SCHEMBL7895381

SCHEMBL7895381

CCCCOC(=O)/C(Cl)=C\C(=O)O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 4/20 0.50
ATM Q13315 1/20 0.47
ALDH1A1 P00352 2/20 0.45
TSHR P16473 5/20 0.44
HPGD P15428 1/20 0.44
NAAA Q02083 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.37
NPSR1 Q6W5P4 2/20 0.37
LMNA P02545 2/20 0.37
SMN1; SMN2 Q16637 2/20 0.37
MAPT P10636 1/20 0.37
RAB9A P51151 1/20 0.37
POLB P06746 1/20 0.37
RAD52 P43351 1/20 0.36
ESR1 P03372 2/20 0.36
EPHX1 P07099 1/20 0.35
CYP1A2 P05177 1/20 0.35
CYP2D6 P10635 1/20 0.35
MAPK1 P28482 1/20 0.35

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
SCHEMBL4251457 0.85 ATM (0.57) HCAR2ATMALDH1A1TSHRHPGD
SCHEMBL4251461 0.85 ATM (0.57) HCAR2ATMALDH1A1TSHRHPGD
SCHEMBL4254653 0.85 ATM (0.57) HCAR2ATMALDH1A1TSHRHPGD
SCHEMBL4437232 0.81 HCAR2 (0.53) HCAR2ATMALDH1A1TSHRHPGD
SCHEMBL4437235 0.81 HCAR2 (0.53) HCAR2ATMALDH1A1TSHRHPGD
SCHEMBL27941983 0.81 ALDH1A1 (0.54) HCAR2ATMALDH1A1TSHRHPGD
SCHEMBL4115120 0.80 NPSR1 (0.47) HCAR2ALDH1A1TSHRTDP1NPSR1
SCHEMBL4115115 0.80 NPSR1 (0.47) HCAR2ALDH1A1TSHRTDP1NPSR1
SCHEMBL27385701 0.80 NPSR1 (0.47) HCAR2ALDH1A1TSHRTDP1NPSR1
SCHEMBL4247950 0.80 HCAR2 (0.51) HCAR2ATMALDH1A1TSHRHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6180315-B1 FORMING POLYMER LAYER CONTAINING PATTERN OR IMAGE OF DISSOLVED PIGMENT PRECURSOR COMPONENT, POLYMER OR NATURAL OR SYNTHETIC RESIN, CATALYST FOR PIGMENT FORMATION; LOCALLY REGENERATING PIGMENT BY CHEMICAL, PHOTOLYTICAL, THERMAL OR LASER MEANS CIBA SPECIALTY CHEMCIALS CORPORATION 2001-01-30 US disclosed
US-6160037-A Reactive extrusion of latent pigments CIBA SPECIALTY CHEMICALS CORPORATION (US) 2000-12-12 US disclosed
US-6040108-A FORMING RESIN LAYER CONTAINING DISSOLVED ORGANIC PIGMENT PRECURSOR, IMAGEWISE PRECIPITATING COLORED NANO-SIZED PIGMENT PARTICLES UPON EXPOSURE TO CHEMICAL, THERMAL, PHOTOLYTIC OR LASER IRRADIATION MEANS CIBA SPECIALTY CHEMICALS CORPORATION (US) 2000-03-21 US disclosed
EP-0654711-B1 Compositions for making structured color images and application thereof CIBA GEIGY AG (CH) 1999-06-02 EP disclosed
US-5879855-A PIGMENT PRECURSOR DISSOLVED IN COMPOSITION WHICH CAN BE TRANSFORMED TO INSOLUBLE PIGMENT, POSITIVE OR NEGATIVE PHOTORESIST WHICH CAN BE MODIFIED CIBA SPECIALTY CHEMICALS CORPORATION (US) 1999-03-09 US disclosed
EP-0892018-A1 Reactive extrusion of latent pigments Ciba SC Holding AG (CH) 1999-01-20 EP disclosed
EP-0654711-A1 Compositions for making structured color images and application thereof CIBA-GEIGY AG (CH) 1995-05-24 EP disclosed