SCHEMBL63531

SCHEMBL63531

COC(=O)c1cnc(Cl)nc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 3/20 0.55
KDM4E B2RXH2 4/20 0.52
L3MBTL1 Q9Y468 2/20 0.52
ALDH1A1 P00352 5/20 0.46
ATM Q13315 1/20 0.46
TSHR P16473 1/20 0.45
CA1 P00915 3/20 0.43
CA2 P00918 3/20 0.43
CA12 O43570 2/20 0.43
CA7 P43166 2/20 0.43
CA9 Q16790 2/20 0.43
CA14 Q9ULX7 2/20 0.43
TDP1 Q9NUW8 2/20 0.43
MAPT P10636 3/20 0.42
KMT2A Q03164 2/20 0.42
MEN1 O00255 1/20 0.42
HPGD P15428 1/20 0.42
XBP1 P17861 1/20 0.42
HTT P42858 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42

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
SCHEMBL14850502 0.80 MAPK1 (0.57) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL4128911 0.80 MAPK1 (0.57) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL14782142 0.80 MAPK1 (0.57) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL14782154 0.79 MAPK1 (0.52) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL23031061 0.78 MAPK1 (0.55) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL27999559 0.78 MAPK1 (0.55) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL4038270 0.78 MAPK1 (0.55) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL27282195 0.78 MAPK1 (0.55) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL18547783 0.78 MAPK1 (0.55) MAPK1KDM4EL3MBTL1ALDH1A1ATM
SCHEMBL1656723 0.78 HDAC1 (0.55) MAPK1KDM4EL3MBTL1ALDH1A1ATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116768857-A EZH2/HDAC double-target inhibitor and preparation method and medical application thereof 中国药科大学 2023-09-19 CN claimed
CN-109232541-B Prolyl hydroxylase and histone deacetylase dual inhibitor and preparation method and application thereof 中国医学科学院放射医学研究所 2020-04-24 CN claimed
CN-109232541-A Prolyl hydroxylase and histon deacetylase (HDAC) double inhibitor and its preparation method and application 中国医学科学院放射医学研究所 2019-01-18 CN claimed
CN-122079878-A Nitrogen-containing heterocyclic derivative inhibitor, preparation method and application thereof 2026-05-26 CN disclosed
US-12637440-B2 Amide derivative useful as diacylglycerol acyltransferase 2 inhibitor, and use thereof LG CHEM, LTD. (KR) 2026-05-26 US disclosed
CN-122079879-A Nitrogen-containing heterocyclic derivative inhibitor, preparation method and application thereof 2026-05-26 CN disclosed
CN-122079880-A Nitrogen-containing heterocyclic derivative inhibitor, preparation method and application thereof 2026-05-26 CN disclosed
US-12630509-B2 Heterocyclic NMDA antagonists TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2026-05-19 US disclosed
CN-122036722-A Hydroxamic acid compound of gamma-tetrahydrocarboline, and preparation method and application thereof 浙江大学 2026-05-15 CN disclosed
US-20260132111-A1 Host-Targeted Pan-Respiratory Antiviral Small Molecule Therapeutics PROSETTA BIOSCIENCES INC (US) 2026-05-14 US disclosed
US-20260125367-A1 CANCER TREATMENTS TARGETING CANCER STEM CELLS REMEDY PLAN, INC. (US) 2026-05-07 US disclosed
WO-2008130320-A2 NOVEL N- (8-HETEROARYLTETRAHYDRONAPHTALENE-2YL) OR N- (5- HETEROARYLCHROMANE-3-YL) CARBOXAMIDE DERIVATIVES FOR THE TREATMENT OF PAIN ASTRAZENECA AB (SE) 2008-10-30 WO disclosed
EP-1981874-A1 AMINOPHENYL DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE Janssen Pharmaceutica, N.V. (BE) 2008-10-22 EP disclosed
WO-2008097428-A2 COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY IRM LLC (BM) 2008-08-14 WO disclosed
WO-2008082490-A2 NOVEL JNK INHIBITORS SCHERING CORPORATION (US) 2008-07-10 WO disclosed
WO-2008075068-A2 ACYLAMINOPYRAZOLES AS FGFR INHIBITORS ASTRAZENECA AB (SE) 2008-06-26 WO disclosed
US-20080153812-A1 Heterocyclic amides as anticancer agents ASTRAZENECA AB (SE) 2008-06-26 US disclosed
WO-2008046226-A1 AZACYCLOALKANE DERIVATIVES AS INHIBITORS OF STEAROYL-COENZYME A DELTA-9 DESATURASE MERCK FROSST CANADA LTD. (CA) 2008-04-24 WO disclosed
WO-2007082878-A1 AMINOPHENYL DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE JANSSEN PHARMACEUTICA N.V. (BE) 2007-07-26 WO disclosed
CN-1993353-A Substituted indolyl alkylamino derivatives as novel inhibitors of histone deacetylase JANSSEN PHARMACEUTICA NV (BE) 2007-07-04 CN 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 (5 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-12630509-B2 Heterocyclic NMDA antagonists GRIN1, GRIN3A, GRIN2B MAPK1 555/4885KDM4E 575/4885L3MBTL1 3347/4885
US-20260132111-A1 Host-Targeted Pan-Respiratory Antiviral Small Molecule Therapeutics NCOR1, HAVCR2, NR3C1 MAPK1 3571/4885KDM4E 4577/4885L3MBTL1 2268/4885
US-20080153812-A1 Heterocyclic amides as anticancer agents HDAC1, HDAC11, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16 MAPK1 105/4885KDM4E 1889/4885L3MBTL1 4499/4885
US-20260125367-A1 CANCER TREATMENTS TARGETING CANCER STEM CELLS MCL1, MALT1, BCL6 MAPK1 3373/4885KDM4E 2690/4885L3MBTL1 177/4885
US-12637440-B2 Amide derivative useful as diacylglycerol acyltransferase 2 inhibitor, and use thereof DGAT2, DGAT1, DLAT MAPK1 2480/4885KDM4E 3064/4885L3MBTL1 991/4885

“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.