SCHEMBL567396

SCHEMBL567396

CCCCCCCCOOC(=O)c1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.54
TSHR P16473 3/20 0.54
ALDH1A1 P00352 3/20 0.54
TDP1 Q9NUW8 1/20 0.53
F2 P00734 1/20 0.52
TP53 P04637 2/20 0.51
CYP3A4 P08684 1/20 0.51
MAPK1 P28482 1/20 0.51
CES2 O00748 2/20 0.50
CES1 P23141 2/20 0.50
NPC1 O15118 1/20 0.50
MAPT P10636 1/20 0.50
RAB9A P51151 1/20 0.50
NAAA Q02083 1/20 0.49
KDM4E B2RXH2 1/20 0.48
POLB P06746 1/20 0.48
HSD17B10 Q99714 1/20 0.48
PLA2G4B P0C869 1/20 0.47
CNR2 P34972 1/20 0.47

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
SCHEMBL27389912 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL11767588 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL28645326 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL6462426 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL825240 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL4284909 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL29105916 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL8756235 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
SCHEMBL6130417 1.00 LMNA (0.54) LMNATSHRALDH1A1TDP1F2
Bicarbonate SCHEMBL28738435 0.98 LMNA (0.53) LMNATSHRALDH1A1TDP1F2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105037193-A Preparation method of otilonium bromide ZHEJIANG SANMEN HYGECON PHARMACEUTICAL CO LTD 2015-11-11 CN claimed
CN-1274783-C Hexahydrogen bonded self-assembled supermolecular yellow-green luminescent material and its synthesizing method UNIV SICHUAN (CN) 2006-09-13 CN claimed
US-6951904-B1 Process for increasing the melt strength of polypropylene POLYMERS AUSTRALIA PTY LIMITED (AU) 2005-10-04 US claimed
CN-1640983-A Hexahydrogen bonded self-assembled supermolecular yellow-green luminescent material and its synthesizing method UNIV SICHUAN (CN) 2005-07-20 CN claimed
EP-1080148-A4 PROCESS FOR INCREASING THE MELT STRENGTH OF POLYPROPYLENE POLYMERS AUSTRALIA PTY LTD (AU) 2003-02-05 EP claimed
EP-1080148-A1 PROCESS FOR INCREASING THE MELT STRENGTH OF POLYPROPYLENE Polymers Australia PTY Limited (AU) 2001-03-07 EP claimed
WO-1999036466-A1 PROCESS FOR INCREASING THE MELT STRENGTH OF POLYPROPYLENE POLYMERS AUSTRALIA PTY LIMITED (AU) 1999-07-22 WO claimed
EP-3753920-B1 METHODS FOR PRODUCING THIOL COMPOUNDS AND SULFIDE COMPOUNDS USING A PHENOL COMPOUND CHEVRON PHILLIPS CHEMICAL CO LP (US) 2025-08-06 EP disclosed
EP-3992180-B1 METHODS FOR PRODUCING THIOL COMPOUNDS AND SULFIDE COMPOUNDS USING A MONO-ALKYL PHENOL COMPOUND CHEVRON PHILLIPS CHEMICAL CO LP (US) 2024-11-27 EP disclosed
CN-112703180-B Amphiphilic mesogenic organic dyes for customized reflective low dimensional materials 索邦大学 2024-01-23 CN disclosed
EP-3510018-B2 METHODS FOR PRODUCING THIOL COMPOUNDS AND SULFIDE COMPOUNDS USING DIPHENYLAMINE OR A PHENOL COMPOUND CHEVRON PHILLIPS CHEMICAL CO LP (US) 2023-11-01 EP disclosed
EP-3712198-B1 METHODS OF MAKING MERCAPTANIZED VINYLNORBORNENE COMPOSITIONS CHEVRON PHILLIPS CHEMICAL CO LP (US) 2023-05-10 EP disclosed
EP-3992180-A1 METHODS FOR PRODUCING THIOL COMPOUNDS AND SULFIDE COMPOUNDS USING A MONO-ALKYL PHENOL COMPOUND Chevron Phillips Chemical Company LP (US) 2022-05-04 EP disclosed
EP-1080148-A1 PROCESS FOR INCREASING THE MELT STRENGTH OF POLYPROPYLENE Polymers Australia PTY Limited (AU) 2001-03-07 EP disclosed
WO-1999036466-A1 PROCESS FOR INCREASING THE MELT STRENGTH OF POLYPROPYLENE POLYMERS AUSTRALIA PTY LIMITED (AU) 1999-07-22 WO disclosed
CN-1166823-A Liquid crystal compounds having perfluoroether terminal portions MINNESOTA MINING & MFG (US) 1997-12-03 CN disclosed
CN-1131673-A Chiral compounds BASF AG (DE) 1996-09-25 CN disclosed
EP-0342666-A2 Novel biphenyl compounds, method of producing the same as well as liquid crystal compositions and light switching elements each containing the same JAPAN ENERGY CORPORATION (JP) 1989-11-23 EP disclosed
CN-1035107-A FLUORINATED OLIGOPHENYL DERIVATIVES MERCK PATENT GMBH (DE) 1989-08-30 CN disclosed
US-4110243-A LIQUID CRYSTAL ADDITIVES THOMSON-CSF (FR) 1978-08-29 US disclosed