SCHEMBL5995274

SCHEMBL5995274

CCP(=O)(C(=O)c1ccc(OC)cc1OC)C(=O)c1c(C)cc(C)cc1C

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC3 O15379 1/20 0.45
HDAC1 Q13547 1/20 0.45
HDAC2 Q92769 1/20 0.45
TP53 P04637 3/20 0.45
NPC1 O15118 6/20 0.45
RAB9A P51151 6/20 0.44
GAA P10253 2/20 0.44
MITF O75030 1/20 0.44
MEN1 O00255 3/20 0.43
KMT2A Q03164 3/20 0.43
ALDH1A1 P00352 3/20 0.43
HTT P42858 2/20 0.43
PKM P14618 1/20 0.43
HPGD P15428 1/20 0.43
SMN1; SMN2 Q16637 4/20 0.42
LMNA P02545 1/20 0.42
TSHR P16473 1/20 0.41
ABCG2 Q9UNQ0 2/20 0.41
CFTR P13569 1/20 0.41
MAPT P10636 1/20 0.41

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
SCHEMBL5994244 0.90 ALDH1A1 (0.46) HDAC3HDAC1HDAC2TP53NPC1
SCHEMBL5995831 0.90 HDAC3 (0.49) HDAC3HDAC1HDAC2TP53NPC1
SCHEMBL5996125 0.89 HDAC3 (0.43) HDAC3HDAC1HDAC2TP53NPC1
SCHEMBL5997395 0.88 TP53 (0.50) HDAC3HDAC1HDAC2TP53NPC1
SCHEMBL5993289 0.87 HDAC3 (0.49) HDAC3HDAC1HDAC2TP53NPC1
SCHEMBL30505227 0.86 NPC1 (0.48) TP53NPC1RAB9AGAAMITF
SCHEMBL5994583 0.85 CYP3A4 (0.42) NPC1RAB9AMEN1KMT2APKM
SCHEMBL5994793 0.85 MAPT (0.51) HDAC3HDAC1HDAC2TP53NPC1
SCHEMBL5997895 0.83 TP53 (0.42) HDAC3HDAC1HDAC2TP53NPC1
SCHEMBL5994796 0.83 PKM (0.38) GAAMEN1KMT2AALDH1A1PKM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7026017-B2 Photoinitiators for acrylic esters; reacting an acyl halide with a metal benzoyl phosphine; cable coatings, screen printing stencils, resist materials, colour filters, electrical encapsulation CIBA SPECIALTY CHEMICALS CORPORATION (US) 2006-04-11 US disclosed
US-6969733-B2 Photoinitiators CIBA SPECIALTY CHEMICALS CORPORATION (US) 2005-11-29 US disclosed
US-6737549-B2 PHOTOINITIATORS FOR ACRYLATE COATINGS CIBA SPECIALTY CHEMICALS CORPORATION 2004-05-18 US disclosed
US-20030139485-A1 Photoinitiators WOLF JEAN-PIERRE (CH) 2003-07-24 US disclosed
US-20030130370-A1 Photoinitiators for acrylic esters; reacting an acyl halide with a metal benzoyl phosphine; cable coatings, screen printing stencils, resist materials, colour filters, electrical encapsulation WOLF JEAN-PIERRE (CH) 2003-07-10 US disclosed
US-20020026049-A1 Photoinitiators for acrylate coatings CIBA SPECIALTY CHEMICALS CORP. 2002-02-28 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 (3 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-20030139485-A1 Photoinitiators DHCR24, NR1I3, CBR1 HDAC3 335/4885HDAC1 1012/4885HDAC2 1649/4885
US-20030130370-A1 Photoinitiators for acrylic esters; reacting an acyl halide with a metal benzoyl phosphine; cable coatings, screen printing stencils, resist materials, colour filters, electrical encapsulation SMARCC1, ARPC5L, DHCR24 HDAC3 1552/4885HDAC1 1863/4885HDAC2 2246/4885
US-20020026049-A1 Photoinitiators for acrylate coatings DHCR24, NR5A1, NR2C2 HDAC3 247/4885HDAC1 645/4885HDAC2 1213/4885

“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.