SCHEMBL149335

SCHEMBL149335

CC(C)(C)N(F)F

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
SCHEMBL23758052 0.74
SCHEMBL5268499 0.74
SCHEMBL11881363 0.74
SCHEMBL19293661 0.74
Hydrochloric Acid SCHEMBL7962854 0.70
SCHEMBL11883341 0.65
SCHEMBL3204686 0.65
SCHEMBL20212016 0.59
SCHEMBL184857 0.59
SCHEMBL124148 0.59

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4479396-A1 PROCESS FOR MANUFACTURING MACROCYCLIC PEPTIDES F. Hoffmann-La Roche AG (CH) 2024-12-25 EP claimed
WO-2023152347-A1 PROCESS FOR MANUFACTURING MACROCYCLIC PEPTIDES F. HOFFMANN-LA ROCHE AG (CH) 2023-08-17 WO claimed
US-7795326-B2 Solution of an amphiphilic copolymer of a nitrogen-containing monomer, such as N-isopropylacrylamide, and a siloxy monomer, preferably 3-(methacryloyloxy)propyltris(trimethylsiloxy)silane in non-stinging, volatile, siloxane, alkane, fluorocarbon, lor iquid or supercritical carbon dioxide; medical devices ROCHAL INDUSTRIES, LLP (US) 2010-09-14 US claimed
JP-2009518145-A 2009-05-07 JP claimed
EP-1968655-A2 CONFORMABLE BANDAGE AND COATING MATERIAL Rochal Industries, LLP (US) 2008-09-17 EP claimed
WO-2007067866-A2 CONFORMABLE BANDAGE AND COATING MATERIAL ROCHAL INDUSTRIES, LLP (US) 2007-06-14 WO claimed
US-20070129474-A1 Solution of an amphiphilic copolymer of a nitrogen-containing monomer, such as N-isopropylacrylamide, and a siloxy monomer, preferably 3-(methacryloyloxy)propyltris(trimethylsiloxy)silane in non-stinging, volatile, siloxane, alkane, fluorocarbon, lor iquid or supercritical carbon dioxide; medical devices ROCHAL INDUSTRIES, LLP. (US) 2007-06-07 US claimed
US-20060173219-A1 Protective groups for crossed aldol condensations EVERETT CHRISTIAN 2006-08-03 US claimed
US-20120059163-A1 Non-linear opticaly active molecules, their synthesis, and use OPTIMER PHOTONICS, INC. (US) 2012-03-08 US disclosed
EP-1968655-B1 CONFORMABLE BANDAGE AND COATING MATERIAL ROCHAL IND LLP (US) 2011-03-02 EP disclosed
US-7795375-B2 Fluoropolyether compound ASAHI GLASS COMPANY, LIMITED (JP) 2010-09-14 US disclosed
US-7795326-B2 Solution of an amphiphilic copolymer of a nitrogen-containing monomer, such as N-isopropylacrylamide, and a siloxy monomer, preferably 3-(methacryloyloxy)propyltris(trimethylsiloxy)silane in non-stinging, volatile, siloxane, alkane, fluorocarbon, lor iquid or supercritical carbon dioxide; medical devices ROCHAL INDUSTRIES, LLP (US) 2010-09-14 US disclosed
EP-1705203-B1 FLUOROPOLYETHER COMPOUND ASAHI GLASS CO LTD (JP) 2009-06-03 EP disclosed
EP-1968655-A2 CONFORMABLE BANDAGE AND COATING MATERIAL Rochal Industries, LLP (US) 2008-09-17 EP disclosed
EP-1742906-A2 NON-LINEAR OPTICALLY ACTIVE MOLECULES, THEIR SYNTHESIS, AND USE Optimer Photonics, Inc. (US) 2007-01-17 EP disclosed
US-20060252910-A1 Fluoropolyether compound ASAHI GLASS COMPANY, LIMITED (JP) 2006-11-09 US disclosed
EP-1705203-A1 FLUOROPOLYETHER COMPOUND Asahi Glass Company, Limited (JP) 2006-09-27 EP disclosed
WO-2005119315-A2 NON-LINEAR OPTICALLY ACTIVE MOLECULES, THEIR SYNTHESIS, AND USE OPTIMER PHOTONICS, INC. (US) 2005-12-15 WO disclosed
US-20050197408-A1 Perfluoropolyether derivative ASAHI GLASS COMPANY LIMITED (JP) 2005-09-08 US disclosed
EP-1553123-A1 PERFLUOROPOLYETHER DERIVATIVES ASAHI GLASS COMPANY LTD. (JP) 2005-07-13 EP disclosed