SCHEMBL2849585

SCHEMBL2849585

O=C(c1ccccc1)C(O)Cl

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES1 P23141 5/20 0.58
CES2 O00748 4/20 0.58
LMNA P02545 2/20 0.58
TDP1 Q9NUW8 3/20 0.54
L3MBTL1 Q9Y468 2/20 0.54
ATM Q13315 3/20 0.52
GAA P10253 2/20 0.52
HSP90AA1 P07900 2/20 0.52
NPC1 O15118 1/20 0.52
RAB9A P51151 1/20 0.52
ALKBH5 Q6P6C2 1/20 0.48
MDM2 Q00987 1/20 0.48
ALDH1A1 P00352 4/20 0.48
TSHR P16473 2/20 0.48
DAO P14920 1/20 0.48
NAPRT Q6XQN6 1/20 0.48
GPR55 Q9Y2T6 2/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
MAPK1 P28482 2/20 0.44

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
Phosphine SCHEMBL27941168 0.98 CES1 (0.56) CES1CES2LMNATDP1L3MBTL1
SCHEMBL2238176 0.82 TDP1 (0.56) CES1CES2LMNATDP1L3MBTL1
SCHEMBL24188 0.82 TDP1 (0.56) CES1CES2LMNATDP1L3MBTL1
SCHEMBL2358014 0.82 ATM (0.64) CES1CES2LMNATDP1L3MBTL1
SCHEMBL11287856 0.80 TDP1 (0.54) CES1CES2LMNATDP1L3MBTL1
Water SCHEMBL27597000 0.80 TDP1 (0.54) CES1CES2LMNATDP1L3MBTL1
Hydrochloric Acid SCHEMBL27977560 0.80 TDP1 (0.54) CES1CES2LMNATDP1L3MBTL1
SCHEMBL7384862 0.80 TDP1 (0.54) CES1CES2LMNATDP1L3MBTL1
SCHEMBL157066 0.79 CES1 (0.62) CES1CES2LMNATDP1L3MBTL1
SCHEMBL1549080 0.79 CES1 (0.62) CES1CES2LMNATDP1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102482649-B Stereospecific carbonyl reductases UNIV RUTGERS 2014-09-03 CN claimed
CN-101857887-B Method for preparing optically pure aryl alcohol with cell-free extracts of recombinant strains by catalytic asymmetric conversion UNIV JIANGNAN 2012-11-14 CN claimed
CN-102482649-A Stereospecific carbonyl reductases UNIV RUTGERS 2012-05-30 CN claimed
CN-101857887-A Method for preparing optically pure aryl alcohol with cell-free extracts of recombinant strains by catalytic asymmetric conversion UNIV JIANGNAN 2010-10-13 CN claimed
CN-109195599-A antifungal composition 株式会社种探索研究所 2019-01-11 CN disclosed
CN-108373444-A Fluorescence viologen derivative and its application and preparation method 上海大学 2018-08-07 CN disclosed
CN-105431427-B Novel PDE 4 inhibitor 明治制果药业株式会社 2017-12-08 CN disclosed
CN-105431427-A Novel PDE4 inhibitor MEIJI SEIKA PHARMA CO LTD 2016-03-23 CN disclosed
CN-105121395-A Method to improve 1,1,3-trichloropropene and/or 3,3,3-trichloropropene selectivity during the dehydrochlorination of 1,1,1,3-tetrachloropropane HONEYWELL INT INC 2015-12-02 CN disclosed
CN-101857887-B Method for preparing optically pure aryl alcohol with cell-free extracts of recombinant strains by catalytic asymmetric conversion UNIV JIANGNAN 2012-11-14 CN disclosed
CN-1688532-B Compositions based on substituted 1, 3-diphenylprop-2-en-1-one derivatives, preparation and use thereof GENFIT 2012-07-11 CN disclosed
CN-102482649-A Stereospecific carbonyl reductases UNIV RUTGERS 2012-05-30 CN disclosed
CN-1013443-B PROCESS FOR PREPARING IMIDAZOLE DERIVATIVES SHIONOGI & CO (JP) 1991-08-07 CN disclosed
EP-0409164-A2 Phenacylpyridiniothiocephalosporins SHIONOGI SEIYAKU KABUSHIKI KAISHA trading under the name of SHIONOGI & CO. LTD. (JP) 1991-01-23 EP disclosed
US-4980496-A Method for producing C1 to C5 alkyl nitrides HOECHST CELANESE CORPORATION, A CORP. OF DE 1990-12-25 US disclosed
EP-0383539-A1 Production of alpha-chloro-alpha-oximino-4-hydroxy-acetophenone HOECHST CELANESE CORPORATION (US) 1990-08-22 EP disclosed
US-4910338-A Production of α-chloro-α-oximino-4-hydroxyacetophenone HOECHST CELANESE CORPORATION (US) 1990-03-20 US disclosed
CN-87100191-A The hydroxy acid derivative of treatment diabetic complication 1987-09-09 CN disclosed
CN-85104009-A The method for preparing imdazole derivatives 1986-11-19 CN disclosed
EP-0066378-A1 Pharmaceutical spiro-hydantoin derivatives IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1982-12-08 EP disclosed