SCHEMBL6135989

SCHEMBL6135989

CCN(CCc1cccc(Cc2c(-c3ccc(O)cc3)ccc3cc(O)ccc23)c1)C(=O)Nc1ccc(Cl)cc1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ GAA P10253 2/20 0.40
▸ TRPV1 Q8NER1 4/20 0.39
▸ NPSR1 Q6W5P4 1/20 0.38
▸ USP2 O75604 2/20 0.35
▸ MAPK1 P28482 2/20 0.35
▸ ESR1 P03372 2/20 0.35
▸ ESR2 Q92731 2/20 0.35
▸ TOP2A P11388 1/20 0.35
▸ TOP2B Q02880 1/20 0.35
▸ KDM4E B2RXH2 1/20 0.34
▸ ALDH1A1 P00352 1/20 0.34
▸ HPGD P15428 1/20 0.34
▸ ALOX15 P16050 1/20 0.34
▸ ALOX12 P18054 1/20 0.34
▸ SMN1; SMN2 Q16637 1/20 0.34
▸ MEN1 O00255 1/20 0.34
▸ MAPT P10636 1/20 0.34
▸ KMT2A Q03164 1/20 0.34
▸ CNR1 P21554 3/20 0.34
▸ ROCK2 O75116 2/20 0.34

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
SCHEMBL6135968 0.96 TRPV1 (0.41) GAATRPV1NPSR1ESR1ESR2
SCHEMBL6136274 0.90 ROCK2 (0.41) TRPV1NPSR1MAPK1ESR1ESR2
SCHEMBL6136057 0.90 NPY5R (0.40) TRPV1ESR1ESR2TOP2ATOP2B
SCHEMBL6136358 0.85 TRPV1 (0.43) GAATRPV1USP2MAPK1ESR1
SCHEMBL6136383 0.85 NPY5R (0.43) TRPV1ESR1ESR2TOP2ATOP2B
SCHEMBL6136266 0.82 MTOR (0.44) TRPV1ESR1ESR2TOP2ATOP2B
SCHEMBL6136184 0.82 CNR1 (0.54) TRPV1SMN1; SMN2MEN1MAPTKMT2A
SCHEMBL6136065 0.81 TRPV1 (0.47) TRPV1ESR1ESR2MEN1KMT2A
SCHEMBL6136417 0.80 NPY5R (0.45) NPSR1ESR1ESR2TOP2ATOP2B
SCHEMBL6136478 0.78 MTOR (0.48) TRPV1ESR1ESR2ROCK2

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
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
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
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