SCHEMBL948161

SCHEMBL948161

CCCCN(C)C(=O)CC(=O)N(C)CCCC

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.46
KDM4C Q9H3R0 7/20 0.44
KDM5A P29375 6/20 0.44
EPHX2 P34913 3/20 0.43
CA12 O43570 2/20 0.43
CA1 P00915 2/20 0.43
CA9 Q16790 2/20 0.43
KDM4A O75164 2/20 0.42
PHF8 Q9UPP1 1/20 0.42
SIGMAR1 Q99720 1/20 0.40
MMP1 P03956 1/20 0.40
MMP2 P08253 1/20 0.40
MMP3 P08254 1/20 0.40
MMP8 P22894 1/20 0.40
CNR1 P21554 1/20 0.40
KDM5C P41229 1/20 0.39
KDM5B Q9UGL1 1/20 0.39
NPC1 O15118 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
DNM1 Q05193 1/20 0.38

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL10341548 0.91 EPHX2 (0.53) KDM4CKDM5AEPHX2KDM4APHF8
SCHEMBL11192785 0.89 KDM4C (0.49) ALDH1A1KDM4CKDM5AEPHX2KDM4A
SCHEMBL12323491 0.89 ALDH1A1 (0.41) ALDH1A1KDM4CKDM5AEPHX2CA12
SCHEMBL15224198 0.87 ALDH1A1 (0.40) ALDH1A1KDM4CKDM5AEPHX2CA12
SCHEMBL14890355 0.87 ALDH1A1 (0.40) ALDH1A1KDM4CKDM5AEPHX2CA12
SCHEMBL4146764 0.85 ALDH1A1 (0.46) ALDH1A1KDM4CKDM5AEPHX2CA12
SCHEMBL18461363 0.85 EPHX2 (0.49) ALDH1A1KDM4CKDM5AEPHX2KDM4A
SCHEMBL11186932 0.83 GAA (0.52) ALDH1A1KDM4CKDM5AEPHX2CA12
SCHEMBL20673423 0.83 ALDH1A1 (0.62) ALDH1A1KDM4CKDM5AEPHX2CA12
SCHEMBL11161106 0.83 EPHX2 (0.50) ALDH1A1KDM4CKDM5AEPHX2CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7879306-B2 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2011-02-01 US claimed
US-20080008643-A1 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2008-01-10 US claimed
CN-117800862-A Synthesis method of N, N '-dimethyl-N, N' -dibutyl-2-tetradecyl malonamide 中核四0四有限公司 2024-04-02 CN disclosed
US-7879306-B2 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2011-02-01 US disclosed
US-7879306-B2 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2011-02-01 US disclosed
US-7879306-B2 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2011-02-01 US disclosed
US-7875257-B2 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2011-01-25 US disclosed
US-7875257-B2 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2011-01-25 US disclosed
US-7875257-B2 Dispersion and separation of nanostructured carbon in organic solvents ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2011-01-25 US disclosed
US-20090320571-A1 A dispersion of nanostructured carbon in an organic solvent, comprising the diamide compound 2-R1,7-R2-perhydrocopyrine(2,7-naphthyridine) where R1 and R2 are independently selected from C1-C6 alkyl and phenyl; mobilizing; purity determination; analysis of electrical, optical and mechanical properties ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2009-12-31 US disclosed
US-20090320571-A1 A dispersion of nanostructured carbon in an organic solvent, comprising the diamide compound 2-R1,7-R2-perhydrocopyrine(2,7-naphthyridine) where R1 and R2 are independently selected from C1-C6 alkyl and phenyl; mobilizing; purity determination; analysis of electrical, optical and mechanical properties ROCHESTER INSTITUTE OF TECHNOLOGY (US) 2009-12-31 US disclosed
EP-0527685-A1 Process for the separation of the actinides from lanthanides by selective extraction of the actinides in an organic solvent comprising a propane diamide COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1993-02-17 EP disclosed
EP-0505277-A1 Method for separating iron and/or zirconium from actinides and/or lanthanides present in an aqueous acid solution using a propane diamide COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1992-09-23 EP disclosed
US-4938871-A Alkylation COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1990-07-03 US disclosed
EP-0210928-B1 EXTRACTING AGENTS AND PROPANE DIAMIDES, THEIR USE TO RECOVER ACTINIDES AND/OR LANTHANIDES AND PROCESS FOR THEIR PREPARATION COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1990-03-14 EP disclosed
US-4770807-A RECOVERY OF ACTINIDES AND-OR LANTHANIDES COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1988-09-13 US disclosed
EP-0110789-B1 PROCESS FOR RECOVERING ACTINIDES AND/OR LANTHANIDES PRESENT IN THEIR TRIVALENT STATE IN AN AQUEOUS ACIDIC SOLUTION COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1987-02-11 EP disclosed
EP-0210928-A1 Extracting agents and propane diamides, their use to recover actinides and/or lanthanides and process for their preparation COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1987-02-04 EP disclosed
US-4572802-A EXTRACTION WITH DIAMIDES COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1986-02-25 US disclosed
EP-0110789-A1 Process for recovering actinides and/or lanthanides present in their trivalent state in an aqueous acidic solution COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 1984-06-13 EP disclosed