Hydroquinone

Hydroquinone

SCHEMBL827468

C=CC(=O)CCCCOc1ccc(C(=O)O)cc1.C=CC(=O)CCCCOc1ccc(C(=O)O)cc1.Oc1ccc(O)cc1

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.58
L3MBTL1 Q9Y468 1/20 0.58
HTT P42858 3/20 0.56
TP53 P04637 1/20 0.52
TSHR P16473 1/20 0.52
PLA2G4B P0C869 5/20 0.51
PKM P14618 1/20 0.50
RARB P10826 3/20 0.49
POLB P06746 1/20 0.49
APEX1 P27695 1/20 0.49
TDP1 Q9NUW8 1/20 0.49
PLA2G4A P47712 1/20 0.47

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
SCHEMBL2107828 0.94 ALDH1A1 (0.65) ALDH1A1L3MBTL1HTTTP53TSHR
SCHEMBL495530 0.93 HTT (0.63) ALDH1A1L3MBTL1HTTTP53TSHR
SCHEMBL27894195 0.93 HTT (0.63) ALDH1A1L3MBTL1HTTTP53TSHR
Hydrochloric Acid SCHEMBL7084259 0.92 HTT (0.62) ALDH1A1L3MBTL1HTTTP53TSHR
SCHEMBL5485757 0.86 LMNA (0.47) ALDH1A1L3MBTL1HTTTSHR
Hydroquinone SCHEMBL7622065 0.83 HTT (0.63) ALDH1A1L3MBTL1HTTTP53TSHR
SCHEMBL7620855 0.83 HTT (0.63) ALDH1A1L3MBTL1HTTTP53TSHR
Hydroquinone SCHEMBL7616531 0.81 HTT (0.59) ALDH1A1L3MBTL1HTTTP53TSHR
SCHEMBL27853261 0.81 ALDH1A1 (0.51) ALDH1A1L3MBTL1HTTTP53TSHR
SCHEMBL13183005 0.81 HDAC1 (0.61)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8142682-B2 Cholesteric multi-layers SICPA HOLDING SA (CH) 2012-03-27 US disclosed
US-7794620-B2 Cholesteric monolayers and monolayer pigments with particular properties, their production and use SICPA HOLDING S.A. (CH) 2010-09-14 US disclosed
EP-2032672-B1 CHOLESTERIC MULTI-LAYERS SICPA HOLDING SA (CH) 2010-09-01 EP disclosed
US-20100178508-A1 Cholesteric Multi-Layers SICPA HOLDING S.A. (CH) 2010-07-15 US disclosed
EP-2032672-A1 CHOLESTERIC MULTI-LAYERS Sicpa Holding S.A. (CH) 2009-03-11 EP disclosed
US-20080305315-A1 Cholesteric Monolayers and Monolayer Pigments with Particular Properties, Their Production and Use SICPA HOLDING S.A. (CH) 2008-12-11 US disclosed
US-7396486-B2 Polymerizable mixtures WACKER CHEMIE AG (DE) 2008-07-08 US disclosed
EP-1831328-B1 CHOLESTERIC MONOLAYERS AND MONOLAYER PIGMENTS WITH PARTICULAR PROPERTIES, THEIR PRODUCTION AND USE SICPA HOLDING SA (CH) 2008-05-14 EP disclosed
EP-1876216-A1 Cholesteric multi-layers Sicpa Holding S.A. (CH) 2008-01-09 EP disclosed
WO-2008000755-A1 CHOLESTERIC MULTI-LAYERS SICPA HOLDING S.A. (CH) 2008-01-03 WO disclosed
US-20060097224-A1 Polymerisable mixtures WACKER CHEMIE AG (DE) 2006-05-11 US disclosed
US-6732961-B2 MATERIAL TO BE PROCESSED INTO PLATELETS IS APPLIED IN A FLOWABLE OR GASEOUS STATE TO A SUBSTRATE, CONSOLIDATED, REMOVED FROM SUBSTRATE, AND SUBJECTED TO CRUSHING OR GRINDING, WHEREIN MATERIAL IS APPLIED IN SUCCEEDING LAYERS CONSORTIUM FUER ELEKTROCHEMISCHE INDUSTRIE, GMBH (DE) 2004-05-11 US disclosed
US-6423246-B1 LIQUID CRYSTAL POLYMERS AND CROSSLINKING CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) 2002-07-23 US disclosed
US-20020086113-A1 Method of producing platelets CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) 2002-07-04 US disclosed