SCHEMBL5685392

SCHEMBL5685392

NC(=O)c1cc(C#Cc2ccccc2)cc(C#Cc2ccccc2)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GRM5 P41594 2/20 0.56
NPC1 O15118 2/20 0.55
RAB9A P51151 2/20 0.55
MAPT P10636 2/20 0.52
POLB P06746 1/20 0.52
CYP3A4 P08684 1/20 0.52
PARP1 P09874 1/20 0.52
TSHR P16473 1/20 0.52
CYP2C19 P33261 1/20 0.52
RECQL P46063 1/20 0.52
BLM P54132 1/20 0.52
PMP22 Q01453 1/20 0.52
HSD17B10 Q99714 1/20 0.52
TDP1 Q9NUW8 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
APP P05067 1/20 0.48
DHODH Q02127 2/20 0.46
PARP10 Q53GL7 1/20 0.46
ASIC3 Q9UHC3 1/20 0.45
AKR1C2 P52895 1/20 0.45

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
SCHEMBL15611234 0.83 GRM5 (0.64) GRM5NPC1RAB9AMAPTPOLB
SCHEMBL4367063 0.83 APP (0.52) NPC1RAB9AMAPTTSHRAPP
SCHEMBL1479638 0.80 GRM5 (0.56) GRM5NPC1RAB9AMAPTPOLB
SCHEMBL4848452 0.80 CES2 (0.56) NPC1RAB9AMAPTAPPAKR1C2
SCHEMBL5684797 0.80 AKR1C2 (0.49) GRM5NPC1RAB9AMAPTAPP
SCHEMBL2707734 0.79 APP (0.52) NPC1RAB9ATSHRAPPDHODH
Hydrochloric Acid SCHEMBL1476861 0.79 GRM5 (0.55) GRM5NPC1RAB9AMAPTPOLB
SCHEMBL4189999 0.78 APP (0.46) GRM5NPC1RAB9AMAPTAPP
SCHEMBL16103102 0.78 RARB (0.56) GRM5MAPTCYP3A4TSHRAPP
Hydrochloric Acid SCHEMBL2709682 0.78 AKR1C2 (0.50) NPC1RAB9ATSHRAPPDHODH

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7109249-B2 Composition containing a cross-linkable matrix precursor and a poragen, and porous matrix prepared therefrom DOW GLOBAL TECHNOLOGIES INC. (US) 2006-09-19 US disclosed
EP-1141128-B1 A COMPOSITION CONTAINING A CROSS-LINKABLE MATRIX PRECURSOR AND A PORAGEN, AND A POROUS MATRIX PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC (US) 2006-04-12 EP disclosed
US-6887910-B2 Composition containing a cross-linkable matrix precursor and a poragen, and a porous matrix prepared therefrom DOW GLOBAL TECHNOLOGIES INC. (US) 2005-05-03 US disclosed
US-20050014855-A1 Composition containing a cross-linkable matrix precursor and a poragen, and a porous matrix prepared therefrom BRUZA KENNETH J (US) 2005-01-20 US disclosed
US-6653358-B2 Electronics; integrated circuits; containing benzocyclobutene polymer DOW GLOBAL TECHNOLOGIES INC. 2003-11-25 US disclosed
US-6630520-B1 Matrix precursor comprises a material selected from cyclopentadienone and acetylene functional compounds, at least some of which have three or more reactive functional groups; partially polymerized reaction products and perfluoroethylenes DOW GLOBAL TECHNOLOGIES INC. 2003-10-07 US disclosed
US-20030092785-A1 Composition containing a cross-linkable matrix precursor and a poragen, and a porous matrix prepared therefrom BRUZA KENNETH J (US) 2003-05-15 US disclosed
US-20030083392-A1 Composition containing a cross-linkable matrix precursor and a poragen, and a porous matrix prepared therefrom BRUZA KENNETH J (US) 2003-05-01 US disclosed
EP-1141128-A1 A COMPOSITION CONTAINING A CROSS-LINKABLE MATRIX PRECURSOR AND A PORAGEN, AND A POROUS MATRIX PREPARED THEREFROM THE DOW CHEMICAL COMPANY (US) 2001-10-10 EP disclosed
WO-2000031183-A1 A COMPOSITION CONTAINING A CROSS-LINKABLE MATRIX PRECURSOR AND A PORAGEN, AND A POROUS MATRIX PREPARED THEREFROM THE DOW CHEMICAL COMPANY (US) 2000-06-02 WO disclosed