SCHEMBL2059634

SCHEMBL2059634

CCCCCOC(=O)c1ccccc1Cl

nearest known ligand 0.78

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 5/20 0.78
MAPK1 P28482 3/20 0.78
CYP3A4 P08684 2/20 0.78
TP53 P04637 1/20 0.78
ALDH1A1 P00352 7/20 0.76
LMNA P02545 3/20 0.76
L3MBTL1 Q9Y468 3/20 0.70
TDP1 Q9NUW8 3/20 0.70
KDM4E B2RXH2 3/20 0.66
HSD17B10 Q99714 2/20 0.66
POLB P06746 1/20 0.66
HPGD P15428 2/20 0.53
MAPT P10636 1/20 0.52
SMN1; SMN2 Q16637 1/20 0.52
KMT2A Q03164 1/20 0.49
CNR2 P34972 1/20 0.49
MMP1 P03956 1/20 0.49
MMP9 P14780 1/20 0.49
MMP12 P39900 1/20 0.49

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
SCHEMBL9342127 0.98 ALDH1A1 (0.79) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL9065267 0.98 ALDH1A1 (0.79) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL6057099 0.98 ALDH1A1 (0.79) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL27571824 0.98 ALDH1A1 (0.79) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL2059607 0.95 TSHR (0.77) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL7937585 0.93 ALDH1A1 (0.70) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL2059610 0.88 ALDH1A1 (0.76) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL29351843 0.88 TSHR (1.00) TSHRMAPK1CYP3A4TP53ALDH1A1
SCHEMBL57859 0.88 TSHR (1.00) TSHRMAPK1CYP3A4TP53ALDH1A1
1,2-Dichlorobenzene SCHEMBL10902521 0.88 ALDH1A1 (0.77) TSHRMAPK1CYP3A4TP53ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2383275-A1 METHOD FOR SYNTHESIZING O-DIPHENYLPHOSPHINO BENZOIC ACID Sinomax Chemical Technology Co., Ltd (CN) 2011-11-02 EP claimed
US-20110077426-A1 METHOD FOR SYNTHESIS OF O-DIPHENYLPHOSPHINOBENZOIC ACID SINOMAX CHEMICAL TECHNOLOGY CO. LTD. (CN) 2011-03-31 US claimed
EP-2383275-A1 METHOD FOR SYNTHESIZING O-DIPHENYLPHOSPHINO BENZOIC ACID Sinomax Chemical Technology Co., Ltd (CN) 2011-11-02 EP disclosed
CN-101018847-B Improvements in or relating to organic compositions RECKITT BENCKISER INC 2011-05-11 CN disclosed
US-20110077426-A1 METHOD FOR SYNTHESIS OF O-DIPHENYLPHOSPHINOBENZOIC ACID SINOMAX CHEMICAL TECHNOLOGY CO. LTD. (CN) 2011-03-31 US disclosed
CN-101481388-B Process for synthesizing O-diphenylphosphinolbenzoic acid SINOMAX BEIJING CHEMICAL TECHNOLOGY CO LTD 2011-02-23 CN disclosed
CN-101481388-A Process for synthesizing O-diphenylphosphinolbenzoic acid SINOMAX BEIJING SOLUTIONS TECH (CN) 2009-07-15 CN disclosed
CN-101018847-A Improvements in or relating to organic compositions RECKITT BENCKISER INC (US) 2007-08-15 CN disclosed
EP-1159315-B1 PROCESS FOR PRODUCING POLYETHYLENE EASTMAN CHEM CO (US) 2006-09-06 EP disclosed
EP-1192196-B1 PROCESS FOR PRODUCING ETHYLENE/OLEFIN INTERPOLYMERS EASTMAN CHEM CO (US) 2005-07-13 EP disclosed
EP-1183284-B1 PROCESS FOR PRODUCING ETHYLENE/OLEFIN INTERPOLYMERS EASTMAN CHEM CO (US) 2005-04-27 EP disclosed
WO-2001051526-A1 PROCATALYSTS COMPRISING BIDENTATE LIGANDS, CATALYST SYSTEMS, AND USE IN OLEFIN POLYMERIZATION EASTMAN CHEMICAL COMPANY (US) 2001-07-19 WO disclosed
WO-2001051527-A1 PROCATALYSTS, CATALYST SYSTEMS, AND USE IN OLEFIN POLYMERIZATION EASTMAN CHEMICAL COMPANY (US) 2001-07-19 WO disclosed
WO-2001051529-A1 PROCATALYSTS COMPRISING BIDENTATE LIGANDS, CATALYST SYSTEMS, AND USE IN OLEFIN POLYMERIZATION EASTMAN CHEMICAL COMPANY (US) 2001-07-19 WO disclosed
WO-2001051528-A1 PROCATALYSTS COMPRISING BIDENTATE LIGANDS, CATALYST SYSTEMS, AND USE IN OLEFIN POLYMERIZATION EASTMAN CHEMICAL COMPANY (US) 2001-07-19 WO disclosed
WO-2000075203-A1 PROCESS FOR PRODUCING ETHYLENE/OLEFIN INTERPOLYMERS EASTMAN CHEMICAL COMPANY (US) 2000-12-14 WO disclosed
WO-2000075202-A1 PROCESS FOR PRODUCING ETHYLENE/OLEFIN INTERPOLYMERS EASTMAN CHEMICAL COMPANY (US) 2000-12-14 WO disclosed
WO-2000075204-A1 PROCESS FOR PRODUCING ETHYLENE/OLEFIN INTERPOLYMERS EASTMAN CHEMICAL COMPANY (US) 2000-12-14 WO disclosed
WO-2000052068-A1 PROCESS FOR PRODUCING POLYETHYLENE EASTMAN CHEMICAL COMPANY (US) 2000-09-08 WO disclosed
US-4454340-A Preparation of aryl 1-hydroxyaryl-2-carboxylates EASTMAN KODAK COMPANY (US) 1984-06-12 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110077426-A1 METHOD FOR SYNTHESIS OF O-DIPHENYLPHOSPHINOBENZOIC ACID PLCB1, DCPS, POF1B TSHR 4780/4885MAPK1 1191/4885CYP3A4 2108/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.