SCHEMBL4853025

SCHEMBL4853025

CCCCCCCCCCC(C(=O)c1ccc(OC)cc1)C(=O)c1ccc(C(C)(C)C)cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.55
LMNA P02545 2/20 0.55
ALOX15 P16050 1/20 0.55
APEX1 P27695 1/20 0.55
MAPK1 P28482 1/20 0.55
RECQL P46063 1/20 0.55
HSD17B10 Q99714 1/20 0.55
TDP1 Q9NUW8 1/20 0.55
MAPT P10636 2/20 0.52
MEN1 O00255 3/20 0.49
KMT2A Q03164 3/20 0.49
HTT P42858 3/20 0.49
NPC1 O15118 2/20 0.49
RAB9A P51151 2/20 0.49
EPHX2 P34913 1/20 0.49
NR1H4 Q96RI1 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49
CYP2D6 P10635 1/20 0.49
HDAC3 O15379 3/20 0.47
HDAC1 Q13547 3/20 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
SCHEMBL20225318 0.99 ALDH1A1 (0.56) ALDH1A1LMNAALOX15APEX1MAPK1
SCHEMBL24260590 0.95 ALDH1A1 (0.57) ALDH1A1LMNAALOX15APEX1MAPK1
SCHEMBL23188134 0.90 ALDH1A1 (0.55) ALDH1A1LMNAALOX15APEX1MAPK1
SCHEMBL9809349 0.84 MEN1 (0.50) ALDH1A1MEN1KMT2AHTTNPC1
SCHEMBL7100665 0.84 ALDH1A1 (0.63) ALDH1A1LMNAALOX15APEX1MAPK1
SCHEMBL20225323 0.83 HDAC3 (0.47) ALDH1A1MAPTMEN1KMT2AEPHX2
SCHEMBL541916 0.80 CES2 (0.54) ALDH1A1LMNAMAPTMEN1KMT2A
SCHEMBL24719139 0.79 ALDH1A1 (0.53) ALDH1A1LMNAALOX15APEX1MAPK1
SCHEMBL9440242 0.78 HTT (0.52) ALDH1A1LMNAMEN1KMT2AHTT
SCHEMBL27457534 0.78 HTT (0.52) ALDH1A1LMNAMEN1KMT2AHTT

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-7446230-B2 Dibenzoylmethane-based compounds, use as photoactivatable sunscreens and cosmetic compositions containing them LABORATOIRE BIODERMA (FR) 2008-11-04 US claimed
US-20070025930-A1 Dibenzoilmethane derivative compounds, the use thereof in the form of photoactivable solar filters and cosmetic compositions containing said compounds UNIVERSITE PAUL SABATIER TOULOUSE 3 (FR) 2007-02-01 US claimed
US-7446230-B2 Dibenzoylmethane-based compounds, use as photoactivatable sunscreens and cosmetic compositions containing them LABORATOIRE BIODERMA (FR) 2008-11-04 US disclosed
US-7446230-B2 Dibenzoylmethane-based compounds, use as photoactivatable sunscreens and cosmetic compositions containing them LABORATOIRE BIODERMA (FR) 2008-11-04 US disclosed
US-20070025930-A1 Dibenzoilmethane derivative compounds, the use thereof in the form of photoactivable solar filters and cosmetic compositions containing said compounds UNIVERSITE PAUL SABATIER TOULOUSE 3 (FR) 2007-02-01 US disclosed
US-20070025930-A1 Dibenzoilmethane derivative compounds, the use thereof in the form of photoactivable solar filters and cosmetic compositions containing said compounds UNIVERSITE PAUL SABATIER TOULOUSE 3 (FR) 2007-02-01 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-20070025930-A1 Dibenzoilmethane derivative compounds, the use thereof in the form of photoactivable solar filters and cosmetic compositions containing said compounds TYR, DSG1, DPM1 ALDH1A1 227/4885LMNA 689/4885ALOX15 988/4885

“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.