SCHEMBL6136267

SCHEMBL6136267

CN(C(=O)NCCc1cccc(Cc2c(-c3ccc(O)cc3)ccc3cc(O)ccc23)c1)c1ccccc1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ OPRM1 P35372 3/20 0.40
▸ OPRD1 P41143 3/20 0.40
▸ OPRK1 P41145 3/20 0.40
▸ MTNR1A P48039 3/20 0.39
▸ MTNR1B P49286 3/20 0.39
▸ TRPV1 Q8NER1 3/20 0.39
▸ ESR1 P03372 2/20 0.37
▸ ESR2 Q92731 2/20 0.37
▸ MAPT P10636 3/20 0.35
▸ MAOB P27338 1/20 0.35
▸ SNCA P37840 1/20 0.35
▸ KDM4E B2RXH2 2/20 0.35
▸ MEN1 O00255 2/20 0.35
▸ GAA P10253 2/20 0.35
▸ KMT2A Q03164 2/20 0.35
▸ ALDH1A1 P00352 1/20 0.35
▸ POLB P06746 1/20 0.35
▸ PKM P14618 1/20 0.35
▸ MAPK1 P28482 1/20 0.35
▸ HTT P42858 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
SCHEMBL6135927 0.96 ESR1 (0.38) OPRM1OPRD1OPRK1MTNR1AMTNR1B
SCHEMBL6136150 0.92 CNR1 (0.39) MTNR1AMTNR1BTRPV1ESR1ESR2
SCHEMBL6136157 0.91 ESR1 (0.40) OPRM1OPRD1OPRK1MTNR1AMTNR1B
SCHEMBL6136484 0.86 ESR1 (0.44) TRPV1ESR1ESR2MAOB
SCHEMBL6136136 0.83 TRPV1 (0.50) TRPV1MAPTKDM4EMEN1KMT2A
SCHEMBL6136101 0.81 ESR1 (0.46) TRPV1ESR1ESR2MAOB
SCHEMBL6136126 0.81 TRPV1 (0.47) TRPV1ESR1ESR2RAB9ATOP2A
SCHEMBL6136266 0.80 MTOR (0.44) OPRM1OPRD1OPRK1TRPV1ESR1
SCHEMBL6136383 0.78 NPY5R (0.43) OPRM1OPRD1OPRK1TRPV1ESR1
SCHEMBL6136002 0.78 ESR1 (0.43) ESR1ESR2MAPTMAOBKDM4E

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
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 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
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