SCHEMBL6136113

SCHEMBL6136113

CCN(Cc1ccc(Cc2c(-c3ccc(O)cc3)ccc3cc(O)ccc23)cc1)C(=O)Nc1cccc(Cl)c1C

nearest known ligand 0.52

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ TRPV1 Q8NER1 6/20 0.52
▸ ESR1 P03372 2/20 0.39
▸ ESR2 Q92731 2/20 0.39
▸ EGFR P00533 2/20 0.38
▸ ERBB2 P04626 2/20 0.38
▸ MT-CO2 P00403 1/20 0.36
▸ ALDH1A1 P00352 3/20 0.36
▸ ROCK1 Q13464 1/20 0.36
▸ HTT P42858 1/20 0.35
▸ SMN1; SMN2 Q16637 1/20 0.35
▸ NPSR1 Q6W5P4 1/20 0.35
▸ THRB P10828 1/20 0.35
▸ LMNA P02545 1/20 0.35
▸ POLB P06746 1/20 0.35
▸ MEN1 O00255 2/20 0.35
▸ KMT2A Q03164 2/20 0.35
▸ HCAR2 Q8TDS4 1/20 0.35
▸ RAB9A P51151 1/20 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
SCHEMBL6136025 0.90 TRPV1 (0.53) TRPV1ESR1ESR2MT-CO2ALDH1A1
SCHEMBL6136065 0.85 TRPV1 (0.47) TRPV1ESR1ESR2EGFRERBB2
SCHEMBL6136358 0.84 TRPV1 (0.43) TRPV1ESR1ESR2EGFRERBB2
SCHEMBL6136359 0.84 KMT2A (0.53) TRPV1MT-CO2HTTPOLBMEN1
SCHEMBL6136144 0.84 TRPV1 (0.44) TRPV1ESR1ESR2EGFRERBB2
SCHEMBL6136103 0.80 ESR1 (0.45) TRPV1ESR1ESR2ROCK1
SCHEMBL6136211 0.79 ESR1 (0.38) TRPV1ESR1ESR2MT-CO2THRB
SCHEMBL6136098 0.77 ESR1 (0.39) TRPV1ESR1ESR2MT-CO2THRB
SCHEMBL6135989 0.74 GAA (0.40) TRPV1ESR1ESR2ALDH1A1SMN1; SMN2
SCHEMBL6135968 0.74 TRPV1 (0.41) TRPV1ESR1ESR2EGFRERBB2

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
Send feedback