SCHEMBL6136103

SCHEMBL6136103

CCN(Cc1ccc(Cc2c(-c3ccc(O)cc3)ccc3cc(O)ccc23)cc1)C(=O)Nc1ccc(OC)cc1

nearest known ligand 0.45

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ ESR1 P03372 3/20 0.45
▸ ESR2 Q92731 2/20 0.45
▸ ROCK2 O75116 3/20 0.43
▸ TRPV1 Q8NER1 1/20 0.42
▸ MAPT P10636 3/20 0.41
▸ SAE1 Q9UBE0 1/20 0.39
▸ UBA2 Q9UBT2 1/20 0.39
▸ PLG P00747 2/20 0.38
▸ KLK1 P06870 2/20 0.38
▸ KLK6 Q92876 2/20 0.38
▸ MAPK1 P28482 1/20 0.38
▸ KDR P35968 2/20 0.38
▸ TSHR P16473 1/20 0.38
▸ BMP1 P13497 1/20 0.37
▸ CYP3A4 P08684 2/20 0.37
▸ CYP2D6 P10635 2/20 0.37
▸ CYP2C9 P11712 2/20 0.37
▸ ROCK1 Q13464 2/20 0.37
▸ CDC42BPA Q5VT25 2/20 0.37

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
SCHEMBL6136065 0.94 TRPV1 (0.47) ESR1ESR2ROCK2TRPV1
SCHEMBL6136144 0.90 TRPV1 (0.44) ESR1ESR2ROCK2TRPV1MAPT
SCHEMBL6136139 0.90 MTOR (0.47) ESR1ESR2ROCK2TRPV1MAPT
SCHEMBL6136358 0.90 TRPV1 (0.43) ESR1ESR2ROCK2TRPV1MAPT
SCHEMBL6136274 0.86 ROCK2 (0.41) ESR1ESR2ROCK2TRPV1MAPT
SCHEMBL6136341 0.82 MTOR (0.53) ESR1ESR2ROCK2TRPV1CYP2C9
SCHEMBL6136146 0.82 SMN1; SMN2 (0.52) ESR1ESR2ROCK2SAE1UBA2
SCHEMBL6136113 0.80 TRPV1 (0.52) ESR1ESR2TRPV1ROCK1
SCHEMBL6136177 0.79 MTOR (0.49) ESR1ESR2ROCK2TRPV1CYP2C9
SCHEMBL6136296 0.79 ESR1 (0.45) ESR1ESR2ROCK2MAPTCYP3A4

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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