SCHEMBL4420728

SCHEMBL4420728

CCCC1=C(c2ccc(O)cc2)C(c2ccccc2)c2cc(O)ccc21

nearest known ligand 0.50

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
ESR2 Q92731 10/20 0.50
ESR1 P03372 9/20 0.50
USP7 Q93009 3/20 0.35
ALOX5 P09917 1/20 0.34
MEN1 O00255 1/20 0.33
ALDH1A1 P00352 1/20 0.33
TSHR P16473 1/20 0.33
MAPK1 P28482 1/20 0.33
KMT2A Q03164 1/20 0.33
HSD17B10 Q99714 1/20 0.33

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
SCHEMBL4418132 0.93 ESR1 (0.48) ESR2ESR1ALDH1A1HSD17B10
SCHEMBL4417339 0.91 ESR1 (0.47) ESR2ESR1ALOX5MEN1ALDH1A1
SCHEMBL4418128 0.90 ESR2 (0.63) ESR2ESR1USP7ALOX5MEN1
SCHEMBL4418943 0.84 ESR2 (0.46) ESR2ESR1ALOX5MEN1ALDH1A1
SCHEMBL4417137 0.80 ESR2 (0.43) ESR2ESR1ALOX5MEN1ALDH1A1
SCHEMBL29242486 0.72 DYRK1A (0.54) ESR2ESR1ALOX5MEN1ALDH1A1
SCHEMBL30901161 0.72 DYRK1A (0.54) ESR2ESR1ALOX5MEN1ALDH1A1
SCHEMBL31570928 0.69 ESR1 (0.59) ESR2ESR1ALOX5MEN1ALDH1A1
SCHEMBL27502889 0.68 ALDH1A1 (0.38) ESR2ESR1ALDH1A1MAPK1KMT2A
SCHEMBL8383765 0.68 ESR1 (0.71) ESR2ESR1USP7MEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands KARO BIO AB (SE) 2009-12-31 US claimed
EP-2074102-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2009-07-01 EP claimed
WO-2008043567-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2008-04-17 WO claimed
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands KARO BIO AB (SE) 2009-12-31 US disclosed
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands KARO BIO AB (SE) 2009-12-31 US disclosed
US-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands KARO BIO AB (SE) 2009-12-31 US disclosed
EP-2074102-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2009-07-01 EP disclosed
WO-2008043567-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2008-04-17 WO disclosed
WO-2008043567-A1 2-PHENYL INDENE DERIVATIVES USEFUL AS ESTROGEN RECEPTOR LIGANDS KARO BIO AB (SE) 2008-04-17 WO 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-20090326018-A1 2-Phenyl indene derivatives useful as estrogen receptor ligands ESR1, GPER1, ESR2 ESR2 3/4885ESR1 1/4885USP7 3727/4885

“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.