SCHEMBL9525319

SCHEMBL9525319

CN1C(=O)c2cc(Cl)c(Cl)cc2C1=O

nearest known ligand 0.50

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.47
HPGD P15428 2/20 0.47
KDM4E B2RXH2 1/20 0.47
MEN1 O00255 2/20 0.44
MAPT P10636 2/20 0.44
KMT2A Q03164 2/20 0.44
HSD17B10 Q99714 2/20 0.44
L3MBTL1 Q9Y468 2/20 0.44
ALOX15 P16050 1/20 0.44
CASP3 P42574 1/20 0.43
APP P05067 3/20 0.42
MAPK1 P28482 2/20 0.42
CA9 Q16790 2/20 0.42
CES1 P23141 1/20 0.41
CA12 O43570 1/20 0.41
CA1 P00915 1/20 0.41
AHR P35869 1/20 0.41

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
SCHEMBL12744258 0.81 ALDH1A1 (0.50) ALDH1A1HPGDKDM4EMEN1MAPT
SCHEMBL19009043 0.80 ALDH1A1 (0.44) ALDH1A1HPGDKDM4EMEN1MAPT
SCHEMBL441605 0.78 CA12 (0.47) ALDH1A1KDM4EMAPTCASP3MAPK1
SCHEMBL9485161 0.78 ALDH1A1 (0.40) ALDH1A1HPGDKDM4EMEN1MAPT
SCHEMBL19009047 0.78 ALDH1A1 (0.43) ALDH1A1HPGDKDM4EMEN1MAPT
SCHEMBL1500415 0.77 ALDH1A1 (0.55) ALDH1A1HPGDKDM4EMEN1MAPT
SCHEMBL17303441 0.75 ALDH1A1 (0.38) ALDH1A1HPGDKDM4EMEN1MAPT
SCHEMBL8730344 0.75 ALDH1A1 (0.38) ALDH1A1HPGDKDM4EMEN1MAPT
SCHEMBL6318641 0.75 CASP3 (0.52) ALDH1A1MEN1KMT2ACASP3CES1
SCHEMBL17193079 0.74 APP (0.48) ALDH1A1HPGDKDM4EMEN1MAPT

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110263540-A1 SMALL-MOLECULE INHIBITORS OF PROTEIN SYNTHESIS INACTIVATING TOXINS MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH 2011-10-27 US disclosed
US-RE41614-E1 Synthetic analogs of ecteinascidin-743 PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2010-08-31 US disclosed
US-RE41614-E1 Synthetic analogs of ecteinascidin-743 PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2010-08-31 US disclosed
EP-0314766-B1 METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM GEN ELECTRIC (US) 1993-11-03 EP disclosed
US-4864015-A OXIDATION RESISTANT COMPOSITES GENERAL ELECTRIC COMPANY (US) 1989-09-05 US disclosed
EP-0314766-A1 METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM. GEN ELECTRIC (US) 1989-05-10 EP disclosed
US-4814466-A FORMING A BISIMIDE FROM AN ALKALI SULFIDE AND AN N-ORGANO-4,5-DIHALOPHTHALIMIDE; HYDROLYSIS AND DEHYDRATION GENERAL ELECTRIC COMPANY (US) 1989-03-21 US disclosed
WO-1988009353-A1 METHOD FOR MAKING THIANTHRENE DIANHYDRIDE AND POLYIMIDES OBTAINED THEREFROM GENERAL ELECTRIC COMPANY (US) 1988-12-01 WO disclosed
US-4681950-A PHOTOSENSITIZERS CIBA-GEIGY CORPORATION (US) 1987-07-21 US disclosed
US-4585876-A PHOTOSENSITIZERS CIBA-GEIGY CORPORATION (US) 1986-04-29 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 (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-20110263540-A1 SMALL-MOLECULE INHIBITORS OF PROTEIN SYNTHESIS INACTIVATING TOXINS MRPS27, MRPS22, MRPS23 ALDH1A1 4637/4885HPGD 3921/4885KDM4E 3689/4885

“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.