SCHEMBL7909113

SCHEMBL7909113

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

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TDP1 Q9NUW8 2/20 0.59
▸ LMNA P02545 2/20 0.56
▸ ALDH1A1 P00352 2/20 0.51
▸ MAPK1 P28482 1/20 0.49
▸ HIF1A Q16665 1/20 0.49
▸ SLC6A2 P23975 1/20 0.49
▸ SLC6A3 Q01959 1/20 0.49
▸ KMT2A Q03164 1/20 0.49
▸ NPC1 O15118 1/20 0.47
▸ RAB9A P51151 1/20 0.47
▸ SMN1; SMN2 Q16637 2/20 0.46
▸ SLC1A5 Q15758 1/20 0.46
▸ KDM4E B2RXH2 1/20 0.46
▸ GAA P10253 1/20 0.46
▸ L3MBTL1 Q9Y468 1/20 0.46
▸ ESR1 P03372 1/20 0.45
▸ ESR2 Q92731 1/20 0.45
▸ TSHR P16473 1/20 0.45
▸ F2 P00734 1/20 0.44
▸ SLC7A5 Q01650 1/20 0.43

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
SCHEMBL7908767 1.00 TDP1 (0.59) TDP1LMNAALDH1A1MAPK1HIF1A
SCHEMBL7905994 0.89 TDP1 (0.51) TDP1LMNAALDH1A1MAPK1HIF1A
SCHEMBL7899570 0.89 TDP1 (0.51) TDP1LMNAALDH1A1MAPK1HIF1A
SCHEMBL28117942 0.84 ALDH1A1 (0.62) TDP1LMNAALDH1A1MAPK1HIF1A
SCHEMBL27286618 0.83 LMNA (0.61) TDP1LMNAALDH1A1MAPK1HIF1A
SCHEMBL31374444 0.83 TDP1 (0.59) TDP1LMNAALDH1A1MAPK1HIF1A
SCHEMBL25362743 0.82 CYP1A2 (0.58) LMNAMAPK1KMT2ASMN1; SMN2
SCHEMBL16015311 0.82 CYP1A2 (0.58) LMNAMAPK1KMT2ASMN1; SMN2
SCHEMBL25362745 0.82 CYP1A2 (0.58) LMNAMAPK1KMT2ASMN1; SMN2
SCHEMBL17629339 0.81 LMNA (0.59) TDP1LMNAALDH1A1MAPK1HIF1A

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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