SCHEMBL6136133

SCHEMBL6136133

Oc1ccc(-c2ccc3cc(O)ccc3c2Cc2ccc(OCC3CCCNC3)cc2)cc1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 4/20 0.57
ESR2 Q92731 4/20 0.57
MAP2K1 Q02750 1/20 0.47
CHEK2 O96017 1/20 0.42
KDM1A O60341 3/20 0.42
PRKCZ Q05513 1/20 0.42
SLC6A2 P23975 3/20 0.41
SLC6A4 P31645 3/20 0.41
SLC6A3 Q01959 1/20 0.40
IKBKB O14920 2/20 0.40
CHUK O15111 2/20 0.40
CHRNB2 P17787 2/20 0.37
CHRNA4 P43681 2/20 0.37
LTA4H P09960 1/20 0.37
GRK2 P25098 1/20 0.36
HPGD P15428 1/20 0.36
CHRNB4 P30926 1/20 0.36
CHRNA3 P32297 1/20 0.36
KCNH2 Q12809 2/20 0.35
RCOR1 Q9UKL0 1/20 0.35

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
SCHEMBL6136145 0.94 ESR1 (0.56) ESR1ESR2MAP2K1CHEK2KDM1A
SCHEMBL6136022 0.91 ESR1 (0.60) ESR1ESR2MAP2K1HPGD
SCHEMBL6136156 0.90 ESR1 (0.59) ESR1ESR2MAP2K1
SCHEMBL6136055 0.89 ESR1 (0.58) ESR1ESR2MAP2K1
SCHEMBL6135973 0.89 ESR1 (0.58) ESR1ESR2CHEK2KDM1APRKCZ
SCHEMBL6136203 0.86 ESR1 (0.59) ESR1ESR2PRKCZLTA4HCHRNB4
SCHEMBL6135921 0.85 ESR1 (0.59) ESR1ESR2CHEK2PRKCZSLC6A2
SCHEMBL6135970 0.84 ESR1 (0.58) ESR1ESR2PRKCZSLC6A2SLC6A4
SCHEMBL6136015 0.84 ESR1 (0.57) ESR1ESR2PRKCZSLC6A2SLC6A4
SCHEMBL6135993 0.83 ESR1 (0.58) ESR1ESR2PRKCZLTA4HCHRNB4

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 7 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
WO-1999007377-A1 1-[4-(SUBSTITUTED ALKOXY)BENZYL]NAPHTHALENE COMPOUNDS HAVING ESTROGEN INHIBITORY ACTIVITY ELI LILLY AND COMPANY (US) 1999-02-18 WO 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