SCHEMBL867753

SCHEMBL867753

CC(C)N(C)CC(=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
Hydrochloric Acid SCHEMBL23357882 0.97 TDP1 (0.38)
SCHEMBL893034 0.83
SCHEMBL1858816 0.79 FFAR3 (0.36)
SCHEMBL14055633 0.79 FFAR3 (0.36)
SCHEMBL7695769 0.78
SCHEMBL10044465 0.78
SCHEMBL17935549 0.77 MAOB (0.41)
SCHEMBL294067 0.77 MAOB (0.41)
SCHEMBL18229248 0.77 FFAR3 (0.35)
Hydrochloric Acid SCHEMBL109328 0.77 FFAR3 (0.35)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6984754-B1 Aliphatic amino carboxylic and amino phosphonic acids amino nitriles and amino tetrazoles as cellular rescue agents UNIVERSITY OF SASKATCHEWAN TECHNOLOGIES INC. (CA) 2006-01-10 US claimed
JP-2002507591-A 2002-03-12 JP claimed
EP-1064254-A2 ALIPHATIC AMINO CARBOXYLIC AND AMINO PHOSPHONIC ACIDS, AMINO NITRILES AND AMINO TETRAZOLES AS CELLULAR RESCUE AGENTS University of Saskatchewan Technologies Inc. (CA) 2001-01-03 EP claimed
WO-1999048858-A2 ALIPHATIC AMINO CARBOXYLIC AND AMINO PHOSPHONIC ACIDS, AMINO NITRILES AND AMINO TETRAZOLES AS CELLULAR RESCUE AGENTS UNIVERSITY OF SASKATCHEWAN TECHNOLOGIES INC. (CA) 1999-09-30 WO claimed
EP-3966226-B1 MASP INHIBITORY COMPOUNDS AND USES THEREOF BAYER AG (DE) 2025-12-24 EP disclosed
US-12503491-B2 MASP inhibitory compounds and uses thereof BAYER AKTIENGESELLSCHAFT (DE) 2025-12-23 US disclosed
CN-114585637-B MASP-inhibitory compounds and uses thereof 拜耳公司 2025-04-15 CN disclosed
US-20240124522-A1 MASP INHIBITORY COMPOUNDS AND USES THEREOF BAYER AKTIENGESELLSCHAFT (DE) 2024-04-18 US disclosed
US-11873291-B2 Quinoline cGAS antagonist compounds IMMUNESENSOR THERAPEUTICS, INC. (US) 2024-01-16 US disclosed
US-20230322731-A1 HETEROARYL-BIPHENYL AMIDES FOR THE TREATMENT OF PD-L1 DISEASES CHEMOCENTRYX, INC. 2023-10-12 US disclosed
US-11760762-B2 Thienopyranones and furanopyranones as kinase, bromodomain, and checkpoint inhibitors SIGNALRX PHARMACEUTICALS, INC. (US) 2023-09-19 US disclosed
US-11713307-B2 Heteroaryl-biphenyl amides for the treatment of PD-L1 diseases CHEMOCENTRYX, INC. (US) 2023-08-01 US disclosed
CN-1105353-A Modular design and synthesis of oxazolone-derived molecules ARQULE PARTNERS L P (US) 1995-07-19 CN disclosed
WO-1995017903-A1 MODULAR DESIGN AND SYNTHESIS OF OXAZOLONE-DERIVED MOLECULES ARQULE PARTNERS, L.P. (US) 1995-07-06 WO disclosed
EP-0649443-A1 OXAZOLONE DERIVED MATERIALS LEGOMER PARTNERS, L.P. (US) 1995-04-26 EP disclosed
WO-1994000509-A9 OXAZOLONE DERIVED MATERIALS 1994-03-17 WO disclosed
WO-1994000509-A1 OXAZOLONE DERIVED MATERIALS LEGOMER PARTNERS, L.P. (US) 1994-01-06 WO disclosed
US-4804500-A Amine dealkylation process MONSANTO COMPANY (US) 1989-02-14 US disclosed
EP-0199702-B1 AMINE DEALKYLATION PROCESS Monsanto Company (US) 1988-12-21 EP disclosed
EP-0199702-A1 Amine dealkylation process Monsanto Company (US) 1986-10-29 EP disclosed