SCHEMBL1884483

SCHEMBL1884483

CCCCCNc1cc(C(=O)O)c(NCCCCC)cc1C(=O)O

nearest known ligand 0.63

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CISD1 Q9NZ45 8/20 0.63
KDM6B O15054 2/20 0.54
KDM4C Q9H3R0 2/20 0.54
HCAR3 P49019 3/20 0.51
PLK1 P53350 4/20 0.51
CA12 O43570 1/20 0.45
CA9 Q16790 1/20 0.45
KDM4E B2RXH2 1/20 0.45
ALDH1A1 P00352 1/20 0.45
MAPT P10636 1/20 0.45
HPGD P15428 1/20 0.45
AKR1C3 P42330 1/20 0.45
AKR1C2 P52895 1/20 0.45
AKR1C1 Q04828 1/20 0.45
HSD17B10 Q99714 1/20 0.45
L3MBTL1 Q9Y468 1/20 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
Valine SCHEMBL4412745 0.85 CISD1 (0.57) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL28110422 0.84 PLK1 (0.67) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL28109945 0.84 PLK1 (0.67) CISD1HCAR3PLK1
SCHEMBL2426202 0.83 CISD1 (0.52) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL17363127 0.83 CISD1 (0.56) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL22097725 0.82 HCAR3 (0.60) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL3781973 0.82 PLK1 (0.62) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL3396063 0.82 KDM4E (0.63) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL7356043 0.82 PLK1 (0.53) CISD1KDM6BKDM4CHCAR3PLK1
SCHEMBL3979546 0.82 CISD1 (0.51) CISD1KDM6BKDM4CHCAR3PLK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114751837-A Preparation method of intermediate 2, 5-diarylamine-terephthalic acid 唐继勇 2022-07-15 CN claimed
CN-103012223-B Method of recovering waste slag in quinacridone production course to prepare 2,2'-disulfonic acid ethyl benzidine UNIV EAST CHINA SCIENCE & TECH 2014-06-11 CN claimed
CN-103012223-A Method of recovering waste slag in quinacridone production course to prepare 2,2'-disulfonic acid ethyl benzidine UNIV EAST CHINA SCIENCE & TECH 2013-04-03 CN claimed
EP-0632106-B2 Process for the production of 2,5-di(arylamino)-3,6- dihydroterephthalic acid dialkyl ester, and process for the production of quinacridone from said ester as intermediate TOYO INK MFG CO (JP) 2009-02-25 EP claimed
EP-1739135-A2 Colorant compounds containing copolymerizable vinyl groups Eastman Chemical Company (US) 2007-01-03 EP claimed
US-7138539-B2 Colorant compounds containing copolymerizable vinyl groups EASTMAN CHEMICAL COMPANY (US) 2006-11-21 US claimed
EP-1307515-B1 COLORANT COMPOUNDS CONTAINING COPOLYMERIZABLE VINYL GROUPS EASTMAN CHEM CO (US) 2006-06-28 EP claimed
US-20060052469-A1 Colorant compounds containing copolymerizable vinyl groups CYR MICHAEL J 2006-03-09 US claimed
US-20040059014-A1 Colorant Compounds containing copolymerizable vinyl groups CYR MICHAEL JOHN (US) 2004-03-25 US claimed
US-20040059124-A1 Colorant compounds containing copolymerizable vinyl groups CYR MICHAEL JOHN (US) 2004-03-25 US claimed
US-20020132874-A1 Colorant compounds containing copolymerizable vinyl groups EASTMAN CHEMICAL COMPANY 2002-09-19 US claimed
WO-2002012402-A2 COLORANT COMPOUNDS CONTAINING COPOLYMERIZABLE VINYL GROUPS EASTMAN CHEMICAL COMPANY (US) 2002-02-14 WO claimed
US-6284890-B1 CYCLIZING A 2,5-DIARYLAMINO-6,13-DIHYDROTEREPHTHALIC ACID WITH POLYPHOSPHORIC ACID AND TREATING THE MELT WITH SULFURIC ACID; SMALL PARTICLE SIZE CIBA SPECIALTY CHEMICALS CORP. 2001-09-04 US claimed
EP-0632106-B1 Process for the production of 2,5-di(arylamino)-3,6- dihydroterephthalic acid dialkyl ester, and process for the production of quinacridone from said ester as intermediate TOYO INK MFG CO (JP) 2001-08-22 EP claimed
CN-1245516-A Method for preparing light-absorbing polymer composition EASTMAN CHEM CO (US) 2000-02-23 CN claimed
US-5817817-A Process for the production of 2,5-di(arylamino)-3,6-dihydroterephthalic acid dialkyl ester, and process for the production of quinacridone from said ester as intermediate TOYO INK MANUFACTURING CO., LTD. (JP) 1998-10-06 US claimed
EP-0632106-A1 Process for the production of 2,5-di(arylamino)-3,6- dihydroterephthalic acid dialkyl ester, and process for the production of quinacridone from said ester as intermediate TOYO INK MANUFACTURING CO., LTD. (JP) 1995-01-04 EP claimed
US-5347038-A Starting material for quinacridone pigments, pollution control, from succinic acid diester and aniline HOECHST AKTIENGESELLSCHAFT (DE) 1994-09-13 US claimed
US-4981997-A Process for the preparation of 2,5-diarylaminoterephthalic acids BAYER AKTIENGESELLSCHAFT (DE) 1991-01-01 US claimed
US-4064129-A Process for making quinacridone and its derivatives HARMON COLORS CORPORATION (US) 1977-12-20 US claimed

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-20060052469-A1 Colorant compounds containing copolymerizable vinyl groups ALOX5, ALAD, EED CISD1 2059/4885KDM6B 1016/4885KDM4C 457/4885
US-20040059124-A1 Colorant compounds containing copolymerizable vinyl groups ALOX5, ALAD, EED CISD1 2059/4885KDM6B 1016/4885KDM4C 457/4885

“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.