SCHEMBL6313128

SCHEMBL6313128

COc1cc(Nc2ncc(-c3ccc4c(c3)N(C(C)=O)CC4(C)C)c(N)n2)cc(OC)c1OC

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 2/20 0.43
AURKA O14965 1/20 0.43
AURKB Q96GD4 1/20 0.43
PDGFRB P09619 2/20 0.40
PTK2 Q05397 9/20 0.40
ZAP70 P43403 6/20 0.39
PRKD3 O94806 3/20 0.39
PRKCG P05129 3/20 0.39
PRKCB P05771 3/20 0.39
LCK P06239 3/20 0.39
PRKCA P17252 3/20 0.39
PRKCH P24723 3/20 0.39
PRKCI P41743 3/20 0.39
PRKCE Q02156 3/20 0.39
PRKCQ Q04759 3/20 0.39
PRKCZ Q05513 3/20 0.39
PRKCD Q05655 3/20 0.39
PRKD1 Q15139 3/20 0.39
EGFR P00533 2/20 0.39
IGF1R P08069 1/20 0.39

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
SCHEMBL6315327 0.78 IGF1R (0.64) KDRAURKAAURKBPTK2ZAP70
SCHEMBL6314234 0.76 KDR (0.57) KDRAURKAAURKBPTK2ZAP70
SCHEMBL27997729 0.72 FYN (0.59) KDRAURKAAURKBPTK2ZAP70
SCHEMBL6317955 0.72 IGF1R (0.57) KDRAURKAAURKBPTK2ZAP70
SCHEMBL6311694 0.70 KDR (0.52) KDRAURKAAURKBPTK2ZAP70
SCHEMBL6312589 0.70 IGF1R (0.59) KDRAURKAAURKBPTK2ZAP70
SCHEMBL6318895 0.69 IGF1R (0.59) KDRAURKAAURKBPTK2ZAP70
SCHEMBL6419728 0.68 KDR (0.49) KDRAURKAAURKBPTK2EGFR
SCHEMBL2205447 0.68 IGF1R (0.63) KDRAURKAAURKBPDGFRBPTK2
SCHEMBL6312279 0.68 EGFR (0.39) EGFRSYK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6979749-B2 Catalytic process for the production of 3,3′, 4,4′-tetraminobiphenyl COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2005-12-27 US claimed
US-20050215823-A1 NOVEL CATALYTIC PROCESS FOR THE PRODUCTION OF 3,3', 4,4'-TETRAMINOBIPHENYL COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2005-09-29 US claimed
US-6979749-B2 Catalytic process for the production of 3,3′, 4,4′-tetraminobiphenyl COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2005-12-27 US disclosed
US-6939874-B2 Substituted pyrimidinyl derivatives and methods of use AMGEN INC. (US) 2005-09-06 US disclosed
US-20040063705-A1 Substituted pyrimidinyl derivatives and methods of use AMGEN INC. 2004-04-01 US disclosed
EP-0369420-B1 PROCESS FOR PREPARING 4,4'-DINITRODIPHENYL AMINE HOECHST AKTIENGESELLSCHAFT (DE) 1993-03-17 EP disclosed
EP-0369420-A1 Process for preparing 4,4'-dinitrodiphenyl amine HOECHST AKTIENGESELLSCHAFT (DE) 1990-05-23 EP disclosed
EP-0330591-A1 Process for preparing aromatic carbamates RHONE-POULENC CHIMIE (FR) 1989-08-30 EP disclosed
EP-0125169-B1 LIQUID COMPOSITION CONTAINING DIISOCYANATES WITH A DIPHENYL METHANE STRUCTURE, AND PROCESS FOR ITS PREPARATION ELF ATOCHEM S.A. (FR) 1987-10-07 EP disclosed
EP-0149388-B1 ISOCYANATE COMPOSITION HAVING A LOW MELTING POINT WITH A DIPHENYL ETHANE STRUCTURE, PROCESS FOR THE PREPARATION THEREOF; USE FOR THE FABRICATION OF POLYURETHANES ELF ATOCHEM S.A. (FR) 1987-08-12 EP disclosed
EP-0078729-B1 PROCESS FOR PREPARING AROMATIC ISOCYANATES BY CARBONYLATION OF NITRO COMPOUNDS IN THE PRESENCE OF SUPPORTED CATALYSTS PREPARED FROM HETEROPOLYMETALLIC COMPLEXES RHONE-POULENC CHIMIE DE BASE (FR) 1986-01-08 EP disclosed
EP-0045710-B1 PROCESS FOR THE SELECTIVE PREPARATION OF META-CHLORINATED ANILINES RHONE-POULENC AGROCHIMIE (FR) 1984-07-04 EP disclosed
EP-0078729-A1 Process for preparing aromatic isocyanates by carbonylation of nitro compounds in the presence of supported catalysts prepared from heteropolymetallic complexes RHONE-POULENC CHIMIE DE BASE (FR) 1983-05-11 EP disclosed
EP-0022387-B1 PROCESS FOR THE PREPARATION OF BENZENE DERIVATIVES BY THE REACTION OF AN ACTIVATED HALOBENZENE WITH AN ORGANIC COMPOUND CONTAINING AN OXYGEN OR SULPHUR ANION RHONE-POULENC SPECIALITES CHIMIQUES (FR) 1983-01-05 EP disclosed
EP-0015220-B1 PROCESS FOR THE PREPARATION OF META-CHLORO ANILINES RHONE-POULENC AGROCHIMIE (FR) 1982-05-12 EP disclosed
EP-0045709-A1 Process for the preparation of meta-chlorinated anilines RHONE-POULENC AGROCHIMIE (FR) 1982-02-10 EP disclosed
EP-0045710-A1 Process for the selective preparation of meta-chlorinated anilines RHONE-POULENC AGROCHIMIE (FR) 1982-02-10 EP disclosed
EP-0015219-B1 PROCESS FOR THE PREPARATION OF META-CHLORO ANILINES RHONE-POULENC AGROCHIMIE (FR) 1981-10-28 EP disclosed
EP-0015220-A1 Process for the preparation of meta-chloro anilines RHONE-POULENC AGROCHIMIE (FR) 1980-09-03 EP disclosed
EP-0015219-A1 Process for the preparation of meta-chloro anilines RHONE-POULENC AGROCHIMIE (FR) 1980-09-03 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 (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-20040063705-A1 Substituted pyrimidinyl derivatives and methods of use DPYD, TYMP, TPMT KDR 2148/4885AURKA 2306/4885AURKB 1715/4885
US-20050215823-A1 NOVEL CATALYTIC PROCESS FOR THE PRODUCTION OF 3,3', 4,4'-TETRAMINOBIPHENYL NNMT, CBR3, POR KDR 1203/4885AURKA 1034/4885AURKB 2487/4885

“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.