SCHEMBL2742745

SCHEMBL2742745

CC=C(CC)OCC

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
SCHEMBL6549394 1.00
SCHEMBL7260856 0.81 FFAR3 (0.30)
SCHEMBL28254075 0.79
SCHEMBL425262 0.77
SCHEMBL21110910 0.77 SOAT1 (0.38)
SCHEMBL9497789 0.77
SCHEMBL9117680 0.77
SCHEMBL18265467 0.77
SCHEMBL8203398 0.77
SCHEMBL16550051 0.77

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2718767-B1 COMPOSITION OF SOLUTIONS AND CONDITIONS FOR USE ENABLING THE STRIPPING AND COMPLETE DISSOLUTION OF PHOTORESISTS TECHNIC FRANCE (FR) 2019-08-07 EP disclosed
EP-2718767-A1 COMPOSITION OF SOLUTIONS AND CONDITIONS FOR USE ENABLING THE STRIPPING AND COMPLETE DISSOLUTION OF PHOTORESISTS Technic France (FR) 2014-04-16 EP disclosed
US-20140076356-A1 COMPOSITION OF SOLUTIONS AND CONDITIONS FOR USE ENABLING THE STRIPPING AND COMPLETE DISSOLUTION OF PHOTORESISTS TECHNIC FRANCE (FR) 2014-03-20 US disclosed
WO-2012168485-A1 COMPOSITION OF SOLUTIONS AND CONDITIONS FOR USE ENABLING THE STRIPPING AND COMPLETE DISSOLUTION OF PHOTORESISTS TECHNIC FRANCE (FR) 2012-12-13 WO disclosed
CN-101583365-B Triazine derivatives and their therapeutical applications ABRAXIS BIOSCIENCE INC 2012-09-26 CN disclosed
US-8088346-B2 Alkene hydrofunctionalization reactions UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2012-01-03 US disclosed
CN-101583365-A Triazine derivatives and their therapeutical applications ABRAXIS BIOSCIENCE INC (US) 2009-11-18 CN disclosed
US-20090069580-A1 Alkene Hydrofunctionalization Reactions NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2009-03-12 US disclosed
EP-1383726-A1 PROCESS FOR THE PREPARATION OF KETONES Degussa AG (DE) 2004-01-28 EP disclosed
EP-1383725-A1 PROCESS FOR THE PREPARATION OF UNSATURATED KETONES Degussa AG (DE) 2004-01-28 EP disclosed
EP-1092700-A1 Process for the preparation of unsaturated 4,5-allene ketones, 3,5-dienketones and the corresponding saturated ketones Degussa-Hüls Aktiengesellschaft (DE) 2001-04-18 EP disclosed
US-6034279-A REACTIG A TERTIARY ALLYL ALCOHOL WITH A ALKEYL ETHER I PRESECE OF ACID CATALYST BASF AKTIENGESELLSCHAFT (DE) 2000-03-07 US disclosed
EP-0897380-A1 METHOD FOR THE PRODUCTION OF $g(g), $g(d)-UNSATURATED KETONES BY REACTING TERTIARY ALLYL ALCOHOLS WITH ALKENYL ALKYL ETHERS BASF AKTIENGESELLSCHAFT (DE) 1999-02-24 EP disclosed
WO-1998023570-A1 METHOD FOR THE PRODUCTION OF η, δ-UNSATURATED KETONES BY REACTING TERTIARY ALLYL ALCOHOLS WITH ALKENYL ALKYL ETHERS BASF AKTIENGESELLSCHAFT (DE) 1998-06-04 WO disclosed
EP-0504812-B1 Aromatic compounds, their production processes and their compositions for the control of insect pests SUMITOMO CHEMICAL CO (JP) 1995-09-06 EP disclosed
US-5262441-A APPLYING INSECTICIDE TO INSECT OR LOCUS WHERE INSECT PROPAGATES SUMITOMO CHEMICAL COMPANY LIMITED (JP) 1993-11-16 US disclosed
EP-0272110-B1 ERYTHROMYCIN A DERIVATIVES AND METHOD FOR THE PREPARATION OF THE SAME TAISHO PHARMACEUTICAL CO. LTD (JP) 1993-04-07 EP disclosed
EP-0504812-A2 Aromatic compounds, their production processes and their compositions for the control of insect pests SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1992-09-23 EP disclosed
US-4990602-A Bactericides TAISHO PHARMACEUTICAL CO., LTD. (JP) 1991-02-05 US disclosed
EP-0272110-A2 Erythromycin a derivatives and method for the preparation of the same TAISHO PHARMACEUTICAL CO. LTD (JP) 1988-06-22 EP disclosed