SCHEMBL7570534

SCHEMBL7570534

CC(=O)Oc1ccc(OC(C)=O)c(C(C)(C)C)c1

nearest known ligand 0.53

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.53
CYP3A4 P08684 1/20 0.49
NR1H4 Q96RI1 2/20 0.48
KMT2A Q03164 1/20 0.48
MAPT P10636 1/20 0.47
MAPK1 P28482 1/20 0.47
LMNA P02545 3/20 0.46
RAB9A P51151 2/20 0.44
NPC1 O15118 1/20 0.44
PKM P14618 1/20 0.44
HTT P42858 1/20 0.44
BACE1 P56817 1/20 0.44
ACHE P22303 1/20 0.44
ALDH1A1 P00352 2/20 0.43
GAA P10253 2/20 0.43
TSHR P16473 1/20 0.43
ATM Q13315 1/20 0.43
ESRRA P11474 2/20 0.43
CFD P00746 1/20 0.42

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
SCHEMBL13688321 0.90 ALDH1A1 (0.54) KDM4ENR1H4KMT2AMAPTNPC1
SCHEMBL21075510 0.84 KDM4E (0.42) KDM4ECYP3A4NR1H4KMT2AMAPT
SCHEMBL3864856 0.82 ALDH1A1 (0.50) KDM4ECYP3A4NR1H4LMNARAB9A
SCHEMBL11143326 0.82 ESRRA (0.62) CYP3A4NR1H4MAPTLMNAHTT
SCHEMBL9247660 0.82 NR1H4 (0.48) KDM4ENR1H4KMT2ALMNARAB9A
SCHEMBL11229207 0.82 APEX1 (0.50) KDM4ENR1H4KMT2ARAB9ABACE1
SCHEMBL26764584 0.81 ELANE (0.46) NR1H4KMT2AMAPTALDH1A1GAA
SCHEMBL22650884 0.81 TSHR (0.50) KDM4ENR1H4KMT2ARAB9AALDH1A1
SCHEMBL22140455 0.79 KDM4E (0.50) KDM4ECYP3A4NR1H4KMT2AMAPT
SCHEMBL17224803 0.79 CYP3A4 (0.46) KDM4ECYP3A4NR1H4KMT2AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0883614-B1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE KEMIRA CHEMICALS OY (FI) 2001-10-24 EP claimed
EP-0883615-A1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE NESTE OY (FI) 1998-12-16 EP claimed
EP-0883614-A1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE NESTE OY (FI) 1998-12-16 EP claimed
WO-1997030039-A1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE NESTE OY (FI) 1997-08-21 WO claimed
WO-1997023474-A1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE NESTE OY (FI) 1997-07-03 WO claimed
US-20190169362-A1 POLYMER, COMPOSITION, MOLDED ARTICLE, CURED PRODUCT, AND LAMINATE JSR CORPORATION (JP) 2019-06-06 US disclosed
US-7595074-B2 Polymeric antioxidants UNIVERSITY OF MASSACHUSETTS LOWELL (US) 2009-09-29 US disclosed
EP-0771337-B1 LIQUID CRYSTALLINE COPOLY(ESTER-IMIDE)S AND A PROCESS FOR THE PREPARATION THEREOF OPTATECH CORP (FI) 2002-09-18 EP disclosed
EP-0883614-B1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE KEMIRA CHEMICALS OY (FI) 2001-10-24 EP disclosed
EP-0883614-A1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE NESTE OY (FI) 1998-12-16 EP disclosed
US-5843541-A Liquid crystalline copoly(ester-imide)s and a process for the preparation thereof OPTATECH CORPORATION (FI) 1998-12-01 US disclosed
WO-1997030039-A1 ADDITIVES USABLE IN PREPARATION OF ALKENYL SUCCINIC ANHYDRIDE NESTE OY (FI) 1997-08-21 WO disclosed
EP-0771337-A1 LIQUID CRYSTALLINE COPOLY(ESTER-IMIDE)S AND A PROCESS FOR THE PREPARATION THEREOF OPTATECH CORPORATION (FI) 1997-05-07 EP disclosed
WO-1996001284-A1 LIQUID CRYSTALLINE COPOLY(ESTER-IMIDE)S AND A PROCESS FOR THE PREPARATION THEREOF OPTATECH CORPORATION (FI) 1996-01-18 WO disclosed
EP-0640108-A1 MELT-PROCESSABLE LIQUID CRYSTALLINE POLYESTER, PROCESS FOR THE PREPARATION THEREOF AND PRODUCTS PREPARED FROM THE POLYESTER NESTE OY (FI) 1995-03-01 EP disclosed
WO-1993023451-A1 MELT-PROCESSABLE LIQUID CRYSTALLINE POLYESTER, PROCESS FOR THE PREPARATION THEREOF AND PRODUCTS PREPARED FROM THE POLYESTER NESTE OY (FI) 1993-11-25 WO disclosed