SCHEMBL9012528

SCHEMBL9012528

CC(=O)C(=O)Oc1c[nH]c2cc(Cl)ccc12

nearest known ligand 0.54

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
NR4A2 P43354 2/20 0.54
SLC22A6 Q4U2R8 1/20 0.48
GPR84 Q9NQS5 1/20 0.44
ABCB11 O95342 1/20 0.42
F7 P08709 1/20 0.42
F3 P13726 1/20 0.42
ALDH1A1 P00352 1/20 0.41
ALOX15 P16050 1/20 0.41
IDO1 P14902 1/20 0.40
AMY1A P0DUB6 1/20 0.39
MTNR1A P48039 1/20 0.39
MTNR1B P49286 1/20 0.39
SLC6A4 P31645 1/20 0.39
SPR P35270 1/20 0.38
PYGL P06737 1/20 0.38
GFER P55789 1/20 0.38
HSD17B10 Q99714 1/20 0.38
HTR2A P28223 1/20 0.38
AVPR1A P37288 1/20 0.38

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
SCHEMBL1614860 0.88 SLC22A6 (0.62) NR4A2SLC22A6GPR84ABCB11F7
SCHEMBL4626534 0.84 NR4A2 (0.52) NR4A2SLC22A6ALDH1A1IDO1MTNR1A
SCHEMBL27591784 0.81 NR4A2 (0.52) NR4A2SLC22A6GPR84ABCB11F7
SCHEMBL9300226 0.80 NR4A2 (0.51) NR4A2SLC22A6GPR84F7F3
SCHEMBL125250 0.78 SLC22A6 (0.76) NR4A2SLC22A6GPR84ALDH1A1
SCHEMBL27920534 0.78 KMT2A (0.53) NR4A2SLC22A6ALDH1A1ALOX15
SCHEMBL3182218 0.76 NR4A2 (0.69) NR4A2GPR84F7F3ALDH1A1
SCHEMBL14527902 0.76 NR4A2 (0.55) NR4A2GPR84ALDH1A1IDO1SLC6A4
SCHEMBL9120206 0.76 SLC22A6 (0.62) NR4A2SLC22A6GPR84ABCB11F7
SCHEMBL9117344 0.75 NR4A2 (0.52) NR4A2SLC22A6GPR84F7F3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0421946-B1 3-indolepyruvic acid derivatives their method of production and therapeutic use POLIFARMA SPA (IT) 1996-11-20 EP disclosed
US-5210215-A Reacting indoles, dimethylamine and formaldehyde to gramines, condensing with malonic compounds to tryptophans, converting to 3-indolepyruvic acids; also preparation from indoles by reaction with alkyl ester oximes of 3-bromopyruvic acid POLIFARMA S.P.A. (IT) 1993-05-11 US disclosed
EP-0421946-A2 3-indolepyruvic acid derivatives their method of production and therapeutic use POLIFARMA S.p.A. (IT) 1991-04-10 EP disclosed