SCHEMBL547698

SCHEMBL547698

O=Cc1ccccc1-c1ccccc1C(=O)O

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.53
KDM4E B2RXH2 2/20 0.53
POLB P06746 1/20 0.53
ALDH1A1 P00352 4/20 0.50
CYP2C9 P11712 2/20 0.50
ALOX15 P16050 1/20 0.50
ERN1 O75460 1/20 0.50
CYP3A4 P08684 1/20 0.50
ALOX12 P18054 1/20 0.50
FOLH1 Q04609 2/20 0.47
CYP1A2 P05177 1/20 0.47
GAA P10253 1/20 0.47
MYC P01106 1/20 0.47
KMT2A Q03164 2/20 0.46
MEN1 O00255 1/20 0.46
THRB P10828 1/20 0.46
BLM P54132 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
EIF4E P06730 1/20 0.45
L3MBTL1 Q9Y468 2/20 0.45

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
SCHEMBL29955778 1.00 LMNA (0.53) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL21003262 0.93 ERN1 (0.52) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL21003172 0.87 FOLH1 (0.55) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL27599322 0.85 ALDH1A1 (0.68) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL2557529 0.84 ALDH1A1 (0.56) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL547697 0.83 ALDH1A1 (0.51) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL29556927 0.83 ALDH1A1 (0.59) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL20448823 0.83 ALDH1A1 (0.59) LMNAKDM4EPOLBALDH1A1CYP2C9
Benzene SCHEMBL28103329 0.83 ALDH1A1 (0.59) LMNAKDM4EPOLBALDH1A1CYP2C9
SCHEMBL78873 0.83 ALDH1A1 (0.59) LMNAKDM4EPOLBALDH1A1CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11091419-B2 Preparation and purification of biphenyldicarboxylic acids EXXONMOBIL CHEMICAL PATENTS INC. (US) 2021-08-17 US claimed
US-20200361847-A1 Preparation and Purification of Biphenyldicarboxylic Acids EXXONMOBIL CHEMICAL PATENTS INC. 2020-11-19 US claimed
US-20200290945-A1 Preparation and Purification of Biphenyldicarboxylic Acids EXXONMOBIL CHEMICAL PATENTS INC (US) 2020-09-17 US claimed
EP-2080750-B1 RADIATION-SENSITIVE COMPOSITION MITSUBISHI GAS CHEMICAL CO (JP) 2020-07-29 EP claimed
WO-2019103759-A1 PREPARATION AND PURIFICATION OF BIPHENYLDICARBOXYLIC ACIDS EXXONMOBIL CHEMICAL PATENTS INC. (US) 2019-05-31 WO claimed
WO-2019103756-A1 PREPARATION AND PURIFICATION OF BIPHENYLDICARBOXYLIC ACIDS EXXONMOBIL CHEMICAL PATENTS INC. (US) 2019-05-31 WO claimed
US-20240368777-A1 ELECTROCHEMICAL REDUCTIVE COUPLING OF PHENOL DERIVATIVES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2024-11-07 US disclosed
WO-2023278766-A1 ELECTROCHEMICAL REDUCTIVE COUPLING OF PHENOL DERIVATIVES WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2023-01-05 WO disclosed
CN-113321628-A N-type organic dye based on benzothiazol and preparation method and application thereof 南京邮电大学 2021-08-31 CN disclosed
US-11091419-B2 Preparation and purification of biphenyldicarboxylic acids EXXONMOBIL CHEMICAL PATENTS INC. (US) 2021-08-17 US disclosed
US-11091419-B2 Preparation and purification of biphenyldicarboxylic acids EXXONMOBIL CHEMICAL PATENTS INC. (US) 2021-08-17 US disclosed
US-20200361847-A1 Preparation and Purification of Biphenyldicarboxylic Acids EXXONMOBIL CHEMICAL PATENTS INC. 2020-11-19 US disclosed
US-20200361847-A1 Preparation and Purification of Biphenyldicarboxylic Acids EXXONMOBIL CHEMICAL PATENTS INC. 2020-11-19 US disclosed
US-6528525-B1 Amidocarboxylic acid derivatives SANKYO COMPANY, LIMITED (JP) 2003-03-04 US disclosed
US-6455731-B2 REACTING AROMATIC ACID WITH AMINE; SALT FROMATION; DECOMPOSITION MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2002-09-24 US disclosed
US-6452047-B1 LOW COLOR, SIMPLE PURIFICATION OF SUCH AS 2,6-NAPHTHALENE-DICARBOXYLIC ACID OR 4,4'-BIPHENYLDICARBOXYLIC ACID; AMINE SALT FORMATION, PRECIPITATION, AND DECOMPOSITION OF SALT BY DISSOLUTION IN WATER MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2002-09-17 US disclosed
US-20020002305-A1 Process for producing a high purity aromatic polycarboxylic acid MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2002-01-03 US disclosed
EP-1157981-A2 Process for producing a high purity aromatic polycarboxylic acid MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2001-11-28 EP disclosed
EP-1055660-A1 Process for producing highly pure aromatic polycarboxylic acid MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2000-11-29 EP disclosed
EP-1026149-A1 AMIDOCARBOXYLIC ACID DERIVATIVES Sankyo Company Limited (JP) 2000-08-09 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 (3 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-20200290945-A1 Preparation and Purification of Biphenyldicarboxylic Acids DDC, MCCC2, ADH1C LMNA 2169/4885KDM4E 1904/4885POLB 1215/4885
US-20200361847-A1 Preparation and Purification of Biphenyldicarboxylic Acids HPD, HMBS, MCCC2 LMNA 3535/4885KDM4E 867/4885POLB 793/4885
US-11091419-B2 Preparation and purification of biphenyldicarboxylic acids HPD, HMBS, MCCC2 LMNA 3535/4885KDM4E 867/4885POLB 793/4885

“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.