SCHEMBL6761980

SCHEMBL6761980

COC(=O)c1cccc2cc3cccc(C(=O)OC)c3cc12

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.54
KDM4E B2RXH2 7/20 0.54
HPGD P15428 4/20 0.54
NPSR1 Q6W5P4 1/20 0.54
LMNA P02545 1/20 0.50
TSHR P16473 1/20 0.50
GAA P10253 1/20 0.50
SLC6A2 P23975 1/20 0.50
SLC6A4 P31645 1/20 0.50
SLC6A3 Q01959 1/20 0.50
HSD17B10 Q99714 2/20 0.48
CFTR P13569 1/20 0.48
MAPT P10636 3/20 0.48
MEN1 O00255 2/20 0.48
KMT2A Q03164 2/20 0.48
MTNR1A P48039 1/20 0.47
POLB P06746 1/20 0.47
ATM Q13315 1/20 0.47
PDE4B Q07343 1/20 0.46
SCN9A Q15858 1/20 0.46

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
SCHEMBL29403597 1.00 ALDH1A1 (0.54) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL19733167 0.94 ALDH1A1 (0.56) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL9984575 0.93 PTPN1 (0.51) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL1164706 0.93 ALDH1A1 (0.61) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL25189907 0.91 ALDH1A1 (0.59) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL27398809 0.87 ALDH1A1 (0.50) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL18906153 0.87 LMNA (0.55) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL6953102 0.86 LMNA (0.58) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL27451761 0.86 KDM4E (0.54) ALDH1A1KDM4EHPGDNPSR1LMNA
SCHEMBL522791 0.82 MAPT (0.63) ALDH1A1KDM4EHPGDNPSR1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114737397-B Preparation method of anthracene structure-containing polyester fabric moisture-absorbing and sweat-releasing finishing agent 广东德美精细化工集团股份有限公司 2024-02-06 CN claimed
CN-114737397-A Preparation method of moisture-absorbing and sweat-releasing finishing agent for polyester fabric containing anthracene structure 广东德美精细化工集团股份有限公司 2022-07-12 CN claimed
EP-2331604-B1 POLYESTER MELT-PHASE COMPOSITIONS HAVING IMPROVED THERMO-OXIDATIVE STABILITY, AND METHODS OF MAKING AND USING THEM GRUPO PETROTEMEX SA DE CV (MX) 2017-12-27 EP claimed
EP-3712922-B1 METHOD, DEVICE AND CARRIER MEDIUM FOR PREPARING MEASUREMENT SAMPLE FOR MALDI MASS SPECTROMETRY, MEASUREMENT SAMPLE FOR MALDI MASS SPECTROMETRY, AND MALDI MASS SPECTROMETRY METHOD RICOH CO LTD (JP) 2025-09-24 EP disclosed
WO-2024247569-A1 COMPOUND, COMPOSITION, SURFACE TREATMENT AGENT, ARTICLE, AND METHOD FOR PRODUCING ARTICLE AGC株式会社 2024-12-05 WO disclosed
EP-3886141-B1 METHOD AND DEVICE FOR PREPARING MEASUREMENT SAMPLE FOR MALDI MASS SPECTROMETRY RICOH CO LTD (JP) 2024-09-18 EP disclosed
EP-3315579-B1 SURFACE TREATMENT AGENT INCLUDING PERFLUORO(POLY)ETHER GROUP-CONTAINING SILANE COMPOUND DAIKIN IND LTD (JP) 2024-05-01 EP disclosed
CN-114737397-B Preparation method of anthracene structure-containing polyester fabric moisture-absorbing and sweat-releasing finishing agent 广东德美精细化工集团股份有限公司 2024-02-06 CN disclosed
CN-114737397-B Preparation method of anthracene structure-containing polyester fabric moisture-absorbing and sweat-releasing finishing agent 广东德美精细化工集团股份有限公司 2024-02-06 CN disclosed
US-11532472-B2 Mass spectrometry RICOH COMPANY, LTD. (JP) 2022-12-20 US disclosed
US-11404261-B2 Method, device, and base for preparing measurement sample for MALDI mass spectrometry RICOH COMPANY, LTD. (JP) 2022-08-02 US disclosed
US-8986630-B2 Gas-generating material and micro pump SEKISUI CHEMICAL CO., LTD. (JP) 2015-03-24 US disclosed
CN-104211930-A Large-dimension aromatic ring structure-containing polyester for powder coating and preparation method of polyester HAIAN HIGH NEW TECHNOLOGY RES INST OF NANJING UNIVERSITY 2014-12-17 CN disclosed
US-20140206094-A1 MALDI MASS SPECTROMETRY METHOD THE NOGUCHI INSTITUTE (JP) 2014-07-24 US disclosed
EP-2752659-A1 MALDI MASS ANALYSIS METHOD The Noguchi Institute (JP) 2014-07-09 EP disclosed
US-20140161687-A1 GAS-GENERATING MATERIAL AND MICRO PUMP SEKISUI CHEMICAL CO., LTD. (JP) 2014-06-12 US disclosed
EP-2397504-A1 (METH)ACRYLATE COMPOUND CONTAINING AROMATIC GROUP Showa Denko K.K. (JP) 2011-12-21 EP disclosed
US-20110294948-A1 AROMATIC GROUP-CONTAINING (METH) ACRYLATE COMPOUND SHOWA DENKO K.K. (JP) 2011-12-01 US disclosed
US-6723870-B2 REACTING A METAL HYDRIDE WITH AN ANTHRAQUINONE, DEKETALIZATION; DYE INTERMEDIATES SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-04-20 US disclosed
US-20030069443-A1 Method for producing anthracenes SUMITOMO CHEMICAL COMPANY, LIMITED 2003-04-10 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 (2 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-20110294948-A1 AROMATIC GROUP-CONTAINING (METH) ACRYLATE COMPOUND ACR, MMAB, ATR ALDH1A1 144/4885KDM4E 279/4885HPGD 4258/4885
US-20030069443-A1 Method for producing anthracenes AKR7A2, ADH1A, CYP2E1 ALDH1A1 23/4885KDM4E 4274/4885HPGD 61/4885

“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.