SCHEMBL21313870

SCHEMBL21313870

O=C(/C=C/c1ccc(OC(F)(F)F)cc1)N1CC=C2CN(C(=O)N3CCc4[nH]nnc4C3)C[C@H]2CC1

nearest known ligand 0.40

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ HRH3 Q9Y5N1 1/20 0.40
▸ CCR2 P41597 1/20 0.39
▸ MAPT P10636 3/20 0.38
▸ ALDH1A1 P00352 1/20 0.38
▸ ENPP2 Q13822 3/20 0.37
▸ ATXN2 Q99700 2/20 0.37
▸ NAMPT P43490 1/20 0.36
▸ CA2 P00918 2/20 0.35
▸ NPC1 O15118 1/20 0.35
▸ HPGD P15428 1/20 0.35
▸ RAB9A P51151 1/20 0.35
▸ SMN1; SMN2 Q16637 1/20 0.35
▸ STAT3 P40763 1/20 0.34
▸ CYP2D6 P10635 1/20 0.34
▸ MCHR1 Q99705 5/20 0.34
▸ GPR183 P32249 1/20 0.34
▸ KCNH2 Q12809 1/20 0.34
▸ TP53 P04637 1/20 0.33

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
SCHEMBL16963158 1.00 HRH3 (0.40) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL16962973 0.89 CCR2 (0.40) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL21313885 0.89 CCR2 (0.40) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL16963747 0.87 ENPP2 (0.40) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL21313879 0.87 ENPP2 (0.40) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL21313827 0.87 ENPP2 (0.40) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL16961684 0.87 ENPP2 (0.40) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL21323305 0.85 CCR2 (0.42) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL16963160 0.85 CCR2 (0.42) HRH3CCR2MAPTALDH1A1ENPP2
SCHEMBL16963155 0.85 CCR2 (0.42) HRH3CCR2MAPTALDH1A1ENPP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2900669-B1 HEXAHYDROPYRROLO[3,4-C]PYRROLE DERIVATIVES AND RELATED COMPOUNDS AS AUTOTAXIN (ATX) INHIBITORS AND AS INHIBITORS OF THE LYSOPHOSPHATIDIC ACID (LPA) PRODUCTION FOR TREATING E.G. RENAL DISEASES HOFFMANN LA ROCHE (CH) 2019-09-04 — — EP disclosed
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