SCHEMBL6858071

SCHEMBL6858071

CNC(=O)C(=O)Nc1ccccc1Cl

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.56
HPGD P15428 1/20 0.56
CYP2C19 P33261 1/20 0.56
MEN1 O00255 1/20 0.55
KMT2A Q03164 1/20 0.55
NPC1 O15118 4/20 0.54
RAB9A P51151 4/20 0.54
PDK1 Q15118 3/20 0.51
PDK2 Q15119 3/20 0.51
PDK3 Q15120 3/20 0.51
PDK4 Q16654 3/20 0.51
ALDH1A1 P00352 3/20 0.51
L3MBTL1 Q9Y468 2/20 0.51
GLA P06280 1/20 0.51
ATM Q13315 1/20 0.51
HTT P42858 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
S1PR4 O95977 1/20 0.51
MAPT P10636 1/20 0.51
PKM P14618 1/20 0.51

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
SCHEMBL6859262 0.92 CYP1A2 (0.64) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL5697344 0.85 ALDH1A1 (0.67) HPGDMEN1KMT2ANPC1RAB9A
SCHEMBL8830517 0.84 SMN1; SMN2 (0.73) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL9168941 0.82 MAPT (0.59) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL8645476 0.82 GPR35 (0.68) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL28440244 0.81 NPC1 (0.47) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL7779068 0.81 CYP1A2 (0.53) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL11786602 0.81 ALDH1A1 (0.53) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL13741589 0.80 CYP1A2 (0.56) CYP1A2HPGDCYP2C19MEN1KMT2A
SCHEMBL646296 0.79 HPGD (0.66) CYP1A2HPGDCYP2C19MEN1KMT2A

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-6737193-B2 ACTIVE MATERIALS IN THE POSITIVE ELECTRODES OF BATTERIES. NOVEL METHODS FOR PREPARING THE TETRAKETOPIPERAZINE UNIT-CONTAINING COMPOUNDS INCLUDE: (I) REACTING AN OXALYL HALIDE AND AN OXAMIDE, AND ADDING WATER OR AN AQUEOUS ALKALI IM&T RESEARCH, INC. 2004-05-18 US disclosed
US-20030148188-A1 Active materials in the positive electrodes of batteries. Novel methods for preparing the tetraketopiperazine unit-containing compounds include: (i) reacting an oxalyl halide and an oxamide, and adding water or an aqueous alkali IM&T RESEARCH, INC. 2003-08-07 US disclosed