SCHEMBL6069562

SCHEMBL6069562

C#CC(c1ccccc1)c1ccccc1.c1cc2ccc1-2

nearest known ligand 0.46

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ CHRNB2 P17787 1/20 0.41
▸ CHRNA4 P43681 1/20 0.41
▸ PTGS2 P35354 1/20 0.39
▸ ALDH1A1 P00352 2/20 0.38
▸ ACP3 P15309 1/20 0.38
▸ DPP4 P27487 2/20 0.36
▸ TSHR P16473 2/20 0.36
▸ F2 P00734 1/20 0.36
▸ MAPK1 P28482 1/20 0.35
▸ CYP1A2 P05177 1/20 0.35
▸ CYP3A4 P08684 1/20 0.35
▸ TAAR1 Q96RJ0 1/20 0.35
▸ HSD17B10 Q99714 1/20 0.35
▸ TDP1 Q9NUW8 1/20 0.35
▸ MMP3 P08254 1/20 0.35
▸ BCL2L1 Q07817 1/20 0.35
▸ TRPA1 O75762 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
SCHEMBL2106150 0.92 TSHR (0.41) ALDH1A1DPP4TSHRF2TAAR1
SCHEMBL11408107 0.80 IDO1 (0.36) ACP3DPP4TSHRF2TAAR1
SCHEMBL5324736 0.79 LMNA (0.50) ALDH1A1
SCHEMBL7493934 0.79 IDO1 (0.48) ALDH1A1TSHRMAPK1CYP1A2CYP3A4
SCHEMBL8886347 0.76 TRPA1 (0.52) CHRNB2CHRNA4PTGS2ALDH1A1ACP3
SCHEMBL16569811 0.74 LMNA (0.35) CHRNB2CHRNA4PTGS2ALDH1A1ACP3
SCHEMBL5174129 0.74 PBRM1 (0.54) ALDH1A1ACP3TSHRMAPK1TDP1
SCHEMBL28385338 0.72 DPP4 (0.38) DPP4TSHRF2TAAR1TRPA1
SCHEMBL11272528 0.72 CYP2C19 (0.42) ALDH1A1TSHRHSD17B10
SCHEMBL6869750 0.72 ACP3 (0.44) ALDH1A1ACP3TSHRCYP3A4

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9926408-B2 Preparation of imide oligomers via concurrent reactive extrusion POLYONE CORPORATION (US) 2018-03-27 — — US claimed
US-20160215095-A1 PREPARATION OF IMIDE OLIGOMERS VIA CONCURRENT REACTIVE EXTRUSION POLYONE CORPORATION (US) 2016-07-28 — — US claimed
US-20160215096-A1 PREPARATION OF IMIDE OLIGOMERS VIA CONCURRENT REACTIVE EXTRUSION POLYONE CORPORATION (US) 2016-07-28 — — US claimed
WO-2015048065-A1 PREPARATION OF IMIDE OLIGOMERS VIA CONCURRENT REACTIVE EXTRUSION POLYONE CORPORATION (US) 2015-04-02 — — WO claimed
US-20140135447-A1 PREPARATION OF IMIDE OLIGOMERS POLYONE CORPORATION (US) 2014-05-15 — — US claimed
WO-2013006621-A2 PREPARATION OF IMIDE OLIGOMERS POLYONE CORPORATION (US) 2013-01-10 — — WO claimed
US-RE43880-E1 Solvent free low-melt viscosity imide oligomers and thermosetting polymide composites THE UNITED STATES OF AMERICA AS REPRESENTED BY THE ADMINISTRATOR OF NATIONAL AERONAUTICS AND SPACE ADMINISTRATION (US) 2012-12-25 — — US claimed
US-7015304-B1 reacting specific aromatic dianhydrides such as 2,3,3',4'-biphenyltetracarboxylic dianydride, and aromatic diamines containing one or two benzene rings with a reactive monofunctional endcap such as phenylethynyl phthalic anhydride; melt processability; transfer molding with fiber preforms THE UNITED STATES OF AMERICA AS REPRESENTED BY THE ADMINISTRATOR OF THE NATIONAL AERONAUTICS AND SPACE ADMINISTRATION (US) 2006-03-21 — — US claimed
US-9926408-B2 Preparation of imide oligomers via concurrent reactive extrusion POLYONE CORPORATION (US) 2018-03-27 — — US disclosed
US-20160215095-A1 PREPARATION OF IMIDE OLIGOMERS VIA CONCURRENT REACTIVE EXTRUSION POLYONE CORPORATION (US) 2016-07-28 — — US disclosed
WO-2015048065-A1 PREPARATION OF IMIDE OLIGOMERS VIA CONCURRENT REACTIVE EXTRUSION POLYONE CORPORATION (US) 2015-04-02 — — WO disclosed
US-20140135447-A1 PREPARATION OF IMIDE OLIGOMERS POLYONE CORPORATION (US) 2014-05-15 — — US disclosed
WO-2013006621-A2 PREPARATION OF IMIDE OLIGOMERS POLYONE CORPORATION (US) 2013-01-10 — — WO disclosed
US-RE43880-E1 Solvent free low-melt viscosity imide oligomers and thermosetting polymide composites THE UNITED STATES OF AMERICA AS REPRESENTED BY THE ADMINISTRATOR OF NATIONAL AERONAUTICS AND SPACE ADMINISTRATION (US) 2012-12-25 — — US disclosed
US-7015304-B1 reacting specific aromatic dianhydrides such as 2,3,3',4'-biphenyltetracarboxylic dianydride, and aromatic diamines containing one or two benzene rings with a reactive monofunctional endcap such as phenylethynyl phthalic anhydride; melt processability; transfer molding with fiber preforms THE UNITED STATES OF AMERICA AS REPRESENTED BY THE ADMINISTRATOR OF THE NATIONAL AERONAUTICS AND SPACE ADMINISTRATION (US) 2006-03-21 — — US disclosed
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