SCHEMBL6136203

SCHEMBL6136203

Oc1ccc(-c2ccc3cc(O)ccc3c2Cc2ccc(OCC3CCCN3)cc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 2/20 0.59
ESR2 Q92731 2/20 0.59
LTA4H P09960 10/20 0.52
CHRNB4 P30926 3/20 0.49
CHRNA3 P32297 3/20 0.49
PRKCZ Q05513 1/20 0.48
PRKAB2 O43741 1/20 0.45
PRKAG1 P54619 1/20 0.45
PRKAA2 P54646 1/20 0.45
PRKAA1 Q13131 1/20 0.45
PRKAG3 Q9UGI9 1/20 0.45
PRKAG2 Q9UGJ0 1/20 0.45
PRKAB1 Q9Y478 1/20 0.45

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
SCHEMBL6135993 0.97 ESR1 (0.58) ESR1ESR2LTA4HCHRNB4CHRNA3
SCHEMBL6136215 0.90 ESR1 (0.65) ESR1ESR2LTA4H
SCHEMBL6135990 0.90 ESR1 (0.64) ESR1ESR2LTA4HPRKCZ
SCHEMBL6136054 0.89 ESR1 (0.63) ESR1ESR2LTA4H
SCHEMBL3714380 0.88 ESR1 (0.64) ESR1ESR2LTA4H
SCHEMBL6135934 0.87 ESR1 (0.63) ESR1ESR2LTA4H
Hydrochloric Acid SCHEMBL5256714 0.87 ESR1 (0.66) ESR1ESR2LTA4H
SCHEMBL6135900 0.86 ESR1 (0.62) ESR1ESR2LTA4H
SCHEMBL6136133 0.86 ESR1 (0.57) ESR1ESR2LTA4HCHRNB4CHRNA3
SCHEMBL6135973 0.85 ESR1 (0.58) ESR1ESR2PRKCZ

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
EP-0895989-B1 1-[4-(Substituted alkoxy)benzyl] naphthalene compounds having estrogen inhibitory activity LILLY CO ELI (US) 2005-05-18 EP claimed
WO-1999007377-A1 1-[4-(SUBSTITUTED ALKOXY)BENZYL]NAPHTHALENE COMPOUNDS HAVING ESTROGEN INHIBITORY ACTIVITY ELI LILLY AND COMPANY (US) 1999-02-18 WO claimed
EP-0895989-A1 1-[4-(Substituted alkoxy)benzyl] naphthalene compounds having estrogen inhibitory activity ELI LILLY AND COMPANY (US) 1999-02-10 EP claimed
EP-0895989-B1 1-[4-(Substituted alkoxy)benzyl] naphthalene compounds having estrogen inhibitory activity LILLY CO ELI (US) 2005-05-18 EP disclosed
US-6509356-B1 Estrogen inhibitory activity method for the treatment of breast cancer in a woman comprising administering to a patient a therapeutically effective amount of a compound ELI LILLY AND COMPANY 2003-01-21 US disclosed
EP-0895989-A1 1-[4-(Substituted alkoxy)benzyl] naphthalene compounds having estrogen inhibitory activity ELI LILLY AND COMPANY (US) 1999-02-10 EP disclosed