SCHEMBL28339059

SCHEMBL28339059

Cc1cc[c]c(N(C)Cc2ccccc2)c1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.42
ALDH1A1 P00352 2/20 0.42
KMT2A Q03164 3/20 0.40
MAPT P10636 2/20 0.40
SMN1; SMN2 Q16637 2/20 0.40
AOC3 Q16853 1/20 0.40
CYP2C19 P33261 1/20 0.40
NPC1 O15118 3/20 0.36
RAB9A P51151 3/20 0.36
KDM4E B2RXH2 1/20 0.36
TSPO P30536 1/20 0.36
ERAP1 Q9NZ08 1/20 0.36
CARM1 Q86X55 1/20 0.36
PRMT6 Q96LA8 1/20 0.36
PRMT8 Q9NR22 1/20 0.36
HTT P42858 2/20 0.35
JAK2 O60674 1/20 0.35
PAX8 Q06710 1/20 0.35
MEN1 O00255 2/20 0.35
ATM Q13315 1/20 0.35

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
SCHEMBL10671402 0.83 SMN1; SMN2 (0.43) TSHRALDH1A1KMT2AMAPTSMN1; SMN2
SCHEMBL28339074 0.82 SMN1; SMN2 (0.45) TSHRALDH1A1KMT2AMAPTSMN1; SMN2
SCHEMBL28339065 0.80 CALM1 (0.46) TSHRKMT2AMAPTKDM4EMEN1
SCHEMBL1045949 0.79 TSHR (0.48) TSHRALDH1A1KMT2AMAPTSMN1; SMN2
SCHEMBL8659969 0.72 ALDH1A1 (0.33) TSHRALDH1A1
SCHEMBL9638314 0.70 RAB9A (0.55) TSHRALDH1A1KMT2AAOC3CYP2C19
SCHEMBL5604665 0.69 TSPO (0.57) TSHRALDH1A1KMT2AMAPTSMN1; SMN2
SCHEMBL921505 0.69 NR1H2 (0.43) TSHRALDH1A1KMT2AMAPTSMN1; SMN2
SCHEMBL2852601 0.68 CALM1 (0.41) TSHRALDH1A1KMT2ASMN1; SMN2CYP2C19
SCHEMBL28147900 0.68 TSHR (0.44) TSHRALDH1A1KMT2AMAPTSMN1; SMN2

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 claimed
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