SCHEMBL3058723

SCHEMBL3058723

NC1=CC=NCN1N

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
SCHEMBL10647140 0.69
SCHEMBL6154657 0.60
SCHEMBL1702448 0.55
SCHEMBL4868723 0.54
Hydrochloric Acid SCHEMBL7932129 0.51
SCHEMBL5888231 0.45
SCHEMBL1300603 0.40
SCHEMBL2362493 0.40 KDM4E (0.41)
SCHEMBL17900003 0.39
SCHEMBL121778 0.37

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105745202-A Novel 2,6-diaminopyrimidine derivative 卡尔那生物科学株式会社 2016-07-06 CN claimed
EP-4536217-A1 CO-AGENTS AS THERAPY AGAINST ANAEROBIC PATHOGENS Fleurir Abx LLC (US) 2025-04-16 EP disclosed
CN-118121707-A Pharmaceutical composition for preventing and treating mental retardation, infection, metabolic syndrome, oral disease, osteoporosis and cancer 林萧水银 2024-06-04 CN disclosed
US-20230398101-A1 Co-agents as Therapy Against Anaerobic Pathogens FLEURIR ABX LLC (US) 2023-12-14 US disclosed
WO-2023239822-A1 CO-AGENTS AS THERAPY AGAINST ANAEROBIC PATHOGENS FLEURIR ABX LLC (US) 2023-12-14 WO disclosed
CN-103946224-A 4-amino-3-phenylamino-6-phenylpyrazolo[3,4-d] pyrimidine derivatives, their manufacture and their use as antiviral active substances DRITTE PATENTPORTFOLIO BETEILI 2014-07-23 CN disclosed
CN-103702989-A Novel compounds as modulators of protein kinases RHIZEN PHARMACEUTICALS SA 2014-04-02 CN disclosed
US-7790730-B2 Imidazo[4,5-d]pyrimidines, their uses and methods of preparation GILEAD SCIENCES, INC. (US) 2010-09-07 US disclosed
US-20100120722-A1 HETEROCYCLIC COMPOUNDS FOR PREVENTING AND TREATING DISORDERS ASSOCIATED WITH EXCESSIVE BONE LOSS SYNTA PHARMACEUTICALS CORP. (US) 2010-05-13 US disclosed
US-20090208456-A1 Imidazo[4,5-d]pyrimidines, their uses and methods of preparation GILEAD SCIENCES, INC. (US) 2009-08-20 US disclosed
WO-2006033703-A1 IMIDAZO[4,5-D]PYRIMIDINES, THEIR USES AND METHODS OF PREPARATION GILEAD SCIENCES, INC. (US) 2006-03-30 WO disclosed
US-20060052602-A1 Imidazo[4,5-d]pyrimidines, their uses and methods of preparation GILEAD SCIENCES, INC. 2006-03-09 US disclosed
EP-1626725-A2 HETEROCYCLIC COMPOUNDS FOR PREVENTING AND TREATING DISORDERS ASSOCIATED WITH EXCESSIVE BONE LOSS Synta Pharmaceuticals Corporation (US) 2006-02-22 EP disclosed
EP-1556140-A2 NOVEL COMPOUNDS Synta Pharmaceuticals Corporation (US) 2005-07-27 EP disclosed
WO-2005000404-A2 HETEROCYCLIC COMPOUNDS FOR PREVENTING AND TREATING DISORDERS ASSOCIATED WITH EXCESSIVE BONE LOSS SYNTA PHARMACEUTICALS, CORP. (US) 2005-01-06 WO disclosed
US-20040198725-A1 A bi-heterocyclic compound e.g 3-methoxyphenyl)-{6-Morpholin-4-yl-2-[2-(pyridin-2-yloxy)-ethoxy]-9H-purin-8-yl}-amine or other derivatives useful for treating an interleukin-12 overproduction-related disorder such as rheumatoid arthritis, sepsis, Crohn's disease, multiple sclerosis, psoriasis or diabetes SYNTA PHARMACEUTICALS CORP. 2004-10-07 US disclosed
WO-2004035740-A2 AROMATIC BICYCLIC HETEROCYLES TO MODULATE 1L - 12 PRODUCTION SYNTA PHARMACEUTICALS CORP. (US) 2004-04-29 WO disclosed
EP-0831855-A1 NUCLEOTIDE ANALOGUES FOR TOPICAL TREATMENT OF PROLIFERATIVE DISEASE OF THE SKIN HOSTETLER, Karl Y. (US) 1998-04-01 EP disclosed
US-5654286-A Nucleotides for topical treatment of psoriasis, and methods for using same HOSTETLER KARL Y (US) 1997-08-05 US disclosed
WO-1996040166-A1 NUCLEOTIDE ANALOGUES FOR TOPICAL TREATMENT OF PROLIFERATIVE DISEASE OF THE SKIN HOSTETLER KARL Y (US) 1996-12-19 WO disclosed