SCHEMBL7908771

SCHEMBL7908771

NC(=O)[C@@H](CCO)Cc1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.57
EPHX1 P07099 1/20 0.53
CPA3 P15088 3/20 0.51
CPA1 P15085 6/20 0.50
FOLH1 Q04609 3/20 0.50
SLC1A3 P43003 1/20 0.50
SLC1A2 P43004 1/20 0.50
SLC1A1 P43005 1/20 0.50
CPB1 P15086 1/20 0.50
CPB2 Q96IY4 1/20 0.50
ALPI P09923 1/20 0.48
PKM P14618 1/20 0.48
PTGS1 P23219 1/20 0.48
XIAP P98170 1/20 0.48
SLC7A5 Q01650 1/20 0.48
CCR1 P32246 1/20 0.46
ALDH1A1 P00352 1/20 0.45
POLB P06746 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45

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
SCHEMBL7907545 1.00 CYP1A2 (0.57) CYP1A2EPHX1CPA3CPA1FOLH1
SCHEMBL4020655 1.00 CYP1A2 (0.57) CYP1A2EPHX1CPA3CPA1FOLH1
SCHEMBL28179819 0.89 FOLH1 (0.54) CYP1A2EPHX1CPA3CPA1FOLH1
SCHEMBL5052372 0.86 CYP1A2 (0.68) CYP1A2EPHX1CPA3CPA1FOLH1
SCHEMBL3044591 0.85 CYP1A2 (0.57) CYP1A2EPHX1CPA3CPA1FOLH1
SCHEMBL27417767 0.85 CYP1A2 (0.57) CYP1A2EPHX1CPA3CPA1FOLH1
SCHEMBL7303315 0.85 CYP1A2 (0.73) CYP1A2CPA3CPA1FOLH1SLC1A3
SCHEMBL7301792 0.85 CYP1A2 (0.73) CYP1A2CPA3CPA1FOLH1SLC1A3
SCHEMBL7667156 0.85 CYP1A2 (0.73) CYP1A2CPA3CPA1FOLH1SLC1A3
SCHEMBL1059561 0.85 CYP1A2 (0.61) CYP1A2EPHX1CPA3CPA1FOLH1

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 4 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
WO-1999032649-A1 METHODS AND PRECURSORS FOR THE PRODUCTION OF CHIRAL 1,3-AMINOALCOHOLS BIOCATALYTICS, INC. (US) 1999-07-01 WO disclosed
US-5916786-A Method for the production of chiral 1,3-aminoalcohols BIOCATALYTICS, INC. (US) 1999-06-29 US disclosed
US-5693650-A TREATING ATHEROSCLEROSIS BAYER AKTIENGESELLSCHAFT (DE) 1997-12-02 US disclosed