SCHEMBL28825258

SCHEMBL28825258

CC(C)(C)c1ccc(CP(=O)(c2ccccc2)c2ccccc2)c(O)c1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HTT P42858 3/20 0.55
▸ MEN1 O00255 2/20 0.54
▸ KMT2A Q03164 2/20 0.54
▸ GAA P10253 1/20 0.54
▸ ALDH1A1 P00352 3/20 0.51
▸ HPGD P15428 3/20 0.51
▸ CYP2D6 P10635 2/20 0.48
▸ L3MBTL1 Q9Y468 1/20 0.44
▸ ALOX15 P16050 1/20 0.43
▸ HSD17B10 Q99714 1/20 0.43
▸ TDP1 Q9NUW8 1/20 0.43
▸ POLB P06746 1/20 0.41
▸ G6PD P11413 1/20 0.41
▸ NR1H4 Q96RI1 1/20 0.40
▸ MAPT P10636 1/20 0.39
▸ MAPK1 P28482 1/20 0.39
▸ SMN1; SMN2 Q16637 1/20 0.39
▸ TSHR P16473 2/20 0.39
▸ HSP90AA1 P07900 1/20 0.38
▸ HSP90AB1 P08238 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
SCHEMBL28825321 0.88 HTT (0.67) HTTMEN1KMT2AGAAALDH1A1
SCHEMBL10910759 0.77 HTT (0.77) HTTMEN1KMT2AGAAALDH1A1
SCHEMBL10824828 0.76 HTT (0.65) HTTMEN1KMT2AGAAALDH1A1
SCHEMBL30956065 0.75 KMT2A (0.43) HTTMEN1KMT2AGAAALDH1A1
SCHEMBL29119880 0.74 MEN1 (0.58) HTTMEN1KMT2AGAAALDH1A1
SCHEMBL26090556 0.74 NPSR1 (0.53) MEN1KMT2AGAAALDH1A1HPGD
SCHEMBL5167762 0.73 ALDH1A1 (0.59) MEN1KMT2AGAAALDH1A1HPGD
SCHEMBL14076377 0.73 RXRA (0.54) MEN1KMT2AGAAALDH1A1HPGD
SCHEMBL51349 0.71 ALDH1A1 (0.61) MEN1KMT2AGAAALDH1A1HPGD
SCHEMBL29152361 0.71 ALDH1A1 (0.68) HTTMEN1KMT2AGAAALDH1A1

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-114933562-B Efficient preparation method of chloroquine based on (2-hydroxybenzyl) disubstituted phosphine oxide catalysis 华东理工大学 2024-07-23 — — CN disclosed
CN-114933562-A Efficient preparation method of chloroquine based on catalysis of (2-hydroxybenzyl) disubstituted phosphine oxide 华东理工大学 2022-08-23 — — CN disclosed
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