Diethylamine

Diethylamine

SCHEMBL2935918

CC.CCNCC

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CCKAR

The experimentally established mechanism targets of Diethylamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

⚠ 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
Diethylamine SCHEMBL27977249 1.00 TP53 (0.89)
Diethylamine SCHEMBL28898169 0.95
Diethylamine SCHEMBL27874841 0.95
Diethylamine SCHEMBL6426924 0.95
Diethylamine SCHEMBL7368833 0.94
Diethylamine SCHEMBL3558785 0.94
Diethylamine SCHEMBL2698 0.94
Diethylamine SCHEMBL7130457 0.94 TP53 (1.00)
Diethylamine SCHEMBL9289074 0.89 TP53 (0.89)
Diethylamine SCHEMBL21585566 0.89

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0539281-B1 Naphthamides, process for their preparation and their application in the therapeutical field INST NAT SANTE RECH MED (FR) 1998-12-30 EP claimed
CN-112125788-B Preparation method of liquid crystal monomer compound containing difluoromethyl ether bridge bond 宁夏中星显示材料有限公司 2023-04-07 CN disclosed
CN-112125788-A Preparation method of liquid crystal monomer compound containing difluoromethyl ether bridge bond 宁夏中星显示材料有限公司 2020-12-25 CN disclosed
CN-1450859-B Method for blocking ethylene response in plants using cyclopropene derivatives UNIV NORTH CAROLINA STATE 2011-08-03 CN disclosed
EP-1582346-B1 Infrared absorbing compounds and their use in imageable elements EASTMAN KODAK CO (US) 2010-09-22 EP disclosed
CN-101828552-A Method with the cyclopropene derivatives blocking ethylene response in plants UNIV NORTH CAROLINA STATE 2010-09-15 CN disclosed
CN-100467611-C Purification of polypeptides GENENTECH INC (US) 2009-03-11 CN disclosed
US-7371454-B2 Imageable element comprising sulfated polymers EASTMAN KODAK COMPANY (US) 2008-05-13 US disclosed
CN-100360669-C Oligomeric compounds that modulate survivin expression SANTARIS PHARMA AS (DK) 2008-01-09 CN disclosed
EP-1555299-B1 Infrared absorbing N-alkylsulfate cyanine compounds EASTMAN KODAK CO (US) 2007-11-14 EP disclosed
CN-1748029-A Oligomeric compounds that modulate survivin expression SANTARIS PHARMA AS (DK) 2006-03-15 CN disclosed
US-20050221215-A1 Infrared absorbing compounds and their use in imageable elements CITICORP NORTH AMERICA, INC., AS AGENT 2005-10-06 US disclosed
EP-1582346-A2 Infrared absorbing compounds and their use in imageable elements Kodak Polychrome Graphics, LLC (US) 2005-10-05 EP disclosed
EP-1555299-A1 Infrared absorbing N-alkylsulfate cyanine compounds Kodak Polychrome Graphics, LLC (US) 2005-07-20 EP disclosed
US-20050130059-A1 Infrared absorbing N-alkylsulfate cyanine compounds CITICORP NORTH AMERICA, INC., AS AGENT 2005-06-16 US disclosed
US-20050129915-A1 Imageable element comprising sulfated polymers KODAK (NEAR EAST) INC. 2005-06-16 US disclosed
WO-2005005146-A1 IMAGEABLE ELEMENT COMPRISING SULFATED POLYMERS KODAK POLYCHROME GRAPHICS LLC (US) 2005-01-20 WO disclosed
US-6774102-B1 LIGANDS ARE OLIGOPEPTIDES CONTAINING ARGININE, LYSINE AND/OR HISTIDINE GAMBRO DIALYSATOREN GMBH & CO. KG (DE) 2004-08-10 US disclosed
EP-1220868-B1 EXTRACORPOREAL ENDOTOXIN REMOVAL METHOD GAMBRO DIALYSATOREN (DE) 2004-02-25 EP disclosed
CN-1450859-A method for blocking ethylene response in plants using cyclopropene derivatives UNIV NORTH CAROLINA STATE (US) 2003-10-22 CN disclosed