SCHEMBL9837295

SCHEMBL9837295

CN(C)Cc1ccc(C(=O)Oc2ccc(-n3cnc4c(=O)[nH]c(=O)[nH]c43)cc2)cc1

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CA2 P00918 1/20 0.38
▸ ALDH1A1 P00352 1/20 0.37
▸ KMT2A Q03164 2/20 0.37
▸ MEN1 O00255 1/20 0.37
▸ XDH P47989 1/20 0.36
▸ LSS P48449 2/20 0.35
▸ HCAR1 Q9BXC0 1/20 0.34
▸ TP53 P04637 1/20 0.33
▸ MCHR1 Q99705 2/20 0.33
▸ SLC6A2 P23975 1/20 0.33
▸ SLC6A4 P31645 1/20 0.33
▸ SLC6A3 Q01959 1/20 0.33
▸ MAPT P10636 3/20 0.33
▸ DHODH Q02127 1/20 0.33
▸ THRB P10828 2/20 0.32
▸ SLC22A2 O15244 1/20 0.32
▸ TMPRSS2 O15393 1/20 0.32
▸ F2 P00734 1/20 0.32
▸ HPN P05981 1/20 0.32
▸ KLK1 P06870 1/20 0.32

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
SCHEMBL9837292 0.71 ADORA2B (0.46) CA2TP53MAPTSMN1; SMN2
SCHEMBL22193385 0.69 PRSS1 (0.52) CA2ALDH1A1KMT2AMEN1SLC6A2
SCHEMBL9837288 0.69 ADORA2A (0.38) CA2KMT2AMEN1LSSTP53
SCHEMBL21318232 0.67 SMN1; SMN2 (0.57) CA2ALDH1A1KMT2AMEN1MAPT
SCHEMBL27365841 0.67 CA2 (0.48) CA2ALDH1A1KMT2AMEN1LSS
SCHEMBL6796630 0.66 ALDH1A1 (0.49) ALDH1A1KMT2AMEN1XDHHCAR1
SCHEMBL9837043 0.64 KMT2A (0.65) ALDH1A1KMT2AMEN1TP53MAPT
SCHEMBL6231216 0.60 HRH3 (0.49) ALDH1A1KMT2AMEN1LSSSMN1; SMN2
SCHEMBL5067508 0.60 LOXL2 (0.61) CA2ALDH1A1KMT2AMEN1LSS
SCHEMBL12154217 0.59 ALDH1A1 (0.57) ALDH1A1KMT2ATP53MAPTTHRB

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-0454773-A1 NOVEL PRODRUG DERIVATIVES OF BIOLOGICALLY ACTIVE AGENTS CONTAINING HYDROXYL GROUPS OR NH-ACIDIC GROUPS Bundgaard, Hans (DK) 1991-11-06 — — EP disclosed
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