SCHEMBL2804547

SCHEMBL2804547

CPC(C)(C)C

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
SCHEMBL5069718 0.94
Iodide SCHEMBL3314506 0.94
Iodide SCHEMBL3288221 0.89
SCHEMBL17714059 0.82
Iodide SCHEMBL3290178 0.78
SCHEMBL13953070 0.67
SCHEMBL19068041 0.67
SCHEMBL14537899 0.67
SCHEMBL18557572 0.67
SCHEMBL16272972 0.64

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3732175-B1 A CATALYST COMPOSITION FOR A PRODUCING PROCESS OF AN UNSATURATED CARBOXYLIC ACID SALT AND ITS DERIVATIVES FROM CARBON DIOXIDE AND OLEFIN PTT GLOBAL CHEMICAL PUBLIC CO LTD (TH) 2023-08-16 EP claimed
CN-104011007-A Continuous process for the carbonylation of ethylene LUCITE INT UK LTD 2014-08-27 CN claimed
CN-119019229-B Synthesis method of beta-gem difluorophenethyl alcohol or beta-gem difluorophenethyl ether compound and analogues thereof 中国科学技术大学 2025-04-29 CN disclosed
CN-119019229-A Synthesis method of beta-gem difluorophenethyl alcohol or beta-gem difluorophenethyl ether compound and analogues thereof 中国科学技术大学 2024-11-26 CN disclosed
CN-114096547-B Optically active bisphosphonylmethane, method for producing same, transition metal complex, and asymmetric catalyst 日本化学工业株式会社 2024-04-30 CN disclosed
CN-111018923-B Carbohydrate monophosphines, method for the production and use thereof 东莞市均成高新材料有限公司 2024-04-19 CN disclosed
US-20230382876-A1 PROTOPORPHYRINOGEN OXIDASE INHIBITORS ENKO CHEM, INC. (US) 2023-11-30 US disclosed
EP-4276092-A1 COMPOUND LIBRARY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-11-15 EP disclosed
CN-110997686-B Method for producing 2, 3-biphosphinylpyrazine derivative and method for producing phosphine transition metal complex 日本化学工业株式会社 2023-11-03 CN disclosed
US-11773120-B2 Method for producing optically active 2, 3-bisphosphinopyrazine derivative and method for producing optically active phosphine transition metal complex NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2023-10-03 US disclosed
CN-112204044-B Process for producing phosphinobenzeborane derivative, process for producing 1, 2-bis (dialkylphosphino) benzene derivative, and transition metal complex 日本化学工业株式会社 2023-08-29 CN disclosed
US-20120022255-A1 SUBSTITUTED 3-HYDROXY-4-PYRIDONE DERIVATIVE SHIONOGI & CO., LTD. (JP) 2012-01-26 US disclosed
US-20110251416-A1 CHIRAL LIGANDS SOLVIAS AG (CH) 2011-10-13 US disclosed
US-20100292421-A1 BRIDGED METALLOCENE COMPOUND, OLEFIN POLYMERIZATION CATALYST CONTAINING THE SAME, AND ETHYLENE POLYMER OBTAINED WITH THE CATALYST MITSUI CHEMICALS, INC. 2010-11-18 US disclosed
EP-1885688-B1 ASYMMETRIC HYDROGENATION FOR THE PREPARATION OF DIPHENYLALANINE DERIVATIVES REDDY S LAB EU LTD DR (GB) 2010-09-22 EP disclosed
EP-2218725-A1 BRIDGED METALLOCENE COMPOUND, OLEFIN POLYMERIZATION CATALYST USING THE COMPOUND AND ETHYLENE POLYMER OBTAINED BY USING THE CATALYST Mitsui Chemicals, Inc. (JP) 2010-08-18 EP disclosed
US-6774265-B2 SALT FORMATION REACTION OF PHOSPHINE AND SECONDARY PHOSPHINE IN ALCOHOLIC SOLVENT NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2004-08-10 US disclosed
US-20040138504-A1 BISPHOSPHONIUM SALT AND PROCESS FOR PRODUCING THE SAME NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2004-07-15 US disclosed
EP-0944666-A1 CATALYST SYSTEMS FOR PRODUCING COPOLYMERS OF CARBON MONOXIDE AND OLEFINICALLY UNSATURATED COMPOUNDS BASF AKTIENGESELLSCHAFT (DE) 1999-09-29 EP disclosed
WO-1998025991-A1 CATALYST SYSTEMS FOR PRODUCING COPOLYMERS OF CARBON MONOXIDE AND OLEFINICALLY UNSATURATED COMPOUNDS BASF AKTIENGESELLSCHAFT (DE) 1998-06-18 WO disclosed