SCHEMBL28339068

SCHEMBL28339068

CN(Cc1ccccc1)CC(O)c1ccccc1Cl

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ AOC3 Q16853 1/20 0.62
▸ KDM4E B2RXH2 2/20 0.51
▸ SMN1; SMN2 Q16637 2/20 0.51
▸ MEN1 O00255 1/20 0.51
▸ KMT2A Q03164 1/20 0.51
▸ ADRB2 P07550 2/20 0.46
▸ ADRB1 P08588 2/20 0.46
▸ DNM1 Q05193 1/20 0.46
▸ CYP2D6 P10635 1/20 0.45
▸ NFKB1 P19838 1/20 0.45
▸ HIF1A Q16665 1/20 0.45
▸ TDP1 Q9NUW8 1/20 0.44
▸ BLM P54132 2/20 0.44
▸ LMNA P02545 2/20 0.44
▸ USP2 O75604 1/20 0.44
▸ CYP3A4 P08684 1/20 0.44
▸ TSHR P16473 1/20 0.44
▸ MAOA P21397 1/20 0.44
▸ MAOB P27338 1/20 0.44
▸ PYCR1 P32322 1/20 0.44

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
SCHEMBL28339057 0.80 KDM4E (0.54) KDM4ESMN1; SMN2MEN1KMT2ADNM1
SCHEMBL28339091 0.78 KDM4E (0.70) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL14274010 0.78 KDM4E (0.70) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL13993320 0.78 KDM4E (0.70) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL25159695 0.78 MEN1 (0.66) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL28169242 0.78 MEN1 (0.66) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL2098159 0.77 DNM1 (0.57) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL1022224 0.77 DNM1 (0.57) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL2098163 0.77 DNM1 (0.57) AOC3KDM4ESMN1; SMN2MEN1KMT2A
SCHEMBL5964083 0.76 CNR2 (0.51) AOC3KDM4ESMN1; SMN2MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107021884-B Method for efficiently synthesizing chiral 1, 2-amino alcohol by catalyzing alpha-aminoketone through Ir/f-amphox 武汉凯特立斯科技有限公司 2019-12-24 — — CN disclosed
CN-107021884-A Method for efficiently synthesizing chiral 1, 2-amino alcohol by catalyzing alpha-aminoketone through Ir/f-amphox 武汉凯特立斯科技有限公司 2017-08-08 — — CN disclosed
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