 0.69 HIF1A (0.50)
SCHEMBL7343489 0.69 CA1 (0.38)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109776509-B N-substituted imidazole formate derivative and application thereof 成都麻沸散医药科技有限公司 2023-07-07 CN disclosed
EP-2935278-B1 TRICYCLIC COMPOUNDS FOR INHIBITING THE CFTR CHANNEL NOVARTIS AG (CH) 2017-03-15 EP disclosed
US-9359381-B2 Tricyclic compounds for inhibiting the CFTR channel NOVARTIS AG (CH) 2016-06-07 US disclosed
US-9359381-B2 Tricyclic compounds for inhibiting the CFTR channel NOVARTIS AG (CH) 2016-06-07 US disclosed
US-9359381-B2 Tricyclic compounds for inhibiting the CFTR channel NOVARTIS AG (CH) 2016-06-07 US disclosed
CN-105143230-A Tricyclic compounds for inhibiting the CFTR channel NOVARTIS AG 2015-12-09 CN disclosed
US-20150336986-A1 TRICYCLIC COMPOUNDS FOR INHIBITING THE CFTR CHANNEL NOVARTIS AG (CH) 2015-11-26 US disclosed
US-20150336986-A1 TRICYCLIC COMPOUNDS FOR INHIBITING THE CFTR CHANNEL NOVARTIS AG (CH) 2015-11-26 US disclosed
US-20150336986-A1 TRICYCLIC COMPOUNDS FOR INHIBITING THE CFTR CHANNEL NOVARTIS AG (CH) 2015-11-26 US disclosed
EP-2935278-A1 TRICYCLIC COMPOUNDS FOR INHIBITING THE CFTR CHANNEL Novartis AG (CH) 2015-10-28 EP disclosed
US-20060270853-A1 Process for the preparation of (S)-4-fluoromethyl-dihydro-furan-2-one useful in the preparation of the DPP-IV inhibitor (S)-1 ((2S,3S,11bS)-2-amino-9,10-dimethoxy-1,3,4,6,7, 11b-hexahydro-2h-pyrido[2,1-a] isoquinolin-3-yl)-4-fluoromethyl-pyrrolidin-2-one HOFFMANN-LA ROCHE INC. 2006-11-30 US disclosed
US-20060270853-A1 Process for the preparation of (S)-4-fluoromethyl-dihydro-furan-2-one useful in the preparation of the DPP-IV inhibitor (S)-1 ((2S,3S,11bS)-2-amino-9,10-dimethoxy-1,3,4,6,7, 11b-hexahydro-2h-pyrido[2,1-a] isoquinolin-3-yl)-4-fluoromethyl-pyrrolidin-2-one HOFFMANN-LA ROCHE INC. 2006-11-30 US disclosed
WO-2003051857-A2 FURANONE SYNTHESIS MERCK PATENT GMBH (DE) 2003-06-26 WO disclosed
US-6451785-B1 SUBSTITUTED 3-(TRIPHENYLMETHYLAMINO)AZETIDIN-2-ONE; COA-INDEPENDENT TRANSACYLASE (COA-IT) INHIBITOR; COADMINISTERED WITH EDELFOSINE (ET-18-OCH3) OR OTHER ALKYL-LYSOPHOSPHOLIPID ANALOG SMITHKLINE BEECHAM CORPORATION 2002-09-17 US disclosed
US-20020082250-A1 BETA LACTAMS AS ANTIPROLIFERATIVE AGENTS WAKE FOREST UNIVERSITY HEALTH SCIENCES 2002-06-27 US disclosed
EP-1011663-A1 BETA-LACTAM INHIBITORS OF CoA-IT SMITHKLINE BEECHAM CORPORATION (US) 2000-06-28 EP disclosed
EP-0982991-A1 BETA LACTAMS AS ANTIPROLIFERATIVE AGENTS SMITHKLINE BEECHAM CORPORATION (US) 2000-03-08 EP disclosed
WO-1998050032-A9 BETA-LACTAM INHIBITORS OF CoA-IT SMITHKLINE BEECHAM CORP (US) 1999-03-25 WO disclosed
WO-1998049897-A1 BETA LACTAMS AS ANTIPROLIFERATIVE AGENTS SMITHKLINE BEECHAM CORPORATION (US) 1998-11-12 WO disclosed
WO-1998050032-A1 BETA-LACTAM INHIBITORS OF CoA-IT SMITHKLINE BEECHAM CORPORATION (US) 1998-11-12 WO disclosed