SCHEMBL13656370

SCHEMBL13656370

C=CCOCCOCC(COc1ccccc1)OCCO

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 1/20 0.42
▸ RECQL P46063 1/20 0.42
▸ LMNA P02545 2/20 0.36
▸ THRB P10828 1/20 0.35
▸ MEN1 O00255 3/20 0.35
▸ KMT2A Q03164 3/20 0.35
▸ KDM4E B2RXH2 1/20 0.35
▸ SMN1; SMN2 Q16637 1/20 0.35
▸ PLA2G2A P14555 2/20 0.34
▸ CASP1 P29466 2/20 0.34
▸ MAPT P10636 1/20 0.34
▸ CYP2D6 P10635 2/20 0.33
▸ GAA P10253 1/20 0.33
▸ SCN4A P35499 2/20 0.33
▸ PLA2G10 O15496 1/20 0.32
▸ PLA2G1B P04054 1/20 0.32
▸ PLA2G5 P39877 1/20 0.32
▸ SLC22A1 O15245 1/20 0.32
▸ CYP1A2 P05177 1/20 0.32
▸ ADRB2 P07550 1/20 0.32

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
SCHEMBL13656373 0.96 ALDH1A1 (0.41) ALDH1A1RECQLLMNATHRBMEN1
SCHEMBL13105510 0.95 ALDH1A1 (0.41) ALDH1A1RECQLLMNATHRBMEN1
SCHEMBL13105514 0.95 ALDH1A1 (0.41) ALDH1A1RECQLLMNATHRBMEN1
SCHEMBL13656374 0.85 LMNA (0.39) ALDH1A1RECQLLMNAMEN1KMT2A
SCHEMBL14168750 0.84 LTA4H (0.41) LMNAMEN1KMT2APLA2G2APLA2G10
SCHEMBL12098568 0.83 ALDH1A1 (0.50) ALDH1A1RECQLLMNAMEN1KMT2A
SCHEMBL27250574 0.83 ALDH1A1 (0.35) ALDH1A1RECQLLMNAMEN1KMT2A
SCHEMBL14436878 0.82 CYP2D6 (0.39) RECQLLMNAMEN1KMT2AKDM4E
SCHEMBL13105537 0.81 LMNA (0.36) ALDH1A1RECQLLMNAMEN1KMT2A
SCHEMBL13105525 0.81 LMNA (0.36) ALDH1A1RECQLLMNAMEN1KMT2A

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 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7605224-B2 Reacting alkylene oxide and glycidy ether to produce OH- or acid-terminated copolymer CLARIANT PRODUKTE (DEUTSCHLAND) GMBH (DE) 2009-10-20 — — US disclosed
US-20080227917-A1 Copolymers made of alkylene oxides and glycidyl ethers and use thereof as polymerizable emulsifiers CLARIANT PRODUKTE (DEUTSCHLAND) GMBH 2008-09-18 — — US disclosed
US-7388068-B2 Copolymers made of alkylene oxides and glycidyl ethers and use thereof as polymerizable emulsifiers CLARIANT PRODUKTE (DEUTSCHLAND) GMBH (DE) 2008-06-17 — — US disclosed
Send feedback