SCHEMBL7924569

SCHEMBL7924569

CC(OCc1ccccc1)C(=O)Cl.CC(OCc1ccccc1)C(=O)O

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.49
CYP1A2 P05177 3/20 0.49
SLC1A3 P43003 2/20 0.49
SLC1A2 P43004 2/20 0.49
SLC1A1 P43005 2/20 0.49
CYP2C9 P11712 2/20 0.49
CYP2C19 P33261 2/20 0.49
MEN1 O00255 1/20 0.49
CYP2D6 P10635 1/20 0.49
ALDH1A1 P00352 4/20 0.49
GLRA1 P23415 1/20 0.44
LMNA P02545 2/20 0.41
L3MBTL1 Q9Y468 2/20 0.41
TSHR P16473 2/20 0.41
MMP9 P14780 1/20 0.40
MMP8 P22894 1/20 0.40
GAA P10253 1/20 0.40
PKM P14618 1/20 0.40
MAPK1 P28482 2/20 0.40
HPGD P15428 1/20 0.40

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
SCHEMBL5169494 0.95 ALDH1A1 (0.53) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
SCHEMBL5168366 0.95 ALDH1A1 (0.53) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
SCHEMBL839677 0.95 ALDH1A1 (0.53) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
SCHEMBL28656889 0.93 ALDH1A1 (0.52) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
SCHEMBL138280 0.91 KMT2A (0.56) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
SCHEMBL138281 0.91 KMT2A (0.56) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
SCHEMBL1706675 0.91 KMT2A (0.56) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
SCHEMBL27757196 0.91 KMT2A (0.56) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL7686303 0.90 KMT2A (0.54) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL8687912 0.90 KMT2A (0.54) KMT2ACYP1A2SLC1A3SLC1A2SLC1A1

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-6300522-B1 CONDENSING 2-CHLOROALKANOIC ACID WITH OPTIONALLY SUBSTITUTED BENZYL ALCOHOL TO FORM 2-BENZYLOXYALKANOIC ACID, CONVERTING TO ACID CHLORIDE, REACTING WITH GRIGNARD REAGENT IN PRESENCE OF CUPROUS COMPOUND, HYDROGENATING TO REMOVE BENZYL GROUP AVECIA LIMITED (GB) 2001-10-09 US disclosed
EP-1080062-A1 PROCESS FOR THE PREPARATION OF 2-HYDROXYALKYL HALOPHENONES Avecia Limited (GB) 2001-03-07 EP disclosed
WO-1999054272-A1 PROCESS FOR THE PREPARATION OF 2-HYDROXYALKYL HALOPHENONES AVECIA LIMITED (GB) 1999-10-28 WO disclosed