SCHEMBL1322

SCHEMBL1322

O=[PH](Cc1ccccc1)Cc1ccccc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOB P27338 1/20 0.46
CALM1 P0DP23 1/20 0.45
ELANE P08246 2/20 0.44
F2 P00734 1/20 0.44
PLG P00747 1/20 0.44
CTSG P08311 1/20 0.44
CMA1 P23946 1/20 0.44
CTRC Q99895 1/20 0.44
EPHX2 P34913 1/20 0.42
CES2 O00748 1/20 0.42
CES1 P23141 1/20 0.42
AKR1B1 P15121 1/20 0.42
TSHR P16473 3/20 0.41
ALDH1A1 P00352 2/20 0.41
IDO1 P14902 1/20 0.41
TP53 P04637 1/20 0.41
LOXL2 Q9Y4K0 1/20 0.41
TRPA1 O75762 1/20 0.41
HPGD P15428 1/20 0.39
ALOX15 P16050 1/20 0.39

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
SCHEMBL7600151 0.85 TP53 (0.46) MAOBCALM1ELANEF2PLG
SCHEMBL11305880 0.81 TP53 (0.42) MAOBCALM1ELANEF2PLG
SCHEMBL777237 0.79 CES1 (0.39) MAOBCALM1ELANEF2PLG
SCHEMBL686789 0.78 CES2 (0.44) MAOBCALM1ELANEF2PLG
SCHEMBL9122325 0.78 TP53 (0.43) MAOBCALM1ELANEF2PLG
SCHEMBL7142036 0.78 F2 (0.46) MAOBCALM1ELANEF2PLG
SCHEMBL29227588 0.78 EPHX2 (0.44) MAOBCALM1ELANEF2PLG
SCHEMBL9120006 0.78 SMN1; SMN2 (0.43) MAOBEPHX2ALDH1A1TP53
SCHEMBL4915443 0.77 MEN1 (0.48) ALDH1A1IDO1HPGDALOX15
SCHEMBL28934022 0.76 MIF (0.35) MAOBCALM1ELANEF2PLG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118996447-A Phosphine-oxide substituted quinoxaline quinazolinone compound, preparation method and application thereof 南阳师范学院 2024-11-22 CN claimed
CN-117447519-A Method for constructing dibenzophosphine oxide by copper-catalyzed P-H bond functionalization 四川轻化工大学 2024-01-26 CN claimed
CN-114181250-A Alkenyl phosphine compound and preparation method thereof 中国石油化工股份有限公司 2022-03-15 CN claimed
EP-2481760-B1 INITIATOR SYSTEM FOR CATIONIC POLYMERIZATION AND POLYMERIZATION METHOD USING SAME CHINA PETROLEUM & CHEM CORP (CN) 2021-05-05 EP claimed
CN-112500441-A Preparation process of high-purity glycosyl phosphate 上海彩迩文生化科技有限公司 2021-03-16 CN claimed
US-9382334-B2 Optical film SK INNOVATION CO., LTD. (KR) 2016-07-05 US claimed
CN-103910758-B The preparation method of a kind of axial chirality dibenzyl phosphine oxide and axial chirality dibenzyl phosphine SUN YAT-SEN UNIVERSITY (CN) 2016-01-20 CN claimed
US-20150004333-A1 Optical Film SK INNOVATION CO., LTD. (KR) 2015-01-01 US claimed
EP-2800779-A1 OPTICAL FILM SK Innovation Co., Ltd. (KR) 2014-11-12 EP claimed
CN-103910758-A Preparation method of axially chiral biaryl phosphine oxide and axially chiral biaryl phosphine UNIV SUN YAT SEN 2014-07-09 CN claimed
WO-2013103251-A1 OPTICAL FILM SK INNOVATION CO.,LTD. (KR) 2013-07-11 WO claimed
CN-103073578-A Dibenzyl phosphinic acid synthetic method UNIV TSINGHUA 2013-05-01 CN claimed
EP-1514542-B1 Medicinal composition comprising Tacrine or Donepezil for improving brain function. TOYAMA CHEMICAL CO LTD (JP) 2012-02-22 EP claimed
US-6624322-B1 Reacting ketones, primary amines and phosphorous compound, then oxidizing the aminophosphonate formed using halogen-free acids in water and solvent mixtures having buffers ATOFINA (FR) 2003-09-23 US claimed
EP-0387747-B1 Process for the preparation of 1,3-substituted tetrahydro-1H-thieno[3,4-d]imidazol-2(3H)-on-4-ylidene-pentanoic ester LONZA AG (CH) 1995-05-17 EP claimed
EP-0270076-B1 IMIDAZOLE DERIVATIVES AND A PROCESS FOR THEIR PREPARATION LONZA AG (CH) 1991-10-09 EP claimed
EP-0362634-A2 Basic dihydropyridines, process for their preparation and their use as intermediates BAYER AG (DE) 1990-04-11 EP claimed
US-4650868-A 7-deazapurine derivatives useful as antitumor agents TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1987-03-17 US claimed
EP-0000745-B1 SALT OF AN OPTICALLY ACTIVE ISOMER OF PHENYLGLYCINE AND AN OPTICALLY ACTIVE ISOMER OF 2-AMINO BUTANOL AND PROCESS FOR ITS PREPARATION HOECHST AKTIENGESELLSCHAFT (DE) 1981-07-15 EP claimed
EP-0000745-A1 Salt of an optically active isomer of phenylglycine and an optically active isomer of 2-amino butanol and process for its preparation HOECHST AKTIENGESELLSCHAFT (DE) 1979-02-21 EP claimed