SCHEMBL5996433

SCHEMBL5996433

Cc1cc(C)c(C(=O)C(CP=O)C(=O)c2c(C)cc(C(C)(C)C)cc2C)c(C)c1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.37
L3MBTL1 Q9Y468 1/20 0.37
RXRB P28702 3/20 0.34
RXRA P19793 2/20 0.34
HPGD P15428 3/20 0.32
ALDH1A1 P00352 3/20 0.32
RAB9A P51151 2/20 0.32
TSHR P16473 1/20 0.32
HTR1D P28221 2/20 0.32
HTR1B P28222 1/20 0.32
GAA P10253 1/20 0.31
LMNA P02545 2/20 0.31
MEN1 O00255 1/20 0.31
KMT2A Q03164 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
NPSR1 Q6W5P4 1/20 0.31
MCOLN3 Q8TDD5 1/20 0.31
MAPT P10636 2/20 0.31
NPC1 O15118 1/20 0.31
POLB P06746 1/20 0.31

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
SCHEMBL6403712 0.95 HTR1D (0.34) KDM4EL3MBTL1RXRBRXRAHPGD
SCHEMBL2499307 0.91 KDM4E (0.36) KDM4EL3MBTL1HPGDALDH1A1RAB9A
SCHEMBL5997921 0.83 KMT2A (0.35) KDM4EL3MBTL1HPGDALDH1A1GAA
SCHEMBL6399267 0.82 CYP3A4 (0.37) HPGDLMNAKMT2ASMN1; SMN2MAPK1
SCHEMBL5994805 0.79 ALDH1A1 (0.35) L3MBTL1ALDH1A1GAAKMT2ASMN1; SMN2
SCHEMBL5996153 0.78 KMT2A (0.35) KDM4EL3MBTL1HPGDALDH1A1GAA
SCHEMBL5996310 0.78 KMT2A (0.41) HPGDALDH1A1RAB9ATSHRGAA
SCHEMBL5994591 0.76 CYP3A4 (0.39) KDM4EL3MBTL1HPGDLMNAMEN1
SCHEMBL7183772 0.74 CYP1A2 (0.37) RXRBRXRAALDH1A1RAB9ATSHR
SCHEMBL152304 0.74 L3MBTL1 (0.36) L3MBTL1HPGDALDH1A1RAB9ALMNA

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 2 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-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

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

For each of this compound's patents that has machine-readable text (1 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-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 KDM4E 662/4885L3MBTL1 1879/4885RXRB 2536/4885

“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.