SCHEMBL982574

SCHEMBL982574

Cc1cccc(C)c1OC(=O)O

nearest known ligand 0.58

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 3/20 0.58
SMN1; SMN2 Q16637 2/20 0.58
ALDH1A1 P00352 4/20 0.55
KDM4E B2RXH2 2/20 0.55
HPGD P15428 2/20 0.55
HSD17B10 Q99714 2/20 0.55
KMT2A Q03164 4/20 0.46
MEN1 O00255 3/20 0.46
ATM Q13315 1/20 0.46
PTPN1 P18031 1/20 0.43
TSHR P16473 1/20 0.42
MYC P01106 1/20 0.39
NPC1 O15118 1/20 0.38
RAB9A P51151 1/20 0.38

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
SCHEMBL16585706 0.87 PTPN1 (0.50) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL29112120 0.87 ALDH1A1 (0.49) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL982695 0.84 TSHR (0.50) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL8764787 0.83 L3MBTL1 (0.55) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL180120 0.82 SMN1; SMN2 (0.47) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL11218319 0.82 HPGD (0.57) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL31465688 0.82 L3MBTL1 (0.55) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL2059537 0.81 KDM4E (0.71) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
Acetic Acid SCHEMBL28743775 0.80 KDM4E (0.70) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD
SCHEMBL982769 0.80 PTPN1 (0.51) L3MBTL1SMN1; SMN2ALDH1A1KDM4EHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2695203-A2 OPTOELECTRONIC DEVICES AND COATINGS THEREFORE, AND METHODS FOR MAKING AND USING THE SAME SABIC Innovative Plastics IP B.V. (NL) 2014-02-12 EP claimed
WO-2012135584-A2 OPTOELECTRONIC DEVICES AND COATINGS THEREFORE, AND METHODS FOR MAKING AND USING THE SAME SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2012-10-04 WO claimed
WO-2021029158-A1 SULFONAMIDE COMPOUND, NONIONIC PHOTOACID GENERATOR, AND PHOTOLITHOGRAPHY RESIN COMPOSITION サンアプロ株式会社 2021-02-18 WO disclosed
EP-2275405-B1 PROCESS FOR PRODUCING ISOCYANATE USING DIARYL CARBONATE ASAHI CHEMICAL IND (JP) 2019-04-24 EP disclosed
US-20180371163-A1 METHOD FOR PRODUCING OLIGOMERS FOR PRODUCING POLYCARBONATES SHELL OIL COMPANY 2018-12-27 US disclosed
EP-2275406-B1 PROCESS FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2018-11-28 EP disclosed
EP-3394147-A1 METHOD FOR PRODUCING OLIGOMERS FOR PRODUCING POLYCARBONATES SHELL INTERNATIONAL RESEARCH MAATSCHAPPIJ B.V. (NL) 2018-10-31 EP disclosed
WO-2017112622-A1 METHOD FOR PRODUCING OLIGOMERS FOR PRODUCING POLYCARBONATES SHELL OIL COMPANY (US) 2017-06-29 WO disclosed
US-9233918-B2 Isocyanate production process ASAHI KASEI CHEMICALS CORPORATION (JP) 2016-01-12 US disclosed
US-8895774-B2 Process for producing isocyanates using diaryl carbonate ASAHI KASEI CHEMICALS CORPORATION (JP) 2014-11-25 US disclosed
CN-101607908-B Process for preparing diaryl carbonates from dialkyl carbonates BAYER MATERIALSCIENCE AG 2014-07-23 CN disclosed
US-20110054211-A1 PROCESS FOR PRODUCING ISOCYANATES USING DIARYL CARBONATE ASAHI KASEI CHEMICALS CORPORATION (JP) 2011-03-03 US disclosed
EP-2275406-A1 PROCESS FOR PRODUCING ISOCYANATE Asahi Kasei Chemicals Corporation (JP) 2011-01-19 EP disclosed
EP-2275405-A1 PROCESS FOR PRODUCING ISOCYANATE USING DIARYL CARBONATE Asahi Kasei Chemicals Corporation (JP) 2011-01-19 EP disclosed
CN-101607908-A Process for preparing diaryl carbonates from dialkyl carbonates BAYER MATERIALSCIENCE AG (DE) 2009-12-23 CN disclosed
CN-101423473-A Method for producing diaryl carbonates and/or alkylaryl carbonates from dialkyl carbonates BAYER MATERIALSCIENCE AG (DE) 2009-05-06 CN disclosed
US-6197918-B1 INTERCHANGE REACTION OF DIALKYL CARBONATE AND AROMATIC ALCOHOL; CATALYSIS WITH TITANIUM HALIDE, ALKOXIDE, ARYLOXIDE, OR ACETOXIDE GENERAL ELECTRIC COMPANY 2001-03-06 US disclosed
EP-0591923-B1 Continuous production of aromatic carbonates DAICEL CHEM (JP) 1998-08-26 EP disclosed
US-5380908-A From alkylaryl carbonates produced from dialkyl carbonates and a phenol, distillation of alcohol DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1995-01-10 US disclosed
EP-0591923-A1 Continuous production of aromatic carbonates DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1994-04-13 EP 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-20110054211-A1 PROCESS FOR PRODUCING ISOCYANATES USING DIARYL CARBONATE PAH, AADAC, PHGDH L3MBTL1 4612/4885SMN1; SMN2 4627/4885ALDH1A1 3223/4885

“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.