SCHEMBL7905025

SCHEMBL7905025

N#CC1CCn2c(C(=O)c3ccccc3)ccc21

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS2 P35354 4/20 0.64
CDC42 P60953 3/20 0.64
RAC1 P63000 3/20 0.64
PTGS1 P23219 2/20 0.64
PAK1 Q13153 2/20 0.64
NPC1 O15118 1/20 0.64
CHRM3 P20309 1/20 0.64
OPRM1 P35372 1/20 0.64
RAB9A P51151 1/20 0.64
ABCC4 O15439 1/20 0.53
HTT P42858 1/20 0.53
BLM P54132 1/20 0.53
LMNA P02545 1/20 0.53
CYP1A2 P05177 1/20 0.53
NFKB1 P19838 1/20 0.53
MAPK1 P28482 1/20 0.53
CA4 P22748 5/20 0.47
CA9 Q16790 4/20 0.47
CA12 O43570 3/20 0.47
CA1 P00915 3/20 0.47

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
SCHEMBL11198807 0.92 PTGS2 (0.58) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL18096529 0.87 PTGS2 (0.66) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11352958 0.86 CDC42 (0.48) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11348019 0.86 NPC1 (0.48) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11533036 0.86 PTGS2 (0.48) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11340159 0.85 CDC42 (0.47) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11535191 0.85 CDC42 (0.47) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11350964 0.85 CDC42 (0.47) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11346567 0.83 CDC42 (0.45) PTGS2CDC42RAC1PTGS1PAK1
SCHEMBL11442232 0.83 CDC42 (0.45) PTGS2CDC42RAC1PTGS1PAK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0000649-B1 5-SUBSTITUTED-1,2-DIHYDRO-3H-PYRROLO(1,2-A)PYRROLE-1-CARBONITRILES AND PROCESS FOR THEIR CONVERSION TO THE CORRESPONDING 1-CARBOXYLIC ACIDS SYNTEX (U.S.A.) INC. (US) 1981-03-25 EP claimed
US-4140698-A 1,2-Dihydro-3H-pyrrolo[1,2-a]pyrrole-1-nitriles SYNTEX (USA) INC. (US) 1979-02-20 US claimed
EP-0000649-A1 5-substituted-1,2-dihydro-3H-pyrrolo(1,2-a)pyrrole-1-carbonitriles and process for their conversion to the corresponding 1-carboxylic acids SYNTEX (U.S.A.) INC. (US) 1979-02-07 EP claimed
US-6191285-B1 PRODUCING KETOROLAC TROMETHAMINE IN A THREE-PART SOLVENT SYSTEM, I.E., IN THE PRESENCE OF A LOWER ALKYL ALCOHOL, A LOWER ALKYL ACETATE AND WATER BY REACTING KETOROLAC ACID AND TROMETHAMINE ABBOTT LABORATORIES 2001-02-20 US disclosed
EP-0053021-B1 PROCESS FOR 5-AROYLATION OF 1,2-DIHYDRO-3H-PYRROLO(1,2-A)PYRROLE-1-CARBOXYLIC ESTERS AND NITRILES SYNTEX (U.S.A.) INC. (US) 1985-05-02 EP disclosed
US-4353829-A AROYL MORPHOLIDE REAGENT SYNTEX (U.S.A.) INC. (US) 1982-10-12 US disclosed
EP-0053021-A2 Process for 5-aroylation of 1,2-dihydro-3H-pyrrolo(1,2-a)pyrrole-1-carboxylic esters and nitriles SYNTEX (U.S.A.) INC. (US) 1982-06-02 EP disclosed
US-4140698-A 1,2-Dihydro-3H-pyrrolo[1,2-a]pyrrole-1-nitriles SYNTEX (USA) INC. (US) 1979-02-20 US disclosed
EP-0000649-A1 5-substituted-1,2-dihydro-3H-pyrrolo(1,2-a)pyrrole-1-carbonitriles and process for their conversion to the corresponding 1-carboxylic acids SYNTEX (U.S.A.) INC. (US) 1979-02-07 EP disclosed