SCHEMBL9398201

SCHEMBL9398201

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

nearest known ligand 0.36

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.36
NAAA Q02083 1/20 0.33
TDP1 Q9NUW8 2/20 0.32
FFAR3 O14843 1/20 0.32
MGAM O43451 1/20 0.31
GAA P10253 1/20 0.31
SI P14410 1/20 0.31
MGAM2 Q2M2H8 1/20 0.31
SOAT1 P35610 1/20 0.31
TSHR P16473 1/20 0.31
CYP1A2 P05177 1/20 0.30
HPGD P15428 1/20 0.30
CYP2C19 P33261 1/20 0.30
BLM P54132 1/20 0.30
WRN Q14191 1/20 0.30
HIF1A Q16665 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
SCHEMBL9398147 0.83 ALDH1A1 (0.61) ALDH1A1NAAAFFAR3TSHR
SCHEMBL8116737 0.83 ALDH1A1 (0.44) ALDH1A1CYP2C19
SCHEMBL5074549 0.79 ALDH1A1 (0.45) ALDH1A1TDP1FFAR3MGAMGAA
SCHEMBL11652667 0.79 ALDH1A1 (0.45) ALDH1A1TDP1FFAR3MGAMGAA
SCHEMBL17181554 0.73 ALDH1A1 (0.33) ALDH1A1NAAATDP1
SCHEMBL9276 0.73
SCHEMBL5075300 0.72 ALDH1A1 (0.41) ALDH1A1TDP1TSHR
SCHEMBL7152292 0.70 ALDH1A1 (0.56) ALDH1A1NAAATDP1FFAR3MGAM
SCHEMBL9350570 0.70 ALDH1A1 (0.56) ALDH1A1NAAATDP1FFAR3MGAM
Propane SCHEMBL20562580 0.70 ALDH1A1 (0.56) ALDH1A1NAAATDP1FFAR3MGAM

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 13 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
EP-0009741-A1 Process for the preparation of butenediol diesters BASF Aktiengesellschaft (DE) 1980-04-16 EP disclosed