SCHEMBL4122875

SCHEMBL4122875

COC(CCC(OC)OC)OC

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
SCHEMBL17121960 0.86 ALDH1A1 (0.32)
SCHEMBL6298010 0.84 SMPD1 (0.32)
SCHEMBL1426982 0.84
SCHEMBL11875781 0.81
SCHEMBL5160133 0.81 SMPD1 (0.36)
SCHEMBL7934735 0.81 SMPD1 (0.36)
SCHEMBL27075810 0.81
SCHEMBL7936797 0.81 SMPD1 (0.36)
SCHEMBL7934687 0.81 SMPD1 (0.36)
SCHEMBL26276 0.81

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119114033-A Low-protein-adsorptivity blood perfusion adsorbent, preparation method thereof and blood perfusion device 泉州师范学院 2024-12-13 CN claimed
CN-117731562-A Composite camellia seed essential oil, preparation method and application thereof in cosmetics 青岛汭野生物科技有限公司 2024-03-22 CN claimed
US-6764589-B1 Method for the electrolytic conversion of furan or furan derivatives BASF AKTIENGESELLSCHAFT (DE) 2004-07-20 US claimed
EP-1230433-B1 METHOD FOR THE ELECTROLYTIC CONVERSION OF FURANE OR FURANE DERIVATIVES BASF AG (DE) 2003-07-09 EP claimed
EP-1230433-A1 METHOD FOR THE ELECTROLYTIC CONVERSION OF FURANE OR FURANE DERIVATIVES BASF AKTIENGESELLSCHAFT (DE) 2002-08-14 EP claimed
WO-2001021857-A1 METHOD FOR THE ELECTROLYTIC CONVERSION OF FURANE OR FURANE DERIVATIVES BASF AKTIENGESELLSCHAFT (DE) 2001-03-29 WO claimed
US-4619668-A FORMALDEHYDE-FREE THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF AGRICULTURE (US) 1986-10-28 US claimed
WO-2025262285-A1 PU BASED ON POLYOLS CONTAINING CLEAVABLE BONDS BASF SE (DE) 2025-12-26 WO disclosed
US-20250326932-A1 LIGNOCELLULOSE- AND CELLULOSE-BASED BIOPRODUCTS NORTH CAROLINA STATE UNIVERSITY (US) 2025-10-23 US disclosed
US-20250206691-A1 PROCESS FOR THE RUTHENIUM-CATALYSED HYDROGENATION OF ALDEHYDE ACETALS EVONIK OXENO GMBH & CO. KG (DE) 2025-06-26 US disclosed
CN-119192666-A Cross-linked zwitterionic modified adsorbent, ultrahigh cross-linked zwitterionic modified adsorbent, preparation method of cross-linked zwitterionic modified adsorbent and blood perfusion device 泉州师范学院 2024-12-27 CN disclosed
CN-119114033-A Low-protein-adsorptivity blood perfusion adsorbent, preparation method thereof and blood perfusion device 泉州师范学院 2024-12-13 CN disclosed
CN-117731562-A Composite camellia seed essential oil, preparation method and application thereof in cosmetics 青岛汭野生物科技有限公司 2024-03-22 CN disclosed
EP-0614869-A1 Hydrogenolytic reduction of peroxidic ozonolysis compounds DSM Chemie Linz GmbH (AT) 1994-09-14 EP disclosed
EP-0147593-B1 PROCESS FOR THE PREPARATION OF MONO- OR BIS-CARBONYL COMPOUNDS Chemie Linz Gesellschaft m.b.H. (AT) 1990-02-28 EP disclosed
US-4769464-A Process for the preparation of monocarbonyl or biscarbonyl compounds CHEMIE LINZ GESELLSCHAFT M.B.H. (AT) 1988-09-06 US disclosed
EP-0203488-A2 7-Azolyl-1-cyclopropyl-1,4-dihydro-4-oxo-3-quinoline carboxylic acids and 1,8-naphthyridine carboxylic acids, process for their preparation and bactericidal agents containing them BAYER AG (DE) 1986-12-03 EP disclosed
US-4619668-A FORMALDEHYDE-FREE THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF AGRICULTURE (US) 1986-10-28 US disclosed
EP-0147593-A2 Process for the preparation of mono- or bis-carbonyl compounds Chemie Linz Gesellschaft m.b.H. (AT) 1985-07-10 EP disclosed
US-4176190-A Diuretic and saliuretic sulphamoylbenzoic acids CIBA-GEIGY CORPORATION (US) 1979-11-27 US disclosed