SCHEMBL29284762

SCHEMBL29284762

COc1ccc2c(c1)ncc1c(C)c3ccccc3n12

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FGFR1 P11362 5/20 0.47
▸ ALDH1A1 P00352 3/20 0.46
▸ KDM4E B2RXH2 2/20 0.46
▸ MEN1 O00255 2/20 0.46
▸ KMT2A Q03164 2/20 0.46
▸ HPGD P15428 2/20 0.46
▸ HTT P42858 2/20 0.46
▸ MAPT P10636 1/20 0.46
▸ HSD17B10 Q99714 1/20 0.46
▸ L3MBTL1 Q9Y468 1/20 0.46
▸ PDE2A O00408 4/20 0.40
▸ PDE10A Q9Y233 4/20 0.40
▸ GABRA1 P14867 1/20 0.40
▸ GABRG2 P18507 1/20 0.40
▸ GABRB3 P28472 1/20 0.40
▸ GABRA5 P31644 1/20 0.40
▸ GABRA3 P34903 1/20 0.40
▸ GABRA2 P47869 1/20 0.40
▸ GABRA6 Q16445 1/20 0.40
▸ NPC1 O15118 1/20 0.40

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
SCHEMBL29284763 0.81 PTGES (0.36) ALDH1A1KDM4EKMT2AHPGDMAPT
SCHEMBL29284761 0.72 HSD17B10 (0.38) ALDH1A1KDM4EMEN1KMT2AHPGD
SCHEMBL29284757 0.72 PDE2A (0.38) ALDH1A1KDM4EMEN1KMT2AHPGD
SCHEMBL29284765 0.68 FGFR1 (0.43) FGFR1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL30963687 0.68 FGFR1 (0.43) FGFR1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL29284758 0.67 PIK3CA (0.38) KDM4EL3MBTL1
SCHEMBL21917497 0.67 MAPT (0.51) ALDH1A1KDM4EMEN1KMT2AHPGD
SCHEMBL10883857 0.67 FGFR1 (0.43) FGFR1ALDH1A1MEN1KMT2AHPGD
SCHEMBL21717819 0.66 ALDH1A1 (0.68) ALDH1A1KDM4EMEN1KMT2AHPGD
SCHEMBL28988465 0.66 KDM4E (0.56) ALDH1A1KDM4EMEN1KMT2AHTT

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
CN-118221684-A Method for preparing quinoxaline derivative through HFIP-promoted defluorination cyclization reaction of difluoro carbene reagent 陕西科技大学 2024-06-21 — — CN disclosed
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