SCHEMBL9398147

SCHEMBL9398147

CCC=C(OC(=O)CCC)OC(=O)CCC

nearest known ligand 0.61

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.61
CES2 O00748 1/20 0.36
CES1 P23141 1/20 0.36
HDAC3 O15379 4/20 0.35
HDAC1 Q13547 4/20 0.35
HDAC2 Q92769 4/20 0.35
HDAC8 Q9BY41 4/20 0.35
FFAR3 O14843 3/20 0.35
LMNA P02545 1/20 0.34
TSHR P16473 1/20 0.33
HDAC6 Q9UBN7 1/20 0.31
NAAA Q02083 1/20 0.30
DGKA P23743 1/20 0.30
BCL9 O00512 1/20 0.30
CTNNB1 P35222 1/20 0.30
CTSD P07339 1/20 0.30

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
SCHEMBL9398201 0.83 ALDH1A1 (0.36) ALDH1A1FFAR3TSHRNAAA
SCHEMBL31534023 0.80 ALDH1A1 (0.58) ALDH1A1CES2CES1HDAC3HDAC1
SCHEMBL20962970 0.80 ALDH1A1 (0.58) ALDH1A1CES2CES1HDAC3HDAC1
SCHEMBL8116737 0.77 ALDH1A1 (0.44) ALDH1A1
SCHEMBL30568759 0.77 ALDH1A1 (1.00) ALDH1A1CES2CES1HDAC3HDAC1
SCHEMBL8158 0.77 ALDH1A1 (1.00) ALDH1A1CES2CES1HDAC3HDAC1
SCHEMBL9556715 0.75 ALDH1A1 (0.94) ALDH1A1CES2CES1HDAC3HDAC1
SCHEMBL10640242 0.75 ALDH1A1 (0.94) ALDH1A1CES2CES1HDAC3HDAC1
SCHEMBL17477083 0.75 ALDH1A1 (0.94) ALDH1A1CES2CES1HDAC3HDAC1
SCHEMBL27743311 0.75 ALDH1A1 (0.94) ALDH1A1CES2CES1HDAC3HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5354887-A Reacting carbon monoxide and water with diacryloxylated butene in polar, aprotic solvent and catalyst RHONE-POULENC CHIMIE (FR) 1994-10-11 US disclosed
EP-0395545-B1 PROCESS FOR PREPARING 1,6-HEXENEDIOIC ACIDS RHONE-POULENC CHIMIE (FR) 1993-07-28 EP disclosed
EP-0433189-B1 PROCESS FOR THE PREPARATION OF DIESTERS OF HEXENEDIOIC ACID RHONE-POULENC CHIMIE (FR) 1993-06-23 EP disclosed
EP-0433190-B1 PROCESS FOR PREPARING 1,6-HEXENDIOIC ACIDS RHONE-POULENC CHIMIE (FR) 1993-04-21 EP disclosed
EP-0347340-B1 PROCESS FOR THE PREPARATION OF DIESTERS OF HEXENEDIOIC ACID RHONE-POULENC CHIMIE (FR) 1992-04-08 EP disclosed
US-5087735-A Reacting carbon monoxide, alcohol and diacyloxylated butene in polar, aprotic solvent and catalyst system RHONE-POULENC CHIMIE (FR) 1992-02-11 US disclosed
US-5077433-A Reacing carbon monoxide, water and diacyloxylated butene in th e presence of palladium and quaternary onium chloride RHONE-POULENC CHIMIE (FR) 1991-12-31 US disclosed
EP-0433190-A1 Process for preparing 1,6-hexendioic acids RHONE-POULENC CHIMIE (FR) 1991-06-19 EP disclosed
EP-0433189-A1 Process for the preparation of diesters of hexenedioic acid RHONE-POULENC CHIMIE (FR) 1991-06-19 EP disclosed
EP-0395545-A2 Process for preparing 1,6-hexenedioic acids RHONE-POULENC CHIMIE (FR) 1990-10-31 EP disclosed
US-4925973-A REACTION OF DIACETOXY BUTENE WITH ALCOHOL AND CARBON MONOXIDE RHONE-POULENC CHIMIE (FR) 1990-05-15 US disclosed
EP-0347340-A1 Process for the preparation of diesters of hexenedioic acid RHONE-POULENC CHIMIE (FR) 1989-12-20 EP disclosed