SCHEMBL6136378

SCHEMBL6136378

O=C(NCc1ccc(Cc2c(-c3ccc(O)cc3)ccc3cc(O)ccc23)cc1)Nc1ccc(O)cc1

nearest known ligand 0.48

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ MTOR P42345 2/20 0.48
▸ ESR1 P03372 2/20 0.47
▸ ESR2 Q92731 2/20 0.47
▸ NPC1 O15118 2/20 0.43
▸ RORC P51449 2/20 0.43
▸ TRPV1 Q8NER1 5/20 0.42
▸ ROCK2 O75116 2/20 0.40
▸ HDAC1 Q13547 1/20 0.40
▸ HDAC6 Q9UBN7 1/20 0.40
▸ ROCK1 Q13464 1/20 0.40
▸ ERCC1 P07992 1/20 0.40
▸ ERCC4 Q92889 1/20 0.40
▸ HIF1A Q16665 1/20 0.40
▸ RAB9A P51151 2/20 0.39
▸ POLB P06746 1/20 0.39
▸ PDK1 Q15118 1/20 0.39

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
SCHEMBL6136280 0.95 ERCC1 (0.49) MTORESR1ESR2NPC1TRPV1
SCHEMBL6136240 0.95 NPC1 (0.53) MTORESR1ESR2NPC1RAB9A
SCHEMBL6136254 0.95 TRPV1 (0.47) MTORESR1ESR2NPC1RORC
SCHEMBL6136146 0.92 SMN1; SMN2 (0.52) ESR1ESR2NPC1ROCK2HDAC1
SCHEMBL6136126 0.83 TRPV1 (0.47) ESR1ESR2NPC1TRPV1ROCK2
SCHEMBL6136359 0.82 KMT2A (0.53) MTORTRPV1RAB9APOLB
SCHEMBL6136101 0.81 ESR1 (0.46) ESR1ESR2TRPV1ROCK2HDAC1
SCHEMBL6136341 0.80 MTOR (0.53) MTORESR1ESR2TRPV1ROCK2
SCHEMBL6136136 0.79 TRPV1 (0.50) NPC1TRPV1ROCK2HDAC1ROCK1
SCHEMBL6136184 0.79 CNR1 (0.54) NPC1TRPV1RAB9A

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
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
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