SCHEMBL12305572

SCHEMBL12305572

C/C=N/c1ccc(C)cc1Br

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 5/20 0.47
▸ RAB9A P51151 5/20 0.47
▸ L3MBTL1 Q9Y468 3/20 0.47
▸ MEN1 O00255 2/20 0.47
▸ KMT2A Q03164 2/20 0.47
▸ HSP90AA1 P07900 1/20 0.47
▸ CYP3A4 P08684 1/20 0.40
▸ ADRA2A P08913 1/20 0.40
▸ MAPT P10636 7/20 0.38
▸ KDM4E B2RXH2 6/20 0.38
▸ LMNA P02545 4/20 0.38
▸ HTT P42858 4/20 0.38
▸ ALDH1A1 P00352 6/20 0.33
▸ GAA P10253 3/20 0.33
▸ POLB P06746 2/20 0.33
▸ ALOX15 P16050 2/20 0.33
▸ HSD17B10 Q99714 2/20 0.33
▸ HPGD P15428 2/20 0.33
▸ THRB P10828 1/20 0.33
▸ PKM P14618 1/20 0.33

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
SCHEMBL11285388 0.79 CYP3A4 (0.68) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL11148348 0.79 NPC1 (0.44) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL11148344 0.79 NPC1 (0.44) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL11285384 0.79 CYP3A4 (0.68) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL21131297 0.78 CYP3A4 (0.62) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL8292092 0.78 CYP3A4 (0.62) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL16130442 0.75 CYP3A4 (0.40) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL12830975 0.75 CYP3A4 (0.40) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL20726017 0.74 DHODH (0.49) NPC1RAB9AL3MBTL1MEN1KMT2A
SCHEMBL21239424 0.73 CYP3A4 (0.39) NPC1RAB9AL3MBTL1CYP3A4ADRA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8785419-B2 Cavity induced allosteric modification of intermolecular interactions and methods of identifying compounds that effect the same THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2014-07-22 — — US disclosed
US-8785419-B2 Cavity induced allosteric modification of intermolecular interactions and methods of identifying compounds that effect the same THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2014-07-22 — — US disclosed
US-8019557-B2 Cavity induced allosteric modification of intermolecular interactions and methods of identifying compounds that effect the same THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2011-09-13 — — US disclosed
US-8019557-B2 Cavity induced allosteric modification of intermolecular interactions and methods of identifying compounds that effect the same THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2011-09-13 — — US disclosed
US-20100151507-A1 Cavity Induced Allosteric Modification Of Intermolecular Interactions And Methods Of Identifying Compounds That Effect The Same NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2010-06-17 — — US disclosed
US-20100151507-A1 Cavity Induced Allosteric Modification Of Intermolecular Interactions And Methods Of Identifying Compounds That Effect The Same NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2010-06-17 — — US disclosed
US-7653495-B1 Comprises series of steps including identifying cavity proximal to functional critical site, determining physical parameters of cavity, identifying functional groups which can be accommodated by cavity, testing compounds comprising such functional groups in an in vitro assay to determine which are active THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2010-01-26 — — US disclosed
US-7653495-B1 Comprises series of steps including identifying cavity proximal to functional critical site, determining physical parameters of cavity, identifying functional groups which can be accommodated by cavity, testing compounds comprising such functional groups in an in vitro assay to determine which are active THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2010-01-26 — — US disclosed
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