SCHEMBL1636716

SCHEMBL1636716

CC1(C)OB(c2ccc3c(c2)CCNC3=O)OC1(C)C

nearest known ligand 0.54

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 11/20 0.54
PARP11 Q9NR21 10/20 0.54
PARP1 P09874 3/20 0.44
PDPK1 O15530 1/20 0.44
GRM5 P41594 7/20 0.44
KDM4E B2RXH2 1/20 0.42
F7 P08709 1/20 0.40
F3 P13726 1/20 0.40

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
SCHEMBL30720809 1.00 PARP10 (0.54) PARP10PARP11PARP1PDPK1GRM5
SCHEMBL29964464 0.92 PARP11 (0.44) PARP10PARP11PARP1PDPK1GRM5
SCHEMBL12077902 0.92 PARP11 (0.44) PARP10PARP11PARP1PDPK1GRM5
SCHEMBL29676875 0.89 PARP10 (0.54) PARP10PARP11PARP1PDPK1KDM4E
SCHEMBL2052209 0.89 PARP10 (0.54) PARP10PARP11PARP1PDPK1KDM4E
SCHEMBL12078239 0.86 PARP10 (0.38) PARP10PARP11PARP1PDPK1GRM5
SCHEMBL274197 0.86 ROCK1 (0.43) GRM5
SCHEMBL15570438 0.84 PARP10 (0.49) PARP10PARP11PARP1PDPK1KDM4E
SCHEMBL12077888 0.82 LPL (0.37) PARP10PARP11
SCHEMBL204451 0.80 LPL (0.46)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260092053-A1 KHK INHIBITORS GILEAD SCIENCES INC (US) 2026-04-02 US disclosed
EP-4681774-A2 KHK INHIBITORS Gilead Sciences, Inc. (US) 2026-01-21 EP disclosed
EP-4313967-B1 KHK INHIBITORS GILEAD SCIENCES INC (US) 2025-11-12 EP disclosed
US-12421228-B2 Naphthyridine derivatives as PRC2 inhibitors Mirati Therapeutics, Inc. (US) 2025-09-23 US disclosed
US-20250282787-A1 SUBSTITUTED IMIDAZO[1,2-c]PYRIMIDINES AS PRC2 INHIBITORS Mirati Therapeutics, Inc. 2025-09-11 US disclosed
US-12410160-B2 KHK inhibitors GILEAD SCIENCES, INC. (US) 2025-09-09 US disclosed
US-12371435-B2 Substituted imidazo[1,2-c]pyrimidines as PRC2 inhibitors Mirati Therapeutics, Inc. (US) 2025-07-29 US disclosed
US-20250179082-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER Mirati Therapeutics, Inc. 2025-06-05 US disclosed
US-12252493-B2 Imidazo[1,2-c]pyrimidine derivatives as PRC2 inhibitors for treating cancer Mirati Therapeutics, Inc. (US) 2025-03-18 US disclosed
WO-2025043191-A1 PRC2 INHIBITORS FOR USE IN TREATING SICKLE CELL DISEASE ORIC PHARMACEUTICALS, INC. (US) 2025-02-27 WO disclosed
WO-2007117607-A2 QUINAZOLINES FOR PDK1 INHIBITION NOVARTIS AG (CH) 2007-10-18 WO disclosed
US-7105509-B2 Benzodiazepine derivatives as APP modulators MERCK SHARP & DOHME LIMITED (GB) 2006-09-12 US disclosed
US-6995155-B2 Benzodiazepine derivatives as inhibitors of gamma secretase MERCK SHARP & DOHME LIMITED (GB) 2006-02-07 US disclosed
EP-1572693-A1 MITOGEN ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE-2 INHIBITING COMPOUNDS Pharmacia Corporation (US) 2005-09-14 EP disclosed
US-20040209897-A1 Mitogen activated protein kinase-activated protein kinase-2 inhibiting compounds PHARMACIA CORPORATION 2004-10-21 US disclosed
WO-2004058762-A1 MITOGEN ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE-2 INHIBITING COMPOUNDS PHARMACIA CORPORATION (US) 2004-07-15 WO disclosed
US-20040082572-A1 Benzodiazepine derivatives as app modulators MERCK SHARPE & DOHME LIMITED (GB) 2004-04-29 US disclosed
US-20040024203-A1 Benzodiazepine derivatives as inhibitors of gamma secretase MERCK SHARP & DOHME LTD. (GB) 2004-02-05 US disclosed
EP-1326849-A1 BENZODIAZEPINE DERIVATIVES AS INHIBITORS OF GAMMA SECRETASE Merck Sharp & Dohme Limited (GB) 2003-07-16 EP disclosed
WO-2002030912-A1 BENZODIAZEPINE DERIVATIVES AS INHIBITORS OF GAMMA SECRETASE MERCK SHARP & DOHME LIMITED (GB) 2002-04-18 WO 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 (10 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-20040082572-A1 Benzodiazepine derivatives as app modulators BACE1, PSEN1, APP PARP10 2420/4885PARP11 1487/4885PARP1 3023/4885
US-12371435-B2 Substituted imidazo[1,2-c]pyrimidines as PRC2 inhibitors EZH2, BMI1, SUZ12 PARP10 327/4885PARP11 158/4885PARP1 124/4885
US-20260092053-A1 KHK INHIBITORS KHK, SLC5A2, HK1 PARP10 4728/4885PARP11 4626/4885PARP1 4713/4885
US-12252493-B2 Imidazo[1,2-c]pyrimidine derivatives as PRC2 inhibitors for treating cancer BMI1, EZH2, SUZ12 PARP10 862/4885PARP11 429/4885PARP1 473/4885
US-20040024203-A1 Benzodiazepine derivatives as inhibitors of gamma secretase BACE1, BACE2, PSEN1 PARP10 2336/4885PARP11 1788/4885PARP1 2822/4885
US-20250282787-A1 SUBSTITUTED IMIDAZO[1,2-c]PYRIMIDINES AS PRC2 INHIBITORS EZH2, BMI1, SUZ12 PARP10 532/4885PARP11 253/4885PARP1 299/4885
US-20040209897-A1 Mitogen activated protein kinase-activated protein kinase-2 inhibiting compounds MAPKAPK2, MAP3K2, MKNK2 PARP10 1719/4885PARP11 2022/4885PARP1 2965/4885
US-12410160-B2 KHK inhibitors KHK, KHDRBS1, NADK PARP10 677/4885PARP11 1170/4885PARP1 1574/4885
US-20250179082-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER BMI1, EZH2, SUZ12 PARP10 862/4885PARP11 429/4885PARP1 473/4885
US-12421228-B2 Naphthyridine derivatives as PRC2 inhibitors BMI1, EZH2, SUZ12 PARP10 682/4885PARP11 285/4885PARP1 396/4885

“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.