SCHEMBL19202619

SCHEMBL19202619

C1=C=Cc2ocnc2C=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
SCHEMBL219313 0.48
SCHEMBL28900303 0.41
Water SCHEMBL28768410 0.32
Water SCHEMBL1954367 0.32
SCHEMBL28861870 0.32
Water SCHEMBL10747940 0.32
Water SCHEMBL31656559 0.32
Water SCHEMBL3091704 0.32
Water SCHEMBL22806512 0.32
Water SCHEMBL8618181 0.32

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

Appears in 6783 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250120971-A1 NOVEL DRUG TREATMENT OF COGNITIVE IMPAIRMENTS ASSOCIATED WITH SCHIZOPHRENIA FLORIDA ATLANTIC UNIV BOARD OF TRUSTEES (US) 2025-04-17 US claimed
US-20250075265-A1 ENHANCEMENT OF NUCLEIC ACID POLYMERIZATION BY AROMATIC COMPOUNDS ROCHE SEQUENCING SOLUTIONS INC (US) 2025-03-06 US claimed
US-20250075147-A1 FRAGRANCE AND FLAVOR COMPOSITIONS COMPRISING NEW FLAVOR AND FRAGRANCE INGREDIENTS OSMO LABS, PBC 2025-03-06 US claimed
US-20250057962-A1 PROCESSABLE COMPOSITIONS AND USE FOR THE SAME RIPPLE THERAPEUTICS CORPORATION (CA) 2025-02-20 US claimed
US-20250011293-A1 LEUKOTRIENE SYNTHESIS INHIBITORS NAEGIS PHARMACEUTICALS INC. (CA) 2025-01-09 US claimed
EP-4426712-A1 PROCESSABLE COMPOSITIONS AND USE FOR THE SAME Ripple Therapeutics Corporation (CA) 2024-09-11 EP claimed
US-12071404-B2 Aza (indole)-, benzothiophene-, and benzofuran-3-sulfonamides UCB PHARMA GMBH (DE) 2024-08-27 US claimed
US-11970489-B1 4-[(substituted 1H-benzimidazol-2-ylsulfanyl)methyl]-6-substituted-2H-chromen-2-ones as larvicidal agents King Faisal University (SA) 2024-04-30 US claimed
US-11970731-B2 Enhancement of nucleic acid polymerization by aromatic compounds Roche Sequencing Solutions, Inc. (US) 2024-04-30 US claimed
EP-4347040-A1 ALLOSTERIC CHROMENONE INHIBITORS OF PHOSPHOINOSITIDE 3-KINASE (PI3K) FOR THE TREATMENT OF CANCER Petra Pharma Corporation (US) 2024-04-10 EP claimed
CN-102690241-A Benzoyl urea compound containing isoxazoline and isoxazole structure, and preparation and application thereof UNIV NANKAI 2012-09-26 CN claimed
EP-2350066-A1 2,5-DISUBSTITUTED PIPERIDINE OREXIN RECEPTOR ANTAGONISTS Merck Sharp & Dohme Corp. (US) 2011-08-03 EP claimed
JP-4675427-B2 2011-04-20 JP claimed
WO-2010048010-A1 2,5-DISUBSTITUTED PIPERIDINE OREXIN RECEPTOR ANTAGONISTS MERCK SHARP & DOHME CORP. (US) 2010-04-29 WO claimed
EP-2089382-A1 SUBSTITUTED DIAZEPAN COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS Merck & Co., Inc. (US) 2009-08-19 EP claimed
WO-2008069997-A1 SUBSTITUTED DIAZEPAN COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS MERCK & CO., INC. (US) 2008-06-12 WO claimed
CN-1226993-C Brightness increasing agent used as whiteness increasing agent OREAL (FR) 2005-11-16 CN claimed
CN-1654464-A N,N'-disubstituted dihydrazides compound and its preparing process and application thereof UNIV NANKAI (CN) 2005-08-17 CN claimed
EP-1200398-A1 3-ARYLSULFONYL-2-(SUBSTITUTED METHYL)PROPANOIC ACID DERIVATES AS MATRIX METALLOPROTEINASE INHIBITORS Pharmacia Italia S.p.A. (IT) 2002-05-02 EP claimed
WO-2001005756-A1 3-ARYLSULFONYL-2-(SUBSTITUTED METHYL)PROPANOIC ACID DERIVATES AS MATRIX METALLOPROTEINASE INHIBITORS PHARMACIA & UPJOHN SPA (IT) 2001-01-25 WO claimed