SCHEMBL5725907

SCHEMBL5725907

O=C(Cc1ccccc1Cl)c1ccc(OCCN2CCCCC2)cc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PSMB1 P20618 5/20 0.61
PSMB5 P28074 5/20 0.61
PSMB2 P49721 4/20 0.61
LTA4H P09960 1/20 0.60
HRH3 Q9Y5N1 3/20 0.56
ESR1 P03372 2/20 0.54
MCHR1 Q99705 1/20 0.54
ALDH1A1 P00352 4/20 0.54
THRB P10828 3/20 0.54
KDM4E B2RXH2 3/20 0.54
LMNA P02545 2/20 0.54
CYP1A2 P05177 1/20 0.54
CHRM2 P08172 1/20 0.54
CHRM4 P08173 1/20 0.54
CHRM5 P08912 1/20 0.54
CYP2D6 P10635 1/20 0.54
CYP2C9 P11712 1/20 0.54
ADRA2C P18825 1/20 0.54
DRD4 P21917 1/20 0.54
ACHE P22303 1/20 0.54

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
SCHEMBL5728349 0.84 L3MBTL1 (0.60) PSMB1PSMB5PSMB2LTA4HHRH3
SCHEMBL10685703 0.83 LTA4H (0.70) PSMB1PSMB5PSMB2LTA4HHRH3
SCHEMBL10676277 0.82 LTA4H (0.71) PSMB1PSMB5PSMB2LTA4HESR1
SCHEMBL7209622 0.81 L3MBTL1 (0.58) PSMB1PSMB5PSMB2LTA4HHRH3
SCHEMBL5725869 0.80 NR4A2 (0.54) MAPTSMN1; SMN2
SCHEMBL7140961 0.80 MCHR1 (0.73) PSMB1PSMB5LTA4HHRH3MCHR1
SCHEMBL5175148 0.78 LTA4H (0.73) PSMB1PSMB5PSMB2LTA4HHRH3
SCHEMBL14287617 0.77 SMN1; SMN2 (0.76) PSMB1PSMB5PSMB2HRH3ALDH1A1
SCHEMBL13305534 0.77 LTA4H (0.97) PSMB1PSMB5PSMB2LTA4HESR1
SCHEMBL1358544 0.77 PSMB1 (0.78) PSMB1PSMB5PSMB2LTA4HHRH3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1705169-A2 Triphenylalkene derivatives and their use as selective estrogen receptor modulators Hormos Medical Ltd. (FI) 2006-09-27 EP disclosed
EP-1235776-B1 TRIPHENYLALKENE DERIVATIVES AND THEIR USE AS SELECTIVE ESTROGEN RECEPTOR MODULATORS HORMOS MEDICAL CORP (FI) 2006-02-08 EP disclosed
US-6875775-B2 Triphenylalkene derivatives and their use as selective estrogen receptor modulators HORMOS MEDICAL OY LTD (FI) 2005-04-05 US disclosed
US-20030225130-A1 Triphenylalkene derivatives and their use as selective estrogen receptor modulators HORMOS MEDICAL OY LTD. 2003-12-04 US disclosed
US-6576645-B1 Such as 3-(4-chloro-1-(4-(2-(2-hydroxyethoxy)ethoxy)phenyl)--2-phenylbut-1 -enyl)phenol; producing tissue specific estro-genic and/or antiestrogenic effect HORMOS MEDICAL OY LTD (FI) 2003-06-10 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-20030225130-A1 Triphenylalkene derivatives and their use as selective estrogen receptor modulators ESR2, ESR1, GPER1 PSMB1 2238/4885PSMB5 1936/4885PSMB2 1710/4885

“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.