P-Xylene

P-Xylene

SCHEMBL2118886

CCCOC(=O)COC.CCOC(=O)CCC(C)=O.Cc1ccc(C)cc1

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.43
TDP1 Q9NUW8 2/20 0.43
LMNA P02545 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.40
HPGD P15428 1/20 0.38
NLRP3 Q96P20 1/20 0.38
TSHR P16473 1/20 0.38
MAPK1 P28482 1/20 0.38
ATM Q13315 1/20 0.38
ALDH1A1 P00352 2/20 0.37
CYP4F2 P78329 1/20 0.37
CYP4A11 Q02928 1/20 0.37
MEN1 O00255 1/20 0.37
KMT2A Q03164 1/20 0.37
RAB9A P51151 1/20 0.36

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
P-Xylene SCHEMBL7180336 0.89 MAPT (0.43) MAPTTDP1LMNASMN1; SMN2NLRP3
P-Xylene SCHEMBL223418 0.87 HPGD (0.46) MAPTTDP1LMNAHPGDNLRP3
P-Xylene SCHEMBL11573033 0.82 NLRP3 (0.50) MAPTLMNASMN1; SMN2NLRP3MEN1
Acetic Acid Butyl Ester SCHEMBL3407993 0.79 ALDH1A1 (0.51) MAPTTDP1LMNASMN1; SMN2HPGD
SCHEMBL166674 0.76 DGKA (0.50) MAPTTDP1LMNAMAPK1ALDH1A1
Toluene SCHEMBL28111602 0.76 SMN1; SMN2 (0.55) SMN1; SMN2TSHRALDH1A1CYP4F2CYP4A11
SCHEMBL2044080 0.74 GAA (0.52) MAPTTDP1LMNASMN1; SMN2TSHR
SCHEMBL29075 0.74
O-Xylene SCHEMBL27841634 0.74 ALDH1A1 (0.49) LMNASMN1; SMN2HPGDNLRP3TSHR
SCHEMBL1871750 0.73 KMT2A (0.56) MAPTTDP1LMNAHPGDTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120095164-A1 CROSSLINKABLE POLYURETHANE DISPERSIONS BAYER MATERIALSCIENCE AG (DE) 2012-04-19 US disclosed
US-7691941-B2 Low-solvent or solvent-free crosslinker dispersions with pyrazole-blocked isocyanate groups BAYER MATERIAL SCIENCE AG (DE) 2010-04-06 US disclosed
US-7589148-B2 Preparation of a polyurethane dispersion with blocked isocyanate groups BAYER MATERIALSCIENCE AG (DE) 2009-09-15 US disclosed
US-20080161487-A1 Cosolvent-free, self-crosslinking PU dispersions BAYER MATERIALSCIENCE AG 2008-07-03 US disclosed
US-20070282062-A1 Low-solvent or solvent-free crosslinker dispersions with pyrazole-blocked isocyanate groups BAYER MATERIALSCIENCE AG 2007-12-06 US disclosed
US-20070265389-A1 Aqueous dispersions with bimodal particle size distribution BAYER MATERIALSCIENCE AG (DE) 2007-11-15 US disclosed
US-20070129488-A1 Preparation of a polyurethane dispersion with blocked isocyanate groups BAYER MATERIALSCIENCE AG 2007-06-07 US disclosed
US-20070032594-A1 Self-crosslinking polyurethane dispersions containing uretdione and isocyanate-reactive groups BAYER MATERIALSCIENCE AG 2007-02-08 US disclosed
US-20070004894-A1 Silicon-free polyisocyanate or polyurethanes having monoamide-containing hydrophilic groups BAYER MATERIALSCIENCE AG 2007-01-04 US disclosed
US-6583216-B1 Crosslinking agents are storage stable with little yellowing; 1,6-diisocyanatohexane blocked with diethyl malonate, 1-amino-3,3,5- trimethyl-5-aminomethylcyclohexane, and formaldehyde BAYER AKTIENGESELLSCHAFT (DE) 2003-06-24 US disclosed
US-6335381-B1 AQUEOUS COATING COMPOSITION COMPRISING REACTION PRODUCT OF POLYISOCYANATE AND MONOHYDRIC ALCOHOL HAVING (METH)ACRYLOYL GROUPS, ULTRAVIOLET RADIATION INITIATOR WHICH INITIATES POLYMERIZATION BY FREE RADICAL MECHANISM, REACTIVE BINDER BAYER AKTIENGESELLSCHAFT (DE) 2002-01-01 US disclosed