SCHEMBL7899570

SCHEMBL7899570

N[C@H](CCOC(=O)c1ccccc1)c1ccc(F)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TDP1 Q9NUW8 2/20 0.51
▸ LMNA P02545 2/20 0.49
▸ NPC1 O15118 2/20 0.46
▸ RAB9A P51151 2/20 0.46
▸ PKM P14618 1/20 0.46
▸ ALDH1A1 P00352 2/20 0.45
▸ BCHE P06276 1/20 0.43
▸ SLC6A3 Q01959 3/20 0.42
▸ KMT2A Q03164 2/20 0.42
▸ MAPK1 P28482 1/20 0.42
▸ HIF1A Q16665 1/20 0.42
▸ SLC6A2 P23975 1/20 0.42
▸ SLC6A4 P31645 2/20 0.41
▸ SMN1; SMN2 Q16637 2/20 0.41
▸ SLC1A5 Q15758 1/20 0.41
▸ PLA2G7 Q13093 1/20 0.41
▸ ALPG P10696 1/20 0.41
▸ HPGD P15428 1/20 0.41
▸ KDM4E B2RXH2 1/20 0.41
▸ GAA P10253 1/20 0.41

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
SCHEMBL7905994 1.00 TDP1 (0.51) TDP1LMNANPC1RAB9APKM
SCHEMBL7909113 0.89 TDP1 (0.59) TDP1LMNANPC1RAB9AALDH1A1
SCHEMBL7908767 0.89 TDP1 (0.59) TDP1LMNANPC1RAB9AALDH1A1
SCHEMBL7907425 0.81 TDP1 (0.44) TDP1LMNANPC1RAB9APKM
SCHEMBL7907430 0.81 TDP1 (0.44) TDP1LMNANPC1RAB9APKM
SCHEMBL27286618 0.76 LMNA (0.61) TDP1LMNANPC1RAB9APKM
SCHEMBL31374444 0.76 TDP1 (0.59) TDP1LMNANPC1RAB9APKM
SCHEMBL14362839 0.76 TDP1 (0.63) TDP1LMNANPC1RAB9APKM
SCHEMBL17061429 0.75 ESR1 (0.64) TDP1LMNANPC1RAB9APKM
SCHEMBL22017039 0.75 PTGFR (0.43) ALDH1A1KMT2AKDM4EGAA

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
US-6207862-B1 PRECURSORS ARE CHIRAL 4-HYDROXYCARBOXAMIDES, 4-HYDROXYHYDROXAMIC ACIDS, OR 4-HYDROXYHYDRAZIDES PRODUCED FROM GAMMA-LACTONES, WHICH IN TURN ARE DERIVED FROM 1,4-DIOLS BY STEREOSELECTIVE OXIDATION, BIOCATALYTICS, INC. 2001-03-27 — — US disclosed
US-5916786-A Method for the production of chiral 1,3-aminoalcohols BIOCATALYTICS, INC. (US) 1999-06-29 — — US disclosed
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