SCHEMBL2461503

SCHEMBL2461503

CC(N(C)C)N(C(C)N(C)C)C(C)N(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
SCHEMBL435361 0.80
Hydrochloric Acid SCHEMBL8044053 0.73
SCHEMBL10935886 0.73
SCHEMBL23699788 0.72
SCHEMBL28924988 0.70
SCHEMBL22114793 0.70
SCHEMBL4864674 0.67
SCHEMBL22350615 0.67
SCHEMBL8756692 0.67
SCHEMBL12995976 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4693687-A1 SEPARATOR OF LITHIUM-ION BATTERY, AND PREPARATION METHOD THEREFOR AND USE THEREOF SVOLT Energy Technology Co., Ltd. (CN) 2026-02-11 EP claimed
WO-2024217474-A1 SEPARATOR OF LITHIUM-ION BATTERY, AND PREPARATION METHOD THEREFOR AND USE THEREOF 蜂巢能源科技股份有限公司 2024-10-24 WO claimed
US-11426496-B2 Method for preparing anti-bacterial surface on medical material surface SOUTH CHINA UNIVERSITY OF TECHNOLOGY 2022-08-30 US claimed
WO-2021109371-A1 METHOD FOR PREPARING POLYETHER MODIFIED POLYORGANOSILOXANE 江苏四新科技应用研究所股份有限公司 2021-06-10 WO claimed
WO-2020228212-A1 DEFOAMER FOR TRANSPARENT LIQUID DETERGENT 江苏四新科技应用研究所股份有限公司 2020-11-19 WO claimed
US-20190328939-A1 Method for Preparing Anti-Bacterial Surface on Medical Material Surface SOUTH CHINA UNIVERSITY OF TECHNOLOGY (CN) 2019-10-31 US claimed
CN-107286288-A A kind of preparation method of slow-setting polycarboxylic acid water reducing agent 江苏中铁奥莱特新材料股份有限公司 2017-10-24 CN claimed
EP-1499672-B1 METHOD FOR ATTACHMENT OF ONE OR MORE ORGANIC GROUPS ONTO A PARTICLE CABOT CORP (US) 2009-09-30 EP claimed
US-20050158271-A1 Pharmaceutical applications of hydrotropic polymer micelles AKINA, INC. 2005-07-21 US claimed
US-6852158-B2 Method for attachment of one or more organic groups onto a particle CABOT CORPORATION (US) 2005-02-08 US claimed
EP-1499672-A1 METHOD FOR ATTACHMENT OF ONE OR MORE ORGANIC GROUPS ONTO A PARTICLE CABOT CORPORATION (US) 2005-01-26 EP claimed
US-20040007161-A1 Method for attachment of one or more organic groups onto a particle CABOT CORPORATION 2004-01-15 US claimed
WO-2003082968-A1 METHOD FOR ATTACHMENT OF ONE OR MORE ORGANIC GROUPS ONTO A PARTICLE CABOT CORPORATION (US) 2003-10-09 WO claimed
US-5342929-A Direct glycosylation leads to the desired glycosides in high yield and relatively short reaction times using metal complex salts; large amounts of the alpha- or beta-form are often obtained CIBA-GEIGY CORPORATION (US) 1994-08-30 US claimed
EP-4742866-A1 PEROVSKITE SOLAR CELL AND PREPARATION METHOD THEREFOR, PHOTOVOLTAIC MODULE, SYSTEM, AND ELECTRIC DEVICE Contemporary Amperex Future Energy Research Institute (Shanghai) Limited (CN) 2026-05-13 EP disclosed
EP-4693687-A1 SEPARATOR OF LITHIUM-ION BATTERY, AND PREPARATION METHOD THEREFOR AND USE THEREOF SVOLT Energy Technology Co., Ltd. (CN) 2026-02-11 EP disclosed
WO-2025011160-A1 PEROVSKITE SOLAR CELL AND PREPARATION METHOD THEREFOR, PHOTOVOLTAIC MODULE, SYSTEM, AND ELECTRIC DEVICE 宁德时代未来能源(上海)研究院有限公司 2025-01-16 WO disclosed
EP-1171496-A1 CATALYTIC PROCESSES FOR THE CONTROLLED POLYMERIZATION OF FREE RADICALLY (CO)POLYMERIZABLE MONOMERS AND FUNCTIONAL POLYMERIC SYSTEMS PREPARED THEREBY CARNEGIE-MELLON UNIVERSITY (US) 2002-01-16 EP disclosed
WO-2000056795-A1 CATALYTIC PROCESSES FOR THE CONTROLLED POLYMERIZATION OF FREE RADICALLY (CO)POLYMERIZABLE MONOMERS AND FUNCTIONAL POLYMERIC SYSTEMS PREPARED THEREBY CARNEGIE MELLON UNIVERSITY (US) 2000-09-28 WO disclosed
US-5342929-A Direct glycosylation leads to the desired glycosides in high yield and relatively short reaction times using metal complex salts; large amounts of the alpha- or beta-form are often obtained CIBA-GEIGY CORPORATION (US) 1994-08-30 US disclosed