SCHEMBL114743

SCHEMBL114743

CC(C)[Si](OS(=O)(=O)C(F)(F)F)(C(C)C)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
SCHEMBL5960750 0.86
SCHEMBL631967 0.81
SCHEMBL537785 0.79
SCHEMBL14981496 0.79
SCHEMBL5960817 0.79 CA1 (0.31)
SCHEMBL6641375 0.78
SCHEMBL5960753 0.77 CA2 (0.37)
SCHEMBL22325672 0.76
SCHEMBL16987250 0.76
SCHEMBL5960772 0.76 CA2 (0.39)

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

Appears in 2108 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4745178-A1 ULTRA-HIGH MOLECULAR WEIGHT POLYGLUTAMIC ACID AND PREPARATION METHOD THEREFOR Imeik Technology Development Co., Ltd. (CN) 2026-05-20 EP claimed
EP-4673424-A1 LIQUID PHASE PEPTIDE SUPPORT SYNTHESIS OF PEPTIDES AND PEPTIDOMIMETICS Regeneron Pharmaceuticals, Inc. (US) 2026-01-07 EP claimed
US-20250289842-A1 Processes for Making NAG-25, a Carbohydrate Targeting Moiety, and its Intermediates AMGEN INC. 2025-09-18 US claimed
US-12331072-B2 Deprotection method and resin removal method in solid-phase reaction for peptide compound or amide compound, and method for producing peptide compound CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-06-17 US claimed
WO-2025104679-A1 PROCESSES FOR MAKING INTERMEDIATES FOR ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2025-05-22 WO claimed
WO-2025083736-A1 NOVEL PROCESS FOR THE PREPARATION OF PIRTOBRUTINIB AND ITS INTERMEDIATES THEREOF MSN LABORATORIES PRIVATE LIMITED, R&D CENTER (IN) 2025-04-24 WO claimed
CN-115976130-B Ruimei gem Process for synthesizing intermediate 奥锐特药业(天津)有限公司 2025-03-28 CN claimed
EP-4519278-A1 PROCESSES FOR MAKING NAG-25, A CARBOHYDRATE TARGETING MOIETY, AND ITS INTERMEDIATES Amgen Inc. (US) 2025-03-12 EP claimed
CN-119562958-A Methods for preparing NAG-25 carbohydrate targeting moieties and intermediates thereof 安进公司 2025-03-04 CN claimed
WO-2025041809-A1 METHOD FOR PRODUCING DEUTERATED COMPOUND 国立大学法人九州大学 2025-02-27 WO claimed
EP-0487602-B1 5-(1-AMINOCYCLOHEXYL)-2(1H)-PYRIDINONE AND RELATED COMPOUNDS HOECHST ROUSSEL PHARMA (US) 1997-07-16 EP claimed
US-5426206-A Stereospecific synthesis of aldols THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1995-06-20 US claimed
US-5264575-A Reacting 1,3-benzodiazocine-8-ol derivative with lutidine/2,6-/, triisoproylsilyltrifluoro methane, formed intermediate reacted with lithium chloride, tetrabutylammonium fluoride and isocyanate HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1993-11-23 US claimed
EP-0487602-A4 5-(1-AMINOCYCLOHEXYL)-2(1H)-PYRIDINONE AND RELATED COMPOUNDS 1993-03-17 EP claimed
EP-0487602-A1 5-(1-AMINOCYCLOHEXYL)-2(1H)-PYRIDINONE AND RELATED COMPOUNDS. HOECHST ROUSSEL PHARMA (US) 1992-06-03 EP claimed
WO-1991002721-A1 5-(1-AMINOCYCLOHEXYL)-2(1H)-PYRIDINONE AND RELATED COMPOUNDS HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1991-03-07 WO claimed
EP-0335292-A2 2,6-Methano-1,3-benzodiazocines, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1989-10-04 EP claimed
EP-0308913-A2 2,6-Methanopyrrolo-3-benzazocines, a process and intermediates for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1989-03-29 EP claimed
US-4772683-A SILYLATION, AZETIDONE THIOLESTERS BRISTOL-MYERS COMPANY (US) 1988-09-20 US claimed
US-4639335-A ANHYDROPENICILLIN INTERMEDIATE BRISTOL-MYERS COMPANY (US) 1987-01-27 US claimed