SCHEMBL1427892

SCHEMBL1427892

COc1c(COC(=O)O)ccc(Cl)c1C

nearest known ligand 0.44

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.44
KDM4E B2RXH2 2/20 0.44
HSD17B10 Q99714 1/20 0.44
TSHR P16473 1/20 0.43
IMPDH2 P12268 3/20 0.40
MRGPRX4 Q96LA9 1/20 0.38
RXFP1 Q9HBX9 1/20 0.37
MEP1B Q16820 1/20 0.36
PKM P14618 1/20 0.36
KMT2A Q03164 1/20 0.36
TAS1R3 Q7RTX0 2/20 0.35
TAS1R1 Q7RTX1 2/20 0.35
TAS1R2 Q8TE23 2/20 0.35
TPMT P51580 1/20 0.34
GAA P10253 1/20 0.34
HDAC8 Q9BY41 1/20 0.33

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
SCHEMBL716643 0.74 TSHR (0.43) ALDH1A1KDM4EHSD17B10TSHRMRGPRX4
SCHEMBL31045837 0.72 MTNR1A (0.44) ALDH1A1KDM4EHSD17B10TSHRIMPDH2
SCHEMBL27621906 0.71 ALOX5 (0.38) ALDH1A1KDM4EHSD17B10TSHRIMPDH2
SCHEMBL28829137 0.71 GPR55 (0.45) ALDH1A1KDM4EKMT2AGAA
SCHEMBL13034124 0.70 TAAR1 (0.43) ALDH1A1KDM4ETSHRIMPDH2KMT2A
SCHEMBL11484541 0.69 ALDH1A1 (0.48) ALDH1A1KDM4EHSD17B10TSHRKMT2A
SCHEMBL28519470 0.68 KDM4A (0.47) ALDH1A1KDM4ETSHRKMT2A
SCHEMBL4374949 0.67 L3MBTL1 (0.59) ALDH1A1PKMKMT2A
SCHEMBL28659748 0.67 KMT2A (0.35) ALDH1A1KDM4EPKMKMT2AGAA
SCHEMBL20460826 0.66 ALDH1A1 (0.71) ALDH1A1KDM4EHSD17B10TSHRMEP1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1724110-B1 Multilayered articles and method of manufacture thereof SABIC GLOBAL TECHNOLOGIES BV (NL) 2019-08-21 EP disclosed
EP-2300414-B1 METHOD FOR PRODUCING PHENOLIC COMPOUND SABIC GLOBAL TECHNOLOGIES BV (NL) 2016-04-27 EP disclosed
EP-1414779-B1 SOLVENTLESS PREPARATION OF ESTER-SUBSTITUTED DIARYL CARBONATES SABIC INNOVATIVE PLASTICS IP (NL) 2015-05-27 EP disclosed
US-8900693-B2 Polycarbonate compositions having infrared absorbance, method of manufacture, and articles prepared therefrom SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2014-12-02 US disclosed
EP-1907465-B1 POLYCARBONATE COMPOSITIONS HAVING INFRARED ABSORBANCE, METHOD OF MANUFACTURE, AND ARTICLES PREPARED THEREFROM SABIC INNOVATIVE PLASTICS IP (NL) 2014-07-23 EP disclosed
EP-1776332-B1 METHOD OF PREPARING ESTER-SUBSTITUTED DIARYL CARBONATES SABIC INNOVATIVE PLASTICS IP (NL) 2013-07-03 EP disclosed
EP-1529632-B1 Multilayered articles and method of manufacture thereof SABIC INNOVATIVE PLASTICS IP (NL) 2012-09-05 EP disclosed
US-8034967-B2 Method of preparing a purified ester-substituted phenol stream Sabic Innnovative Plastics IP B.V. (NL) 2011-10-11 US disclosed
EP-2215045-B1 METHOD OF PREPARING A PURIFIED ESTER-SUBSTITUTED PHENOL STREAM SABIC INNOVATIVE PLASTICS IP (NL) 2011-08-03 EP disclosed
EP-2300414-A1 METHOD FOR PRODUCING PHENOLIC COMPOUND SABIC Innovative Plastics IP B.V. (NL) 2011-03-30 EP disclosed
US-20030149223-A1 Method of polycarbonate preparation GENERAL ELECTRIC COMPANY 2003-08-07 US disclosed
US-6548623-B2 Melt reaction of bisphenol A and bis-methyl salicyl carbonate using alkali or alkaline earth metal catalyst and quaternary ammonium or phosphonium compound; Fries suppression; by-product inhibition GENERAL ELECTRIC COMPANY 2003-04-15 US disclosed
US-20030060649-A1 Solventless preparation of ester-substituted diaryl carbonates GENERAL ELECTRIC COMPANY 2003-03-27 US disclosed
US-20030050427-A1 METHOD OF POLYCARBONATE PREPARATION GENERAL ELECTRIC COMPANY 2003-03-13 US disclosed
WO-2003010218-A1 METHOD OF POLYCARBONATE PREPARATION GENERAL ELECTRIC COMPANY (US) 2003-02-06 WO disclosed
WO-2003010123-A1 SOLVENTLESS PREPARATION OF ESTER-SUBSTITUTED DIARYL CARBONATES GENERAL ELECTRIC COMPANY (US) 2003-02-06 WO disclosed
WO-2003010122-A1 INTERFACIAL METHOD OF PREPARING ESTER-SUBSTITUTED DIARYL CARBONATES GENERAL ELECTRIC COMPANY (US) 2003-02-06 WO disclosed
US-6469192-B1 NO SOLVENT OTHER THAN WATER OR STARTING ESTER- SUBSTITUTED PHENOL IS PRESENT IN THE REACTION MIXTURE DURING THE REACTION OF ESTER-SUBSTITUTED PHENOL WITH PHOSGENE GENERAL ELECTRIC COMPANY 2002-10-22 US disclosed
US-6420512-B1 SCREW EXTRUSION AND ESTER INTERCHANGE GENERAL ELECTRIC COMPANY 2002-07-16 US disclosed
US-6420588-B1 REACTION OF PHENOL WITH PHOSGENE AND PHASE TRANSFER AGENT GENERAL ELECTRIC COMPANY 2002-07-16 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-20030060649-A1 Solventless preparation of ester-substituted diaryl carbonates CDS2, ASH2L, PGGT1B ALDH1A1 4720/4885KDM4E 339/4885HSD17B10 1755/4885

“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.