SCHEMBL48989

SCHEMBL48989

CCC(CO)NC(C)=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
SCHEMBL5669163 1.00 — —
SCHEMBL14970377 1.00 — —
SCHEMBL1861994 0.87 — —
SCHEMBL422585 0.87 — —
SCHEMBL14007401 0.81 PLA2G2C (0.40) —
SCHEMBL1437055 0.80 — —
SCHEMBL5112339 0.80 — —
SCHEMBL4578510 0.80 — —
SCHEMBL5197140 0.80 — —
SCHEMBL2417291 0.79 TDP1 (0.43) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1951686-B1 QUINAZOLINE DERIVATIVES AS A MULTIPLEX INHIBITOR AND METHOD FOR THE PREPARATION THEREOF HANMI PHARM IND CO LTD (KR) 2013-04-03 — — EP claimed
US-20080318950-A1 Quinazoline Derivatives as a Multiplex Inhibitor and Method For the Preparation Thereof HANMI PHARM. CO., LTD (KR) 2008-12-25 — — US claimed
CN-101304978-A Quinazoline derivatives as multiplex inhibitors and process for their preparation HANMI PHARM IND CO LTD (KR) 2008-11-12 — — CN claimed
EP-1951686-A1 QUINAZOLINE DERIVATIVES AS A MULTIPLEX INHIBITOR AND METHOD FOR THE PREPARATION THEREOF Hanmi Pharm. Co., Ltd. (KR) 2008-08-06 — — EP claimed
WO-2007055514-A1 QUINAZOLINE DERIVATIVES AS A MULTIPLEX INHIBITOR AND METHOD FOR THE PREPARATION THEREOF HANMI PHARM. CO., LTD. (KR) 2007-05-18 — — WO claimed
EP-4630410-A1 POLQ INHIBITORS Astrazeneca AB (SE) 2025-10-15 — — EP disclosed
CN-120020116-A Process for the preparation of N-alkenylamides 中国石油化工股份有限公司 2025-05-20 — — CN disclosed
WO-2024121753-A1 POLQ INHIBITORS ASTRAZENECA AB (SE) 2024-06-13 — — WO disclosed
WO-2023072974-A1 TRICYCLIC HETEROCYCLES MERCK PATENT GMBH (DE) 2023-05-04 — — WO disclosed
WO-2021224291-A1 TRICYCLIC HETEROCYCLES USEFUL AS TEAD BINDERS MERCK PATENT GMBH (DE) 2021-11-11 — — WO disclosed
EP-3089971-B1 COMPOUNDS AND METHODS OF USE MEDIVATION TECH LLC (US) 2020-07-29 — — EP disclosed
WO-2020012357-A1 HETEROCYCLIC COMPOUNDS AND METHODS OF USE INTEGRAL BIOSCIENCES PVT. LTD. (IN) 2020-01-16 — — WO disclosed
EP-0239122-B1 PROCESS FOR THE ENZYMATIC RESOLUTION OF RACEMIC 2-AMINO-1-ALKANOLS Montedison S.p.A. (IT) 1992-06-17 — — EP disclosed
EP-0404146-A2 Enantiomeric enrichment and stereoselective synthesis of chiral amines CELGENE CORPORATION (US) 1990-12-27 — — EP disclosed
US-4950606-A CONTACTING IN AN AQUEOUS MEDIUM IN THE PRESENCE OF AN AMINO ACCEPTOR WITH AN OMEGA-AMINO ACID TRANSAMINASE TO CONVERT ONE OF AMINES TO KETONE CELGENE CORPORATION (US) 1990-08-21 — — US disclosed
EP-0239122-A2 Process for the enzymatic resolution of racemic 2-amino-1-alkanols Montedison S.p.A. (IT) 1987-09-30 — — EP disclosed
US-3944618-A DI-1-AMINO-2-BUTANOL, ETHYLENE DICHLORIDE AMERICAN CYANAMID COMPANY (US) 1976-03-16 — — US disclosed
US-3944619-A ISOLATION FROM L ISOMER USING L(+)-TARTARIC ACID AMERICAN CYANAMID COMPANY (US) 1976-03-16 — — US disclosed
US-3944617-A HYDROLYSIS OF N-(1-(CHLOROMETHYL)-PROPYL)ACETAMIDE AMERICAN CYANAMID COMPANY (US) 1976-03-16 — — US disclosed
US-3944608-A Synthesis of N-[1-(chloromethyl)propyl]acetamide AMERICAN CYANAMID COMPANY (US) 1976-03-16 — — US disclosed
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