SCHEMBL4408919

SCHEMBL4408919

CSNC(C)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
SCHEMBL4408920 1.00
SCHEMBL7185807 0.80 TP53 (0.40)
SCHEMBL7185803 0.80 TP53 (0.40)
SCHEMBL2858074 0.80 TP53 (0.40)
SCHEMBL28767303 0.74 TP53 (0.35)
SCHEMBL8548242 0.74
SCHEMBL21844017 0.74 SMN1; SMN2 (0.37)
SCHEMBL29625187 0.74 SLC7A5 (0.36)
SCHEMBL13529015 0.72
SCHEMBL24996113 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7560482-B2 Inhibitors of plasmepsins THE JOHNS HOPKINS UNIVERSITY (US) 2009-07-14 US claimed
US-20050037953-A1 Inhibitors of plasmepsins NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2005-02-17 US claimed
WO-2002074719-A2 INHIBITORS OF PLASMEPSINS THE JOHNS HOPKINS UNIVERSITY (US) 2002-09-26 WO claimed
EP-0490667-B1 HIV protease inhibitors JAPAN ENERGY CORP (JP) 1999-06-09 EP claimed
US-7560482-B2 Inhibitors of plasmepsins THE JOHNS HOPKINS UNIVERSITY (US) 2009-07-14 US disclosed
US-20050037953-A1 Inhibitors of plasmepsins NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2005-02-17 US disclosed
WO-2002074719-A2 INHIBITORS OF PLASMEPSINS THE JOHNS HOPKINS UNIVERSITY (US) 2002-09-26 WO disclosed
US-6291432-B1 (R)-N-(2-METHYLBENZYL)-3-((2S, 3S)-3-(N-(2-CHROMONECARBONYL)-L-ASPARAGINYL)AMINO-2-HYDROXY-4-PHENYLBUTANO YL)-5,5-DIMETHYL-1,3-THIAZOLIDINE-4-CARBOXAMIDE CAN BE GIVEN AS A TYPICAL EXAMPLE OF THIS COMPOUND. JAPAN ENERGY CORPORATION (JP) 2001-09-18 US disclosed
EP-0490667-B1 HIV protease inhibitors JAPAN ENERGY CORP (JP) 1999-06-09 EP disclosed
EP-0900566-A1 NOVEL TRIPEPTIDE COMPOUNDS AND ANTI-AIDS DRUGS JAPAN ENERGY CORPORATION (JP) 1999-03-10 EP disclosed
EP-0574135-B1 Process for producing peptide derivatives and salts thereof JAPAN ENERGY CORP (JP) 1998-11-18 EP disclosed
US-5644028-A Process for producing peptide derivatives and salts therefor JAPAN ENERGY CORPORATION (JP) 1997-07-01 US disclosed
EP-0574135-A1 Process for producing peptide derivatives and salts thereof JAPAN ENERGY CORPORATION (JP) 1993-12-15 EP disclosed