SCHEMBL7624006

SCHEMBL7624006

NC(=O)c1ccccc1[C@@H](N)[CH]c1ccccc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.46
ALDH1A1 P00352 4/20 0.46
HPGD P15428 4/20 0.46
MAPT P10636 4/20 0.46
LMNA P02545 1/20 0.46
SIRT2 Q8IXJ6 1/20 0.42
BCAT2 O15382 1/20 0.42
PARP1 P09874 2/20 0.41
TSHR P16473 2/20 0.41
HSD17B10 Q99714 2/20 0.41
NPC1 O15118 2/20 0.40
SIRT1 Q96EB6 2/20 0.40
METAP2 P50579 1/20 0.39
CTNNB1 P35222 1/20 0.39
RAB9A P51151 2/20 0.38
IRAK4 Q9NWZ3 1/20 0.38
KEAP1 Q14145 1/20 0.38
NFE2L2 Q16236 1/20 0.38
HDAC3 O15379 1/20 0.37
TNKS O95271 1/20 0.37

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
SCHEMBL3210135 1.00 KDM4E (0.46) KDM4EALDH1A1HPGDMAPTLMNA
SCHEMBL3658524 0.83 KDM4E (0.46) KDM4EALDH1A1HPGDMAPTLMNA
SCHEMBL2762810 0.83 KDM4E (0.46) KDM4EALDH1A1HPGDMAPTLMNA
SCHEMBL4553803 0.79 KDM4E (0.44) KDM4EALDH1A1HPGDMAPTLMNA
SCHEMBL3831520 0.73 BCAT2 (0.46) KDM4EALDH1A1HPGDMAPTLMNA
SCHEMBL731619 0.72 IRAK4 (0.52) KDM4EALDH1A1HPGDMAPTBCAT2
SCHEMBL105262 0.71 IRAK4 (0.55) KDM4EALDH1A1HPGDMAPTLMNA
SCHEMBL31632660 0.71 IRAK4 (0.55) KDM4EALDH1A1HPGDMAPTLMNA
SCHEMBL4431290 0.71 KDM4E (0.47) KDM4EALDH1A1HPGDMAPTBCAT2
Hydrochloric Acid SCHEMBL3683840 0.71 IRAK4 (0.50) KDM4EALDH1A1HPGDMAPTLMNA

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0915076-B1 Process for the preparation of trans-(R,R)-actinol HOFFMANN LA ROCHE (CH) 2002-01-16 EP claimed
US-6187961-B1 HYDROGENATING (R)-LEVODIONE IN PRESENCE OF HYDROGEN DONAR AND A SOLVENT OR IN PRESENCE OF HYDROGEN DONOR WHICH SIMULTANEOUSLY USED AS THE SOLVENT, AND AN AMINO-AMIDE-RUTHENIUM COMPLEX ROCHE VITAMINS INC. 2001-02-13 US claimed
EP-0915076-A1 Process for the preparation of trans-(R,R)-actinol F. HOFFMANN-LA ROCHE AG (CH) 1999-05-12 EP claimed
EP-0915076-B1 Process for the preparation of trans-(R,R)-actinol HOFFMANN LA ROCHE (CH) 2002-01-16 EP disclosed
US-6300509-B1 CATALYST FOR DIASTEREOSELECTIVE TRANSFER HYDROGENATION OF (R)-LEVODIONE TO TRANS-(R,R)-ACTINOL IN PRESENCE OF HYDROGEN DONOR, WHICH SIMULTANEOUSLY CAN BE USED AS SOLVENT ROCHE VITAMINS INC. 2001-10-09 US disclosed
US-6187961-B1 HYDROGENATING (R)-LEVODIONE IN PRESENCE OF HYDROGEN DONAR AND A SOLVENT OR IN PRESENCE OF HYDROGEN DONOR WHICH SIMULTANEOUSLY USED AS THE SOLVENT, AND AN AMINO-AMIDE-RUTHENIUM COMPLEX ROCHE VITAMINS INC. 2001-02-13 US disclosed
EP-0915076-A1 Process for the preparation of trans-(R,R)-actinol F. HOFFMANN-LA ROCHE AG (CH) 1999-05-12 EP disclosed