SCHEMBL4355959

SCHEMBL4355959

Cc1cc(C(=O)c2ccc(F)c(C)c2)ccc1F

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.53
HTT P42858 1/20 0.53
HSD17B1 P14061 3/20 0.53
HSD17B2 P37059 3/20 0.53
PIM1 P11309 1/20 0.49
LMNA P02545 3/20 0.47
NPC1 O15118 1/20 0.47
MITF O75030 1/20 0.47
POLB P06746 1/20 0.47
CES2 O00748 1/20 0.46
CES1 P23141 1/20 0.46
ALDH1A1 P00352 4/20 0.46
HSD17B14 Q9BPX1 2/20 0.46
MAPT P10636 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
HDAC1 Q13547 1/20 0.46
HDAC6 Q9UBN7 1/20 0.46
MAOA P21397 1/20 0.43
MAOB P27338 1/20 0.43
CYP1A2 P05177 1/20 0.42

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
SCHEMBL13991056 0.94 CES2 (0.57) SMN1; SMN2HTTHSD17B1HSD17B2PIM1
SCHEMBL11110423 0.92 SMN1; SMN2 (0.52) SMN1; SMN2HTTHSD17B1HSD17B2PIM1
SCHEMBL7815583 0.90 ATM (0.55) SMN1; SMN2HTTHSD17B1HSD17B2LMNA
SCHEMBL11114087 0.90 SRD5A2 (0.52) SMN1; SMN2HTTHSD17B1HSD17B2PIM1
SCHEMBL385343 0.84 LMNA (0.53) SMN1; SMN2HTTPIM1LMNAPOLB
SCHEMBL1924482 0.84 PIM1 (0.47) HSD17B1PIM1LMNANPC1CES2
SCHEMBL29602493 0.84 PIM1 (0.47) HSD17B1PIM1LMNANPC1CES2
SCHEMBL5981059 0.84 CES2 (0.47) SMN1; SMN2HTTHSD17B1HSD17B2PIM1
SCHEMBL25759474 0.84 HSD17B1 (0.42) SMN1; SMN2HTTHSD17B1HSD17B2PIM1
Hydrochloric Acid SCHEMBL1478519 0.83 LMNA (0.52) SMN1; SMN2HTTPIM1LMNAPOLB

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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107611322-A A kind of High-strength lithium battery diaphragm and its production technology 界首市天鸿新材料股份有限公司 2018-01-19 CN claimed
WO-2020032019-A1 POSITIVE OSMOSIS MEMBRANE AND APPLICATION FOR SAME 三井化学株式会社 2020-02-13 WO disclosed
WO-2019189547-A1 FORWARD OSMOSIS MEMBRANE AND USE THEREOF 三井化学株式会社 2019-10-03 WO disclosed
WO-2019189548-A1 METHOD FOR PRODUCING SOLUTION HAVING REDUCED SOLUTE CONCENTRATION 三井化学株式会社 2019-10-03 WO disclosed
CN-107611322-A A kind of High-strength lithium battery diaphragm and its production technology 界首市天鸿新材料股份有限公司 2018-01-19 CN disclosed
US-8288058-B2 Binder for fuel cell, composition for forming electrode, electrode, and fuel cell using the electrode MITSUI CHEMICALS, INC. (JP) 2012-10-16 US disclosed
EP-1788649-B1 BINDER FOR FUEL CELL, COMPOSITION FOR ELECTRODE FORMATION, ELECTRODE, AND FUEL CELL USING THE ELECTRODE MITSUI CHEMICALS INC (JP) 2012-09-26 EP disclosed
US-20100167165-A1 COPOLYMER, POLYMER ELECTROLYTE, AND USE THEREOF SUMITOMO CHEMICAL COMPANY , LIMITED (JP) 2010-07-01 US disclosed
US-7645856-B2 Ether nitrile co-polymers containing sulfonic acid groups for PEM application NATIONAL RESEARCH COUNCIL OF CANADA (CA) 2010-01-12 US disclosed
EP-1457511-B1 CROSSLINKABLE AROMATIC RESINS HAVING PROTONIC ACID GROUPS AND ION CONDUCTIVE POLYMER MEMBRANES BINDERS AND FUEL CELLS MADE BY USING THE SAME MITSUI CHEMICALS INC (JP) 2009-07-15 EP disclosed
US-20070148467-A1 THERMAL MANAGEMENT CIRCUIT MATERIALS, METHOD OF MANUFACTURE THEREOF, AND ARTICLES FORMED THEREFROM WORLD PROPERTIES, INC. (US) 2007-06-28 US disclosed
EP-1788649-A1 BINDER FOR FUEL CELL, COMPOSITION FOR ELECTRODE FORMATION, ELECTRODE, AND FUEL CELL USING THE ELECTRODE Mitsui Chemicals, Inc. (JP) 2007-05-23 EP disclosed
US-20040191602-A1 Crosslinkable aromatic resin having protonic acid group, and ion conductive polymer membrane, binder and fuel cell using the resin MITSUI CHEMICALS, INC. (JP) 2004-09-30 US disclosed
EP-1457511-A1 CROSSLINKABLE AROMATIC RESINS HAVING PROTONIC ACID GROUPS AND ION CONDUCTIVE POLYMER MEMBRANES BINDERS AND FUEL CELLS MADE BY USING THE SAME Mitsui Chemicals, Inc. (JP) 2004-09-15 EP disclosed
US-5110940-A Inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A reductase BRISTOL-MYERS COMPANY (US) 1992-05-05 US disclosed
US-5068346-A Anticholesterol agents BRISTOL-MYERS COMPANY (US) 1991-11-26 US disclosed
US-4939265-A Intermediates and process for the preparation of antihypercholesterolemic tetrazole compounds BRISTOL-MYERS COMPANY (US) 1990-07-03 US disclosed
US-4898949-A Intermediates for the preparation of antihypercholesterolemic tetrazole compounds BRISTOL-MYERS COMPANY (US) 1990-02-06 US disclosed
US-4897490-A DERIVATIVES OF BETA-HYDROXY,OMEGA-DIPHENYL,TETRAZOL-5-YL ALK-OMEGA-ENOIC ACID, ESTER OR LACTONE BRISTOL-MEYERS COMPANY (US) 1990-01-30 US disclosed
WO-1988006584-A1 ANTIHYPERCHOLESTEROLEMIC TETRAZOLE COMPOUNDS BRISTOL-MYERS COMPANY (US) 1988-09-07 WO disclosed