SCHEMBL29236568

SCHEMBL29236568

CSc1ccc([C@@H](O)CN2C(=O)c3ccccc3C2=O)cc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 6/20 0.47
▸ MMP2 P08253 2/20 0.46
▸ MMP9 P14780 2/20 0.46
▸ KMT2A Q03164 3/20 0.44
▸ MAPK1 P28482 1/20 0.42
▸ MAPT P10636 2/20 0.41
▸ RAB9A P51151 2/20 0.40
▸ CA12 O43570 1/20 0.39
▸ CA9 Q16790 1/20 0.39
▸ NPC1 O15118 1/20 0.39
▸ CASP3 P42574 1/20 0.39
▸ SMN1; SMN2 Q16637 1/20 0.39
▸ SENP8 Q96LD8 1/20 0.39
▸ SENP7 Q9BQF6 1/20 0.39
▸ SENP6 Q9GZR1 1/20 0.39
▸ PLIN1 O60240 1/20 0.38
▸ HPGD P15428 1/20 0.38
▸ ALOX15 P16050 1/20 0.38
▸ PLIN5 Q00G26 1/20 0.38
▸ ABHD5 Q8WTS1 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
SCHEMBL29236545 1.00 ALDH1A1 (0.47) ALDH1A1MMP2MMP9KMT2AMAPK1
SCHEMBL29236534 0.84 ALDH1A1 (0.51) ALDH1A1KMT2AMAPK1MAPTHPGD
SCHEMBL29236536 0.84 ALDH1A1 (0.51) ALDH1A1KMT2AMAPK1MAPTHPGD
SCHEMBL9773949 0.82 ALDH1A1 (0.56) ALDH1A1KMT2AMAPK1MAPTRAB9A
SCHEMBL24032681 0.82 MMP2 (0.51) ALDH1A1MMP2MMP9KMT2AMAPK1
SCHEMBL29236538 0.81 RPS6KA2 (0.52) ALDH1A1MMP2MMP9KMT2AMAPK1
SCHEMBL29236539 0.81 RPS6KA2 (0.52) ALDH1A1MMP2MMP9KMT2AMAPK1
SCHEMBL29236527 0.80 CASP3 (0.53) ALDH1A1KMT2AMAPK1MAPTRAB9A
SCHEMBL29236529 0.80 CASP3 (0.53) ALDH1A1KMT2AMAPK1MAPTRAB9A
SCHEMBL24032602 0.80 MMP2 (0.44) ALDH1A1MMP2MMP9KMT2AMAPT

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-118184477-A Method for preparing chiral amino alcohol compound by catalyzing amino ketone with nickel metal by using water as hydrogen source 云南民族大学 2024-06-14 — — CN disclosed
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