SCHEMBL194525

SCHEMBL194525

C=C(CCCCCCC)C(=O)N(CC)CC

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 4/20 0.46
CES1 P23141 4/20 0.46
GPR84 Q9NQS5 7/20 0.45
PPARG P37231 7/20 0.45
PPARD Q03181 7/20 0.45
PPARA Q07869 7/20 0.45
HDAC11 Q96DB2 5/20 0.45
TSHR P16473 5/20 0.45
PTPN1 P18031 3/20 0.45
ALDH1A1 P00352 3/20 0.45
TLR2 O60603 2/20 0.45
TDP1 Q9NUW8 2/20 0.45
FABP4 P15090 2/20 0.45
SLC22A6 Q4U2R8 1/20 0.45
SLC22A8 Q8TCC7 1/20 0.45
MEN1 O00255 1/20 0.45
ESR1 P03372 1/20 0.45
ALOX15 P16050 1/20 0.45
PDE4A P27815 1/20 0.45
KMT2A Q03164 1/20 0.45

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
SCHEMBL648954 1.00 CES2 (0.46) CES2CES1GPR84PPARGPPARD
SCHEMBL1628754 0.92 LMNA (0.43) CES2CES1GPR84PPARGPPARD
SCHEMBL11243264 0.87 LMNA (0.52) TSHRALDH1A1MEN1ALOX15PDE4A
SCHEMBL1079303 0.84 CES2 (0.43) CES2CES1GPR84PPARGPPARD
SCHEMBL6142622 0.84 CA12 (0.45) CES2CES1GPR84PPARGPPARD
SCHEMBL476918 0.83 MGLL (0.49) CES2CES1GPR84PPARGPPARD
SCHEMBL1629859 0.83 LMNA (0.41) CES2CES1TSHRALDH1A1MEN1
SCHEMBL1629808 0.82 MGLL (0.43) CES2CES1GPR84PPARGPPARD
SCHEMBL2505688 0.82 BLM (0.43) HDAC11TSHRALDH1A1MEN1ALOX15
SCHEMBL10867506 0.82 CES2 (0.48) CES2CES1GPR84PPARGPPARD

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 29 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9365515-B2 Oxime ester photoinitiators BASF SE (DE) 2016-06-14 US disclosed
US-9310677-B2 Polymerizable composition comprising an oxime sulfonate as thermal curing agent BASF (DE) 2016-04-12 US disclosed
US-20140334027-A1 OXIME ESTER PHOTOINITIATORS BASF SE (DE) 2014-11-13 US disclosed
US-20130308219-A1 POLYMERIZABLE COMPOSITION COMPRISING AN OXIME SULFONATE AS THERMAL CURING AGENT BASF SE (DE) 2013-11-21 US disclosed
US-8524425-B2 Oxime ester photoinitiators BASF SE (DE) 2013-09-03 US disclosed
US-8349548-B2 Oxime ester photoinitiators BASF SE (DE) 2013-01-08 US disclosed
US-8148358-B2 Blue colour filters with enhanced contrast BASF SE (DE) 2012-04-03 US disclosed
US-20120038996-A1 PHOTORESIST COMPOSITIONS BASF SE (DE) 2012-02-16 US disclosed
EP-2285836-B1 PHOTOINITIATOR MIXTURES BASF SE (DE) 2012-01-18 EP disclosed
EP-2402315-A1 Oxime ester photoinitiators BASF SE (DE) 2012-01-04 EP disclosed
US-20100317819-A1 SURFACE-MODIFIED NANOPARTICLES COMPRISING A CATIONIC COLORANT FOR USE IN COLOR FILTERS CIBA CORPORATION (US) 2010-12-16 US disclosed
US-20100227199-A1 Blue Colour Filters with Enhanced Contrast CIBA CORPORATION 2010-09-09 US disclosed
US-7731791-B2 Use of pyrimido[5,4-g]pteridines as shading component in color filter colorant compositions CIBA SPECIALTY CHEMICALS CORPORATION (US) 2010-06-08 US disclosed
US-20100136467-A1 OXIME ESTER PHOTOINITIATORS BASF SE (DE) 2010-06-03 US disclosed
US-20100086881-A1 OXIME ESTER PHOTOINITIATORS BASF SE (DE) 2010-04-08 US disclosed
US-7648738-B2 for photopolymerization; photography, relief imaging; color filters CIBA SPECIALTY CHEMICALS CORPORATION (US) 2010-01-19 US disclosed
US-20090293769-A1 BLUE PHTHALOCYANINE PIGMENT COMPOSITION AND ITS PREPARATION CIBA CORPORATION (US) 2009-12-03 US disclosed
US-20080206658-A1 Compositions Containing Anthraquinone Dyes HUNTSMAN INTERNATIONAL LLC (US) 2008-08-28 US disclosed
US-20080095950-A1 Compositions Containing Phthalocyanine Dyes HUNTSMAN INTERNATIONAL LLC (US) 2008-04-24 US disclosed
US-20060241259-A1 Oxime ester photoinitiators with heteroaromatic groups CIBA CORPORATION 2006-10-26 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100136467-A1 OXIME ESTER PHOTOINITIATORS CHRM4, NR2E3, CYP3A4 CES2 172/4885CES1 393/4885GPR84 424/4885
US-20100086881-A1 OXIME ESTER PHOTOINITIATORS CYP3A4, CHRM1, PPOX CES2 810/4885CES1 558/4885GPR84 1811/4885
US-20120038996-A1 PHOTORESIST COMPOSITIONS HAAO, CBR3, AKR1B10 CES2 661/4885CES1 825/4885GPR84 994/4885
US-20100227199-A1 Blue Colour Filters with Enhanced Contrast NR1H4, NR1D1, NR1D2 CES2 2032/4885CES1 2668/4885GPR84 959/4885
US-20100317819-A1 SURFACE-MODIFIED NANOPARTICLES COMPRISING A CATIONIC COLORANT FOR USE IN COLOR FILTERS CD63, CD59, ITGAM CES2 2326/4885CES1 3783/4885GPR84 2618/4885
US-20080095950-A1 Compositions Containing Phthalocyanine Dyes ZKSCAN2, INCENP, CRY2 CES2 3451/4885CES1 2373/4885GPR84 2790/4885
US-20140334027-A1 OXIME ESTER PHOTOINITIATORS CBR3, OR10J3, CHRM1 CES2 425/4885CES1 458/4885GPR84 865/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.