SCHEMBL6851008

SCHEMBL6851008

CNC(=O)C(=O)Nc1ccccc1F

nearest known ligand 0.64

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 7/20 0.64
NPC1 O15118 5/20 0.64
SMN1; SMN2 Q16637 5/20 0.64
MEN1 O00255 2/20 0.64
KMT2A Q03164 2/20 0.64
ALDH1A1 P00352 4/20 0.54
HTT P42858 2/20 0.53
PDK1 Q15118 1/20 0.53
PDK2 Q15119 1/20 0.53
PDK3 Q15120 1/20 0.53
PDK4 Q16654 1/20 0.53
MAPT P10636 2/20 0.52
KDM4E B2RXH2 1/20 0.52
LMNA P02545 2/20 0.51
POLB P06746 1/20 0.51
RECQL P46063 1/20 0.50
NPSR1 Q6W5P4 1/20 0.50
GAA P10253 1/20 0.50

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
SCHEMBL6850971 0.92 RAB9A (0.75) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL5697344 0.85 ALDH1A1 (0.67) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL824564 0.84 SMN1; SMN2 (0.77) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL7098684 0.84 RAB9A (0.64) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL440095 0.82 RAB9A (0.67) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL29179553 0.80 RAB9A (0.64) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL2605749 0.79 KMT2A (0.63) RAB9ANPC1SMN1; SMN2KMT2AALDH1A1
SCHEMBL1430533 0.79 RAB9A (0.69) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL29408738 0.79 RAB9A (0.69) RAB9ANPC1SMN1; SMN2MEN1KMT2A
SCHEMBL30851501 0.79 RAB9A (1.00) RAB9ANPC1SMN1; SMN2MEN1KMT2A

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