SCHEMBL8487315

SCHEMBL8487315

NC(=O)[C@H]1O[C@@H]1c1ccccc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ EPHX1 P07099 6/20 0.62
▸ TSHR P16473 2/20 0.53
▸ F13A1 P00488 3/20 0.50
▸ TGM2 P21980 3/20 0.50
▸ CYP2C19 P33261 2/20 0.50
▸ MEN1 O00255 1/20 0.50
▸ TP53 P04637 1/20 0.50
▸ CYP1A2 P05177 1/20 0.50
▸ CYP2C9 P11712 1/20 0.50
▸ HPGD P15428 1/20 0.50
▸ KMT2A Q03164 1/20 0.50
▸ LMNA P02545 1/20 0.42
▸ POLB P06746 1/20 0.39
▸ CYP3A4 P08684 1/20 0.39
▸ PARP1 P09874 1/20 0.39
▸ MAPT P10636 1/20 0.39
▸ RECQL P46063 1/20 0.39
▸ BLM P54132 1/20 0.39
▸ PMP22 Q01453 1/20 0.39
▸ HSD17B10 Q99714 1/20 0.39

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
SCHEMBL8339724 1.00 EPHX1 (0.62) EPHX1TSHRF13A1TGM2CYP2C19
SCHEMBL8376293 1.00 EPHX1 (0.62) EPHX1TSHRF13A1TGM2CYP2C19
SCHEMBL1692473 0.82 EPHX1 (0.67) EPHX1TSHRCYP2C19MEN1TP53
SCHEMBL5598863 0.82 EPHX1 (0.67) EPHX1TSHRF13A1TGM2CYP2C19
SCHEMBL3343090 0.82 EPHX1 (0.67) EPHX1TSHRCYP2C19MEN1TP53
SCHEMBL14571889 0.82 EPHX1 (0.67) EPHX1TSHRF13A1TGM2CYP2C19
SCHEMBL6689012 0.82 EPHX1 (0.67) EPHX1TSHRCYP2C19MEN1TP53
SCHEMBL5598408 0.82 EPHX1 (0.67) EPHX1TSHRF13A1TGM2CYP2C19
SCHEMBL5598404 0.82 EPHX1 (0.67) EPHX1TSHRF13A1TGM2CYP2C19
SCHEMBL4071198 0.82 EPHX1 (0.67) EPHX1TSHRCYP2C19MEN1TP53

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-5883264-A SUBJECTING RACEMIC TRANS-3-PHENYLGLYCIDAMIDE COMPOUND TO OPTICAL RESOLUTION USING A MICROORGANISM HAVING ABILITY OF PREFERENTIALLY HYDROLYZING ONE OF (2S,3R) ISOMER OR (2R,3S) ISOMER THEREOF TANABE SEIYAKU CO., LTD. (JP) 1999-03-16 — — US disclosed
EP-0795609-A2 Process for preparing optically active trans-3-phenylglycidamide compounds TANABE SEIYAKU CO., LTD. (JP) 1997-09-17 — — EP disclosed
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