SCHEMBL8199516

SCHEMBL8199516

Cc1ccc(N(c2ccc(-c3ccccc3)cc2)c2ccc(C(C)(c3ccc(O)cc3)c3ccc(O)cc3)cc2)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ESR1 P03372 5/20 0.56
▸ ESR2 Q92731 4/20 0.56
▸ MMP3 P08254 1/20 0.46
▸ BCL2L1 Q07817 1/20 0.46
▸ CYP3A4 P08684 2/20 0.43
▸ ALDH1A1 P00352 2/20 0.43
▸ ACHE P22303 1/20 0.39
▸ MEN1 O00255 2/20 0.37
▸ KMT2A Q03164 2/20 0.37
▸ KIF11 P52732 2/20 0.37
▸ PDE4A P27815 1/20 0.36
▸ PDE4B Q07343 1/20 0.36
▸ PDE4C Q08493 1/20 0.36
▸ PDE4D Q08499 1/20 0.36
▸ LMNA P02545 1/20 0.36
▸ TYR P14679 1/20 0.36
▸ AR P10275 1/20 0.36
▸ HPGD P15428 1/20 0.36
▸ TSHR P16473 1/20 0.36
▸ SLC6A2 P23975 1/20 0.36

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
SCHEMBL22182772 0.89 MMP3 (0.58) ESR1ESR2MMP3BCL2L1ALDH1A1
SCHEMBL14173660 0.89 MMP3 (0.58) ESR1ESR2MMP3BCL2L1ALDH1A1
SCHEMBL23789718 0.89 MMP3 (0.58) ESR1ESR2MMP3BCL2L1ALDH1A1
SCHEMBL411554 0.89 ESR1 (0.53) ESR1ESR2CYP3A4ALDH1A1ACHE
SCHEMBL8279198 0.85 MMP3 (0.52) ESR1ESR2MMP3BCL2L1CYP3A4
SCHEMBL8279203 0.85 MMP3 (0.52) ESR1ESR2MMP3BCL2L1CYP3A4
SCHEMBL23789720 0.85 MMP3 (0.52) ESR1ESR2MMP3BCL2L1CYP3A4
SCHEMBL13879196 0.85 MMP3 (0.52) ESR1ESR2MMP3BCL2L1CYP3A4
SCHEMBL8206761 0.85 ESR1 (0.70) ESR1ESR2CYP3A4ALDH1A1MEN1
SCHEMBL8211247 0.85 ESR2 (0.49) ESR1ESR2MMP3BCL2L1CYP3A4

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
US-9859505-B2 Charge-transporting molecular glass mixtures, luminescent molecular glass mixtures, or combinations thereof or organic light emitting diodes and other organic electronics and photonics applications MOLECULAR GLASSES, INC. (US) 2018-01-02 — — US disclosed
US-20150179714-A1 Crosslinkable, /Polymerizable and Combinations Thereof Charge-transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications and Mothod of Making Same. Molaire Consulting 2015-06-25 — — US disclosed
US-20150179714-A1 Crosslinkable, /Polymerizable and Combinations Thereof Charge-transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications and Mothod of Making Same. Molaire Consulting 2015-06-25 — — US disclosed
US-20150053894-A1 Charge-transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications Molaire Consulting 2015-02-26 — — US disclosed
US-20150053894-A1 Charge-transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications Molaire Consulting 2015-02-26 — — US disclosed
US-6093784-A (CO)POLYCARBONATE CONTAINING DIARYLAMINOPHENYL-SUBSTITUTED BISPHENOL UNITS; DURABILITY, HEAT RESISTANCE, RADIATION TRANSPARENCY RICOH COMPANY, LTD. (JP) 2000-07-25 — — US disclosed
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